Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23041 |
| ensemblid | ENSG00000061987.16 |
| hgncid | 29177 |
| symbol | MON2 |
| name | MON2 homolog, regulator of endosome-to-Golgi trafficking |
| refseq_nuc | NM_015026.3 |
| refseq_prot | NP_055841.2 |
| ensembl_nuc | ENST00000393630.8 |
| ensembl_prot | ENSP00000377250.4 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 62466826 |
| end | 62600476 |
| strand | + |
| ver | v1.2 |
| region | chr12:62466826-62600476 |
| region5000 | chr12:62461826-62605476 |
| regionname0 | MON2_chr12_62466826_62600476 |
| regionname5000 | MON2_chr12_62461826_62605476 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1717 | 201 | 59 | 44 | 72 | 5 | 19 | 57 | MON2_chr12_62461826_62605476 | MON2 | MSGTS others(1712): Show |
chr12 | 62461826 | 62605476 |
| a0002 | 0/0 | 1717 | 118 | 28 | 13 | 57 | 6 | 14 | 45 | MON2_chr12_62461826_62605476 | MON2 | MSGTS others(1712): Show |
chr12 | 62461826 | 62605476 |
| a0003 | 0/0 | 1717 | 33 | 2 | 8 | 18 | 3 | 2 | 16 | MON2_chr12_62461826_62605476 | MON2 | MSGTS others(1712): Show |
chr12 | 62461826 | 62605476 |
| a0004 | 0/0 | 1717 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | MON2_chr12_62461826_62605476 | MON2 | MSGTS others(1712): Show |
chr12 | 62461826 | 62605476 |
| a0005 | 0/0 | 1717 | 4 | 1 | 0 | 3 | 0 | 0 | 3 | MON2_chr12_62461826_62605476 | MON2 | MSGTS others(1712): Show |
chr12 | 62461826 | 62605476 |
| a0006 | 0/0 | 1717 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | MSGTS others(1712): Show |
chr12 | 62461826 | 62605476 |
| a0007 | 0/0 | 1717 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | MSGTS others(1712): Show |
chr12 | 62461826 | 62605476 |
| a0008 | 0/0 | 1717 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | MSGTS others(1712): Show |
chr12 | 62461826 | 62605476 |
| a0009 | 0/0 | 1717 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | MSGTS others(1712): Show |
chr12 | 62461826 | 62605476 |
| a0010 | 0/0 | 1717 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | MSGTS others(1712): Show |
chr12 | 62461826 | 62605476 |
| a0011 | 0/0 | 1717 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | MSGTS others(1712): Show |
chr12 | 62461826 | 62605476 |
| a0012 | 0/0 | 1717 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | MSGTS others(1712): Show |
chr12 | 62461826 | 62605476 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 1/0 | 5151 | 78 | 19 | 19 | 28 | 3 | 8 | MON2_chr12_62461826_62605476 | MON2 | ATGTC others(5146): Show |
chr12 | 62461826 | 62605476 | ||
| a0001c0003 | 0/1 | 5151 | 69 | 11 | 9 | 41 | 1 | 6 | MON2_chr12_62461826_62605476 | MON2 | ATGTC others(5146): Show |
chr12 | 62461826 | 62605476 | ||
| a0001c0005 | 0/0 | 5151 | 24 | 2 | 13 | 3 | 1 | 5 | MON2_chr12_62461826_62605476 | MON2 | ATGTC others(5146): Show |
chr12 | 62461826 | 62605476 | ||
| a0001c0006 | 0/0 | 5151 | 24 | 23 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | ATGTC others(5146): Show |
chr12 | 62461826 | 62605476 | ||
| a0001c0009 | 0/0 | 5151 | 2 | 2 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | ATGTC others(5146): Show |
chr12 | 62461826 | 62605476 | ||
| a0001c0016 | 0/0 | 5151 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | ATGTC others(5146): Show |
chr12 | 62461826 | 62605476 | ||
| a0001c0017 | 0/0 | 5151 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | ATGTC others(5146): Show |
chr12 | 62461826 | 62605476 | ||
| a0001c0018 | 0/0 | 5151 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | ATGTC others(5146): Show |
chr12 | 62461826 | 62605476 | ||
| a0001c0020 | 0/0 | 5151 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | ATGTC others(5146): Show |
chr12 | 62461826 | 62605476 | ||
| a0002c0001 | 0/0 | 5151 | 117 | 28 | 13 | 57 | 6 | 13 | MON2_chr12_62461826_62605476 | MON2 | ATGTC others(5146): Show |
chr12 | 62461826 | 62605476 | ||
| a0002c0015 | 0/0 | 5151 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | ATGTC others(5146): Show |
chr12 | 62461826 | 62605476 | ||
| a0003c0004 | 0/0 | 5151 | 33 | 2 | 8 | 18 | 3 | 2 | MON2_chr12_62461826_62605476 | MON2 | ATGTC others(5146): Show |
chr12 | 62461826 | 62605476 | ||
| a0004c0007 | 0/0 | 5151 | 4 | 0 | 0 | 4 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | ATGTC others(5146): Show |
chr12 | 62461826 | 62605476 | ||
| a0005c0008 | 0/0 | 5151 | 4 | 1 | 0 | 3 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | ATGTC others(5146): Show |
chr12 | 62461826 | 62605476 | ||
| a0006c0010 | 0/0 | 5151 | 2 | 0 | 0 | 0 | 2 | 0 | MON2_chr12_62461826_62605476 | MON2 | ATGTC others(5146): Show |
chr12 | 62461826 | 62605476 | ||
| a0007c0014 | 0/0 | 5151 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | ATGTC others(5146): Show |
chr12 | 62461826 | 62605476 | ||
| a0008c0019 | 0/0 | 5151 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | ATGTC others(5146): Show |
chr12 | 62461826 | 62605476 | ||
| a0009c0013 | 0/0 | 5151 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | ATGTC others(5146): Show |
chr12 | 62461826 | 62605476 | ||
| a0010c0011 | 0/0 | 5151 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | ATGTC others(5146): Show |
chr12 | 62461826 | 62605476 | ||
| a0011c0021 | 0/0 | 5151 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | ATGTC others(5146): Show |
chr12 | 62461826 | 62605476 | ||
| a0012c0012 | 0/0 | 5151 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | ATGTC others(5146): Show |
chr12 | 62461826 | 62605476 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0002 | 0/0 | 13263 | 40 | 3 | 11 | 20 | 1 | 5 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0001c0002t0003 | 0/0 | 13263 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0001c0002t0005 | 0/0 | 13263 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0001c0002t0010 | 0/0 | 13263 | 5 | 5 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0001c0002t0011 | 1/0 | 13263 | 5 | 0 | 0 | 3 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0001c0002t0013 | 0/0 | 13263 | 4 | 1 | 3 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0001c0002t0014 | 0/0 | 13263 | 4 | 1 | 1 | 0 | 2 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0001c0002t0015 | 0/0 | 13264 | 4 | 0 | 0 | 3 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13259): Show |
chr12 | 62461826 | 62605476 |
| a0001c0002t0017 | 0/0 | 13263 | 3 | 2 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0001c0002t0020 | 0/0 | 13263 | 2 | 0 | 2 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0001c0002t0022 | 0/0 | 13263 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0001c0002t0026 | 0/0 | 13263 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0001c0002t0031 | 0/0 | 13263 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0001c0002t0035 | 0/0 | 13263 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0001c0002t0037 | 0/0 | 13263 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0001c0002t0039 | 0/0 | 13263 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0001c0002t0045 | 0/0 | 13263 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0001c0002t0047 | 0/0 | 13263 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0001c0002t0048 | 0/0 | 13263 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0001c0003t0002 | 0/0 | 13263 | 15 | 0 | 3 | 12 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0001c0003t0003 | 0/0 | 13263 | 8 | 3 | 1 | 4 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0001c0003t0005 | 0/1 | 13263 | 28 | 8 | 2 | 11 | 1 | 5 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0001c0003t0008 | 0/0 | 13263 | 11 | 0 | 0 | 11 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0001c0003t0021 | 0/0 | 13263 | 2 | 0 | 2 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0001c0003t0023 | 0/0 | 13264 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13259): Show |
chr12 | 62461826 | 62605476 |
| a0001c0003t0036 | 0/0 | 13263 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0001c0003t0041 | 0/0 | 13263 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0001c0003t0049 | 0/0 | 13264 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13259): Show |
chr12 | 62461826 | 62605476 |
| a0001c0003t0050 | 0/0 | 13263 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0001c0005t0003 | 0/0 | 13263 | 19 | 2 | 10 | 3 | 0 | 4 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0001c0005t0016 | 0/0 | 13263 | 3 | 0 | 3 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0001c0005t0040 | 0/0 | 13263 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0001c0005t0043 | 0/0 | 13263 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0001c0006t0003 | 0/0 | 13263 | 9 | 9 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0001c0006t0007 | 0/0 | 13262 | 12 | 11 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13257): Show |
chr12 | 62461826 | 62605476 |
| a0001c0006t0033 | 0/0 | 13262 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13257): Show |
chr12 | 62461826 | 62605476 |
| a0001c0006t0034 | 0/0 | 13262 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13257): Show |
chr12 | 62461826 | 62605476 |
| a0001c0006t0042 | 0/0 | 13263 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0001c0009t0019 | 0/0 | 13263 | 2 | 2 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0001c0016t0032 | 0/0 | 13262 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13257): Show |
chr12 | 62461826 | 62605476 |
| a0001c0017t0002 | 0/0 | 13263 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0001c0018t0002 | 0/0 | 13263 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0001c0020t0038 | 0/0 | 13263 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0002c0001t0001 | 0/0 | 13262 | 82 | 25 | 9 | 39 | 4 | 5 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13257): Show |
chr12 | 62461826 | 62605476 |
| a0002c0001t0006 | 0/0 | 13262 | 20 | 0 | 2 | 16 | 0 | 2 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13257): Show |
chr12 | 62461826 | 62605476 |
| a0002c0001t0009 | 0/0 | 13262 | 4 | 0 | 1 | 0 | 0 | 3 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13257): Show |
chr12 | 62461826 | 62605476 |
| a0002c0001t0012 | 0/0 | 13263 | 4 | 2 | 0 | 1 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0002c0001t0018 | 0/0 | 13262 | 2 | 0 | 1 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13257): Show |
chr12 | 62461826 | 62605476 |
| a0002c0001t0025 | 0/0 | 13263 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0002c0001t0027 | 0/0 | 13262 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13257): Show |
chr12 | 62461826 | 62605476 |
| a0002c0001t0028 | 0/0 | 13262 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13257): Show |
chr12 | 62461826 | 62605476 |
| a0002c0001t0029 | 0/0 | 13262 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13257): Show |
chr12 | 62461826 | 62605476 |
| a0002c0001t0030 | 0/0 | 13262 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13257): Show |
chr12 | 62461826 | 62605476 |
| a0002c0015t0024 | 0/0 | 13262 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13257): Show |
chr12 | 62461826 | 62605476 |
| a0003c0004t0004 | 0/0 | 13263 | 31 | 1 | 8 | 17 | 3 | 2 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0003c0004t0022 | 0/0 | 13263 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0003c0004t0044 | 0/0 | 13263 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0004c0007t0002 | 0/0 | 13263 | 3 | 0 | 0 | 3 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0004c0007t0046 | 0/0 | 13263 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0005c0008t0002 | 0/0 | 13263 | 3 | 1 | 0 | 2 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0005c0008t0023 | 0/0 | 13264 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13259): Show |
chr12 | 62461826 | 62605476 |
| a0006c0010t0002 | 0/0 | 13263 | 2 | 0 | 0 | 0 | 2 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0007c0014t0009 | 0/0 | 13262 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13257): Show |
chr12 | 62461826 | 62605476 |
| a0008c0019t0003 | 0/0 | 13263 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0009c0013t0006 | 0/0 | 13262 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13257): Show |
chr12 | 62461826 | 62605476 |
| a0010c0011t0005 | 0/0 | 13263 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13258): Show |
chr12 | 62461826 | 62605476 |
| a0011c0021t0001 | 0/0 | 13262 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13257): Show |
chr12 | 62461826 | 62605476 |
| a0012c0012t0001 | 0/0 | 13262 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | GACTC others(13257): Show |
chr12 | 62461826 | 62605476 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0002g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0005g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0010g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0010g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0010g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0010g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0010g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0011g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0011g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0011g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0011g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0011g0307 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0013g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0013g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0013g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0013g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0014g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0014g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0014g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0014g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0015g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0015g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0015g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0015g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0017g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0017g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0017g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0020g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0020g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0022g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0026g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0031g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0035g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0037g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0039g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0045g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0047g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0002t0048g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0044 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0005g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0008g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0008g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0008g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0008g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0008g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0008g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0008g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0008g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0008g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0008g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0008g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0021g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0023g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0036g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0041g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0049g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0003t0050g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0003g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0016g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0016g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0016g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0040g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0005t0043g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0003g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0003g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0007g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0007g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0007g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0007g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0007g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0007g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0007g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0007g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0007g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0007g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0007g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0007g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0033g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0034g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0006t0042g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0009t0019g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0009t0019g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0016t0032g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0017t0002g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0018t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0001c0020t0038g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0006g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0006g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0006g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0006g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0006g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0006g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0006g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0006g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0006g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0006g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0006g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0006g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0006g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0006g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0006g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0006g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0006g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0006g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0006g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0006g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0009g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0009g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0009g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0009g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0012g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0012g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0012g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0012g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0018g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0018g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0025g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0027g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0028g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0029g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0001t0030g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0002c0015t0024g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0004g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0022g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0003c0004t0044g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0004c0007t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0004c0007t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0004c0007t0002g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0004c0007t0046g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0005c0008t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0005c0008t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0005c0008t0002g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0005c0008t0023g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0006c0010t0002g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0006c0010t0002g0350 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0007c0014t0009g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0008c0019t0003g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0009c0013t0006g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0010c0011t0005g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0011c0021t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| a0012c0012t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0001 | t0001 | g0155 | EUR | GBR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00099 | hp2 | a0001 | c0002 | t0014 | g0288 | EUR | GBR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00140 | hp1 | a0001 | c0003 | t0005 | g0065 | EUR | GBR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00140 | hp2 | a0002 | c0001 | t0018 | g0177 | EUR | GBR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00280 | hp1 | a0003 | c0004 | t0004 | g0270 | EUR | FIN | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00280 | hp2 | a0002 | c0001 | t0001 | g0157 | EUR | FIN | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00323 | hp1 | a0002 | c0001 | t0001 | g0180 | EUR | FIN | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00323 | hp2 | a0003 | c0004 | t0004 | g0262 | EUR | FIN | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00423 | hp1 | a0002 | c0001 | t0001 | g0212 | EAS | CHS | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00423 | hp2 | a0001 | c0002 | t0002 | g0323 | EAS | CHS | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00438 | hp1 | a0001 | c0002 | t0048 | g0320 | EAS | CHS | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00438 | hp2 | a0002 | c0001 | t0006 | g0232 | EAS | CHS | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00544 | hp1 | a0001 | c0003 | t0002 | g0088 | EAS | CHS | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00544 | hp2 | a0002 | c0001 | t0001 | g0249 | EAS | CHS | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00597 | hp1 | a0002 | c0001 | t0001 | g0248 | EAS | CHS | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00597 | hp2 | a0001 | c0003 | t0005 | g0101 | EAS | CHS | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00621 | hp1 | a0001 | c0003 | t0005 | g0087 | EAS | CHS | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0256 | EAS | CHS | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00639 | hp1 | a0003 | c0004 | t0004 | g0365 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00639 | hp2 | a0001 | c0003 | t0005 | g0080 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00642 | hp1 | a0007 | c0014 | t0009 | g0237 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00642 | hp2 | a0001 | c0002 | t0002 | g0346 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00673 | hp1 | a0002 | c0001 | t0001 | g0169 | EAS | CHS | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00673 | hp2 | a0003 | c0004 | t0004 | g0260 | EAS | CHS | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00733 | hp1 | a0002 | c0001 | t0009 | g0197 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00733 | hp2 | a0003 | c0004 | t0004 | g0268 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00735 | hp1 | a0001 | c0017 | t0002 | g0344 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00735 | hp2 | a0001 | c0005 | t0016 | g0115 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00738 | hp1 | a0002 | c0001 | t0001 | g0168 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00738 | hp2 | a0001 | c0005 | t0003 | g0122 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00741 | hp1 | a0002 | c0001 | t0001 | g0225 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG00741 | hp2 | a0001 | c0003 | t0005 | g0098 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01069 | hp1 | a0001 | c0003 | t0021 | g0001 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01069 | hp2 | a0003 | c0004 | t0004 | g0272 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01070 | hp1 | a0001 | c0002 | t0020 | g0287 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01070 | hp2 | a0003 | c0004 | t0004 | g0269 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01071 | hp1 | a0001 | c0003 | t0021 | g0001 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01071 | hp2 | a0001 | c0002 | t0020 | g0292 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01074 | hp1 | a0001 | c0002 | t0013 | g0306 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01074 | hp2 | a0003 | c0004 | t0004 | g0285 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01081 | hp1 | a0001 | c0005 | t0003 | g0123 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01081 | hp2 | a0002 | c0001 | t0001 | g0146 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01099 | hp1 | a0001 | c0006 | t0007 | g0015 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01099 | hp2 | a0001 | c0002 | t0002 | g0303 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01106 | hp1 | a0001 | c0005 | t0016 | g0114 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01106 | hp2 | a0002 | c0001 | t0001 | g0182 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01109 | hp1 | a0001 | c0005 | t0003 | g0130 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01109 | hp2 | a0001 | c0002 | t0017 | g0033 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01167 | hp1 | a0003 | c0004 | t0004 | g0258 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01167 | hp2 | a0001 | c0020 | t0038 | g0305 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01168 | hp1 | a0002 | c0001 | t0001 | g0161 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01168 | hp2 | a0001 | c0005 | t0003 | g0109 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01169 | hp1 | a0001 | c0005 | t0003 | g0110 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01169 | hp2 | a0003 | c0004 | t0004 | g0259 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01192 | hp1 | a0001 | c0005 | t0003 | g0125 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01192 | hp2 | a0001 | c0003 | t0002 | g0084 | AMR | PUR | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01255 | hp1 | a0001 | c0005 | t0003 | g0120 | AMR | CLM | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0363 | AMR | CLM | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01256 | hp1 | a0001 | c0002 | t0013 | g0312 | AMR | CLM | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01256 | hp2 | a0001 | c0005 | t0003 | g0129 | AMR | CLM | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01257 | hp1 | a0002 | c0001 | t0001 | g0174 | AMR | CLM | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0345 | AMR | CLM | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01258 | hp1 | a0001 | c0005 | t0003 | g0128 | AMR | CLM | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0349 | AMR | CLM | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01261 | hp1 | a0001 | c0005 | t0016 | g0116 | AMR | CLM | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01261 | hp2 | a0002 | c0001 | t0006 | g0201 | AMR | CLM | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01346 | hp1 | a0001 | c0005 | t0003 | g0124 | AMR | CLM | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01346 | hp2 | a0002 | c0001 | t0018 | g0247 | AMR | CLM | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01361 | hp1 | a0001 | c0002 | t0002 | g0348 | AMR | CLM | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01361 | hp2 | a0001 | c0003 | t0003 | g0035 | AMR | CLM | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01496 | hp1 | a0001 | c0003 | t0002 | g0072 | AMR | CLM | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0343 | AMR | CLM | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01516 | hp1 | a0002 | c0001 | t0028 | g0184 | EUR | IBS | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01516 | hp2 | a0006 | c0010 | t0002 | g0350 | EUR | IBS | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01517 | hp1 | a0006 | c0010 | t0002 | g0336 | EUR | IBS | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01517 | hp2 | a0002 | c0001 | t0001 | g0227 | EUR | IBS | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01884 | hp1 | a0003 | c0004 | t0022 | g0295 | AFR | ACB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01884 | hp2 | a0002 | c0001 | t0001 | g0213 | AFR | ACB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01891 | hp1 | a0002 | c0001 | t0001 | g0246 | AFR | ACB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01891 | hp2 | a0001 | c0006 | t0007 | g0011 | AFR | ACB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01928 | hp1 | a0002 | c0001 | t0006 | g0192 | AMR | PEL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01928 | hp2 | a0001 | c0002 | t0002 | g0347 | AMR | PEL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01934 | hp1 | a0002 | c0001 | t0001 | g0241 | AMR | PEL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01934 | hp2 | a0001 | c0002 | t0002 | g0358 | AMR | PEL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01975 | hp1 | a0002 | c0001 | t0001 | g0240 | AMR | PEL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG01975 | hp2 | a0001 | c0003 | t0002 | g0057 | AMR | PEL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02004 | hp1 | a0001 | c0002 | t0013 | g0308 | AMR | PEL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02004 | hp2 | a0002 | c0001 | t0001 | g0242 | AMR | PEL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02015 | hp1 | a0002 | c0001 | t0006 | g0188 | EAS | KHV | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02015 | hp2 | a0001 | c0002 | t0002 | g0317 | EAS | KHV | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02027 | hp1 | a0001 | c0002 | t0002 | g0318 | EAS | KHV | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02027 | hp2 | a0002 | c0001 | t0001 | g0163 | EAS | KHV | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02055 | hp1 | a0002 | c0001 | t0001 | g0142 | AFR | ACB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02055 | hp2 | a0001 | c0006 | t0003 | g0106 | AFR | ACB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02071 | hp1 | a0002 | c0001 | t0006 | g0204 | EAS | KHV | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0356 | EAS | KHV | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02074 | hp1 | a0001 | c0003 | t0005 | g0097 | EAS | KHV | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02074 | hp2 | a0002 | c0001 | t0006 | g0222 | EAS | KHV | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02083 | hp1 | a0002 | c0001 | t0006 | g0191 | EAS | KHV | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02083 | hp2 | a0001 | c0003 | t0005 | g0086 | EAS | KHV | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02135 | hp1 | a0002 | c0001 | t0001 | g0179 | EAS | KHV | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0352 | EAS | KHV | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02145 | hp1 | a0002 | c0001 | t0012 | g0141 | AFR | ACB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02145 | hp2 | a0001 | c0002 | t0010 | g0031 | AFR | ACB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02148 | hp1 | a0001 | c0002 | t0005 | g0362 | AMR | PEL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02148 | hp2 | a0001 | c0003 | t0049 | g0096 | AMR | PEL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02165 | hp1 | a0001 | c0003 | t0050 | g0078 | EAS | CDX | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02165 | hp2 | a0004 | c0007 | t0002 | g0327 | EAS | CDX | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02257 | hp1 | a0001 | c0003 | t0003 | g0036 | AFR | ACB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02257 | hp2 | a0001 | c0006 | t0003 | g0102 | AFR | ACB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02258 | hp1 | a0003 | c0004 | t0004 | g0286 | AFR | ACB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02258 | hp2 | a0001 | c0003 | t0005 | g0039 | AFR | ACB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02280 | hp1 | a0001 | c0002 | t0047 | g0301 | AFR | ACB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02280 | hp2 | a0001 | c0002 | t0035 | g0025 | AFR | ACB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02293 | hp1 | a0001 | c0002 | t0002 | g0354 | AMR | PEL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02293 | hp2 | a0003 | c0004 | t0004 | g0296 | AMR | PEL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02300 | hp1 | a0001 | c0002 | t0014 | g0290 | AMR | PEL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02300 | hp2 | a0001 | c0002 | t0002 | g0357 | AMR | PEL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02523 | hp1 | a0003 | c0004 | t0004 | g0264 | EAS | KHV | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02523 | hp2 | a0001 | c0003 | t0036 | g0049 | EAS | KHV | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02572 | hp1 | a0001 | c0006 | t0007 | g0010 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02572 | hp2 | a0001 | c0018 | t0002 | g0299 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02602 | hp1 | a0002 | c0001 | t0001 | g0137 | SAS | PJL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02602 | hp2 | a0008 | c0019 | t0003 | g0113 | SAS | PJL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02615 | hp1 | a0002 | c0001 | t0001 | g0208 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02615 | hp2 | a0001 | c0003 | t0003 | g0100 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02622 | hp1 | a0002 | c0001 | t0001 | g0229 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02622 | hp2 | a0001 | c0005 | t0003 | g0117 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02630 | hp1 | a0002 | c0001 | t0001 | g0139 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02630 | hp2 | a0001 | c0002 | t0010 | g0027 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02647 | hp1 | a0001 | c0006 | t0007 | g0019 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02647 | hp2 | a0002 | c0001 | t0012 | g0251 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02717 | hp1 | a0001 | c0002 | t0039 | g0311 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02717 | hp2 | a0001 | c0006 | t0007 | g0021 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02723 | hp1 | a0001 | c0002 | t0022 | g0294 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02723 | hp2 | a0001 | c0003 | t0003 | g0099 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02735 | hp1 | a0001 | c0005 | t0003 | g0127 | SAS | PJL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02735 | hp2 | a0001 | c0002 | t0011 | g0255 | SAS | PJL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02809 | hp1 | a0001 | c0006 | t0007 | g0016 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02809 | hp2 | a0001 | c0009 | t0019 | g0108 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02886 | hp1 | a0002 | c0001 | t0001 | g0217 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02886 | hp2 | a0001 | c0003 | t0005 | g0047 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02895 | hp1 | a0002 | c0001 | t0001 | g0205 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02895 | hp2 | a0001 | c0002 | t0002 | g0026 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02896 | hp1 | a0002 | c0001 | t0001 | g0003 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02896 | hp2 | a0001 | c0006 | t0007 | g0009 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02897 | hp1 | a0002 | c0001 | t0001 | g0003 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02897 | hp2 | a0001 | c0002 | t0002 | g0030 | AFR | GWD | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02922 | hp1 | a0002 | c0001 | t0001 | g0224 | AFR | ESN | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02922 | hp2 | a0001 | c0006 | t0007 | g0018 | AFR | ESN | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02970 | hp1 | a0001 | c0002 | t0017 | g0032 | AFR | ESN | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02970 | hp2 | a0002 | c0001 | t0001 | g0223 | AFR | ESN | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02976 | hp1 | a0001 | c0006 | t0003 | g0006 | AFR | ESN | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02976 | hp2 | a0001 | c0006 | t0007 | g0014 | AFR | ESN | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03017 | hp1 | a0001 | c0005 | t0003 | g0121 | SAS | PJL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03017 | hp2 | a0001 | c0003 | t0041 | g0054 | SAS | PJL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03098 | hp1 | a0001 | c0009 | t0019 | g0107 | AFR | MSL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03098 | hp2 | a0002 | c0001 | t0030 | g0140 | AFR | MSL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03130 | hp1 | a0001 | c0002 | t0017 | g0024 | AFR | ESN | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03130 | hp2 | a0001 | c0006 | t0003 | g0105 | AFR | ESN | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03139 | hp1 | a0002 | c0001 | t0001 | g0138 | AFR | ESN | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03139 | hp2 | a0001 | c0006 | t0034 | g0020 | AFR | ESN | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03195 | hp1 | a0001 | c0006 | t0042 | g0004 | AFR | ESN | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03195 | hp2 | a0001 | c0006 | t0003 | g0104 | AFR | ESN | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03209 | hp1 | a0001 | c0006 | t0003 | g0005 | AFR | MSL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03209 | hp2 | a0002 | c0001 | t0001 | g0148 | AFR | MSL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03225 | hp1 | a0001 | c0002 | t0031 | g0136 | AFR | MSL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03225 | hp2 | a0001 | c0016 | t0032 | g0252 | AFR | MSL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03239 | hp1 | a0003 | c0004 | t0004 | g0273 | SAS | PJL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03239 | hp2 | a0002 | c0001 | t0009 | g0196 | SAS | PJL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03453 | hp1 | a0001 | c0006 | t0033 | g0022 | AFR | MSL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03453 | hp2 | a0002 | c0001 | t0001 | g0206 | AFR | MSL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03486 | hp1 | a0001 | c0002 | t0026 | g0310 | AFR | MSL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03486 | hp2 | a0002 | c0001 | t0001 | g0215 | AFR | MSL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03490 | hp1 | a0001 | c0002 | t0037 | g0313 | SAS | PJL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03490 | hp2 | a0002 | c0001 | t0006 | g0194 | SAS | PJL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03491 | hp1 | a0001 | c0002 | t0002 | g0325 | SAS | PJL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03491 | hp2 | a0002 | c0001 | t0001 | g0214 | SAS | PJL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03516 | hp1 | a0001 | c0002 | t0003 | g0135 | AFR | ESN | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03516 | hp2 | a0001 | c0002 | t0010 | g0028 | AFR | ESN | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03579 | hp1 | a0001 | c0006 | t0007 | g0017 | AFR | MSL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03579 | hp2 | a0002 | c0001 | t0001 | g0218 | AFR | MSL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03654 | hp1 | a0001 | c0003 | t0005 | g0067 | SAS | PJL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03654 | hp2 | a0002 | c0001 | t0029 | g0151 | SAS | PJL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03669 | hp1 | a0001 | c0005 | t0003 | g0118 | SAS | PJL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03669 | hp2 | a0002 | c0001 | t0001 | g0235 | SAS | PJL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03688 | hp1 | a0001 | c0003 | t0005 | g0081 | SAS | STU | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03688 | hp2 | a0002 | c0001 | t0001 | g0167 | SAS | STU | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03704 | hp1 | a0001 | c0003 | t0005 | g0058 | SAS | PJL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03704 | hp2 | a0001 | c0002 | t0002 | g0330 | SAS | PJL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03834 | hp1 | a0002 | c0015 | t0024 | g0187 | SAS | BEB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03834 | hp2 | a0001 | c0003 | t0005 | g0074 | SAS | BEB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03927 | hp1 | a0002 | c0001 | t0012 | g0211 | SAS | BEB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03927 | hp2 | a0001 | c0002 | t0015 | g0319 | SAS | BEB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03942 | hp1 | a0002 | c0001 | t0009 | g0228 | SAS | BEB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03942 | hp2 | a0001 | c0002 | t0002 | g0254 | SAS | BEB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG04115 | hp1 | a0002 | c0001 | t0006 | g0203 | SAS | STU | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0342 | SAS | STU | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0335 | SAS | BEB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG04184 | hp2 | a0001 | c0005 | t0040 | g0134 | SAS | BEB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG04199 | hp1 | a0001 | c0003 | t0005 | g0089 | SAS | STU | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG04199 | hp2 | a0002 | c0001 | t0009 | g0195 | SAS | STU | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG04228 | hp1 | a0002 | c0001 | t0025 | g0189 | SAS | STU | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG04228 | hp2 | a0003 | c0004 | t0004 | g0293 | SAS | STU | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18522 | hp1 | a0002 | c0001 | t0001 | g0219 | AFR | YRI | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18522 | hp2 | a0001 | c0006 | t0007 | g0012 | AFR | YRI | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18612 | hp1 | a0001 | c0002 | t0045 | g0360 | EAS | CHB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18612 | hp2 | a0002 | c0001 | t0001 | g0152 | EAS | CHB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18906 | hp1 | a0001 | c0006 | t0003 | g0007 | AFR | YRI | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18906 | hp2 | a0001 | c0002 | t0010 | g0029 | AFR | YRI | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18939 | hp1 | a0001 | c0002 | t0011 | g0300 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18939 | hp2 | a0002 | c0001 | t0001 | g0162 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18940 | hp1 | a0001 | c0002 | t0002 | g0359 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18940 | hp2 | a0002 | c0001 | t0001 | g0149 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18941 | hp1 | a0001 | c0003 | t0005 | g0052 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18941 | hp2 | a0002 | c0001 | t0006 | g0233 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18942 | hp1 | a0002 | c0001 | t0001 | g0143 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18942 | hp2 | a0001 | c0003 | t0002 | g0055 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18943 | hp1 | a0002 | c0001 | t0027 | g0165 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18943 | hp2 | a0004 | c0007 | t0046 | g0326 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0338 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18944 | hp2 | a0003 | c0004 | t0004 | g0278 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18945 | hp1 | a0001 | c0003 | t0008 | g0060 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18945 | hp2 | a0001 | c0002 | t0002 | g0322 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18946 | hp1 | a0002 | c0001 | t0001 | g0183 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18946 | hp2 | a0001 | c0003 | t0005 | g0092 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18949 | hp1 | a0004 | c0007 | t0002 | g0361 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18949 | hp2 | a0009 | c0013 | t0006 | g0199 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18951 | hp1 | a0001 | c0002 | t0002 | g0333 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18951 | hp2 | a0002 | c0001 | t0001 | g0159 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18954 | hp1 | a0001 | c0003 | t0005 | g0071 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18954 | hp2 | a0002 | c0001 | t0001 | g0144 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18956 | hp1 | a0001 | c0003 | t0023 | g0066 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18956 | hp2 | a0002 | c0001 | t0001 | g0156 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18957 | hp1 | a0001 | c0003 | t0002 | g0073 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18957 | hp2 | a0002 | c0001 | t0001 | g0171 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18962 | hp1 | a0001 | c0003 | t0002 | g0068 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18962 | hp2 | a0001 | c0002 | t0002 | g0329 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18963 | hp1 | a0002 | c0001 | t0001 | g0111 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18963 | hp2 | a0001 | c0003 | t0008 | g0061 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18966 | hp1 | a0005 | c0008 | t0002 | g0340 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18966 | hp2 | a0002 | c0001 | t0006 | g0250 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18967 | hp1 | a0003 | c0004 | t0004 | g0284 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18967 | hp2 | a0001 | c0003 | t0005 | g0091 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18968 | hp1 | a0001 | c0002 | t0002 | g0339 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18968 | hp2 | a0002 | c0001 | t0001 | g0147 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18969 | hp1 | a0002 | c0001 | t0001 | g0185 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18969 | hp2 | a0001 | c0005 | t0003 | g0133 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18971 | hp1 | a0002 | c0001 | t0006 | g0200 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18971 | hp2 | a0001 | c0003 | t0002 | g0056 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18972 | hp1 | a0001 | c0002 | t0002 | g0353 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18972 | hp2 | a0002 | c0001 | t0001 | g0164 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18973 | hp1 | a0001 | c0003 | t0005 | g0050 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18973 | hp2 | a0002 | c0001 | t0001 | g0153 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18975 | hp1 | a0003 | c0004 | t0004 | g0283 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18975 | hp2 | a0004 | c0007 | t0002 | g0328 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18977 | hp1 | a0002 | c0001 | t0001 | g0253 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18977 | hp2 | a0001 | c0005 | t0003 | g0131 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18983 | hp1 | a0002 | c0001 | t0001 | g0172 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18983 | hp2 | a0003 | c0004 | t0004 | g0266 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18986 | hp1 | a0001 | c0003 | t0008 | g0090 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18986 | hp2 | a0003 | c0004 | t0004 | g0265 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18987 | hp1 | a0003 | c0004 | t0004 | g0282 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18987 | hp2 | a0001 | c0003 | t0002 | g0077 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18988 | hp1 | a0001 | c0002 | t0002 | g0331 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18988 | hp2 | a0001 | c0003 | t0002 | g0095 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18990 | hp1 | a0001 | c0002 | t0015 | g0315 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18990 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18994 | hp1 | a0001 | c0002 | t0011 | g0257 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18994 | hp2 | a0001 | c0003 | t0008 | g0059 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18995 | hp1 | a0003 | c0004 | t0004 | g0277 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18995 | hp2 | a0001 | c0003 | t0008 | g0083 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18998 | hp1 | a0001 | c0003 | t0008 | g0075 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18998 | hp2 | a0002 | c0001 | t0006 | g0193 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19001 | hp1 | a0002 | c0001 | t0001 | g0160 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19001 | hp2 | a0001 | c0002 | t0015 | g0316 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19003 | hp1 | a0002 | c0001 | t0001 | g0221 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19003 | hp2 | a0001 | c0002 | t0002 | g0298 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19004 | hp1 | a0002 | c0001 | t0001 | g0166 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19004 | hp2 | a0001 | c0003 | t0003 | g0041 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19005 | hp1 | a0001 | c0002 | t0002 | g0341 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19005 | hp2 | a0002 | c0001 | t0001 | g0178 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19007 | hp1 | a0001 | c0002 | t0002 | g0355 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19007 | hp2 | a0002 | c0001 | t0001 | g0150 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19009 | hp1 | a0003 | c0004 | t0004 | g0279 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19009 | hp2 | a0002 | c0001 | t0001 | g0245 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19010 | hp1 | a0001 | c0003 | t0002 | g0082 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19010 | hp2 | a0003 | c0004 | t0004 | g0275 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19011 | hp1 | a0001 | c0005 | t0003 | g0132 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19011 | hp2 | a0001 | c0003 | t0002 | g0079 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19030 | hp1 | a0001 | c0006 | t0003 | g0008 | AFR | LWK | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19030 | hp2 | a0002 | c0001 | t0001 | g0226 | AFR | LWK | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19043 | hp1 | a0002 | c0001 | t0001 | g0238 | AFR | LWK | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19043 | hp2 | a0001 | c0002 | t0013 | g0309 | AFR | LWK | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19054 | hp1 | a0001 | c0003 | t0003 | g0048 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19054 | hp2 | a0002 | c0001 | t0001 | g0175 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19055 | hp1 | a0002 | c0001 | t0006 | g0202 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19055 | hp2 | a0001 | c0002 | t0002 | g0332 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19056 | hp1 | a0002 | c0001 | t0001 | g0239 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19056 | hp2 | a0001 | c0003 | t0008 | g0062 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19057 | hp1 | a0002 | c0001 | t0006 | g0145 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19057 | hp2 | a0001 | c0002 | t0002 | g0324 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19060 | hp1 | a0005 | c0008 | t0002 | g0334 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19060 | hp2 | a0002 | c0001 | t0006 | g0198 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19062 | hp1 | a0003 | c0004 | t0004 | g0271 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19062 | hp2 | a0002 | c0001 | t0001 | g0244 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19064 | hp1 | a0010 | c0011 | t0005 | g0093 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19064 | hp2 | a0001 | c0002 | t0011 | g0302 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19065 | hp1 | a0001 | c0003 | t0005 | g0053 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19065 | hp2 | a0011 | c0021 | t0001 | g0337 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19066 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19066 | hp2 | a0001 | c0003 | t0005 | g0051 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19068 | hp1 | a0012 | c0012 | t0001 | g0154 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19068 | hp2 | a0003 | c0004 | t0004 | g0267 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19070 | hp1 | a0002 | c0001 | t0001 | g0181 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19070 | hp2 | a0001 | c0003 | t0003 | g0042 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19074 | hp1 | a0002 | c0001 | t0001 | g0170 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19074 | hp2 | a0001 | c0002 | t0015 | g0314 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19075 | hp1 | a0003 | c0004 | t0004 | g0276 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19075 | hp2 | a0002 | c0001 | t0006 | g0186 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19077 | hp1 | a0003 | c0004 | t0004 | g0281 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19077 | hp2 | a0001 | c0003 | t0008 | g0076 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19080 | hp1 | a0002 | c0001 | t0006 | g0231 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19080 | hp2 | a0001 | c0003 | t0008 | g0064 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19081 | hp1 | a0001 | c0003 | t0003 | g0043 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19081 | hp2 | a0001 | c0002 | t0002 | g0351 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19082 | hp1 | a0002 | c0001 | t0001 | g0158 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19082 | hp2 | a0003 | c0004 | t0004 | g0261 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19083 | hp1 | a0003 | c0004 | t0004 | g0280 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19083 | hp2 | a0002 | c0001 | t0001 | g0173 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19085 | hp1 | a0001 | c0003 | t0002 | g0069 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19085 | hp2 | a0002 | c0001 | t0006 | g0190 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19086 | hp1 | a0001 | c0003 | t0008 | g0063 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19086 | hp2 | a0002 | c0001 | t0006 | g0234 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19087 | hp1 | a0005 | c0008 | t0023 | g0297 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19087 | hp2 | a0003 | c0004 | t0044 | g0263 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19088 | hp1 | a0001 | c0003 | t0002 | g0070 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19088 | hp2 | a0002 | c0001 | t0001 | g0209 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19090 | hp1 | a0001 | c0003 | t0002 | g0094 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19090 | hp2 | a0002 | c0001 | t0001 | g0176 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0304 | AFR | YRI | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA19240 | hp2 | a0001 | c0003 | t0005 | g0040 | AFR | YRI | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA20129 | hp1 | a0002 | c0001 | t0001 | g0243 | AFR | ASW | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA20129 | hp2 | a0001 | c0003 | t0005 | g0038 | AFR | ASW | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA20752 | hp1 | a0001 | c0002 | t0002 | g0321 | EUR | TSI | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA20752 | hp2 | a0001 | c0005 | t0043 | g0112 | EUR | TSI | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA20805 | hp1 | a0003 | c0004 | t0004 | g0274 | EUR | TSI | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA20805 | hp2 | a0001 | c0002 | t0014 | g0291 | EUR | TSI | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA20905 | hp1 | a0002 | c0001 | t0001 | g0210 | SAS | GIH | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA20905 | hp2 | a0001 | c0005 | t0003 | g0119 | SAS | GIH | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02109 | hp1 | a0001 | c0003 | t0005 | g0046 | AFR | ACB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02109 | hp2 | a0002 | c0001 | t0001 | g0216 | AFR | ACB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02486 | hp1 | a0002 | c0001 | t0001 | g0207 | AFR | ACB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02486 | hp2 | a0001 | c0006 | t0003 | g0103 | AFR | ACB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02559 | hp1 | a0001 | c0006 | t0007 | g0013 | AFR | ACB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG02559 | hp2 | a0002 | c0001 | t0001 | g0230 | AFR | ACB | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03471 | hp1 | a0002 | c0001 | t0001 | g0236 | AFR | MSL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG03471 | hp2 | a0001 | c0003 | t0005 | g0037 | AFR | MSL | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG06807 | hp1 | a0001 | c0003 | t0005 | g0034 | AFR | USA | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| HG06807 | hp2 | a0001 | c0002 | t0014 | g0289 | AFR | USA | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18955 | hp1 | a0002 | c0001 | t0012 | g0220 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA18955 | hp2 | a0001 | c0003 | t0008 | g0085 | EAS | JPT | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA20300 | hp1 | a0001 | c0005 | t0003 | g0126 | AFR | USA | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA20300 | hp2 | a0005 | c0008 | t0002 | g0364 | AFR | USA | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA21309 | hp1 | a0001 | c0003 | t0005 | g0045 | AFR | LWK | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| NA21309 | hp2 | a0001 | c0002 | t0010 | g0023 | AFR | LWK | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0005 | g0044 | REF | REF | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0011 | g0307 | REF | REF | MON2_chr12_62461826_62605476 | MON2 | chr12 | 62461826 | 62605476 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:62467263 | G | A | 1 | a0004 | 4 | HG02165.hp2 NA18943.hp2 NA18949.hp1 others(1): Show |
missense_variant | MODERATE | c.56G>A | p.Ser19Asn | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/35 | 438/13263 | 56/5154 | 19/1717 | chr12 | 62467263 | |||
| chr12:62534853 | G | A | 4 | a0002 a0007 a0009 others(1): Show |
121 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(118): Show |
missense_variant | MODERATE | c.1642G>A | p.Ala548Thr | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 13/35 | 2024/13263 | 1642/5154 | 548/1717 | chr12 | 62534853 | |||
| chr12:62535626 | C | T | 1 | a0011 | 1 | NA19065.hp2 | missense_variant | MODERATE | c.1817C>T | p.Thr606Ile | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/35 | 2199/13263 | 1817/5154 | 606/1717 | chr12 | 62535626 | |||
| chr12:62535709 | T | C | 1 | a0012 | 1 | NA19068.hp1 | missense_variant&splice_region_variant | MODERATE | c.1900T>C | p.Ser634Pro | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/35 | 2282/13263 | 1900/5154 | 634/1717 | chr12 | 62535709 | |||
| chr12:62543155 | G | C | 1 | a0009 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.2423G>C | p.Arg808Pro | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 20/35 | 2805/13263 | 2423/5154 | 808/1717 | chr12 | 62543155 | |||
| chr12:62547024 | G | T | 1 | a0008 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.2705G>T | p.Gly902Val | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/35 | 3087/13263 | 2705/5154 | 902/1717 | chr12 | 62547024 | |||
| chr12:62552959 | A | C | 1 | a0005 | 4 | NA18966.hp1 NA19060.hp1 NA19087.hp1 others(1): Show |
missense_variant | MODERATE | c.2995A>C | p.Lys999Gln | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 24/35 | 3377/13263 | 2995/5154 | 999/1717 | chr12 | 62552959 | |||
| chr12:62556022 | G | A | 1 | a0006 | 2 | HG01516.hp2 HG01517.hp1 |
missense_variant | MODERATE | c.3239G>A | p.Arg1080Gln | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/35 | 3621/13263 | 3239/5154 | 1080/1717 | chr12 | 62556022 | |||
| chr12:62565357 | A | G | 1 | a0003 | 33 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(30): Show |
missense_variant | MODERATE | c.4153A>G | p.Ile1385Val | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 27/35 | 4535/13263 | 4153/5154 | 1385/1717 | chr12 | 62565357 | |||
| chr12:62571501 | G | A | 1 | a0010 | 1 | NA19064.hp1 | missense_variant | MODERATE | c.4433G>A | p.Arg1478Gln | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/35 | 4815/13263 | 4433/5154 | 1478/1717 | chr12 | 62571501 | |||
| chr12:62585472 | A | C | 1 | a0007 | 1 | HG00642.hp1 | missense_variant | MODERATE | c.4878A>C | p.Glu1626Asp | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 33/35 | 5260/13263 | 4878/5154 | 1626/1717 | chr12 | 62585472 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:62500856 | T | A | 2 | a0001c0003 a0010c0011 |
69 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(66): Show |
synonymous_variant | LOW | c.639T>A | p.Ala213Ala | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 6/35 | 1021/13263 | 639/5154 | 213/1717 | chr12 | 62500856 | |||
| chr12:62532618 | G | A | 7 | a0001c0009 a0001c0016 a0002c0001 others(4): Show |
124 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
synonymous_variant | LOW | c.1581G>A | p.Ser527Ser | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/35 | 1963/13263 | 1581/5154 | 527/1717 | chr12 | 62532618 | |||
| chr12:62537158 | C | T | 1 | a0001c0006 | 24 | HG01099.hp1 HG01891.hp2 HG02055.hp2 others(21): Show |
synonymous_variant | LOW | c.1908C>T | p.Ser636Ser | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 15/35 | 2290/13263 | 1908/5154 | 636/1717 | chr12 | 62537158 | |||
| chr12:62537616 | T | C | 1 | a0001c0017 | 1 | HG00735.hp1 | synonymous_variant | LOW | c.2028T>C | p.Asn676Asn | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 16/35 | 2410/13263 | 2028/5154 | 676/1717 | chr12 | 62537616 | |||
| chr12:62537637 | A | G | 1 | a0010c0011 | 1 | NA19064.hp1 | synonymous_variant | LOW | c.2049A>G | p.Leu683Leu | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 16/35 | 2431/13263 | 2049/5154 | 683/1717 | chr12 | 62537637 | |||
| chr12:62537661 | G | T | 1 | a0001c0020 | 1 | HG01167.hp2 | synonymous_variant | LOW | c.2073G>T | p.Gly691Gly | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 16/35 | 2455/13263 | 2073/5154 | 691/1717 | chr12 | 62537661 | |||
| chr12:62556101 | C | T | 1 | a0001c0016 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.3318C>T | p.Thr1106Thr | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/35 | 3700/13263 | 3318/5154 | 1106/1717 | chr12 | 62556101 | |||
| chr12:62561035 | T | C | 1 | a0001c0018 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.3954T>C | p.Phe1318Phe | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/35 | 4336/13263 | 3954/5154 | 1318/1717 | chr12 | 62561035 | |||
| chr12:62561053 | C | T | 1 | a0002c0015 | 1 | HG03834.hp1 | synonymous_variant | LOW | c.3972C>T | p.Thr1324Thr | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/35 | 4354/13263 | 3972/5154 | 1324/1717 | chr12 | 62561053 | |||
| chr12:62585436 | G | A | 2 | a0001c0005 a0008c0019 |
25 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(22): Show |
synonymous_variant | LOW | c.4842G>A | p.Arg1614Arg | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 33/35 | 5224/13263 | 4842/5154 | 1614/1717 | chr12 | 62585436 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:62466937 | G | A | 6 | a0002c0001t0006 a0002c0001t0009 a0002c0001t0025 others(3): Show |
28 | HG00438.hp2 HG00642.hp1 HG00733.hp1 others(25): Show |
5_prime_UTR_variant | MODIFIER | c.-271G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/35 | 271 | chr12 | 62466937 | ||||||
| chr12:62466990 | G | A | 1 | a0001c0002t0026 | 1 | HG03486.hp1 | 5_prime_UTR_variant | MODIFIER | c.-218G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/35 | 218 | chr12 | 62466990 | ||||||
| chr12:62467014 | G | A | 1 | a0002c0001t0018 | 2 | HG00140.hp2 HG01346.hp2 |
5_prime_UTR_variant | MODIFIER | c.-194G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/35 | 194 | chr12 | 62467014 | ||||||
| chr12:62592840 | G | A | 20 | a0001c0002t0031 a0001c0006t0007 a0001c0006t0033 others(17): Show |
138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*91G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 91 | chr12 | 62592840 | ||||||
| chr12:62592981 | G | A | 1 | a0001c0002t0035 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*232G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 232 | chr12 | 62592981 | ||||||
| chr12:62593218 | T | C | 1 | a0001c0003t0008 | 11 | NA18945.hp1 NA18955.hp2 NA18963.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*469T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 469 | chr12 | 62593218 | ||||||
| chr12:62593509 | T | G | 1 | a0001c0003t0036 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*760T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 760 | chr12 | 62593509 | ||||||
| chr12:62594045 | A | T | 1 | a0001c0003t0050 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1296A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 1296 | chr12 | 62594045 | ||||||
| chr12:62594079 | G | A | 1 | a0001c0002t0037 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1330G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 1330 | chr12 | 62594079 | ||||||
| chr12:62594305 | T | C | 1 | a0001c0020t0038 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1556T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 1556 | chr12 | 62594305 | ||||||
| chr12:62594508 | G | A | 15 | a0002c0001t0001 a0002c0001t0006 a0002c0001t0009 others(12): Show |
122 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*1759G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 1759 | chr12 | 62594508 | ||||||
| chr12:62594645 | G | A | 48 | a0001c0002t0003 a0001c0002t0005 a0001c0002t0013 others(45): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
3_prime_UTR_variant | MODIFIER | c.*1896G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 1896 | chr12 | 62594645 | ||||||
| chr12:62595141 | G | GT | 5 | a0001c0003t0023 a0001c0003t0049 a0002c0001t0012 others(2): Show |
8 | HG02145.hp1 HG02148.hp2 HG02647.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2408dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 2409 | INFO_REALIGN_3_PRIME | chr12 | 62595141 | |||||
| chr12:62595146 | T | G | 4 | a0001c0002t0013 a0001c0002t0026 a0001c0002t0037 others(1): Show |
7 | HG01074.hp1 HG01256.hp1 HG02004.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2397T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 2397 | chr12 | 62595146 | ||||||
| chr12:62595315 | T | A | 1 | a0002c0001t0027 | 1 | NA18943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2566T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 2566 | chr12 | 62595315 | ||||||
| chr12:62595330 | A | C | 24 | a0001c0002t0022 a0001c0002t0031 a0001c0006t0007 others(21): Show |
172 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
3_prime_UTR_variant | MODIFIER | c.*2581A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 2581 | chr12 | 62595330 | ||||||
| chr12:62595348 | T | G | 1 | a0003c0004t0044 | 1 | NA19087.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2599T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 2599 | chr12 | 62595348 | ||||||
| chr12:62595361 | T | A | 1 | a0001c0005t0040 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2612T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 2612 | chr12 | 62595361 | ||||||
| chr12:62595488 | G | A | 1 | a0001c0006t0007 | 12 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2739G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 2739 | chr12 | 62595488 | ||||||
| chr12:62595578 | T | G | 1 | a0001c0002t0017 | 3 | HG01109.hp2 HG02970.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2829T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 2829 | chr12 | 62595578 | ||||||
| chr12:62595633 | T | C | 1 | a0001c0003t0036 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2884T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 2884 | chr12 | 62595633 | ||||||
| chr12:62595662 | A | T | 1 | a0001c0002t0048 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2913A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 2913 | chr12 | 62595662 | ||||||
| chr12:62595902 | C | G | 1 | a0001c0002t0047 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3153C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 3153 | chr12 | 62595902 | ||||||
| chr12:62596142 | G | A | 2 | a0002c0001t0009 a0007c0014t0009 |
5 | HG00642.hp1 HG00733.hp1 HG03239.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3393G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 3393 | chr12 | 62596142 | ||||||
| chr12:62596623 | A | G | 24 | a0001c0002t0022 a0001c0002t0031 a0001c0006t0007 others(21): Show |
172 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
3_prime_UTR_variant | MODIFIER | c.*3874A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 3874 | chr12 | 62596623 | ||||||
| chr12:62596635 | T | C | 24 | a0001c0002t0022 a0001c0002t0031 a0001c0006t0007 others(21): Show |
172 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
3_prime_UTR_variant | MODIFIER | c.*3886T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 3886 | chr12 | 62596635 | ||||||
| chr12:62597091 | C | A | 20 | a0001c0002t0031 a0001c0006t0007 a0001c0006t0033 others(17): Show |
138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*4342C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 4342 | chr12 | 62597091 | ||||||
| chr12:62597166 | G | A | 1 | a0001c0009t0019 | 2 | HG02809.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4417G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 4417 | chr12 | 62597166 | ||||||
| chr12:62597208 | C | T | 1 | a0001c0006t0034 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4459C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 4459 | chr12 | 62597208 | ||||||
| chr12:62597265 | C | T | 3 | a0001c0006t0007 a0001c0006t0033 a0001c0006t0034 |
14 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4516C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 4516 | chr12 | 62597265 | ||||||
| chr12:62597266 | G | A | 3 | a0001c0002t0010 a0001c0002t0017 a0001c0002t0035 |
9 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4517G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 4517 | chr12 | 62597266 | ||||||
| chr12:62597468 | G | A | 1 | a0002c0001t0028 | 1 | HG01516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4719G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 4719 | chr12 | 62597468 | ||||||
| chr12:62597838 | A | G | 1 | a0001c0003t0049 | 1 | HG02148.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5089A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 5089 | chr12 | 62597838 | ||||||
| chr12:62597891 | T | G | 1 | a0001c0003t0041 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5142T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 5142 | chr12 | 62597891 | ||||||
| chr12:62598221 | G | A | 65 | a0001c0002t0002 a0001c0002t0003 a0001c0002t0005 others(62): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
3_prime_UTR_variant | MODIFIER | c.*5472G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 5472 | chr12 | 62598221 | ||||||
| chr12:62598248 | A | C | 1 | a0001c0005t0016 | 3 | HG00735.hp2 HG01106.hp1 HG01261.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5499A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 5499 | chr12 | 62598248 | ||||||
| chr12:62598467 | T | C | 1 | a0001c0002t0020 | 2 | HG01070.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5718T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 5718 | chr12 | 62598467 | ||||||
| chr12:62598582 | G | A | 1 | a0001c0002t0014 | 4 | HG00099.hp2 HG02300.hp1 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5833G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 5833 | chr12 | 62598582 | ||||||
| chr12:62598706 | C | T | 1 | a0002c0001t0030 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5957C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 5957 | chr12 | 62598706 | ||||||
| chr12:62598762 | G | A | 1 | a0001c0006t0042 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6013G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 6013 | chr12 | 62598762 | ||||||
| chr12:62598847 | T | C | 1 | a0001c0002t0045 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6098T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 6098 | chr12 | 62598847 | ||||||
| chr12:62598879 | T | A | 1 | a0002c0015t0024 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6130T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 6130 | chr12 | 62598879 | ||||||
| chr12:62598984 | T | TA | 1 | a0001c0002t0015 | 4 | HG03927.hp2 NA18990.hp1 NA19001.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6235_*6236insA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 6236 | chr12 | 62598984 | ||||||
| chr12:62599077 | T | C | 1 | a0001c0003t0021 | 2 | HG01069.hp1 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6328T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 6328 | chr12 | 62599077 | ||||||
| chr12:62599116 | GA | G | 19 | a0001c0006t0007 a0001c0006t0033 a0001c0006t0034 others(16): Show |
137 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*6377delA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 6377 | INFO_REALIGN_3_PRIME | chr12 | 62599116 | |||||
| chr12:62599151 | T | C | 1 | a0004c0007t0046 | 1 | NA18943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6402T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 6402 | chr12 | 62599151 | ||||||
| chr12:62599244 | G | A | 1 | a0001c0002t0047 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6495G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 6495 | chr12 | 62599244 | ||||||
| chr12:62599290 | A | G | 1 | a0001c0005t0043 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6541A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 6541 | chr12 | 62599290 | ||||||
| chr12:62599434 | A | G | 1 | a0002c0001t0029 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6685A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 6685 | chr12 | 62599434 | ||||||
| chr12:62599493 | A | T | 1 | a0001c0002t0031 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6744A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 6744 | chr12 | 62599493 | ||||||
| chr12:62600013 | G | A | 15 | a0002c0001t0001 a0002c0001t0006 a0002c0001t0009 others(12): Show |
122 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*7264G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 7264 | chr12 | 62600013 | ||||||
| chr12:62600156 | C | T | 39 | a0001c0002t0003 a0001c0002t0013 a0001c0002t0014 others(36): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
3_prime_UTR_variant | MODIFIER | c.*7407C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 7407 | chr12 | 62600156 | ||||||
| chr12:62600162 | G | A | 2 | a0003c0004t0004 a0003c0004t0044 |
32 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*7413G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 35/35 | 7413 | chr12 | 62600162 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:62467331 | T | C | 252 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0003g0135 others(249): Show |
255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.111+13T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62467331 | |||||||
| chr12:62467531 | T | C | 1 | a0001c0002t0002g0254 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.111+213T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62467531 | |||||||
| chr12:62467538 | G | A | 19 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(16): Show |
19 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.111+220G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62467538 | |||||||
| chr12:62467741 | T | C | 1 | a0001c0002t0011g0255 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.111+423T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62467741 | |||||||
| chr12:62467891 | G | C | 11 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(8): Show |
11 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.111+573G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62467891 | |||||||
| chr12:62467964 | TC | T | 79 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(76): Show |
80 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.111+648delC | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62467964 | ||||||
| chr12:62467965 | C | T | 172 | a0001c0002t0031g0136 a0001c0005t0003g0109 a0001c0005t0003g0110 others(169): Show |
174 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.111+647C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62467965 | |||||||
| chr12:62468155 | T | TA | 9 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(6): Show |
9 | HG02145.hp2 HG02280.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.111+849dupA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62468155 | ||||||
| chr12:62468155 | TA | T | 119 | a0001c0016t0032g0252 a0002c0001t0001g0002 a0002c0001t0001g0003 others(116): Show |
121 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.111+849delA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62468155 | ||||||
| chr12:62468180 | C | A | 97 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(94): Show |
98 | HG00140.hp1 HG00544.hp1 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.111+862C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62468180 | |||||||
| chr12:62468585 | A | G | 7 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0027 others(4): Show |
7 | HG02145.hp2 HG02280.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.111+1267A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62468585 | |||||||
| chr12:62468656 | C | G | 1 | a0003c0004t0004g0365 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.111+1338C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62468656 | |||||||
| chr12:62468666 | A | G | 11 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(8): Show |
11 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.111+1348A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62468666 | |||||||
| chr12:62468800 | C | T | 1 | a0002c0001t0001g0253 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.111+1482C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62468800 | |||||||
| chr12:62468932 | G | A | 1 | a0001c0003t0005g0034 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.111+1614G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62468932 | |||||||
| chr12:62468959 | T | G | 128 | a0001c0005t0003g0109 a0001c0005t0003g0110 a0001c0006t0003g0102 others(125): Show |
130 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.111+1641T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62468959 | |||||||
| chr12:62469075 | G | A | 1 | a0001c0002t0002g0256 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.111+1757G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62469075 | |||||||
| chr12:62469100 | A | G | 2 | a0001c0003t0003g0099 a0001c0003t0003g0100 |
2 | HG02615.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.111+1782A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62469100 | |||||||
| chr12:62469113 | G | A | 1 | a0001c0002t0011g0257 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.111+1795G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62469113 | |||||||
| chr12:62469115 | C | CT | 6 | a0001c0002t0002g0256 a0001c0002t0002g0363 a0001c0002t0005g0362 others(3): Show |
6 | HG00621.hp2 HG01255.hp2 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.111+1815dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62469115 | ||||||
| chr12:62469115 | CT | C | 64 | a0001c0002t0003g0135 a0001c0002t0022g0294 a0001c0003t0002g0055 others(61): Show |
64 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.111+1815delT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62469115 | ||||||
| chr12:62469115 | CTT | C | 221 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(218): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.111+1814_111+1815d others(4): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62469115 | ||||||
| chr12:62469428 | G | C | 2 | a0003c0004t0004g0258 a0003c0004t0004g0259 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.111+2110G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62469428 | |||||||
| chr12:62469576 | T | C | 19 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(16): Show |
19 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.111+2258T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62469576 | |||||||
| chr12:62469735 | G | A | 251 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(248): Show |
254 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.111+2417G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62469735 | |||||||
| chr12:62469881 | A | ATTTT | 36 | a0001c0002t0002g0254 a0001c0002t0002g0256 a0001c0002t0002g0329 others(33): Show |
36 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.111+2564_111+2567d others(6): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62469881 | ||||||
| chr12:62469882 | T | TTTTA | 6 | a0001c0002t0002g0303 a0001c0002t0011g0255 a0001c0002t0011g0257 others(3): Show |
6 | HG01099.hp2 HG02280.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.111+2604_111+2607d others(6): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62469882 | ||||||
| chr12:62469882 | T | TTTTATTT others(1): Show |
3 | a0001c0002t0002g0298 a0001c0002t0045g0360 a0001c0018t0002g0299 |
3 | HG02572.hp2 NA18612.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.111+2600_111+2607d others(10): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62469882 | ||||||
| chr12:62469882 | T | TTTTTTTT others(1): Show |
13 | a0001c0002t0002g0317 a0001c0002t0002g0318 a0001c0002t0002g0321 others(10): Show |
13 | HG00423.hp2 HG00438.hp1 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.111+2567_111+2568i others(10): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62469882 | ||||||
| chr12:62469882 | T | TTTTTTTT others(5): Show |
3 | a0001c0002t0015g0314 a0001c0002t0015g0315 a0001c0002t0015g0316 |
3 | NA18990.hp1 NA19001.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.111+2567_111+2568i others(14): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62469882 | ||||||
| chr12:62469886 | A | T | 1 | a0001c0005t0040g0134 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.111+2568A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62469886 | |||||||
| chr12:62469910 | ATTTATTT others(6): Show |
A | 19 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(16): Show |
19 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.111+2595_111+2607d others(15): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62469910 | ||||||
| chr12:62469914 | ATTTATTT others(2): Show |
A | 83 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(80): Show |
84 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.111+2599_111+2607d others(11): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62469914 | ||||||
| chr12:62469918 | ATTTAT | A | 127 | a0001c0002t0003g0135 a0001c0002t0014g0290 a0001c0006t0003g0102 others(124): Show |
128 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.111+2603_111+2607d others(7): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62469918 | ||||||
| chr12:62469922 | AT | A | 32 | a0001c0002t0014g0288 a0001c0002t0014g0289 a0001c0002t0014g0291 others(29): Show |
33 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(30): Show |
intron_variant | MODIFIER | c.111+2607delT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62469922 | ||||||
| chr12:62469923 | T | TTTA | 7 | a0002c0001t0001g0210 a0002c0001t0001g0223 a0002c0001t0001g0224 others(4): Show |
7 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(4): Show |
intron_variant | MODIFIER | c.111+2607_111+2608i others(5): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62469923 | ||||||
| chr12:62469923 | T | TTTATTTA | 10 | a0001c0002t0013g0306 a0001c0002t0013g0308 a0001c0002t0013g0309 others(7): Show |
10 | HG01074.hp1 HG01256.hp1 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.111+2607_111+2608i others(9): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62469923 | ||||||
| chr12:62469923 | T | TTTATTTA others(4): Show |
18 | a0001c0005t0003g0109 a0001c0005t0003g0110 a0001c0005t0003g0117 others(15): Show |
18 | HG00735.hp2 HG00738.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.111+2607_111+2608i others(13): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62469923 | ||||||
| chr12:62469923 | T | TTTATTTA others(8): Show |
3 | a0001c0005t0040g0134 a0001c0005t0043g0112 a0008c0019t0003g0113 |
3 | HG02602.hp2 HG04184.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.111+2607_111+2608i others(17): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62469923 | ||||||
| chr12:62469923 | T | TTTATTTA others(12): Show |
1 | a0001c0005t0003g0130 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.111+2607_111+2608i others(21): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62469923 | ||||||
| chr12:62470040 | G | A | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.111+2722G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62470040 | |||||||
| chr12:62470153 | C | T | 19 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(16): Show |
19 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.111+2835C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62470153 | |||||||
| chr12:62470363 | A | G | 4 | a0002c0001t0001g0240 a0002c0001t0001g0241 a0002c0001t0001g0242 others(1): Show |
4 | HG01934.hp1 HG01975.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.111+3045A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62470363 | |||||||
| chr12:62470421 | T | G | 1 | a0001c0002t0002g0304 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.111+3103T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62470421 | |||||||
| chr12:62470468 | T | C | 251 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(248): Show |
254 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.111+3150T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62470468 | |||||||
| chr12:62470469 | G | A | 1 | a0001c0003t0021g0001 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.111+3151G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62470469 | |||||||
| chr12:62470476 | A | G | 2 | a0002c0001t0001g0111 a0002c0001t0001g0239 |
2 | NA18963.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.111+3158A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62470476 | |||||||
| chr12:62470526 | G | T | 1 | a0001c0006t0033g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.111+3208G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62470526 | |||||||
| chr12:62470637 | A | C | 98 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(95): Show |
99 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.111+3319A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62470637 | |||||||
| chr12:62470748 | G | A | 1 | a0001c0002t0031g0136 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.111+3430G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62470748 | |||||||
| chr12:62471004 | A | G | 6 | a0001c0002t0014g0288 a0001c0002t0014g0289 a0001c0002t0014g0290 others(3): Show |
6 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.111+3686A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62471004 | |||||||
| chr12:62471031 | G | C | 5 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(2): Show |
5 | HG02976.hp1 HG03195.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.111+3713G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62471031 | |||||||
| chr12:62471097 | A | T | 26 | a0001c0002t0031g0136 a0001c0005t0003g0109 a0001c0005t0003g0110 others(23): Show |
26 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.111+3779A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62471097 | |||||||
| chr12:62471105 | C | T | 1 | a0001c0002t0002g0359 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.111+3787C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62471105 | |||||||
| chr12:62471151 | A | G | 26 | a0001c0002t0031g0136 a0001c0005t0003g0109 a0001c0005t0003g0110 others(23): Show |
26 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.111+3833A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62471151 | |||||||
| chr12:62471312 | A | G | 6 | a0001c0002t0014g0288 a0001c0002t0014g0289 a0001c0002t0014g0290 others(3): Show |
6 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.111+3994A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62471312 | |||||||
| chr12:62471328 | G | A | 27 | a0001c0002t0031g0136 a0001c0003t0021g0001 a0001c0005t0003g0109 others(24): Show |
28 | HG00735.hp2 HG00738.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.111+4010G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62471328 | |||||||
| chr12:62471329 | C | T | 1 | a0002c0001t0001g0238 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.111+4011C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62471329 | |||||||
| chr12:62471372 | C | T | 127 | a0001c0006t0003g0102 a0001c0006t0003g0103 a0001c0006t0003g0104 others(124): Show |
129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.111+4054C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62471372 | |||||||
| chr12:62471430 | C | T | 1 | a0001c0002t0002g0358 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.111+4112C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62471430 | |||||||
| chr12:62471464 | G | C | 1 | a0001c0003t0005g0045 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.111+4146G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62471464 | |||||||
| chr12:62471508 | T | C | 1 | a0002c0001t0001g0137 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.111+4190T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62471508 | |||||||
| chr12:62471511 | G | A | 124 | a0001c0006t0003g0102 a0001c0006t0003g0103 a0001c0006t0003g0104 others(121): Show |
126 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.111+4193G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62471511 | |||||||
| chr12:62471565 | T | C | 26 | a0001c0002t0031g0136 a0001c0005t0003g0109 a0001c0005t0003g0110 others(23): Show |
26 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.111+4247T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62471565 | |||||||
| chr12:62471648 | A | G | 1 | a0007c0014t0009g0237 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.111+4330A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62471648 | |||||||
| chr12:62471680 | G | A | 1 | a0001c0005t0043g0112 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.111+4362G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62471680 | |||||||
| chr12:62471955 | T | A | 1 | a0003c0004t0004g0260 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.111+4637T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62471955 | |||||||
| chr12:62472178 | C | T | 251 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(248): Show |
254 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.111+4860C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62472178 | |||||||
| chr12:62472224 | A | C | 1 | a0002c0001t0001g0236 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.111+4906A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62472224 | |||||||
| chr12:62472279 | G | A | 2 | a0001c0005t0003g0109 a0001c0005t0003g0110 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.111+4961G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62472279 | |||||||
| chr12:62472339 | G | T | 1 | a0001c0006t0033g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.111+5021G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62472339 | |||||||
| chr12:62472601 | T | G | 2 | a0001c0003t0005g0046 a0001c0003t0005g0047 |
2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.111+5283T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62472601 | |||||||
| chr12:62472761 | A | G | 1 | a0003c0004t0004g0286 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.111+5443A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62472761 | |||||||
| chr12:62472987 | A | AT | 52 | a0001c0003t0002g0055 a0001c0003t0002g0056 a0001c0003t0002g0057 others(49): Show |
52 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.111+5672dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62472987 | ||||||
| chr12:62473022 | A | G | 1 | a0001c0002t0002g0357 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.111+5704A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62473022 | |||||||
| chr12:62473203 | G | A | 3 | a0001c0006t0003g0102 a0001c0006t0003g0103 a0001c0006t0003g0104 |
3 | HG02257.hp2 HG02486.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.111+5885G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62473203 | |||||||
| chr12:62473208 | T | G | 1 | a0001c0002t0002g0317 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.111+5890T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62473208 | |||||||
| chr12:62473241 | A | G | 2 | a0001c0005t0003g0132 a0001c0005t0003g0133 |
2 | NA18969.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.111+5923A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62473241 | |||||||
| chr12:62473316 | AAAATGGT others(2): Show |
A | 252 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0003g0135 others(249): Show |
255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.111+6015_111+6023d others(11): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62473316 | ||||||
| chr12:62473427 | T | C | 1 | a0001c0002t0010g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.111+6109T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62473427 | |||||||
| chr12:62474318 | A | T | 153 | a0001c0002t0031g0136 a0001c0005t0003g0109 a0001c0005t0003g0110 others(150): Show |
155 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.111+7000A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62474318 | |||||||
| chr12:62474494 | G | A | 1 | a0001c0020t0038g0305 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.111+7176G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62474494 | |||||||
| chr12:62474518 | G | A | 98 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(95): Show |
99 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.111+7200G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62474518 | |||||||
| chr12:62474557 | T | G | 6 | a0001c0002t0014g0288 a0001c0002t0014g0289 a0001c0002t0014g0290 others(3): Show |
6 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.111+7239T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62474557 | |||||||
| chr12:62474610 | G | A | 2 | a0003c0004t0004g0261 a0003c0004t0004g0293 |
2 | HG04228.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.111+7292G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62474610 | |||||||
| chr12:62474613 | G | A | 1 | a0001c0002t0003g0135 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.111+7295G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62474613 | |||||||
| chr12:62474675 | C | T | 127 | a0001c0006t0003g0102 a0001c0006t0003g0103 a0001c0006t0003g0104 others(124): Show |
129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.111+7357C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62474675 | |||||||
| chr12:62474719 | C | T | 127 | a0001c0006t0003g0102 a0001c0006t0003g0103 a0001c0006t0003g0104 others(124): Show |
129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.111+7401C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62474719 | |||||||
| chr12:62474720 | A | C | 127 | a0001c0006t0003g0102 a0001c0006t0003g0103 a0001c0006t0003g0104 others(124): Show |
129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.111+7402A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62474720 | |||||||
| chr12:62475105 | T | G | 24 | a0001c0002t0031g0136 a0001c0005t0003g0117 a0001c0005t0003g0118 others(21): Show |
24 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.111+7787T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62475105 | |||||||
| chr12:62475107 | C | T | 1 | a0002c0001t0001g0235 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.111+7789C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62475107 | |||||||
| chr12:62475449 | C | T | 11 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(8): Show |
11 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.111+8131C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62475449 | |||||||
| chr12:62475470 | CTATCTT | C | 51 | a0001c0003t0002g0055 a0001c0003t0002g0056 a0001c0003t0002g0057 others(48): Show |
51 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.111+8155_111+8160d others(8): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62475470 | ||||||
| chr12:62475572 | G | A | 6 | a0001c0002t0014g0288 a0001c0002t0014g0289 a0001c0002t0014g0290 others(3): Show |
6 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.111+8254G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62475572 | |||||||
| chr12:62475749 | C | A | 5 | a0002c0001t0001g0138 a0002c0001t0001g0139 a0002c0001t0001g0142 others(2): Show |
5 | HG02055.hp1 HG02145.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.112-8421C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62475749 | |||||||
| chr12:62475883 | C | T | 4 | a0004c0007t0002g0327 a0004c0007t0002g0328 a0004c0007t0002g0361 others(1): Show |
4 | HG02165.hp2 NA18943.hp2 NA18949.hp1 others(1): Show |
intron_variant | MODIFIER | c.112-8287C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62475883 | |||||||
| chr12:62475959 | C | T | 19 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(16): Show |
19 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.112-8211C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62475959 | |||||||
| chr12:62476012 | AAAAAG | A | 24 | a0001c0002t0031g0136 a0001c0005t0003g0117 a0001c0005t0003g0118 others(21): Show |
24 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.112-8147_112-8143d others(7): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62476012 | ||||||
| chr12:62476024 | AAAGG | A | 34 | a0001c0002t0022g0294 a0003c0004t0004g0258 a0003c0004t0004g0259 others(31): Show |
34 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.112-8139_112-8136d others(6): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62476024 | ||||||
| chr12:62476218 | A | C | 1 | a0001c0006t0033g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.112-7952A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62476218 | |||||||
| chr12:62476268 | G | C | 2 | a0001c0002t0002g0363 a0001c0002t0005g0362 |
2 | HG01255.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.112-7902G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62476268 | |||||||
| chr12:62476333 | A | T | 79 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(76): Show |
80 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.112-7837A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62476333 | |||||||
| chr12:62476594 | A | C | 251 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(248): Show |
254 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.112-7576A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62476594 | |||||||
| chr12:62476625 | C | T | 2 | a0001c0009t0019g0107 a0001c0009t0019g0108 |
2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.112-7545C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62476625 | |||||||
| chr12:62476639 | G | A | 11 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(8): Show |
11 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.112-7531G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62476639 | |||||||
| chr12:62476703 | G | A | 1 | a0002c0001t0001g0137 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.112-7467G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62476703 | |||||||
| chr12:62476730 | C | G | 24 | a0001c0002t0031g0136 a0001c0005t0003g0117 a0001c0005t0003g0118 others(21): Show |
24 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.112-7440C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62476730 | |||||||
| chr12:62476756 | C | G | 24 | a0001c0002t0031g0136 a0001c0005t0003g0117 a0001c0005t0003g0118 others(21): Show |
24 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.112-7414C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62476756 | |||||||
| chr12:62476794 | C | G | 129 | a0001c0005t0003g0109 a0001c0005t0003g0110 a0001c0006t0003g0102 others(126): Show |
131 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.112-7376C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62476794 | |||||||
| chr12:62476951 | T | A | 1 | a0001c0002t0002g0329 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.112-7219T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62476951 | |||||||
| chr12:62476992 | A | C | 2 | a0001c0009t0019g0107 a0001c0009t0019g0108 |
2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.112-7178A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62476992 | |||||||
| chr12:62477034 | C | T | 1 | a0001c0002t0003g0135 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.112-7136C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62477034 | |||||||
| chr12:62477044 | G | A | 2 | a0001c0005t0003g0109 a0001c0005t0003g0110 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.112-7126G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62477044 | |||||||
| chr12:62477511 | G | A | 4 | a0001c0003t0003g0035 a0001c0003t0003g0036 a0001c0003t0003g0099 others(1): Show |
4 | HG01361.hp2 HG02257.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.112-6659G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62477511 | |||||||
| chr12:62477581 | A | AT | 6 | a0001c0002t0003g0135 a0001c0003t0005g0091 a0001c0003t0021g0001 others(3): Show |
7 | HG00673.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.112-6571dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62477581 | ||||||
| chr12:62477581 | AT | A | 10 | a0001c0002t0002g0330 a0001c0002t0013g0306 a0001c0002t0020g0287 others(7): Show |
10 | HG01070.hp1 HG01074.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.112-6571delT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62477581 | ||||||
| chr12:62477588 | T | TC | 24 | a0001c0002t0031g0136 a0001c0005t0003g0117 a0001c0005t0003g0118 others(21): Show |
24 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.112-6582_112-6581i others(3): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62477588 | |||||||
| chr12:62477629 | C | CT | 300 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0003g0135 others(297): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.112-6541_112-6540i others(3): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62477629 | |||||||
| chr12:62477636 | G | A | 1 | a0001c0002t0014g0288 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.112-6534G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62477636 | |||||||
| chr12:62477676 | A | G | 1 | a0001c0003t0008g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.112-6494A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62477676 | |||||||
| chr12:62477695 | C | T | 1 | a0001c0006t0003g0008 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.112-6475C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62477695 | |||||||
| chr12:62477772 | G | A | 3 | a0002c0001t0001g0147 a0002c0001t0001g0244 a0002c0001t0001g0245 |
3 | NA18968.hp2 NA19009.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.112-6398G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62477772 | |||||||
| chr12:62478041 | T | G | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.112-6129T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62478041 | |||||||
| chr12:62478047 | T | A | 6 | a0001c0002t0014g0288 a0001c0002t0014g0289 a0001c0002t0014g0290 others(3): Show |
6 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.112-6123T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62478047 | |||||||
| chr12:62478082 | C | A | 4 | a0001c0002t0014g0288 a0001c0002t0014g0289 a0001c0002t0014g0290 others(1): Show |
4 | HG00099.hp2 HG02300.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.112-6088C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62478082 | |||||||
| chr12:62478092 | G | A | 4 | a0001c0003t0003g0035 a0001c0003t0003g0036 a0001c0003t0003g0099 others(1): Show |
4 | HG01361.hp2 HG02257.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.112-6078G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62478092 | |||||||
| chr12:62478121 | T | TTG | 74 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(71): Show |
74 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.112-6025_112-6024d others(4): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62478121 | ||||||
| chr12:62478121 | T | TTGTG | 7 | a0001c0002t0002g0356 a0001c0006t0003g0005 a0001c0006t0003g0006 others(4): Show |
7 | HG01081.hp2 HG02071.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.112-6027_112-6024d others(6): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62478121 | ||||||
| chr12:62478121 | T | TTGTGTG | 22 | a0001c0005t0003g0117 a0001c0005t0003g0118 a0001c0005t0003g0119 others(19): Show |
22 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.112-6029_112-6024d others(8): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62478121 | ||||||
| chr12:62478228 | T | C | 1 | a0001c0002t0002g0359 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.112-5942T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62478228 | |||||||
| chr12:62478291 | A | C | 5 | a0001c0003t0003g0041 a0001c0003t0003g0042 a0001c0003t0003g0043 others(2): Show |
6 | HG01069.hp1 HG01071.hp1 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.112-5879A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62478291 | |||||||
| chr12:62478431 | C | T | 24 | a0001c0002t0031g0136 a0001c0005t0003g0117 a0001c0005t0003g0118 others(21): Show |
24 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.112-5739C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62478431 | |||||||
| chr12:62478482 | A | G | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.112-5688A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62478482 | |||||||
| chr12:62478554 | T | A | 7 | a0001c0002t0013g0306 a0001c0002t0013g0308 a0001c0002t0013g0309 others(4): Show |
7 | HG01074.hp1 HG01256.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.112-5616T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62478554 | |||||||
| chr12:62479093 | G | T | 1 | a0003c0004t0004g0285 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.112-5077G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62479093 | |||||||
| chr12:62479176 | A | C | 1 | a0001c0002t0031g0136 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.112-4994A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62479176 | |||||||
| chr12:62479265 | C | A | 4 | a0001c0003t0003g0035 a0001c0003t0003g0036 a0001c0003t0003g0099 others(1): Show |
4 | HG01361.hp2 HG02257.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.112-4905C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62479265 | |||||||
| chr12:62479286 | A | G | 2 | a0001c0009t0019g0107 a0001c0009t0019g0108 |
2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.112-4884A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62479286 | |||||||
| chr12:62479289 | T | G | 6 | a0001c0002t0014g0288 a0001c0002t0014g0289 a0001c0002t0014g0290 others(3): Show |
6 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.112-4881T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62479289 | |||||||
| chr12:62479335 | T | A | 6 | a0001c0002t0014g0288 a0001c0002t0014g0289 a0001c0002t0014g0290 others(3): Show |
6 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.112-4835T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62479335 | |||||||
| chr12:62479397 | G | A | 293 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0002g0331 others(290): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.112-4773G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62479397 | |||||||
| chr12:62479428 | A | G | 27 | a0001c0002t0002g0355 a0001c0002t0031g0136 a0001c0005t0003g0109 others(24): Show |
27 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.112-4742A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62479428 | |||||||
| chr12:62479431 | T | TC | 15 | a0001c0002t0002g0317 a0001c0002t0002g0325 a0001c0002t0002g0351 others(12): Show |
15 | HG00544.hp1 HG00621.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.112-4725dupC | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62479431 | ||||||
| chr12:62479431 | TC | T | 81 | a0001c0002t0002g0318 a0001c0002t0010g0031 a0001c0002t0013g0309 others(78): Show |
81 | HG00438.hp2 HG00639.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.112-4725delC | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62479431 | ||||||
| chr12:62479431 | TCC | T | 157 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0003g0135 others(154): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.112-4726_112-4725d others(4): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62479431 | ||||||
| chr12:62479431 | TCCC | T | 15 | a0001c0002t0014g0288 a0001c0002t0014g0289 a0001c0002t0014g0290 others(12): Show |
15 | HG00099.hp2 HG00741.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.112-4727_112-4725d others(5): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62479431 | ||||||
| chr12:62479433 | C | A | 26 | a0001c0002t0031g0136 a0001c0005t0003g0109 a0001c0005t0003g0110 others(23): Show |
26 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.112-4737C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62479433 | |||||||
| chr12:62479434 | C | T | 26 | a0001c0002t0031g0136 a0001c0005t0003g0109 a0001c0005t0003g0110 others(23): Show |
26 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.112-4736C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62479434 | |||||||
| chr12:62479566 | C | G | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.112-4604C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62479566 | |||||||
| chr12:62479639 | G | A | 59 | a0002c0001t0001g0002 a0002c0001t0001g0111 a0002c0001t0001g0143 others(56): Show |
60 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.112-4531G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62479639 | |||||||
| chr12:62479863 | G | A | 1 | a0001c0002t0003g0135 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.112-4307G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62479863 | |||||||
| chr12:62480093 | G | A | 24 | a0001c0002t0031g0136 a0001c0005t0003g0117 a0001c0005t0003g0118 others(21): Show |
24 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.112-4077G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62480093 | |||||||
| chr12:62480231 | T | A | 1 | a0001c0018t0002g0299 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.112-3939T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62480231 | |||||||
| chr12:62480374 | C | G | 3 | a0001c0005t0003g0131 a0001c0005t0003g0132 a0001c0005t0003g0133 |
3 | NA18969.hp2 NA18977.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.112-3796C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62480374 | |||||||
| chr12:62480460 | G | C | 1 | a0001c0002t0031g0136 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.112-3710G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62480460 | |||||||
| chr12:62480649 | G | A | 1 | a0001c0002t0003g0135 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.112-3521G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62480649 | |||||||
| chr12:62480680 | A | G | 19 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(16): Show |
19 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.112-3490A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62480680 | |||||||
| chr12:62480707 | G | C | 30 | a0001c0005t0003g0109 a0001c0005t0003g0110 a0002c0001t0006g0145 others(27): Show |
30 | HG00438.hp2 HG00642.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.112-3463G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62480707 | |||||||
| chr12:62480708 | A | T | 30 | a0001c0005t0003g0109 a0001c0005t0003g0110 a0002c0001t0006g0145 others(27): Show |
30 | HG00438.hp2 HG00642.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.112-3462A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62480708 | |||||||
| chr12:62481169 | T | G | 1 | a0001c0002t0048g0320 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.112-3001T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62481169 | |||||||
| chr12:62481198 | A | G | 1 | a0001c0006t0034g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.112-2972A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62481198 | |||||||
| chr12:62481302 | G | A | 34 | a0001c0002t0022g0294 a0003c0004t0004g0258 a0003c0004t0004g0259 others(31): Show |
34 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.112-2868G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62481302 | |||||||
| chr12:62481333 | T | A | 1 | a0001c0006t0003g0008 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.112-2837T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62481333 | |||||||
| chr12:62481487 | G | A | 5 | a0001c0006t0003g0102 a0001c0006t0003g0103 a0001c0006t0003g0104 others(2): Show |
5 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.112-2683G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62481487 | |||||||
| chr12:62481510 | C | T | 52 | a0001c0003t0002g0055 a0001c0003t0002g0056 a0001c0003t0002g0057 others(49): Show |
52 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.112-2660C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62481510 | |||||||
| chr12:62481515 | C | CA | 137 | a0001c0002t0002g0030 a0001c0002t0002g0298 a0001c0002t0002g0318 others(134): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.112-2635dupA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62481515 | ||||||
| chr12:62481515 | C | CAA | 92 | a0001c0002t0002g0026 a0001c0002t0003g0135 a0001c0002t0010g0023 others(89): Show |
93 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.112-2636_112-2635d others(4): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62481515 | ||||||
| chr12:62481515 | C | CAAA | 10 | a0001c0002t0017g0033 a0001c0003t0002g0055 a0001c0003t0002g0056 others(7): Show |
10 | HG01106.hp1 HG01109.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.112-2637_112-2635d others(5): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62481515 | ||||||
| chr12:62481515 | CA | C | 12 | a0001c0002t0037g0313 a0001c0006t0007g0009 a0001c0006t0007g0012 others(9): Show |
12 | HG01099.hp1 HG01516.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.112-2635delA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62481515 | ||||||
| chr12:62481636 | C | T | 19 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(16): Show |
19 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.112-2534C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62481636 | |||||||
| chr12:62481704 | A | G | 2 | a0003c0004t0004g0258 a0003c0004t0004g0259 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.112-2466A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62481704 | |||||||
| chr12:62481907 | A | G | 4 | a0001c0005t0003g0128 a0001c0005t0003g0129 a0001c0005t0003g0130 others(1): Show |
4 | HG01109.hp1 HG01256.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.112-2263A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62481907 | |||||||
| chr12:62482059 | C | T | 128 | a0001c0005t0003g0109 a0001c0005t0003g0110 a0001c0006t0003g0102 others(125): Show |
130 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.112-2111C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62482059 | |||||||
| chr12:62482130 | T | A | 251 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(248): Show |
254 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.112-2040T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62482130 | |||||||
| chr12:62482323 | C | G | 79 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(76): Show |
80 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.112-1847C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62482323 | |||||||
| chr12:62482425 | C | T | 11 | a0001c0002t0002g0303 a0001c0002t0002g0343 a0001c0002t0002g0345 others(8): Show |
11 | HG00642.hp2 HG00735.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.112-1745C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62482425 | |||||||
| chr12:62482478 | G | C | 1 | a0002c0001t0001g0142 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.112-1692G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62482478 | |||||||
| chr12:62482488 | A | C | 1 | a0001c0002t0002g0342 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.112-1682A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62482488 | |||||||
| chr12:62482658 | A | G | 1 | a0003c0004t0004g0365 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.112-1512A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62482658 | |||||||
| chr12:62482717 | C | T | 299 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0003g0135 others(296): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.112-1453C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62482717 | |||||||
| chr12:62482811 | C | T | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.112-1359C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62482811 | |||||||
| chr12:62482907 | AC | A | 5 | a0001c0003t0003g0041 a0001c0003t0003g0042 a0001c0003t0003g0043 others(2): Show |
6 | HG01069.hp1 HG01071.hp1 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.112-1261delC | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62482907 | ||||||
| chr12:62482933 | C | T | 34 | a0001c0002t0022g0294 a0003c0004t0004g0258 a0003c0004t0004g0259 others(31): Show |
34 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.112-1237C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62482933 | |||||||
| chr12:62483207 | G | C | 19 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(16): Show |
19 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.112-963G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62483207 | |||||||
| chr12:62483256 | A | G | 24 | a0001c0002t0031g0136 a0001c0005t0003g0117 a0001c0005t0003g0118 others(21): Show |
24 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.112-914A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62483256 | |||||||
| chr12:62483391 | A | G | 1 | a0001c0002t0003g0135 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.112-779A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62483391 | |||||||
| chr12:62483429 | G | A | 2 | a0001c0003t0005g0046 a0001c0003t0005g0047 |
2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.112-741G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62483429 | |||||||
| chr12:62483485 | G | T | 19 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(16): Show |
19 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.112-685G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62483485 | |||||||
| chr12:62483651 | G | A | 2 | a0001c0002t0013g0309 a0001c0002t0026g0310 |
2 | HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.112-519G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | chr12 | 62483651 | |||||||
| chr12:62483774 | A | AT | 8 | a0001c0006t0007g0009 a0001c0006t0007g0010 a0001c0006t0007g0011 others(5): Show |
8 | HG01891.hp2 HG02572.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.112-389dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr12 | 62483774 | ||||||
| chr12:62484370 | A | G | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.175+137A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62484370 | |||||||
| chr12:62484502 | C | T | 1 | a0001c0002t0031g0136 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.175+269C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62484502 | |||||||
| chr12:62484590 | T | G | 1 | a0001c0005t0003g0131 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.175+357T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62484590 | |||||||
| chr12:62484631 | A | G | 1 | a0002c0001t0028g0184 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.175+398A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62484631 | |||||||
| chr12:62484915 | CT | C | 17 | a0001c0002t0002g0298 a0001c0002t0002g0303 a0001c0002t0002g0321 others(14): Show |
17 | HG01074.hp1 HG01099.hp2 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.175+702delT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr12 | 62484915 | ||||||
| chr12:62484915 | CTT | C | 51 | a0001c0002t0013g0309 a0001c0002t0014g0288 a0001c0002t0014g0289 others(48): Show |
52 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.175+701_175+702del others(2): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr12 | 62484915 | ||||||
| chr12:62484915 | CTTT | C | 227 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(224): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.175+700_175+702del others(3): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr12 | 62484915 | ||||||
| chr12:62484915 | CTTTT | C | 12 | a0001c0003t0002g0057 a0001c0003t0005g0058 a0001c0003t0036g0049 others(9): Show |
12 | HG01081.hp2 HG01168.hp2 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.175+699_175+702del others(4): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr12 | 62484915 | ||||||
| chr12:62484938 | G | A | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.175+705G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62484938 | |||||||
| chr12:62485083 | A | G | 1 | a0002c0001t0001g0249 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.175+850A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62485083 | |||||||
| chr12:62485131 | T | C | 1 | a0001c0003t0008g0085 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.175+898T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62485131 | |||||||
| chr12:62485132 | G | C | 1 | a0001c0002t0003g0135 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.175+899G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62485132 | |||||||
| chr12:62485190 | T | C | 292 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0003g0135 others(289): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.175+957T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62485190 | |||||||
| chr12:62485435 | C | T | 1 | a0001c0003t0005g0045 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.175+1202C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62485435 | |||||||
| chr12:62485437 | G | T | 3 | a0001c0005t0003g0131 a0001c0005t0003g0132 a0001c0005t0003g0133 |
3 | NA18969.hp2 NA18977.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.175+1204G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62485437 | |||||||
| chr12:62485485 | G | A | 1 | a0005c0008t0002g0334 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.175+1252G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62485485 | |||||||
| chr12:62485579 | CAT | C | 23 | a0001c0005t0003g0117 a0001c0005t0003g0118 a0001c0005t0003g0119 others(20): Show |
23 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.175+1347_175+1348d others(4): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62485579 | |||||||
| chr12:62485710 | T | C | 3 | a0001c0003t0005g0086 a0001c0003t0005g0087 a0001c0003t0005g0101 |
3 | HG00597.hp2 HG00621.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.175+1477T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62485710 | |||||||
| chr12:62485860 | C | T | 1 | a0001c0002t0002g0349 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.175+1627C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62485860 | |||||||
| chr12:62486009 | G | A | 2 | a0001c0009t0019g0107 a0001c0009t0019g0108 |
2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.175+1776G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62486009 | |||||||
| chr12:62486121 | C | T | 5 | a0001c0003t0003g0035 a0001c0003t0003g0036 a0001c0003t0003g0099 others(2): Show |
5 | HG01361.hp2 HG02257.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.175+1888C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62486121 | |||||||
| chr12:62486183 | C | A | 1 | a0001c0018t0002g0299 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.175+1950C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62486183 | |||||||
| chr12:62486184 | G | A | 1 | a0001c0002t0002g0332 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.175+1951G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62486184 | |||||||
| chr12:62486244 | A | T | 2 | a0001c0009t0019g0107 a0001c0009t0019g0108 |
2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.175+2011A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62486244 | |||||||
| chr12:62486255 | T | TAAAAAAA others(317): Show |
1 | a0001c0002t0031g0136 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.175+2039_175+2040i others(326): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr12 | 62486255 | ||||||
| chr12:62486255 | T | TAAAAAAA others(323): Show |
3 | a0001c0005t0016g0114 a0001c0005t0016g0115 a0001c0005t0016g0116 |
3 | HG00735.hp2 HG01106.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.175+2039_175+2040i others(332): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr12 | 62486255 | ||||||
| chr12:62486255 | T | TAAAAAAA others(319): Show |
4 | a0001c0005t0003g0124 a0001c0005t0003g0125 a0001c0005t0003g0126 others(1): Show |
4 | HG01192.hp1 HG01346.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.175+2039_175+2040i others(328): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr12 | 62486255 | ||||||
| chr12:62486255 | T | TAAAAAAA others(320): Show |
7 | a0001c0005t0003g0109 a0001c0005t0003g0110 a0001c0005t0003g0121 others(4): Show |
7 | HG00738.hp2 HG01081.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.175+2039_175+2040i others(329): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr12 | 62486255 | ||||||
| chr12:62486255 | T | TAAAAAAA others(321): Show |
4 | a0001c0005t0003g0120 a0001c0005t0003g0128 a0001c0005t0003g0129 others(1): Show |
4 | HG01255.hp1 HG01256.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.175+2039_175+2040i others(330): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr12 | 62486255 | ||||||
| chr12:62486255 | T | TAAAAAAA others(322): Show |
6 | a0001c0005t0003g0118 a0001c0005t0003g0119 a0001c0005t0003g0131 others(3): Show |
6 | HG03669.hp1 NA18969.hp2 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.175+2039_175+2040i others(331): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr12 | 62486255 | ||||||
| chr12:62486255 | T | TAAAAAAA others(323): Show |
1 | a0001c0005t0003g0117 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.175+2039_175+2040i others(332): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr12 | 62486255 | ||||||
| chr12:62486482 | G | A | 12 | a0001c0006t0007g0009 a0001c0006t0007g0010 a0001c0006t0007g0011 others(9): Show |
12 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.175+2249G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62486482 | |||||||
| chr12:62486496 | C | G | 128 | a0001c0005t0003g0109 a0001c0005t0003g0110 a0001c0006t0003g0102 others(125): Show |
130 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.175+2263C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62486496 | |||||||
| chr12:62486651 | A | G | 3 | a0001c0003t0005g0086 a0001c0003t0005g0087 a0001c0003t0005g0101 |
3 | HG00597.hp2 HG00621.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.175+2418A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62486651 | |||||||
| chr12:62487306 | G | A | 1 | a0001c0006t0003g0106 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.175+3073G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62487306 | |||||||
| chr12:62487439 | C | T | 1 | a0001c0002t0031g0136 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.175+3206C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62487439 | |||||||
| chr12:62487440 | G | A | 2 | a0003c0004t0004g0265 a0003c0004t0004g0266 |
2 | NA18983.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.175+3207G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62487440 | |||||||
| chr12:62487547 | G | A | 1 | a0001c0003t0003g0035 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.175+3314G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62487547 | |||||||
| chr12:62487955 | T | A | 300 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0003g0135 others(297): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.175+3722T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62487955 | |||||||
| chr12:62487996 | G | T | 2 | a0001c0009t0019g0107 a0001c0009t0019g0108 |
2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.175+3763G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62487996 | |||||||
| chr12:62488202 | C | A | 1 | a0001c0006t0033g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.175+3969C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62488202 | |||||||
| chr12:62488202 | C | G | 18 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(15): Show |
18 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.175+3969C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62488202 | |||||||
| chr12:62488293 | A | G | 1 | a0001c0005t0003g0130 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.175+4060A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62488293 | |||||||
| chr12:62488485 | T | C | 1 | a0001c0002t0002g0298 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.175+4252T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62488485 | |||||||
| chr12:62488516 | T | C | 3 | a0001c0002t0002g0298 a0001c0002t0002g0322 a0001c0002t0002g0331 |
3 | NA18945.hp2 NA18988.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.175+4283T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62488516 | |||||||
| chr12:62488645 | A | G | 79 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(76): Show |
80 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.175+4412A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62488645 | |||||||
| chr12:62488741 | A | T | 122 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(119): Show |
123 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(120): Show |
intron_variant | MODIFIER | c.175+4508A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62488741 | |||||||
| chr12:62489009 | G | T | 1 | a0001c0006t0007g0015 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.175+4776G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62489009 | |||||||
| chr12:62489287 | T | C | 1 | a0001c0002t0003g0135 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.176-4628T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62489287 | |||||||
| chr12:62489336 | A | G | 1 | a0001c0002t0002g0317 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.176-4579A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62489336 | |||||||
| chr12:62489689 | A | C | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.176-4226A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62489689 | |||||||
| chr12:62489690 | A | G | 122 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(119): Show |
123 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(120): Show |
intron_variant | MODIFIER | c.176-4225A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62489690 | |||||||
| chr12:62489829 | C | T | 6 | a0001c0002t0014g0288 a0001c0002t0014g0289 a0001c0002t0014g0290 others(3): Show |
6 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.176-4086C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62489829 | |||||||
| chr12:62489864 | G | T | 1 | a0002c0001t0001g0182 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.176-4051G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62489864 | |||||||
| chr12:62489882 | T | C | 79 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(76): Show |
80 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.176-4033T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62489882 | |||||||
| chr12:62490145 | C | T | 4 | a0001c0003t0003g0035 a0001c0003t0003g0036 a0001c0003t0003g0099 others(1): Show |
4 | HG01361.hp2 HG02257.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.176-3770C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62490145 | |||||||
| chr12:62490210 | C | CT | 252 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0003g0135 others(249): Show |
255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.176-3704dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr12 | 62490210 | ||||||
| chr12:62490328 | G | GT | 7 | a0001c0002t0014g0288 a0001c0002t0014g0289 a0001c0002t0014g0290 others(4): Show |
7 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.176-3578dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr12 | 62490328 | ||||||
| chr12:62490329 | T | G | 1 | a0002c0001t0001g0150 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.176-3586T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62490329 | |||||||
| chr12:62490343 | G | T | 3 | a0001c0003t0005g0037 a0001c0003t0005g0038 a0001c0003t0005g0039 |
3 | HG02258.hp2 HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.176-3572G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62490343 | |||||||
| chr12:62490370 | A | C | 1 | a0002c0001t0001g0181 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.176-3545A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62490370 | |||||||
| chr12:62490406 | G | A | 79 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(76): Show |
80 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.176-3509G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62490406 | |||||||
| chr12:62490589 | G | A | 4 | a0001c0003t0003g0035 a0001c0003t0003g0036 a0001c0003t0003g0099 others(1): Show |
4 | HG01361.hp2 HG02257.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.176-3326G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62490589 | |||||||
| chr12:62490694 | A | G | 1 | a0001c0002t0002g0330 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.176-3221A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62490694 | |||||||
| chr12:62490731 | A | G | 1 | a0001c0018t0002g0299 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.176-3184A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62490731 | |||||||
| chr12:62490762 | T | C | 251 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(248): Show |
254 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.176-3153T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62490762 | |||||||
| chr12:62490772 | A | G | 251 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(248): Show |
254 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.176-3143A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62490772 | |||||||
| chr12:62490821 | A | C | 1 | a0001c0002t0003g0135 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.176-3094A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62490821 | |||||||
| chr12:62490852 | T | C | 252 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0003g0135 others(249): Show |
255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.176-3063T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62490852 | |||||||
| chr12:62490934 | ATTT | A | 129 | a0001c0005t0003g0109 a0001c0005t0003g0110 a0001c0006t0003g0102 others(126): Show |
131 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.176-2979_176-2977d others(5): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr12 | 62490934 | ||||||
| chr12:62491153 | G | A | 1 | a0002c0001t0029g0151 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.176-2762G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62491153 | |||||||
| chr12:62491192 | G | A | 128 | a0001c0005t0003g0109 a0001c0005t0003g0110 a0001c0006t0003g0102 others(125): Show |
130 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.176-2723G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62491192 | |||||||
| chr12:62491436 | A | C | 2 | a0002c0001t0001g0152 a0002c0001t0001g0183 |
2 | NA18612.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.176-2479A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62491436 | |||||||
| chr12:62491436 | A | T | 249 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(246): Show |
252 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.176-2479A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62491436 | |||||||
| chr12:62491537 | A | G | 1 | a0001c0018t0002g0299 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.176-2378A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62491537 | |||||||
| chr12:62491566 | C | A | 2 | a0002c0001t0001g0223 a0002c0001t0001g0224 |
2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.176-2349C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62491566 | |||||||
| chr12:62491672 | G | A | 1 | a0002c0001t0001g0221 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.176-2243G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62491672 | |||||||
| chr12:62491709 | C | T | 122 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(119): Show |
123 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(120): Show |
intron_variant | MODIFIER | c.176-2206C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62491709 | |||||||
| chr12:62492012 | A | G | 1 | a0002c0001t0001g0215 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.176-1903A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62492012 | |||||||
| chr12:62492101 | A | C | 1 | a0002c0001t0001g0230 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.176-1814A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62492101 | |||||||
| chr12:62492174 | C | T | 6 | a0001c0002t0014g0288 a0001c0002t0014g0289 a0001c0002t0014g0290 others(3): Show |
6 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.176-1741C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62492174 | |||||||
| chr12:62492221 | T | A | 129 | a0001c0005t0003g0109 a0001c0005t0003g0110 a0001c0006t0003g0102 others(126): Show |
131 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.176-1694T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62492221 | |||||||
| chr12:62492334 | C | T | 1 | a0002c0001t0001g0180 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.176-1581C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62492334 | |||||||
| chr12:62492343 | A | G | 24 | a0001c0002t0031g0136 a0001c0005t0003g0117 a0001c0005t0003g0118 others(21): Show |
24 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.176-1572A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62492343 | |||||||
| chr12:62492348 | T | G | 1 | a0001c0002t0013g0306 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.176-1567T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62492348 | |||||||
| chr12:62492362 | C | CT | 197 | a0001c0002t0002g0026 a0001c0002t0014g0288 a0001c0002t0014g0289 others(194): Show |
199 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.176-1533dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr12 | 62492362 | ||||||
| chr12:62492362 | C | CTA | 6 | a0001c0003t0008g0059 a0001c0003t0008g0060 a0001c0003t0008g0061 others(3): Show |
6 | NA18945.hp1 NA18955.hp2 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.176-1552_176-1551i others(4): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr12 | 62492362 | ||||||
| chr12:62492362 | C | CTT | 22 | a0001c0002t0002g0030 a0001c0002t0003g0135 a0001c0002t0010g0027 others(19): Show |
22 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.176-1534_176-1533d others(4): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr12 | 62492362 | ||||||
| chr12:62492399 | C | G | 1 | a0002c0001t0001g0219 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.176-1516C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62492399 | |||||||
| chr12:62492404 | G | A | 19 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(16): Show |
19 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.176-1511G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62492404 | |||||||
| chr12:62492404 | GC | G | 24 | a0001c0002t0031g0136 a0001c0005t0003g0117 a0001c0005t0003g0118 others(21): Show |
24 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.176-1508delC | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr12 | 62492404 | ||||||
| chr12:62492413 | G | A | 2 | a0001c0002t0002g0322 a0001c0002t0002g0331 |
2 | NA18945.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.176-1502G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62492413 | |||||||
| chr12:62492547 | A | G | 1 | a0002c0001t0001g0218 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.176-1368A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62492547 | |||||||
| chr12:62492592 | C | G | 129 | a0001c0005t0003g0109 a0001c0005t0003g0110 a0001c0006t0003g0102 others(126): Show |
131 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.176-1323C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62492592 | |||||||
| chr12:62492618 | G | T | 19 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(16): Show |
19 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.176-1297G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62492618 | |||||||
| chr12:62492632 | A | G | 1 | a0001c0003t0005g0081 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.176-1283A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62492632 | |||||||
| chr12:62492685 | T | C | 1 | a0001c0005t0003g0133 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.176-1230T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62492685 | |||||||
| chr12:62492701 | C | T | 1 | a0001c0005t0003g0127 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.176-1214C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62492701 | |||||||
| chr12:62492836 | G | A | 1 | a0001c0006t0033g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.176-1079G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62492836 | |||||||
| chr12:62492861 | C | T | 5 | a0001c0006t0003g0102 a0001c0006t0003g0103 a0001c0006t0003g0104 others(2): Show |
5 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.176-1054C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62492861 | |||||||
| chr12:62492869 | C | T | 129 | a0001c0005t0003g0109 a0001c0005t0003g0110 a0001c0006t0003g0102 others(126): Show |
131 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.176-1046C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62492869 | |||||||
| chr12:62492979 | G | A | 240 | a0001c0002t0031g0136 a0001c0003t0002g0055 a0001c0003t0002g0056 others(237): Show |
243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.176-936G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62492979 | |||||||
| chr12:62492999 | C | A | 1 | a0002c0001t0029g0151 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.176-916C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62492999 | |||||||
| chr12:62493038 | TACAC | T | 24 | a0001c0002t0031g0136 a0001c0005t0003g0117 a0001c0005t0003g0118 others(21): Show |
24 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.176-869_176-866del others(4): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr12 | 62493038 | ||||||
| chr12:62493043 | A | C | 1 | a0002c0001t0001g0214 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.176-872A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62493043 | |||||||
| chr12:62493047 | A | T | 1 | a0001c0003t0003g0035 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.176-868A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62493047 | |||||||
| chr12:62493149 | T | C | 1 | a0001c0002t0002g0357 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.176-766T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62493149 | |||||||
| chr12:62493227 | TGTGCATT others(10): Show |
T | 1 | a0001c0002t0011g0257 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.176-670_176-654del others(17): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr12 | 62493227 | ||||||
| chr12:62493489 | A | C | 2 | a0001c0003t0005g0058 a0001c0003t0005g0080 |
2 | HG00639.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.176-426A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62493489 | |||||||
| chr12:62493698 | A | C | 16 | a0003c0004t0004g0260 a0003c0004t0004g0264 a0003c0004t0004g0265 others(13): Show |
16 | HG00673.hp2 HG02523.hp1 NA18944.hp2 others(13): Show |
intron_variant | MODIFIER | c.176-217A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62493698 | |||||||
| chr12:62493828 | C | T | 64 | a0001c0003t0002g0055 a0001c0003t0002g0056 a0001c0003t0002g0057 others(61): Show |
65 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.176-87C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62493828 | |||||||
| chr12:62493865 | T | G | 12 | a0001c0006t0007g0009 a0001c0006t0007g0010 a0001c0006t0007g0011 others(9): Show |
12 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.176-50T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62493865 | |||||||
| chr12:62493905 | C | T | 1 | a0003c0004t0004g0273 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.176-10C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 2/34 | chr12 | 62493905 | |||||||
| chr12:62494158 | C | T | 6 | a0001c0002t0014g0288 a0001c0002t0014g0289 a0001c0002t0014g0290 others(3): Show |
6 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.303+116C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 3/34 | chr12 | 62494158 | |||||||
| chr12:62494282 | T | G | 2 | a0001c0009t0019g0107 a0001c0009t0019g0108 |
2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.303+240T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 3/34 | chr12 | 62494282 | |||||||
| chr12:62494353 | G | A | 292 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0003g0135 others(289): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.303+311G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 3/34 | chr12 | 62494353 | |||||||
| chr12:62494371 | TTATATGG others(4): Show |
T | 1 | a0002c0015t0024g0187 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.303+330_303+340del others(11): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 3/34 | chr12 | 62494371 | |||||||
| chr12:62494439 | A | C | 128 | a0001c0005t0003g0109 a0001c0005t0003g0110 a0001c0006t0003g0102 others(125): Show |
130 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.303+397A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 3/34 | chr12 | 62494439 | |||||||
| chr12:62494531 | G | A | 251 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(248): Show |
254 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.304-485G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 3/34 | chr12 | 62494531 | |||||||
| chr12:62494617 | G | T | 1 | a0001c0003t0041g0054 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.304-399G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 3/34 | chr12 | 62494617 | |||||||
| chr12:62494669 | A | T | 1 | a0005c0008t0002g0334 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.304-347A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 3/34 | chr12 | 62494669 | |||||||
| chr12:62494718 | A | G | 5 | a0001c0003t0003g0041 a0001c0003t0003g0042 a0001c0003t0003g0043 others(2): Show |
6 | HG01069.hp1 HG01071.hp1 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.304-298A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 3/34 | chr12 | 62494718 | |||||||
| chr12:62494862 | A | G | 251 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(248): Show |
254 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.304-154A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 3/34 | chr12 | 62494862 | |||||||
| chr12:62494867 | T | C | 24 | a0001c0002t0031g0136 a0001c0005t0003g0117 a0001c0005t0003g0118 others(21): Show |
24 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.304-149T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 3/34 | chr12 | 62494867 | |||||||
| chr12:62494878 | A | G | 1 | a0002c0001t0001g0217 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.304-138A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 3/34 | chr12 | 62494878 | |||||||
| chr12:62494949 | C | T | 251 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(248): Show |
254 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.304-67C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 3/34 | chr12 | 62494949 | |||||||
| chr12:62494961 | G | A | 1 | a0001c0002t0002g0321 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.304-55G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 3/34 | chr12 | 62494961 | |||||||
| chr12:62495260 | A | G | 1 | a0001c0002t0011g0302 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.435+113A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62495260 | |||||||
| chr12:62495290 | C | T | 19 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(16): Show |
19 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.435+143C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62495290 | |||||||
| chr12:62495439 | G | A | 1 | a0002c0001t0001g0236 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.435+292G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62495439 | |||||||
| chr12:62495607 | G | A | 1 | a0003c0004t0004g0274 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.435+460G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62495607 | |||||||
| chr12:62495622 | A | G | 126 | a0001c0005t0003g0109 a0001c0005t0003g0110 a0001c0006t0003g0102 others(123): Show |
128 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.435+475A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62495622 | |||||||
| chr12:62495629 | G | A | 126 | a0001c0005t0003g0109 a0001c0005t0003g0110 a0001c0006t0003g0102 others(123): Show |
128 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.435+482G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62495629 | |||||||
| chr12:62495689 | C | CA | 8 | a0001c0002t0002g0317 a0001c0002t0002g0318 a0001c0002t0002g0335 others(5): Show |
8 | HG00735.hp1 HG02015.hp2 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.435+568dupA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chr12 | 62495689 | ||||||
| chr12:62495689 | CA | C | 63 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0002g0329 others(60): Show |
63 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.435+568delA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chr12 | 62495689 | ||||||
| chr12:62495689 | CAA | C | 91 | a0001c0002t0031g0136 a0001c0003t0002g0055 a0001c0003t0002g0056 others(88): Show |
91 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.435+567_435+568del others(2): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chr12 | 62495689 | ||||||
| chr12:62495689 | CAAA | C | 10 | a0001c0003t0003g0035 a0001c0003t0003g0041 a0001c0003t0003g0042 others(7): Show |
11 | HG01069.hp1 HG01071.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.435+566_435+568del others(3): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chr12 | 62495689 | ||||||
| chr12:62495689 | CAAAAAAA others(6): Show |
C | 129 | a0001c0005t0003g0109 a0001c0005t0003g0110 a0001c0006t0003g0102 others(126): Show |
131 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.435+556_435+568del others(13): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chr12 | 62495689 | ||||||
| chr12:62495754 | C | T | 2 | a0002c0001t0001g0226 a0002c0001t0001g0229 |
2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.435+607C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62495754 | |||||||
| chr12:62495854 | A | G | 5 | a0001c0002t0002g0317 a0005c0008t0002g0334 a0005c0008t0002g0340 others(2): Show |
5 | HG02015.hp2 NA18966.hp1 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.435+707A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62495854 | |||||||
| chr12:62495961 | T | G | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.435+814T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62495961 | |||||||
| chr12:62495975 | T | G | 1 | a0001c0002t0002g0329 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.435+828T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62495975 | |||||||
| chr12:62496015 | A | G | 1 | a0001c0003t0002g0079 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.435+868A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62496015 | |||||||
| chr12:62496096 | T | C | 1 | a0002c0001t0001g0153 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.435+949T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62496096 | |||||||
| chr12:62496380 | T | C | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.435+1233T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62496380 | |||||||
| chr12:62496436 | G | C | 34 | a0001c0002t0022g0294 a0003c0004t0004g0258 a0003c0004t0004g0259 others(31): Show |
34 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.435+1289G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62496436 | |||||||
| chr12:62496495 | G | A | 1 | a0003c0004t0004g0272 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.435+1348G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62496495 | |||||||
| chr12:62496577 | T | C | 2 | a0001c0003t0002g0055 a0001c0003t0002g0088 |
2 | HG00544.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.435+1430T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62496577 | |||||||
| chr12:62496620 | A | G | 1 | a0001c0002t0017g0024 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.435+1473A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62496620 | |||||||
| chr12:62496711 | C | A | 126 | a0001c0005t0003g0109 a0001c0005t0003g0110 a0001c0006t0003g0102 others(123): Show |
128 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.435+1564C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62496711 | |||||||
| chr12:62496743 | G | C | 52 | a0001c0003t0002g0055 a0001c0003t0002g0056 a0001c0003t0002g0057 others(49): Show |
52 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.435+1596G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62496743 | |||||||
| chr12:62496823 | C | T | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.435+1676C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62496823 | |||||||
| chr12:62496959 | A | G | 1 | a0002c0001t0001g0229 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.435+1812A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62496959 | |||||||
| chr12:62497067 | A | G | 122 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(119): Show |
123 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(120): Show |
intron_variant | MODIFIER | c.436-1852A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62497067 | |||||||
| chr12:62497073 | C | T | 252 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(249): Show |
255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.436-1846C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62497073 | |||||||
| chr12:62497169 | A | AG | 14 | a0001c0002t0002g0303 a0001c0002t0002g0339 a0001c0002t0002g0353 others(11): Show |
14 | HG00423.hp1 HG01099.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.436-1744dupG | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chr12 | 62497169 | ||||||
| chr12:62497176 | A | G | 1 | a0002c0001t0001g0248 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.436-1743A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62497176 | |||||||
| chr12:62497281 | T | A | 1 | a0001c0002t0003g0135 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.436-1638T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62497281 | |||||||
| chr12:62497365 | G | A | 19 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(16): Show |
19 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.436-1554G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62497365 | |||||||
| chr12:62497413 | C | T | 5 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(2): Show |
5 | HG02976.hp1 HG03195.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.436-1506C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62497413 | |||||||
| chr12:62497549 | A | G | 24 | a0001c0002t0031g0136 a0001c0005t0003g0117 a0001c0005t0003g0118 others(21): Show |
24 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.436-1370A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62497549 | |||||||
| chr12:62497558 | A | T | 1 | a0001c0003t0002g0082 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.436-1361A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62497558 | |||||||
| chr12:62497626 | T | C | 79 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(76): Show |
80 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.436-1293T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62497626 | |||||||
| chr12:62497632 | T | G | 24 | a0001c0002t0031g0136 a0001c0005t0003g0117 a0001c0005t0003g0118 others(21): Show |
24 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.436-1287T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62497632 | |||||||
| chr12:62497638 | A | G | 7 | a0001c0002t0013g0306 a0001c0002t0013g0308 a0001c0002t0013g0309 others(4): Show |
7 | HG01074.hp1 HG01256.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.436-1281A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62497638 | |||||||
| chr12:62497819 | T | C | 1 | a0012c0012t0001g0154 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.436-1100T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62497819 | |||||||
| chr12:62498004 | C | G | 2 | a0001c0005t0003g0123 a0001c0005t0003g0126 |
2 | HG01081.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.436-915C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62498004 | |||||||
| chr12:62498048 | CT | C | 132 | a0001c0002t0045g0360 a0001c0005t0003g0109 a0001c0005t0003g0110 others(129): Show |
134 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.436-857delT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chr12 | 62498048 | ||||||
| chr12:62498325 | G | C | 59 | a0001c0003t0002g0055 a0001c0003t0002g0056 a0001c0003t0002g0057 others(56): Show |
59 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.436-594G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62498325 | |||||||
| chr12:62498330 | G | C | 1 | a0002c0001t0001g0238 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.436-589G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62498330 | |||||||
| chr12:62498332 | G | A | 12 | a0001c0006t0007g0009 a0001c0006t0007g0010 a0001c0006t0007g0011 others(9): Show |
12 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.436-587G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62498332 | |||||||
| chr12:62498377 | G | A | 2 | a0001c0005t0003g0109 a0001c0005t0003g0110 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.436-542G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62498377 | |||||||
| chr12:62498393 | T | C | 251 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(248): Show |
254 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.436-526T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62498393 | |||||||
| chr12:62498498 | C | G | 1 | a0005c0008t0002g0340 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.436-421C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62498498 | |||||||
| chr12:62498822 | T | C | 7 | a0001c0003t0005g0050 a0001c0003t0005g0051 a0001c0003t0005g0052 others(4): Show |
7 | NA18941.hp1 NA18946.hp2 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.436-97T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 4/34 | chr12 | 62498822 | |||||||
| chr12:62499079 | G | T | 1 | a0001c0003t0003g0035 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.565+31G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 5/34 | chr12 | 62499079 | |||||||
| chr12:62499125 | C | G | 251 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(248): Show |
254 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.565+77C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 5/34 | chr12 | 62499125 | |||||||
| chr12:62499190 | C | A | 3 | a0001c0002t0002g0298 a0001c0002t0002g0322 a0001c0002t0002g0331 |
3 | NA18945.hp2 NA18988.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.565+142C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 5/34 | chr12 | 62499190 | |||||||
| chr12:62499344 | G | A | 2 | a0001c0003t0003g0099 a0001c0003t0003g0100 |
2 | HG02615.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.565+296G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 5/34 | chr12 | 62499344 | |||||||
| chr12:62499387 | C | A | 5 | a0001c0006t0003g0102 a0001c0006t0003g0103 a0001c0006t0003g0104 others(2): Show |
5 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.565+339C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 5/34 | chr12 | 62499387 | |||||||
| chr12:62499419 | T | C | 24 | a0001c0002t0031g0136 a0001c0005t0003g0117 a0001c0005t0003g0118 others(21): Show |
24 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.565+371T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 5/34 | chr12 | 62499419 | |||||||
| chr12:62499472 | C | T | 3 | a0001c0002t0003g0135 a0001c0003t0003g0099 a0001c0003t0003g0100 |
3 | HG02615.hp2 HG02723.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.565+424C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 5/34 | chr12 | 62499472 | |||||||
| chr12:62499525 | C | T | 1 | a0002c0001t0001g0239 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.565+477C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 5/34 | chr12 | 62499525 | |||||||
| chr12:62499749 | T | A | 2 | a0001c0002t0013g0309 a0001c0002t0026g0310 |
2 | HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.565+701T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 5/34 | chr12 | 62499749 | |||||||
| chr12:62499884 | A | T | 5 | a0001c0002t0003g0135 a0001c0003t0005g0037 a0001c0003t0005g0038 others(2): Show |
5 | HG02258.hp2 HG02572.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.565+836A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 5/34 | chr12 | 62499884 | |||||||
| chr12:62499885 | T | A | 6 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(3): Show |
6 | HG02976.hp1 HG03195.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.565+837T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 5/34 | chr12 | 62499885 | |||||||
| chr12:62499893 | A | T | 300 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0002g0333 others(297): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.565+845A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 5/34 | chr12 | 62499893 | |||||||
| chr12:62500075 | C | T | 1 | a0001c0003t0050g0078 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.566-708C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 5/34 | chr12 | 62500075 | |||||||
| chr12:62500101 | T | A | 251 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(248): Show |
254 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.566-682T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 5/34 | chr12 | 62500101 | |||||||
| chr12:62500278 | A | G | 128 | a0001c0005t0003g0109 a0001c0005t0003g0110 a0001c0006t0003g0102 others(125): Show |
130 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.566-505A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 5/34 | chr12 | 62500278 | |||||||
| chr12:62500634 | C | T | 1 | a0001c0002t0035g0025 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.566-149C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 5/34 | chr12 | 62500634 | |||||||
| chr12:62500671 | A | C | 2 | a0001c0006t0003g0006 a0001c0006t0003g0007 |
2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.566-112A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 5/34 | chr12 | 62500671 | |||||||
| chr12:62500778 | T | C | 1 | a0001c0003t0008g0064 | 1 | NA19080.hp2 | splice_region_variant&intron_variant | LOW | c.566-5T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 5/34 | chr12 | 62500778 | |||||||
| chr12:62500917 | T | C | 2 | a0001c0003t0005g0046 a0001c0003t0005g0047 |
2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.663+37T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 6/34 | chr12 | 62500917 | |||||||
| chr12:62501000 | GTAT | G | 34 | a0001c0002t0022g0294 a0003c0004t0004g0258 a0003c0004t0004g0259 others(31): Show |
34 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.663+123_663+125del others(3): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 6/34 | INFO_REALIGN_3_PRIME | chr12 | 62501000 | ||||||
| chr12:62501145 | A | G | 1 | a0001c0003t0021g0001 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.663+265A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 6/34 | chr12 | 62501145 | |||||||
| chr12:62501294 | G | C | 24 | a0001c0002t0031g0136 a0001c0005t0003g0117 a0001c0005t0003g0118 others(21): Show |
24 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.664-279G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 6/34 | chr12 | 62501294 | |||||||
| chr12:62502189 | C | T | 32 | a0003c0004t0004g0258 a0003c0004t0004g0259 a0003c0004t0004g0260 others(29): Show |
32 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.789+491C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62502189 | |||||||
| chr12:62502240 | A | C | 1 | a0001c0006t0033g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.789+542A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62502240 | |||||||
| chr12:62502248 | T | A | 1 | a0002c0001t0001g0111 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.789+550T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62502248 | |||||||
| chr12:62502343 | C | T | 1 | a0002c0001t0006g0186 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.789+645C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62502343 | |||||||
| chr12:62502407 | T | TA | 32 | a0001c0002t0022g0294 a0003c0004t0004g0258 a0003c0004t0004g0259 others(29): Show |
32 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.789+723dupA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr12 | 62502407 | ||||||
| chr12:62502538 | A | C | 1 | a0001c0002t0003g0135 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.789+840A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62502538 | |||||||
| chr12:62503186 | G | A | 11 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(8): Show |
11 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+1488G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62503186 | |||||||
| chr12:62503294 | A | C | 1 | a0001c0002t0013g0312 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.789+1596A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62503294 | |||||||
| chr12:62503470 | G | A | 251 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(248): Show |
254 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.789+1772G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62503470 | |||||||
| chr12:62503488 | T | C | 251 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(248): Show |
254 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.789+1790T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62503488 | |||||||
| chr12:62503800 | G | A | 1 | a0001c0002t0002g0342 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.789+2102G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62503800 | |||||||
| chr12:62503957 | G | GAC | 35 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(32): Show |
35 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.789+2272_789+2273d others(4): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr12 | 62503957 | ||||||
| chr12:62504150 | G | A | 126 | a0001c0005t0003g0109 a0001c0005t0003g0110 a0001c0006t0003g0102 others(123): Show |
128 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.789+2452G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62504150 | |||||||
| chr12:62504216 | C | T | 250 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(247): Show |
253 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.789+2518C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62504216 | |||||||
| chr12:62504245 | C | CT | 100 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0002g0359 others(97): Show |
101 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.789+2564dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr12 | 62504245 | ||||||
| chr12:62504245 | CT | C | 119 | a0001c0005t0003g0109 a0001c0005t0003g0110 a0001c0006t0003g0102 others(116): Show |
121 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.789+2564delT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr12 | 62504245 | ||||||
| chr12:62504303 | C | T | 2 | a0001c0002t0047g0301 a0001c0020t0038g0305 |
2 | HG01167.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.789+2605C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62504303 | |||||||
| chr12:62504331 | G | A | 129 | a0001c0005t0003g0109 a0001c0005t0003g0110 a0001c0006t0003g0102 others(126): Show |
131 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.789+2633G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62504331 | |||||||
| chr12:62504537 | G | A | 1 | a0001c0002t0010g0027 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.789+2839G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62504537 | |||||||
| chr12:62504683 | C | CT | 126 | a0001c0005t0003g0109 a0001c0005t0003g0110 a0001c0006t0003g0102 others(123): Show |
128 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.789+2992dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr12 | 62504683 | ||||||
| chr12:62504710 | C | T | 126 | a0001c0005t0003g0109 a0001c0005t0003g0110 a0001c0006t0003g0102 others(123): Show |
128 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.789+3012C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62504710 | |||||||
| chr12:62505328 | T | C | 1 | a0004c0007t0046g0326 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.790-2958T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62505328 | |||||||
| chr12:62505433 | G | A | 1 | a0001c0006t0003g0008 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.790-2853G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62505433 | |||||||
| chr12:62505725 | T | TA | 52 | a0001c0002t0022g0294 a0001c0006t0003g0005 a0001c0006t0003g0006 others(49): Show |
52 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.790-2547dupA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr12 | 62505725 | ||||||
| chr12:62505726 | A | T | 1 | a0001c0005t0003g0119 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.790-2560A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62505726 | |||||||
| chr12:62505769 | G | T | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.790-2517G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62505769 | |||||||
| chr12:62505977 | G | A | 24 | a0001c0002t0031g0136 a0001c0005t0003g0117 a0001c0005t0003g0118 others(21): Show |
24 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.790-2309G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62505977 | |||||||
| chr12:62506003 | G | C | 1 | a0001c0003t0005g0091 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.790-2283G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62506003 | |||||||
| chr12:62506515 | A | T | 1 | a0001c0002t0011g0255 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.790-1771A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62506515 | |||||||
| chr12:62506725 | C | CA | 244 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0002g0353 others(241): Show |
247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.790-1548dupA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr12 | 62506725 | ||||||
| chr12:62506748 | A | T | 1 | a0002c0001t0001g0185 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.790-1538A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62506748 | |||||||
| chr12:62506823 | T | C | 5 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(2): Show |
5 | HG02976.hp1 HG03195.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.790-1463T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62506823 | |||||||
| chr12:62506968 | A | C | 1 | a0005c0008t0002g0334 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.790-1318A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62506968 | |||||||
| chr12:62507016 | A | G | 1 | a0001c0002t0003g0135 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.790-1270A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62507016 | |||||||
| chr12:62507069 | T | C | 1 | a0002c0001t0006g0204 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.790-1217T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62507069 | |||||||
| chr12:62507259 | A | G | 1 | a0001c0003t0041g0054 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.790-1027A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62507259 | |||||||
| chr12:62507315 | C | CT | 26 | a0001c0002t0002g0353 a0001c0002t0031g0136 a0001c0003t0002g0094 others(23): Show |
26 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.790-959dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chr12 | 62507315 | ||||||
| chr12:62507372 | G | A | 240 | a0001c0002t0031g0136 a0001c0003t0002g0055 a0001c0003t0002g0056 others(237): Show |
243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.790-914G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62507372 | |||||||
| chr12:62507754 | T | C | 11 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(8): Show |
11 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.790-532T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62507754 | |||||||
| chr12:62507901 | T | G | 1 | a0001c0002t0011g0257 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.790-385T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62507901 | |||||||
| chr12:62508055 | G | A | 1 | a0001c0020t0038g0305 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.790-231G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62508055 | |||||||
| chr12:62508117 | C | A | 1 | a0001c0003t0005g0089 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.790-169C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 7/34 | chr12 | 62508117 | |||||||
| chr12:62508640 | C | T | 128 | a0001c0005t0003g0109 a0001c0005t0003g0110 a0001c0006t0003g0102 others(125): Show |
130 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.984+160C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62508640 | |||||||
| chr12:62508643 | T | C | 1 | a0001c0003t0005g0034 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.984+163T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62508643 | |||||||
| chr12:62508770 | T | C | 24 | a0001c0002t0031g0136 a0001c0005t0003g0117 a0001c0005t0003g0118 others(21): Show |
24 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.984+290T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62508770 | |||||||
| chr12:62508858 | C | T | 1 | a0001c0005t0003g0125 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.984+378C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62508858 | |||||||
| chr12:62509053 | A | G | 240 | a0001c0002t0031g0136 a0001c0003t0002g0055 a0001c0003t0002g0056 others(237): Show |
243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.984+573A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62509053 | |||||||
| chr12:62509095 | C | T | 45 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(42): Show |
45 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.984+615C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62509095 | |||||||
| chr12:62509116 | C | CT | 13 | a0001c0002t0002g0359 a0001c0002t0014g0288 a0001c0002t0014g0289 others(10): Show |
13 | HG00099.hp2 HG00642.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.984+652dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | INFO_REALIGN_3_PRIME | chr12 | 62509116 | ||||||
| chr12:62509116 | CT | C | 7 | a0001c0002t0039g0311 a0001c0003t0023g0066 a0002c0001t0001g0180 others(4): Show |
7 | HG00323.hp1 HG02717.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.984+652delT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | INFO_REALIGN_3_PRIME | chr12 | 62509116 | ||||||
| chr12:62509184 | G | A | 1 | a0001c0002t0022g0294 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.984+704G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62509184 | |||||||
| chr12:62509368 | A | G | 2 | a0001c0009t0019g0107 a0001c0009t0019g0108 |
2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.984+888A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62509368 | |||||||
| chr12:62509515 | A | T | 68 | a0001c0003t0002g0055 a0001c0003t0002g0056 a0001c0003t0002g0057 others(65): Show |
69 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.984+1035A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62509515 | |||||||
| chr12:62509638 | T | C | 59 | a0001c0003t0002g0055 a0001c0003t0002g0056 a0001c0003t0002g0057 others(56): Show |
59 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.984+1158T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62509638 | |||||||
| chr12:62509736 | G | T | 2 | a0001c0009t0019g0107 a0001c0009t0019g0108 |
2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.984+1256G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62509736 | |||||||
| chr12:62509859 | A | G | 128 | a0001c0005t0003g0109 a0001c0005t0003g0110 a0001c0006t0003g0102 others(125): Show |
130 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.984+1379A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62509859 | |||||||
| chr12:62509875 | G | GT | 129 | a0001c0005t0003g0109 a0001c0005t0003g0110 a0001c0005t0043g0112 others(126): Show |
131 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.984+1405dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | INFO_REALIGN_3_PRIME | chr12 | 62509875 | ||||||
| chr12:62510013 | A | G | 128 | a0001c0005t0003g0109 a0001c0005t0003g0110 a0001c0006t0003g0102 others(125): Show |
130 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.984+1533A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62510013 | |||||||
| chr12:62510207 | C | T | 4 | a0001c0003t0003g0035 a0001c0003t0003g0036 a0001c0003t0003g0099 others(1): Show |
4 | HG01361.hp2 HG02257.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.984+1727C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62510207 | |||||||
| chr12:62510472 | C | T | 129 | a0001c0005t0003g0109 a0001c0005t0003g0110 a0001c0006t0003g0102 others(126): Show |
131 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.984+1992C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62510472 | |||||||
| chr12:62510492 | A | G | 2 | a0001c0002t0002g0363 a0001c0002t0005g0362 |
2 | HG01255.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.984+2012A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62510492 | |||||||
| chr12:62510499 | A | G | 5 | a0001c0006t0003g0102 a0001c0006t0003g0103 a0001c0006t0003g0104 others(2): Show |
5 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.984+2019A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62510499 | |||||||
| chr12:62510524 | A | G | 45 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(42): Show |
45 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.984+2044A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62510524 | |||||||
| chr12:62510635 | T | C | 68 | a0001c0003t0002g0055 a0001c0003t0002g0056 a0001c0003t0002g0057 others(65): Show |
69 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.984+2155T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62510635 | |||||||
| chr12:62510640 | C | G | 1 | a0001c0002t0002g0298 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.984+2160C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62510640 | |||||||
| chr12:62510737 | C | T | 2 | a0001c0003t0005g0034 a0001c0003t0005g0040 |
2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.984+2257C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62510737 | |||||||
| chr12:62510852 | T | C | 5 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(2): Show |
5 | HG02976.hp1 HG03195.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.984+2372T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62510852 | |||||||
| chr12:62510926 | T | G | 1 | a0001c0002t0002g0330 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.984+2446T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62510926 | |||||||
| chr12:62511116 | A | G | 1 | a0001c0002t0003g0135 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.984+2636A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62511116 | |||||||
| chr12:62511192 | C | A | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.984+2712C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62511192 | |||||||
| chr12:62511287 | C | T | 1 | a0001c0003t0021g0001 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.984+2807C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62511287 | |||||||
| chr12:62511545 | A | G | 59 | a0001c0003t0002g0055 a0001c0003t0002g0056 a0001c0003t0002g0057 others(56): Show |
59 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.984+3065A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62511545 | |||||||
| chr12:62511600 | CA | C | 126 | a0001c0005t0003g0109 a0001c0005t0003g0110 a0001c0006t0003g0102 others(123): Show |
128 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.984+3126delA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | INFO_REALIGN_3_PRIME | chr12 | 62511600 | ||||||
| chr12:62511719 | G | A | 240 | a0001c0002t0031g0136 a0001c0003t0002g0055 a0001c0003t0002g0056 others(237): Show |
243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.984+3239G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62511719 | |||||||
| chr12:62511727 | A | G | 1 | a0001c0003t0002g0055 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.984+3247A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62511727 | |||||||
| chr12:62511909 | T | C | 3 | a0002c0001t0001g0152 a0002c0001t0001g0179 a0002c0001t0001g0183 |
3 | HG02135.hp1 NA18612.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.984+3429T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62511909 | |||||||
| chr12:62511943 | G | A | 34 | a0001c0002t0022g0294 a0003c0004t0004g0258 a0003c0004t0004g0259 others(31): Show |
34 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.984+3463G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62511943 | |||||||
| chr12:62511992 | A | AC | 128 | a0001c0005t0003g0109 a0001c0005t0003g0110 a0001c0006t0003g0102 others(125): Show |
130 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.984+3518dupC | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | INFO_REALIGN_3_PRIME | chr12 | 62511992 | ||||||
| chr12:62512048 | G | A | 7 | a0002c0001t0001g0148 a0002c0001t0001g0155 a0002c0001t0001g0180 others(4): Show |
7 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(4): Show |
intron_variant | MODIFIER | c.984+3568G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62512048 | |||||||
| chr12:62512102 | C | T | 19 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(16): Show |
19 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.984+3622C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62512102 | |||||||
| chr12:62512139 | C | T | 1 | a0002c0001t0001g0137 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.984+3659C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62512139 | |||||||
| chr12:62512538 | T | C | 7 | a0001c0003t0005g0050 a0001c0003t0005g0051 a0001c0003t0005g0052 others(4): Show |
7 | NA18941.hp1 NA18946.hp2 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.984+4058T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62512538 | |||||||
| chr12:62512677 | C | T | 2 | a0002c0001t0001g0226 a0002c0001t0001g0229 |
2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.984+4197C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62512677 | |||||||
| chr12:62512708 | G | A | 128 | a0001c0005t0003g0109 a0001c0005t0003g0110 a0001c0006t0003g0102 others(125): Show |
130 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.984+4228G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62512708 | |||||||
| chr12:62512782 | C | T | 3 | a0002c0001t0001g0226 a0002c0001t0001g0229 a0002c0001t0001g0230 |
3 | HG02559.hp2 HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.984+4302C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62512782 | |||||||
| chr12:62512851 | T | A | 1 | a0003c0004t0004g0293 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.984+4371T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62512851 | |||||||
| chr12:62513071 | G | A | 19 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(16): Show |
19 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.984+4591G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62513071 | |||||||
| chr12:62513185 | C | G | 24 | a0001c0002t0031g0136 a0001c0005t0003g0117 a0001c0005t0003g0118 others(21): Show |
24 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.984+4705C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62513185 | |||||||
| chr12:62513267 | C | T | 1 | a0002c0001t0001g0175 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.984+4787C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62513267 | |||||||
| chr12:62513312 | G | A | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.984+4832G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62513312 | |||||||
| chr12:62513328 | T | C | 4 | a0001c0003t0003g0035 a0001c0003t0003g0036 a0001c0003t0003g0099 others(1): Show |
4 | HG01361.hp2 HG02257.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.984+4848T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62513328 | |||||||
| chr12:62513371 | G | A | 68 | a0001c0003t0002g0055 a0001c0003t0002g0056 a0001c0003t0002g0057 others(65): Show |
69 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.984+4891G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62513371 | |||||||
| chr12:62513386 | C | T | 19 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(16): Show |
19 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.984+4906C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62513386 | |||||||
| chr12:62513422 | C | T | 152 | a0001c0002t0031g0136 a0001c0005t0003g0109 a0001c0005t0003g0110 others(149): Show |
154 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.984+4942C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62513422 | |||||||
| chr12:62513518 | G | A | 34 | a0001c0002t0022g0294 a0003c0004t0004g0258 a0003c0004t0004g0259 others(31): Show |
34 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.984+5038G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62513518 | |||||||
| chr12:62513692 | ATCCCAGC others(388): Show |
A | 54 | a0002c0001t0001g0002 a0002c0001t0001g0111 a0002c0001t0001g0143 others(51): Show |
55 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.984+5215_984+5609d others(2): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | INFO_REALIGN_3_PRIME | chr12 | 62513692 | ||||||
| chr12:62513752 | G | A | 1 | a0001c0002t0031g0136 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.984+5272G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62513752 | |||||||
| chr12:62513842 | G | C | 186 | a0001c0002t0031g0136 a0001c0003t0002g0055 a0001c0003t0002g0056 others(183): Show |
188 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.984+5362G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62513842 | |||||||
| chr12:62513888 | T | C | 24 | a0001c0002t0031g0136 a0001c0005t0003g0117 a0001c0005t0003g0118 others(21): Show |
24 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.984+5408T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62513888 | |||||||
| chr12:62513892 | A | G | 68 | a0001c0003t0002g0055 a0001c0003t0002g0056 a0001c0003t0002g0057 others(65): Show |
69 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.984+5412A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62513892 | |||||||
| chr12:62513898 | C | T | 68 | a0001c0003t0002g0055 a0001c0003t0002g0056 a0001c0003t0002g0057 others(65): Show |
69 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.984+5418C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62513898 | |||||||
| chr12:62513936 | C | T | 2 | a0001c0005t0003g0109 a0001c0005t0003g0110 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.984+5456C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62513936 | |||||||
| chr12:62513937 | G | A | 1 | a0001c0002t0003g0135 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.984+5457G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62513937 | |||||||
| chr12:62513945 | A | G | 2 | a0001c0003t0002g0073 a0001c0003t0002g0079 |
2 | NA18957.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.984+5465A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62513945 | |||||||
| chr12:62513957 | A | G | 1 | a0003c0004t0004g0279 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.984+5477A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62513957 | |||||||
| chr12:62514012 | C | T | 5 | a0001c0003t0003g0041 a0001c0003t0003g0042 a0001c0003t0003g0043 others(2): Show |
6 | HG01069.hp1 HG01071.hp1 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.984+5532C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62514012 | |||||||
| chr12:62514131 | A | G | 75 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(72): Show |
76 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.984+5651A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62514131 | |||||||
| chr12:62514284 | G | A | 1 | a0001c0005t0003g0132 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.984+5804G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62514284 | |||||||
| chr12:62514540 | C | T | 1 | a0001c0002t0002g0254 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.984+6060C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62514540 | |||||||
| chr12:62514543 | T | C | 2 | a0001c0009t0019g0107 a0001c0009t0019g0108 |
2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.984+6063T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62514543 | |||||||
| chr12:62514609 | A | G | 1 | a0001c0006t0033g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.984+6129A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62514609 | |||||||
| chr12:62514643 | G | A | 1 | a0002c0001t0001g0178 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.984+6163G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62514643 | |||||||
| chr12:62514702 | G | T | 6 | a0001c0002t0014g0288 a0001c0002t0014g0289 a0001c0002t0014g0290 others(3): Show |
6 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.984+6222G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62514702 | |||||||
| chr12:62514927 | A | G | 1 | a0001c0002t0010g0027 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.984+6447A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62514927 | |||||||
| chr12:62515003 | G | A | 1 | a0001c0002t0003g0135 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.984+6523G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62515003 | |||||||
| chr12:62515016 | G | T | 1 | a0001c0018t0002g0299 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.984+6536G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62515016 | |||||||
| chr12:62515314 | G | A | 68 | a0001c0003t0002g0055 a0001c0003t0002g0056 a0001c0003t0002g0057 others(65): Show |
69 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.984+6834G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62515314 | |||||||
| chr12:62515399 | T | C | 45 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(42): Show |
45 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.984+6919T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62515399 | |||||||
| chr12:62515684 | G | A | 2 | a0001c0009t0019g0107 a0001c0009t0019g0108 |
2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.984+7204G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62515684 | |||||||
| chr12:62515750 | C | T | 1 | a0001c0006t0033g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.984+7270C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62515750 | |||||||
| chr12:62515810 | C | T | 111 | a0001c0002t0031g0136 a0001c0003t0002g0055 a0001c0003t0002g0056 others(108): Show |
112 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.984+7330C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62515810 | |||||||
| chr12:62515977 | T | A | 5 | a0001c0002t0013g0306 a0001c0002t0013g0308 a0001c0002t0013g0312 others(2): Show |
5 | HG01074.hp1 HG01256.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.984+7497T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62515977 | |||||||
| chr12:62516066 | A | G | 292 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0003g0135 others(289): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.984+7586A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62516066 | |||||||
| chr12:62516635 | C | T | 1 | a0001c0002t0002g0335 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.985-7880C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62516635 | |||||||
| chr12:62516934 | A | T | 126 | a0001c0005t0003g0109 a0001c0005t0003g0110 a0001c0006t0003g0102 others(123): Show |
128 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.985-7581A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62516934 | |||||||
| chr12:62517052 | C | A | 5 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(2): Show |
5 | HG02976.hp1 HG03195.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.985-7463C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62517052 | |||||||
| chr12:62517069 | G | A | 6 | a0001c0002t0014g0288 a0001c0002t0014g0289 a0001c0002t0014g0290 others(3): Show |
6 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.985-7446G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62517069 | |||||||
| chr12:62517385 | T | C | 1 | a0001c0003t0005g0067 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.985-7130T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62517385 | |||||||
| chr12:62517717 | G | A | 11 | a0001c0002t0002g0318 a0001c0002t0002g0323 a0001c0002t0015g0314 others(8): Show |
11 | HG00423.hp2 HG02027.hp1 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.985-6798G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62517717 | |||||||
| chr12:62518050 | A | T | 2 | a0001c0003t0005g0034 a0001c0003t0005g0040 |
2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.985-6465A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62518050 | |||||||
| chr12:62518204 | A | G | 1 | a0001c0003t0002g0077 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.985-6311A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62518204 | |||||||
| chr12:62518279 | G | A | 241 | a0001c0002t0003g0135 a0001c0002t0031g0136 a0001c0003t0002g0055 others(238): Show |
244 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.985-6236G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62518279 | |||||||
| chr12:62518346 | T | A | 68 | a0001c0003t0002g0055 a0001c0003t0002g0056 a0001c0003t0002g0057 others(65): Show |
69 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.985-6169T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62518346 | |||||||
| chr12:62518471 | C | T | 4 | a0001c0005t0003g0128 a0001c0005t0003g0129 a0001c0005t0003g0130 others(1): Show |
4 | HG01109.hp1 HG01256.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.985-6044C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62518471 | |||||||
| chr12:62518485 | T | C | 19 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(16): Show |
19 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.985-6030T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62518485 | |||||||
| chr12:62518514 | T | C | 1 | a0001c0005t0043g0112 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.985-6001T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62518514 | |||||||
| chr12:62518586 | A | G | 3 | a0002c0001t0001g0210 a0002c0001t0001g0235 a0002c0001t0012g0211 |
3 | HG03669.hp2 HG03927.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.985-5929A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62518586 | |||||||
| chr12:62518775 | C | T | 5 | a0001c0003t0003g0041 a0001c0003t0003g0042 a0001c0003t0003g0043 others(2): Show |
6 | HG01069.hp1 HG01071.hp1 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.985-5740C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62518775 | |||||||
| chr12:62518951 | A | C | 2 | a0001c0002t0013g0309 a0001c0002t0026g0310 |
2 | HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.985-5564A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62518951 | |||||||
| chr12:62519009 | C | T | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.985-5506C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62519009 | |||||||
| chr12:62519293 | C | T | 1 | a0001c0002t0003g0135 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.985-5222C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62519293 | |||||||
| chr12:62519295 | C | A | 1 | a0001c0002t0002g0304 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.985-5220C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62519295 | |||||||
| chr12:62519308 | A | C | 2 | a0001c0002t0002g0338 a0001c0002t0002g0353 |
2 | NA18944.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.985-5207A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62519308 | |||||||
| chr12:62519680 | T | C | 2 | a0001c0009t0019g0107 a0001c0009t0019g0108 |
2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.985-4835T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62519680 | |||||||
| chr12:62519871 | C | T | 1 | a0001c0002t0011g0255 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.985-4644C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62519871 | |||||||
| chr12:62519917 | G | A | 11 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(8): Show |
11 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.985-4598G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62519917 | |||||||
| chr12:62519960 | C | T | 2 | a0001c0002t0031g0136 a0002c0001t0006g0200 |
2 | HG03225.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.985-4555C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62519960 | |||||||
| chr12:62519981 | A | G | 1 | a0001c0005t0043g0112 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.985-4534A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62519981 | |||||||
| chr12:62520106 | A | G | 1 | a0001c0006t0003g0008 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.985-4409A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62520106 | |||||||
| chr12:62520138 | C | G | 1 | a0003c0004t0004g0365 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.985-4377C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62520138 | |||||||
| chr12:62520285 | A | G | 4 | a0002c0001t0001g0226 a0002c0001t0001g0229 a0002c0001t0001g0230 others(1): Show |
4 | HG02559.hp2 HG02622.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.985-4230A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62520285 | |||||||
| chr12:62520420 | A | G | 1 | a0002c0001t0001g0174 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.985-4095A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62520420 | |||||||
| chr12:62520429 | C | A | 20 | a0003c0004t0004g0260 a0003c0004t0004g0261 a0003c0004t0004g0264 others(17): Show |
20 | HG00673.hp2 HG02523.hp1 HG04228.hp2 others(17): Show |
intron_variant | MODIFIER | c.985-4086C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62520429 | |||||||
| chr12:62520430 | G | A | 1 | a0001c0002t0003g0135 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.985-4085G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62520430 | |||||||
| chr12:62520433 | C | CTTTG | 251 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(248): Show |
254 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.985-4079_985-4078i others(6): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | INFO_REALIGN_3_PRIME | chr12 | 62520433 | ||||||
| chr12:62520507 | G | T | 240 | a0001c0002t0031g0136 a0001c0003t0002g0055 a0001c0003t0002g0056 others(237): Show |
243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.985-4008G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62520507 | |||||||
| chr12:62520552 | T | A | 1 | a0002c0001t0001g0156 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.985-3963T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62520552 | |||||||
| chr12:62520593 | A | G | 56 | a0001c0002t0002g0254 a0001c0002t0002g0256 a0001c0002t0002g0298 others(53): Show |
56 | HG00423.hp2 HG00438.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.985-3922A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62520593 | |||||||
| chr12:62520905 | CA | C | 82 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0002g0353 others(79): Show |
83 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.985-3599delA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | INFO_REALIGN_3_PRIME | chr12 | 62520905 | ||||||
| chr12:62520968 | T | C | 52 | a0001c0003t0002g0055 a0001c0003t0002g0056 a0001c0003t0002g0057 others(49): Show |
52 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.985-3547T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62520968 | |||||||
| chr12:62520996 | TA | T | 121 | a0001c0009t0019g0107 a0001c0009t0019g0108 a0002c0001t0001g0002 others(118): Show |
123 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.985-3509delA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | INFO_REALIGN_3_PRIME | chr12 | 62520996 | ||||||
| chr12:62520997 | A | T | 5 | a0001c0002t0002g0333 a0001c0002t0013g0309 a0001c0002t0026g0310 others(2): Show |
5 | HG03486.hp1 NA18951.hp1 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.985-3518A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62520997 | |||||||
| chr12:62521056 | A | G | 26 | a0001c0002t0031g0136 a0001c0005t0003g0109 a0001c0005t0003g0110 others(23): Show |
26 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.985-3459A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62521056 | |||||||
| chr12:62521069 | G | T | 1 | a0001c0003t0002g0082 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.985-3446G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62521069 | |||||||
| chr12:62521177 | A | T | 1 | a0001c0003t0002g0082 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.985-3338A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62521177 | |||||||
| chr12:62521239 | C | T | 42 | a0002c0001t0001g0137 a0002c0001t0001g0206 a0002c0001t0001g0207 others(39): Show |
42 | HG00423.hp1 HG00438.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.985-3276C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62521239 | |||||||
| chr12:62521309 | C | T | 1 | a0001c0003t0003g0035 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.985-3206C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62521309 | |||||||
| chr12:62521501 | C | T | 1 | a0002c0001t0006g0232 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.985-3014C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62521501 | |||||||
| chr12:62521971 | T | A | 1 | a0001c0006t0034g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.985-2544T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62521971 | |||||||
| chr12:62522091 | G | A | 1 | a0001c0003t0003g0041 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.985-2424G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62522091 | |||||||
| chr12:62522093 | ACAAGAAT others(9): Show |
A | 24 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(21): Show |
24 | HG01099.hp1 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.985-2420_985-2405d others(18): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | INFO_REALIGN_3_PRIME | chr12 | 62522093 | ||||||
| chr12:62522274 | G | A | 1 | a0002c0001t0025g0189 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.985-2241G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62522274 | |||||||
| chr12:62522279 | A | T | 1 | a0001c0002t0002g0352 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.985-2236A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62522279 | |||||||
| chr12:62522364 | G | T | 240 | a0001c0002t0031g0136 a0001c0003t0002g0055 a0001c0003t0002g0056 others(237): Show |
243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.985-2151G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62522364 | |||||||
| chr12:62522386 | C | T | 3 | a0001c0003t0005g0086 a0001c0003t0005g0087 a0001c0003t0005g0101 |
3 | HG00597.hp2 HG00621.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.985-2129C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62522386 | |||||||
| chr12:62522521 | A | T | 1 | a0001c0003t0008g0061 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.985-1994A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62522521 | |||||||
| chr12:62522650 | T | C | 299 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0003g0135 others(296): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.985-1865T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62522650 | |||||||
| chr12:62522750 | G | A | 1 | a0001c0002t0002g0304 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.985-1765G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62522750 | |||||||
| chr12:62522770 | A | G | 45 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(42): Show |
45 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.985-1745A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62522770 | |||||||
| chr12:62522774 | C | G | 1 | a0002c0001t0001g0238 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.985-1741C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62522774 | |||||||
| chr12:62522966 | G | A | 8 | a0001c0006t0007g0009 a0001c0006t0007g0010 a0001c0006t0007g0011 others(5): Show |
8 | HG01891.hp2 HG02572.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.985-1549G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62522966 | |||||||
| chr12:62522999 | C | T | 11 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(8): Show |
11 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.985-1516C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62522999 | |||||||
| chr12:62523035 | A | G | 12 | a0001c0006t0007g0009 a0001c0006t0007g0010 a0001c0006t0007g0011 others(9): Show |
12 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.985-1480A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62523035 | |||||||
| chr12:62523051 | C | A | 1 | a0001c0002t0031g0136 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.985-1464C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62523051 | |||||||
| chr12:62523086 | A | G | 6 | a0001c0002t0014g0288 a0001c0002t0014g0289 a0001c0002t0014g0290 others(3): Show |
6 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.985-1429A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62523086 | |||||||
| chr12:62523260 | C | A | 4 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(1): Show |
4 | HG02976.hp1 HG03195.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.985-1255C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62523260 | |||||||
| chr12:62523563 | T | A | 1 | a0001c0002t0010g0031 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.985-952T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62523563 | |||||||
| chr12:62523851 | T | A | 118 | a0001c0002t0031g0136 a0001c0003t0002g0055 a0001c0003t0002g0056 others(115): Show |
119 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(116): Show |
intron_variant | MODIFIER | c.985-664T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62523851 | |||||||
| chr12:62523924 | A | G | 119 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0111 others(116): Show |
121 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.985-591A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62523924 | |||||||
| chr12:62524058 | A | G | 45 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(42): Show |
45 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.985-457A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62524058 | |||||||
| chr12:62524390 | G | C | 45 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(42): Show |
45 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.985-125G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 8/34 | chr12 | 62524390 | |||||||
| chr12:62524725 | C | T | 1 | a0002c0001t0012g0220 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1109+86C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 9/34 | chr12 | 62524725 | |||||||
| chr12:62524768 | A | G | 1 | a0001c0002t0002g0303 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1109+129A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 9/34 | chr12 | 62524768 | |||||||
| chr12:62525000 | A | G | 26 | a0001c0002t0031g0136 a0001c0005t0003g0109 a0001c0005t0003g0110 others(23): Show |
26 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.1110-84A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 9/34 | chr12 | 62525000 | |||||||
| chr12:62525260 | G | A | 1 | a0001c0006t0034g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1246+40G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 10/34 | chr12 | 62525260 | |||||||
| chr12:62525504 | A | C | 1 | a0002c0001t0001g0155 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1246+284A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 10/34 | chr12 | 62525504 | |||||||
| chr12:62525575 | GTCA | G | 299 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0003g0135 others(296): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1246+357_1246+359d others(5): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 10/34 | INFO_REALIGN_3_PRIME | chr12 | 62525575 | ||||||
| chr12:62525579 | T | C | 1 | a0001c0002t0002g0341 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1246+359T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 10/34 | chr12 | 62525579 | |||||||
| chr12:62525663 | T | C | 68 | a0001c0003t0002g0055 a0001c0003t0002g0056 a0001c0003t0002g0057 others(65): Show |
69 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.1247-286T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 10/34 | chr12 | 62525663 | |||||||
| chr12:62525673 | C | T | 68 | a0001c0003t0002g0055 a0001c0003t0002g0056 a0001c0003t0002g0057 others(65): Show |
69 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.1247-276C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 10/34 | chr12 | 62525673 | |||||||
| chr12:62525717 | C | T | 241 | a0001c0002t0003g0135 a0001c0002t0031g0136 a0001c0003t0002g0055 others(238): Show |
244 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.1247-232C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 10/34 | chr12 | 62525717 | |||||||
| chr12:62526154 | T | C | 1 | a0003c0004t0004g0272 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1400+52T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62526154 | |||||||
| chr12:62526328 | C | A | 24 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(21): Show |
24 | HG01099.hp1 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.1400+226C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62526328 | |||||||
| chr12:62526853 | A | G | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1400+751A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62526853 | |||||||
| chr12:62526987 | A | T | 252 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0003g0135 others(249): Show |
255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.1400+885A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62526987 | |||||||
| chr12:62527018 | C | T | 1 | a0001c0006t0033g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1400+916C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62527018 | |||||||
| chr12:62527080 | C | G | 119 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0111 others(116): Show |
121 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.1400+978C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62527080 | |||||||
| chr12:62527088 | T | C | 24 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(21): Show |
24 | HG01099.hp1 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.1400+986T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62527088 | |||||||
| chr12:62527170 | A | G | 79 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(76): Show |
80 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.1400+1068A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62527170 | |||||||
| chr12:62527248 | C | T | 1 | a0001c0002t0017g0024 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1400+1146C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62527248 | |||||||
| chr12:62527282 | G | A | 292 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0003g0135 others(289): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.1400+1180G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62527282 | |||||||
| chr12:62527477 | C | T | 119 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0111 others(116): Show |
121 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.1400+1375C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62527477 | |||||||
| chr12:62527643 | A | G | 1 | a0001c0006t0034g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1400+1541A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62527643 | |||||||
| chr12:62527676 | C | T | 52 | a0001c0003t0002g0055 a0001c0003t0002g0056 a0001c0003t0002g0057 others(49): Show |
52 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.1400+1574C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62527676 | |||||||
| chr12:62527727 | G | A | 11 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(8): Show |
11 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1400+1625G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62527727 | |||||||
| chr12:62527901 | A | T | 79 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(76): Show |
80 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.1400+1799A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62527901 | |||||||
| chr12:62528085 | T | C | 1 | a0002c0001t0006g0188 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1400+1983T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62528085 | |||||||
| chr12:62528198 | A | G | 25 | a0001c0005t0003g0109 a0001c0005t0003g0110 a0001c0005t0003g0117 others(22): Show |
25 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.1400+2096A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62528198 | |||||||
| chr12:62528363 | G | A | 121 | a0001c0009t0019g0107 a0001c0009t0019g0108 a0002c0001t0001g0002 others(118): Show |
123 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.1400+2261G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62528363 | |||||||
| chr12:62528406 | A | C | 105 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(102): Show |
106 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.1400+2304A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62528406 | |||||||
| chr12:62528649 | A | G | 24 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(21): Show |
24 | HG01099.hp1 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.1400+2547A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62528649 | |||||||
| chr12:62528810 | G | A | 1 | a0002c0001t0001g0174 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1400+2708G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62528810 | |||||||
| chr12:62528975 | A | G | 2 | a0001c0003t0005g0046 a0001c0003t0005g0047 |
2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1400+2873A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62528975 | |||||||
| chr12:62528999 | T | C | 1 | a0001c0002t0002g0330 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1400+2897T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62528999 | |||||||
| chr12:62529123 | G | A | 1 | a0001c0003t0005g0067 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1400+3021G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62529123 | |||||||
| chr12:62529126 | G | A | 1 | a0003c0004t0022g0295 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1400+3024G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62529126 | |||||||
| chr12:62529560 | T | C | 26 | a0001c0002t0031g0136 a0001c0005t0003g0109 a0001c0005t0003g0110 others(23): Show |
26 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.1401-2878T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62529560 | |||||||
| chr12:62529891 | G | A | 1 | a0001c0002t0003g0135 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1401-2547G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62529891 | |||||||
| chr12:62530049 | T | C | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1401-2389T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62530049 | |||||||
| chr12:62530057 | C | T | 68 | a0001c0003t0002g0055 a0001c0003t0002g0056 a0001c0003t0002g0057 others(65): Show |
69 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.1401-2381C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62530057 | |||||||
| chr12:62530175 | A | G | 26 | a0001c0002t0031g0136 a0001c0005t0003g0109 a0001c0005t0003g0110 others(23): Show |
26 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.1401-2263A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62530175 | |||||||
| chr12:62530227 | A | AT | 23 | a0001c0002t0002g0332 a0001c0002t0002g0341 a0001c0002t0002g0358 others(20): Show |
23 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.1401-2190dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | INFO_REALIGN_3_PRIME | chr12 | 62530227 | ||||||
| chr12:62530227 | AT | A | 45 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0027 others(42): Show |
45 | HG01074.hp1 HG01099.hp1 HG01255.hp1 others(42): Show |
intron_variant | MODIFIER | c.1401-2190delT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | INFO_REALIGN_3_PRIME | chr12 | 62530227 | ||||||
| chr12:62530262 | G | A | 1 | a0001c0005t0003g0130 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1401-2176G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62530262 | |||||||
| chr12:62530316 | T | C | 14 | a0001c0006t0007g0009 a0001c0006t0007g0010 a0001c0006t0007g0011 others(11): Show |
14 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.1401-2122T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62530316 | |||||||
| chr12:62530520 | C | T | 2 | a0001c0002t0013g0309 a0001c0002t0026g0310 |
2 | HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1401-1918C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62530520 | |||||||
| chr12:62530784 | C | G | 1 | a0003c0004t0004g0262 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1401-1654C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62530784 | |||||||
| chr12:62530850 | A | G | 2 | a0002c0001t0001g0223 a0002c0001t0001g0224 |
2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1401-1588A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62530850 | |||||||
| chr12:62530970 | TC | T | 4 | a0001c0003t0003g0035 a0001c0003t0003g0036 a0001c0003t0003g0099 others(1): Show |
4 | HG01361.hp2 HG02257.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1401-1465delC | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | INFO_REALIGN_3_PRIME | chr12 | 62530970 | ||||||
| chr12:62531285 | C | T | 1 | a0001c0006t0034g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1401-1153C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62531285 | |||||||
| chr12:62531292 | C | G | 1 | a0002c0001t0001g0185 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1401-1146C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62531292 | |||||||
| chr12:62531490 | C | T | 292 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0003g0135 others(289): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.1401-948C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62531490 | |||||||
| chr12:62531962 | G | A | 1 | a0001c0002t0017g0024 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1401-476G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62531962 | |||||||
| chr12:62532004 | C | T | 34 | a0001c0002t0022g0294 a0003c0004t0004g0258 a0003c0004t0004g0259 others(31): Show |
34 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.1401-434C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62532004 | |||||||
| chr12:62532167 | A | G | 2 | a0001c0003t0005g0046 a0001c0003t0005g0047 |
2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1401-271A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62532167 | |||||||
| chr12:62532169 | G | A | 1 | a0001c0003t0005g0098 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1401-269G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62532169 | |||||||
| chr12:62532229 | G | T | 1 | a0001c0005t0003g0117 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1401-209G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62532229 | |||||||
| chr12:62532337 | G | A | 4 | a0001c0006t0007g0012 a0001c0006t0007g0013 a0001c0006t0007g0014 others(1): Show |
4 | HG01099.hp1 HG02559.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1401-101G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 11/34 | chr12 | 62532337 | |||||||
| chr12:62532993 | G | C | 68 | a0001c0003t0002g0055 a0001c0003t0002g0056 a0001c0003t0002g0057 others(65): Show |
69 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.1633+323G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62532993 | |||||||
| chr12:62533243 | A | G | 1 | a0001c0005t0003g0121 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1633+573A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62533243 | |||||||
| chr12:62533292 | T | G | 11 | a0003c0004t0004g0258 a0003c0004t0004g0259 a0003c0004t0004g0262 others(8): Show |
11 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.1633+622T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62533292 | |||||||
| chr12:62533378 | A | G | 1 | a0002c0015t0024g0187 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1633+708A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62533378 | |||||||
| chr12:62533765 | G | C | 240 | a0001c0002t0031g0136 a0001c0003t0002g0055 a0001c0003t0002g0056 others(237): Show |
243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.1634-1080G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62533765 | |||||||
| chr12:62533783 | C | T | 4 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0028 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1634-1062C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62533783 | |||||||
| chr12:62533822 | T | C | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1634-1023T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62533822 | |||||||
| chr12:62533915 | A | G | 11 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(8): Show |
11 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1634-930A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62533915 | |||||||
| chr12:62534218 | C | T | 1 | a0001c0003t0050g0078 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1634-627C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534218 | |||||||
| chr12:62534226 | T | TA | 148 | a0001c0003t0005g0037 a0001c0003t0005g0038 a0001c0003t0005g0039 others(145): Show |
150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.1634-608dupA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534226 | ||||||
| chr12:62534404 | A | G | 1 | a0011c0021t0001g0337 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1634-441A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534404 | |||||||
| chr12:62534465 | G | A | 4 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(1): Show |
4 | HG02976.hp1 HG03195.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1634-380G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534465 | |||||||
| chr12:62534517 | G | T | 240 | a0001c0002t0031g0136 a0001c0003t0002g0055 a0001c0003t0002g0056 others(237): Show |
243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.1634-328G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534517 | |||||||
| chr12:62534518 | CAAAAAAA others(2): Show |
C | 6 | a0001c0002t0011g0255 a0001c0002t0011g0257 a0001c0002t0011g0300 others(3): Show |
6 | HG01167.hp2 HG02004.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.1634-310_1634-302d others(11): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534518 | ||||||
| chr12:62534518 | CAAAAAAA others(3): Show |
C | 1 | a0002c0001t0001g0172 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1634-311_1634-302d others(12): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534518 | ||||||
| chr12:62534531 | A | T | 6 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(3): Show |
6 | HG02055.hp2 HG02976.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1634-314A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534531 | |||||||
| chr12:62534532 | A | T | 15 | a0001c0003t0005g0052 a0001c0003t0005g0053 a0001c0003t0005g0065 others(12): Show |
15 | HG00140.hp1 NA18941.hp1 NA18945.hp1 others(12): Show |
intron_variant | MODIFIER | c.1634-313A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534532 | |||||||
| chr12:62534532 | AAAAAAAA others(5): Show |
A | 6 | a0002c0001t0001g0174 a0002c0001t0001g0207 a0002c0001t0001g0215 others(3): Show |
6 | HG00733.hp1 HG01257.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1634-311_1634-300d others(14): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534532 | ||||||
| chr12:62534533 | A | AATATATA others(3): Show |
7 | a0001c0006t0007g0011 a0001c0006t0007g0015 a0001c0006t0007g0016 others(4): Show |
7 | HG01099.hp1 HG01891.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1634-311_1634-310i others(12): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534533 | ||||||
| chr12:62534533 | A | ATATATAT others(8): Show |
1 | a0001c0006t0034g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1634-312_1634-311i others(17): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534533 | |||||||
| chr12:62534533 | A | T | 10 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(7): Show |
10 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1634-312A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534533 | |||||||
| chr12:62534533 | AAAAAAAA others(4): Show |
A | 9 | a0001c0003t0003g0036 a0002c0001t0001g0155 a0002c0001t0001g0171 others(6): Show |
9 | HG00099.hp1 HG00140.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.1634-310_1634-300d others(13): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534533 | ||||||
| chr12:62534533 | AAAAAAAA others(6): Show |
A | 3 | a0001c0009t0019g0107 a0001c0009t0019g0108 a0002c0001t0001g0146 |
3 | HG01081.hp2 HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1634-310_1634-298d others(15): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534533 | ||||||
| chr12:62534534 | A | ATATATAT others(4): Show |
1 | a0002c0001t0012g0141 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1634-311_1634-310i others(13): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534534 | |||||||
| chr12:62534534 | A | T | 35 | a0001c0002t0003g0135 a0001c0003t0002g0084 a0001c0003t0005g0034 others(32): Show |
35 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.1634-311A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534534 | |||||||
| chr12:62534534 | AAAAAAAA others(3): Show |
A | 32 | a0002c0001t0001g0002 a0002c0001t0001g0143 a0002c0001t0001g0149 others(29): Show |
33 | HG00544.hp2 HG00597.hp1 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.1634-309_1634-300d others(12): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534534 | ||||||
| chr12:62534534 | AAAAAAAA others(5): Show |
A | 58 | a0002c0001t0001g0003 a0002c0001t0001g0111 a0002c0001t0001g0137 others(55): Show |
59 | HG00423.hp1 HG00438.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.1634-309_1634-298d others(14): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534534 | ||||||
| chr12:62534534 | AAAAAAAA others(7): Show |
A | 1 | a0002c0001t0012g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1634-309_1634-296d others(16): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534534 | ||||||
| chr12:62534535 | A | AATATATA others(3): Show |
3 | a0001c0006t0007g0012 a0001c0006t0007g0013 a0001c0006t0007g0014 |
3 | HG02559.hp1 HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1634-309_1634-308i others(12): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534535 | ||||||
| chr12:62534535 | A | T | 20 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(17): Show |
20 | HG01099.hp1 HG01891.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.1634-310A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534535 | |||||||
| chr12:62534535 | AAAAAAAA others(4): Show |
A | 4 | a0001c0003t0003g0035 a0001c0005t0003g0128 a0001c0005t0003g0129 others(1): Show |
4 | HG00323.hp1 HG01256.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1634-308_1634-298d others(13): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534535 | ||||||
| chr12:62534536 | A | T | 64 | a0001c0002t0003g0135 a0001c0003t0002g0055 a0001c0003t0002g0056 others(61): Show |
64 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.1634-309A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534536 | |||||||
| chr12:62534536 | AAAAAAAA others(3): Show |
A | 3 | a0001c0003t0003g0099 a0001c0003t0003g0100 a0001c0005t0003g0133 |
3 | HG02615.hp2 HG02723.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.1634-307_1634-298d others(12): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534536 | ||||||
| chr12:62534536 | AAAAAAAA others(5): Show |
A | 3 | a0002c0001t0001g0157 a0002c0001t0001g0216 a0002c0001t0006g0204 |
3 | HG00280.hp2 HG02071.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1634-307_1634-296d others(14): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534536 | ||||||
| chr12:62534537 | A | T | 23 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(20): Show |
23 | HG01099.hp1 HG01891.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.1634-308A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534537 | |||||||
| chr12:62534537 | AAAAAAAT others(4): Show |
A | 20 | a0001c0005t0003g0109 a0001c0005t0003g0110 a0001c0005t0003g0117 others(17): Show |
20 | HG00735.hp2 HG00738.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.1634-306_1634-296d others(13): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534537 | ||||||
| chr12:62534538 | A | T | 70 | a0001c0002t0003g0135 a0001c0003t0002g0055 a0001c0003t0002g0056 others(67): Show |
70 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.1634-307A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534538 | |||||||
| chr12:62534538 | AAAAAATA others(3): Show |
A | 2 | a0001c0005t0003g0123 a0001c0005t0003g0126 |
2 | HG01081.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1634-305_1634-296d others(12): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534538 | ||||||
| chr12:62534539 | A | T | 23 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(20): Show |
23 | HG01099.hp1 HG01891.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.1634-306A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534539 | |||||||
| chr12:62534540 | A | AT | 16 | a0001c0002t0002g0324 a0001c0002t0002g0331 a0001c0002t0002g0332 others(13): Show |
16 | HG00642.hp2 HG01255.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1634-305_1634-304i others(3): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534540 | |||||||
| chr12:62534540 | A | ATATATAT others(6): Show |
2 | a0003c0004t0004g0286 a0003c0004t0004g0365 |
2 | HG00639.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1634-305_1634-304i others(15): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534540 | |||||||
| chr12:62534540 | A | ATATATAT others(11): Show |
1 | a0003c0004t0004g0279 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1634-305_1634-304i others(20): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534540 | |||||||
| chr12:62534540 | A | ATATATAT others(7): Show |
4 | a0001c0006t0003g0102 a0001c0006t0003g0103 a0001c0006t0003g0104 others(1): Show |
4 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1634-305_1634-304i others(16): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534540 | |||||||
| chr12:62534540 | A | T | 76 | a0001c0002t0002g0318 a0001c0002t0002g0322 a0001c0002t0002g0325 others(73): Show |
76 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.1634-305A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534540 | |||||||
| chr12:62534541 | A | T | 20 | a0001c0002t0002g0303 a0001c0006t0003g0005 a0001c0006t0003g0006 others(17): Show |
20 | HG01099.hp1 HG01099.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1634-304A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534541 | |||||||
| chr12:62534542 | A | AAAAAAAA others(98): Show |
1 | a0001c0002t0035g0025 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1634-302_1634-301i others(107): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | ||||||
| chr12:62534542 | A | AAAAAAAA others(22): Show |
1 | a0001c0002t0037g0313 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1634-302_1634-301i others(31): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | ||||||
| chr12:62534542 | A | AAAAAAAA others(62): Show |
1 | a0001c0002t0017g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1634-302_1634-301i others(71): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | ||||||
| chr12:62534542 | A | AAAAAAAA others(64): Show |
1 | a0001c0002t0017g0024 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1634-302_1634-301i others(73): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | ||||||
| chr12:62534542 | A | AAAAAAAA others(37): Show |
1 | a0001c0002t0010g0027 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1634-302_1634-301i others(46): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | ||||||
| chr12:62534542 | A | AAAAAAAA others(62): Show |
1 | a0001c0002t0010g0031 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1634-302_1634-301i others(71): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | ||||||
| chr12:62534542 | A | AAAAAAAA others(13): Show |
1 | a0001c0002t0026g0310 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1634-302_1634-301i others(22): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | ||||||
| chr12:62534542 | A | AAAAAAAA others(59): Show |
1 | a0001c0002t0017g0033 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1634-302_1634-301i others(68): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | ||||||
| chr12:62534542 | A | AAAAAAAT others(8): Show |
1 | a0001c0002t0014g0290 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1634-302_1634-301i others(17): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | ||||||
| chr12:62534542 | A | AAAAAAAT others(54): Show |
1 | a0001c0002t0010g0028 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1634-302_1634-301i others(63): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | ||||||
| chr12:62534542 | A | AAAAAAAT others(56): Show |
1 | a0001c0002t0002g0030 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1634-302_1634-301i others(65): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | ||||||
| chr12:62534542 | A | AAAAAATA others(7): Show |
1 | a0001c0002t0014g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1634-302_1634-301i others(16): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | ||||||
| chr12:62534542 | A | AAAAAATA others(15): Show |
2 | a0001c0002t0013g0308 a0001c0002t0013g0309 |
2 | HG02004.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1634-302_1634-301i others(24): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | ||||||
| chr12:62534542 | A | AAAAAATA others(17): Show |
1 | a0001c0002t0039g0311 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1634-302_1634-301i others(26): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | ||||||
| chr12:62534542 | A | AAAAAATA others(23): Show |
1 | a0001c0002t0013g0306 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1634-302_1634-301i others(32): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | ||||||
| chr12:62534542 | A | AAAAAATA others(57): Show |
1 | a0001c0002t0010g0029 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1634-302_1634-301i others(66): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | ||||||
| chr12:62534542 | A | AAAAAATA others(55): Show |
1 | a0001c0002t0002g0026 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1634-302_1634-301i others(64): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | ||||||
| chr12:62534542 | A | AAAATATA others(3): Show |
2 | a0001c0002t0020g0287 a0001c0002t0020g0292 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1634-302_1634-301i others(12): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | ||||||
| chr12:62534542 | A | AAAATATA others(7): Show |
2 | a0001c0002t0014g0291 a0003c0004t0004g0281 |
2 | NA19077.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1634-302_1634-301i others(16): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | ||||||
| chr12:62534542 | A | AAATATAT others(6): Show |
5 | a0001c0002t0014g0288 a0003c0004t0004g0258 a0003c0004t0004g0259 others(2): Show |
5 | HG00099.hp2 HG01074.hp2 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.1634-302_1634-301i others(15): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | ||||||
| chr12:62534542 | A | AAATATAT others(8): Show |
4 | a0003c0004t0004g0264 a0003c0004t0004g0280 a0003c0004t0004g0284 others(1): Show |
4 | HG02523.hp1 NA18967.hp1 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.1634-302_1634-301i others(17): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | ||||||
| chr12:62534542 | A | AAATATAT others(24): Show |
1 | a0003c0004t0004g0272 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1634-302_1634-301i others(33): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | ||||||
| chr12:62534542 | A | AATATATA others(7): Show |
1 | a0003c0004t0004g0271 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1634-290_1634-277d others(16): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | ||||||
| chr12:62534542 | A | AATATATA others(9): Show |
1 | a0003c0004t0004g0277 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1634-292_1634-277d others(18): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | ||||||
| chr12:62534542 | A | AATATATA others(13): Show |
1 | a0003c0004t0022g0295 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1634-296_1634-277d others(22): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534542 | ||||||
| chr12:62534542 | A | ATATATAT others(6): Show |
1 | a0003c0004t0004g0262 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1634-303_1634-302i others(15): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534542 | |||||||
| chr12:62534542 | A | ATATATAT others(8): Show |
5 | a0003c0004t0004g0261 a0003c0004t0004g0266 a0003c0004t0004g0275 others(2): Show |
5 | NA18975.hp1 NA18983.hp2 NA18987.hp1 others(2): Show |
intron_variant | MODIFIER | c.1634-303_1634-302i others(17): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534542 | |||||||
| chr12:62534542 | A | ATATATAT others(10): Show |
6 | a0003c0004t0004g0265 a0003c0004t0004g0267 a0003c0004t0004g0268 others(3): Show |
6 | HG00280.hp1 HG00733.hp2 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.1634-303_1634-302i others(19): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534542 | |||||||
| chr12:62534542 | A | ATATATAT others(12): Show |
3 | a0003c0004t0004g0273 a0003c0004t0004g0274 a0003c0004t0004g0278 |
3 | HG03239.hp1 NA18944.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1634-303_1634-302i others(21): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534542 | |||||||
| chr12:62534542 | A | ATATATAT others(16): Show |
1 | a0003c0004t0004g0276 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1634-303_1634-302i others(25): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534542 | |||||||
| chr12:62534542 | A | ATATATAT others(44): Show |
1 | a0001c0002t0002g0303 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1634-303_1634-302i others(53): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534542 | |||||||
| chr12:62534542 | A | ATATATAT others(7): Show |
1 | a0001c0006t0003g0008 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1634-303_1634-302i others(16): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534542 | |||||||
| chr12:62534542 | A | ATATATAT others(5): Show |
6 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(3): Show |
6 | HG02572.hp1 HG02976.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1634-303_1634-302i others(14): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534542 | |||||||
| chr12:62534542 | A | T | 127 | a0001c0002t0002g0256 a0001c0002t0002g0298 a0001c0002t0002g0317 others(124): Show |
127 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.1634-303A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534542 | |||||||
| chr12:62534543 | A | AATATATA others(21): Show |
1 | a0001c0002t0002g0335 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1634-302_1634-301i others(30): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534543 | |||||||
| chr12:62534543 | A | ATATATAT others(8): Show |
1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1634-289_1634-288i others(17): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534543 | ||||||
| chr12:62534543 | A | ATATATAT others(35): Show |
1 | a0002c0001t0001g0142 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1634-289_1634-288i others(44): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534543 | ||||||
| chr12:62534543 | A | T | 13 | a0001c0002t0002g0303 a0001c0006t0007g0009 a0001c0006t0007g0011 others(10): Show |
13 | HG01099.hp1 HG01099.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1634-302A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534543 | |||||||
| chr12:62534544 | T | A | 3 | a0001c0002t0013g0312 a0006c0010t0002g0336 a0006c0010t0002g0350 |
3 | HG01256.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1634-301T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534544 | |||||||
| chr12:62534545 | A | ATATATAT others(50): Show |
1 | a0001c0003t0005g0065 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1634-285_1634-284i others(59): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534545 | ||||||
| chr12:62534545 | A | ATATATAT others(33): Show |
1 | a0001c0006t0033g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1634-287_1634-286i others(42): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534545 | ||||||
| chr12:62534545 | A | ATATATAT others(6): Show |
3 | a0002c0001t0001g0138 a0002c0001t0001g0219 a0002c0001t0030g0140 |
3 | HG03098.hp2 HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1634-289_1634-288i others(15): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534545 | ||||||
| chr12:62534545 | A | ATATATAT others(31): Show |
1 | a0002c0001t0001g0139 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1634-289_1634-288i others(40): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534545 | ||||||
| chr12:62534546 | T | A | 1 | a0001c0002t0013g0312 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1634-299T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534546 | |||||||
| chr12:62534547 | A | ATATATAT others(43): Show |
2 | a0006c0010t0002g0336 a0006c0010t0002g0350 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1634-261_1634-260i others(52): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534547 | ||||||
| chr12:62534547 | A | ATATATAT others(12): Show |
1 | a0001c0003t0003g0042 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1634-281_1634-280i others(21): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534547 | ||||||
| chr12:62534547 | A | ATATATAT others(52): Show |
2 | a0001c0003t0002g0070 a0001c0003t0002g0077 |
2 | NA18987.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1634-281_1634-280i others(61): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534547 | ||||||
| chr12:62534547 | A | ATATATAT others(69): Show |
1 | a0001c0003t0005g0045 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1634-283_1634-282i others(78): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534547 | ||||||
| chr12:62534547 | A | ATATATAT others(58): Show |
1 | a0001c0003t0008g0063 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1634-285_1634-284i others(67): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534547 | ||||||
| chr12:62534547 | A | ATATATAT others(56): Show |
1 | a0001c0003t0008g0061 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1634-285_1634-284i others(65): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534547 | ||||||
| chr12:62534547 | A | ATATATAT others(54): Show |
6 | a0001c0003t0008g0060 a0001c0003t0008g0062 a0001c0003t0008g0075 others(3): Show |
6 | NA18945.hp1 NA18955.hp2 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.1634-285_1634-284i others(63): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534547 | ||||||
| chr12:62534547 | A | ATATATAT others(50): Show |
1 | a0001c0003t0008g0083 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1634-285_1634-284i others(59): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534547 | ||||||
| chr12:62534547 | A | ATATATAT others(48): Show |
14 | a0001c0003t0002g0055 a0001c0003t0002g0068 a0001c0003t0002g0069 others(11): Show |
14 | HG00544.hp1 HG00597.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.1634-285_1634-284i others(57): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534547 | ||||||
| chr12:62534547 | A | ATATATAT others(46): Show |
3 | a0001c0003t0005g0067 a0001c0003t0005g0097 a0001c0003t0050g0078 |
3 | HG02074.hp1 HG02165.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1634-285_1634-284i others(55): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534547 | ||||||
| chr12:62534547 | A | ATATATAT others(48): Show |
1 | a0001c0003t0005g0086 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1634-285_1634-284i others(57): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534547 | ||||||
| chr12:62534547 | A | ATATATAT others(46): Show |
2 | a0001c0003t0002g0073 a0001c0003t0002g0079 |
2 | NA18957.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1634-285_1634-284i others(55): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534547 | ||||||
| chr12:62534547 | A | ATATATAT others(46): Show |
1 | a0001c0003t0005g0058 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1634-287_1634-286i others(55): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534547 | ||||||
| chr12:62534548 | T | A | 1 | a0001c0002t0013g0312 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1634-297T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534548 | |||||||
| chr12:62534549 | A | ATATATAT others(50): Show |
2 | a0001c0003t0005g0046 a0001c0003t0005g0047 |
2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1634-281_1634-280i others(59): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534549 | ||||||
| chr12:62534549 | A | ATATATAT others(143): Show |
3 | a0001c0003t0005g0037 a0001c0003t0005g0038 a0001c0003t0005g0039 |
3 | HG02258.hp2 HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1634-283_1634-282i others(152): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534549 | ||||||
| chr12:62534549 | A | ATATATAT others(48): Show |
4 | a0001c0003t0005g0050 a0001c0003t0005g0051 a0001c0003t0005g0092 others(1): Show |
4 | NA18946.hp2 NA18973.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.1634-283_1634-282i others(57): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534549 | ||||||
| chr12:62534549 | A | ATATATAT others(46): Show |
1 | a0001c0003t0005g0053 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1634-283_1634-282i others(55): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534549 | ||||||
| chr12:62534549 | A | ATATATAT others(46): Show |
2 | a0001c0003t0005g0034 a0001c0003t0005g0040 |
2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1634-283_1634-282i others(55): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534549 | ||||||
| chr12:62534549 | A | ATATATAT others(52): Show |
2 | a0001c0003t0008g0059 a0001c0003t0008g0064 |
2 | NA18994.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1634-285_1634-284i others(61): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534549 | ||||||
| chr12:62534549 | A | ATATATAT others(46): Show |
2 | a0001c0003t0005g0087 a0001c0003t0005g0091 |
2 | HG00621.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.1634-285_1634-284i others(55): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534549 | ||||||
| chr12:62534549 | A | ATATATAT others(44): Show |
1 | a0001c0003t0005g0074 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1634-285_1634-284i others(53): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534549 | ||||||
| chr12:62534549 | A | ATATATAT others(44): Show |
1 | a0001c0003t0005g0080 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1634-287_1634-286i others(53): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534549 | ||||||
| chr12:62534551 | A | ATATATAT others(74): Show |
1 | a0001c0002t0010g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1634-277_1634-276i others(83): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534551 | ||||||
| chr12:62534551 | A | ATATATAT others(46): Show |
1 | a0001c0003t0005g0052 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1634-283_1634-282i others(55): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534551 | ||||||
| chr12:62534551 | A | ATATATAT others(44): Show |
5 | a0001c0003t0002g0056 a0001c0003t0002g0072 a0001c0003t0002g0082 others(2): Show |
5 | HG01192.hp2 HG01496.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.1634-285_1634-284i others(53): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534551 | ||||||
| chr12:62534551 | A | ATATATAT others(42): Show |
1 | a0001c0003t0002g0057 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1634-287_1634-286i others(51): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534551 | ||||||
| chr12:62534551 | A | ATTT | 6 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0029 others(3): Show |
6 | HG02145.hp2 HG02280.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1634-293_1634-292i others(5): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534551 | ||||||
| chr12:62534552 | T | TATATTTT others(15): Show |
1 | a0002c0001t0001g0148 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1634-289_1634-288i others(24): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534552 | ||||||
| chr12:62534553 | A | ATTT | 4 | a0001c0002t0010g0027 a0001c0002t0010g0028 a0001c0002t0017g0032 others(1): Show |
4 | HG01109.hp2 HG02630.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1634-291_1634-290i others(5): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr12 | 62534553 | ||||||
| chr12:62534553 | A | T | 1 | a0001c0002t0003g0135 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1634-292A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534553 | |||||||
| chr12:62534569 | T | A | 1 | a0001c0006t0003g0008 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1634-276T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534569 | |||||||
| chr12:62534672 | G | A | 11 | a0001c0002t0002g0318 a0001c0002t0002g0323 a0001c0002t0015g0314 others(8): Show |
11 | HG00423.hp2 HG02027.hp1 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.1634-173G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 12/34 | chr12 | 62534672 | |||||||
| chr12:62534959 | G | A | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1715+33G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 13/34 | chr12 | 62534959 | |||||||
| chr12:62535038 | T | C | 2 | a0001c0003t0002g0070 a0001c0003t0002g0077 |
2 | NA18987.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1715+112T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 13/34 | chr12 | 62535038 | |||||||
| chr12:62535242 | T | C | 2 | a0001c0009t0019g0107 a0001c0009t0019g0108 |
2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1716-283T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 13/34 | chr12 | 62535242 | |||||||
| chr12:62535248 | G | A | 1 | a0002c0001t0001g0148 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1716-277G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 13/34 | chr12 | 62535248 | |||||||
| chr12:62535884 | G | T | 4 | a0001c0005t0003g0118 a0001c0005t0003g0120 a0001c0005t0003g0121 others(1): Show |
4 | HG01255.hp1 HG02602.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1900+175G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/34 | chr12 | 62535884 | |||||||
| chr12:62535947 | A | G | 1 | a0001c0003t0005g0081 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1900+238A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/34 | chr12 | 62535947 | |||||||
| chr12:62536008 | A | G | 1 | a0001c0006t0003g0005 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1900+299A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/34 | chr12 | 62536008 | |||||||
| chr12:62536047 | G | C | 26 | a0001c0002t0031g0136 a0001c0005t0003g0109 a0001c0005t0003g0110 others(23): Show |
26 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.1900+338G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/34 | chr12 | 62536047 | |||||||
| chr12:62536051 | A | G | 1 | a0001c0003t0003g0036 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1900+342A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/34 | chr12 | 62536051 | |||||||
| chr12:62536053 | A | G | 2 | a0001c0009t0019g0107 a0001c0009t0019g0108 |
2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1900+344A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/34 | chr12 | 62536053 | |||||||
| chr12:62536109 | G | A | 1 | a0004c0007t0002g0327 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1900+400G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/34 | chr12 | 62536109 | |||||||
| chr12:62536203 | A | T | 1 | a0008c0019t0003g0113 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1900+494A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/34 | chr12 | 62536203 | |||||||
| chr12:62536224 | A | AT | 173 | a0001c0002t0002g0030 a0001c0002t0003g0135 a0001c0002t0031g0136 others(170): Show |
175 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.1900+524dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr12 | 62536224 | ||||||
| chr12:62536269 | T | C | 1 | a0001c0002t0047g0301 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1900+560T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/34 | chr12 | 62536269 | |||||||
| chr12:62536309 | A | T | 7 | a0001c0003t0005g0050 a0001c0003t0005g0051 a0001c0003t0005g0052 others(4): Show |
7 | NA18941.hp1 NA18946.hp2 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.1900+600A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/34 | chr12 | 62536309 | |||||||
| chr12:62536484 | T | C | 1 | a0001c0002t0002g0304 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1901-667T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/34 | chr12 | 62536484 | |||||||
| chr12:62536506 | T | C | 1 | a0001c0002t0035g0025 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1901-645T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/34 | chr12 | 62536506 | |||||||
| chr12:62536550 | A | C | 2 | a0001c0005t0003g0128 a0001c0005t0003g0129 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1901-601A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/34 | chr12 | 62536550 | |||||||
| chr12:62536694 | G | GTT | 24 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(21): Show |
24 | HG01099.hp1 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.1901-445_1901-444d others(4): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr12 | 62536694 | ||||||
| chr12:62536775 | G | A | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1901-376G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/34 | chr12 | 62536775 | |||||||
| chr12:62536780 | C | G | 1 | a0001c0002t0003g0135 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1901-371C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/34 | chr12 | 62536780 | |||||||
| chr12:62536800 | TG | T | 3 | a0002c0001t0006g0145 a0002c0001t0006g0190 a0002c0001t0006g0198 |
3 | NA19057.hp1 NA19060.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1901-350delG | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/34 | chr12 | 62536800 | |||||||
| chr12:62536823 | A | G | 5 | a0001c0003t0003g0041 a0001c0003t0003g0042 a0001c0003t0003g0043 others(2): Show |
6 | HG01069.hp1 HG01071.hp1 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.1901-328A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/34 | chr12 | 62536823 | |||||||
| chr12:62536841 | G | A | 122 | a0001c0002t0003g0135 a0001c0009t0019g0107 a0001c0009t0019g0108 others(119): Show |
124 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.1901-310G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/34 | chr12 | 62536841 | |||||||
| chr12:62537018 | C | T | 122 | a0001c0002t0003g0135 a0001c0009t0019g0107 a0001c0009t0019g0108 others(119): Show |
124 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.1901-133C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 14/34 | chr12 | 62537018 | |||||||
| chr12:62537303 | C | G | 26 | a0001c0002t0031g0136 a0001c0005t0003g0109 a0001c0005t0003g0110 others(23): Show |
26 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.2013+40C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 15/34 | chr12 | 62537303 | |||||||
| chr12:62537376 | A | C | 3 | a0002c0001t0001g0144 a0002c0001t0001g0169 a0002c0001t0001g0170 |
3 | HG00673.hp1 NA18954.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.2013+113A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 15/34 | chr12 | 62537376 | |||||||
| chr12:62537418 | A | G | 1 | a0001c0006t0034g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2013+155A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 15/34 | chr12 | 62537418 | |||||||
| chr12:62537515 | C | A | 1 | a0001c0002t0015g0314 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2014-87C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 15/34 | chr12 | 62537515 | |||||||
| chr12:62537531 | G | T | 4 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(1): Show |
4 | HG02976.hp1 HG03195.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2014-71G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 15/34 | chr12 | 62537531 | |||||||
| chr12:62537870 | G | A | 1 | a0001c0003t0005g0091 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2118+164G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 16/34 | chr12 | 62537870 | |||||||
| chr12:62537910 | T | G | 26 | a0001c0002t0031g0136 a0001c0005t0003g0109 a0001c0005t0003g0110 others(23): Show |
26 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.2119-186T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 16/34 | chr12 | 62537910 | |||||||
| chr12:62537951 | A | T | 1 | a0001c0006t0034g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2119-145A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 16/34 | chr12 | 62537951 | |||||||
| chr12:62538003 | G | C | 24 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(21): Show |
24 | HG01099.hp1 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.2119-93G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 16/34 | chr12 | 62538003 | |||||||
| chr12:62538066 | ATTTGT | A | 122 | a0001c0002t0003g0135 a0001c0009t0019g0107 a0001c0009t0019g0108 others(119): Show |
124 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.2119-25_2119-21del others(5): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 16/34 | INFO_REALIGN_3_PRIME | chr12 | 62538066 | ||||||
| chr12:62538249 | C | A | 24 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(21): Show |
24 | HG01099.hp1 HG01891.hp2 HG02055.hp2 others(21): Show |
splice_region_variant&intron_variant | LOW | c.2200-3C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 17/34 | chr12 | 62538249 | |||||||
| chr12:62538598 | A | G | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2364+93A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62538598 | |||||||
| chr12:62538646 | T | C | 79 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(76): Show |
80 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.2364+141T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62538646 | |||||||
| chr12:62538828 | AT | A | 25 | a0001c0005t0003g0109 a0001c0005t0003g0110 a0001c0005t0003g0117 others(22): Show |
25 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.2364+326delT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | INFO_REALIGN_3_PRIME | chr12 | 62538828 | ||||||
| chr12:62538997 | G | A | 173 | a0001c0002t0003g0135 a0001c0002t0031g0136 a0001c0005t0003g0109 others(170): Show |
175 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.2364+492G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62538997 | |||||||
| chr12:62539006 | G | T | 1 | a0002c0001t0001g0148 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2364+501G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62539006 | |||||||
| chr12:62539036 | A | G | 119 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0111 others(116): Show |
121 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.2364+531A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62539036 | |||||||
| chr12:62539090 | A | G | 299 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0003g0135 others(296): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.2364+585A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62539090 | |||||||
| chr12:62539246 | A | G | 1 | a0001c0002t0003g0135 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2364+741A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62539246 | |||||||
| chr12:62539298 | C | T | 1 | a0001c0006t0003g0104 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2364+793C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62539298 | |||||||
| chr12:62539337 | G | A | 2 | a0001c0009t0019g0107 a0001c0009t0019g0108 |
2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2364+832G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62539337 | |||||||
| chr12:62539420 | C | T | 1 | a0001c0006t0007g0019 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2364+915C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62539420 | |||||||
| chr12:62539513 | C | T | 10 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(7): Show |
10 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.2364+1008C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62539513 | |||||||
| chr12:62539537 | G | GATTACAG others(18): Show |
1 | a0002c0001t0001g0152 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2364+1033_2364+105 others(29): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | INFO_REALIGN_3_PRIME | chr12 | 62539537 | ||||||
| chr12:62539557 | G | A | 1 | a0001c0005t0003g0130 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2364+1052G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62539557 | |||||||
| chr12:62539558 | C | T | 1 | a0005c0008t0002g0340 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2364+1053C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62539558 | |||||||
| chr12:62539754 | C | T | 1 | a0001c0003t0005g0040 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2364+1249C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62539754 | |||||||
| chr12:62539901 | G | A | 1 | a0002c0001t0001g0246 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2364+1396G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62539901 | |||||||
| chr12:62539984 | T | A | 1 | a0001c0006t0003g0005 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2364+1479T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62539984 | |||||||
| chr12:62540037 | T | C | 1 | a0002c0001t0012g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2364+1532T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62540037 | |||||||
| chr12:62540259 | G | A | 21 | a0001c0002t0002g0303 a0001c0002t0002g0329 a0001c0002t0002g0332 others(18): Show |
21 | HG00642.hp2 HG00735.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.2364+1754G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62540259 | |||||||
| chr12:62540662 | G | A | 173 | a0001c0002t0003g0135 a0001c0002t0031g0136 a0001c0005t0003g0109 others(170): Show |
175 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.2364+2157G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62540662 | |||||||
| chr12:62540805 | A | G | 1 | a0001c0006t0034g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2365-2292A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62540805 | |||||||
| chr12:62541046 | G | A | 1 | a0003c0004t0004g0296 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2365-2051G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62541046 | |||||||
| chr12:62541066 | T | C | 1 | a0001c0006t0007g0012 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2365-2031T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62541066 | |||||||
| chr12:62541170 | C | T | 1 | a0001c0002t0002g0304 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2365-1927C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62541170 | |||||||
| chr12:62541374 | C | CA | 9 | a0001c0002t0002g0358 a0001c0003t0003g0041 a0001c0003t0003g0042 others(6): Show |
10 | HG01069.hp1 HG01071.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.2365-1705dupA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | INFO_REALIGN_3_PRIME | chr12 | 62541374 | ||||||
| chr12:62541374 | CA | C | 120 | a0001c0002t0002g0298 a0001c0002t0003g0135 a0001c0002t0014g0288 others(117): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.2365-1705delA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | INFO_REALIGN_3_PRIME | chr12 | 62541374 | ||||||
| chr12:62541464 | A | C | 5 | a0001c0003t0003g0041 a0001c0003t0003g0042 a0001c0003t0003g0043 others(2): Show |
6 | HG01069.hp1 HG01071.hp1 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.2365-1633A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62541464 | |||||||
| chr12:62541542 | A | G | 1 | a0001c0005t0003g0120 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2365-1555A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62541542 | |||||||
| chr12:62541557 | G | T | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2365-1540G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62541557 | |||||||
| chr12:62541645 | G | A | 7 | a0001c0002t0013g0306 a0001c0002t0013g0308 a0001c0002t0013g0309 others(4): Show |
7 | HG01074.hp1 HG01256.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.2365-1452G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62541645 | |||||||
| chr12:62541863 | G | A | 30 | a0001c0002t0022g0294 a0003c0004t0004g0258 a0003c0004t0004g0259 others(27): Show |
30 | HG00639.hp1 HG00673.hp2 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.2365-1234G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62541863 | |||||||
| chr12:62541908 | A | G | 11 | a0001c0002t0002g0318 a0001c0002t0002g0323 a0001c0002t0015g0314 others(8): Show |
11 | HG00423.hp2 HG02027.hp1 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.2365-1189A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62541908 | |||||||
| chr12:62541925 | C | T | 119 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0111 others(116): Show |
121 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.2365-1172C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62541925 | |||||||
| chr12:62541931 | A | G | 1 | a0003c0004t0004g0261 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2365-1166A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62541931 | |||||||
| chr12:62542087 | A | G | 2 | a0002c0001t0001g0003 a0002c0001t0001g0217 |
3 | HG02886.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2365-1010A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62542087 | |||||||
| chr12:62542151 | T | C | 1 | a0001c0002t0003g0135 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2365-946T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62542151 | |||||||
| chr12:62542222 | C | T | 15 | a0001c0006t0007g0009 a0001c0006t0007g0010 a0001c0006t0007g0011 others(12): Show |
15 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.2365-875C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62542222 | |||||||
| chr12:62542254 | A | G | 1 | a0002c0001t0012g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2365-843A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62542254 | |||||||
| chr12:62542387 | A | G | 2 | a0001c0003t0003g0099 a0001c0003t0003g0100 |
2 | HG02615.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.2365-710A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62542387 | |||||||
| chr12:62542486 | A | G | 291 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0003g0135 others(288): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.2365-611A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62542486 | |||||||
| chr12:62542633 | G | A | 1 | a0001c0002t0013g0306 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2365-464G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62542633 | |||||||
| chr12:62542974 | C | T | 10 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(7): Show |
10 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.2365-123C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 19/34 | chr12 | 62542974 | |||||||
| chr12:62543204 | TTC | T | 10 | a0001c0006t0007g0010 a0001c0006t0007g0011 a0001c0006t0007g0012 others(7): Show |
10 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.2466+10_2466+11del others(2): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr12 | 62543204 | ||||||
| chr12:62543220 | T | C | 1 | a0002c0001t0006g0201 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2466+22T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 20/34 | chr12 | 62543220 | |||||||
| chr12:62543318 | G | A | 1 | a0002c0001t0009g0196 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2466+120G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 20/34 | chr12 | 62543318 | |||||||
| chr12:62543364 | G | T | 1 | a0001c0002t0002g0325 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2466+166G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 20/34 | chr12 | 62543364 | |||||||
| chr12:62543408 | A | G | 1 | a0001c0002t0014g0291 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2466+210A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 20/34 | chr12 | 62543408 | |||||||
| chr12:62543479 | A | G | 139 | a0001c0002t0011g0255 a0001c0002t0011g0257 a0001c0002t0011g0300 others(136): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.2466+281A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 20/34 | chr12 | 62543479 | |||||||
| chr12:62543568 | T | G | 129 | a0001c0002t0002g0329 a0001c0002t0003g0135 a0001c0002t0013g0306 others(126): Show |
131 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.2466+370T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 20/34 | chr12 | 62543568 | |||||||
| chr12:62543609 | C | T | 213 | a0001c0002t0002g0321 a0001c0002t0010g0023 a0001c0002t0010g0027 others(210): Show |
215 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.2466+411C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 20/34 | chr12 | 62543609 | |||||||
| chr12:62543677 | G | A | 3 | a0001c0003t0005g0037 a0001c0003t0005g0038 a0001c0003t0005g0039 |
3 | HG02258.hp2 HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2466+479G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 20/34 | chr12 | 62543677 | |||||||
| chr12:62543691 | G | A | 1 | a0001c0002t0011g0257 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2466+493G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 20/34 | chr12 | 62543691 | |||||||
| chr12:62543752 | C | T | 147 | a0001c0002t0002g0256 a0001c0002t0010g0027 a0001c0002t0031g0136 others(144): Show |
149 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.2466+554C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 20/34 | chr12 | 62543752 | |||||||
| chr12:62543992 | T | C | 1 | a0002c0001t0006g0222 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2466+794T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 20/34 | chr12 | 62543992 | |||||||
| chr12:62544114 | T | C | 1 | a0001c0003t0003g0042 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2467-784T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 20/34 | chr12 | 62544114 | |||||||
| chr12:62544250 | G | T | 2 | a0003c0004t0004g0282 a0003c0004t0004g0283 |
2 | NA18975.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.2467-648G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 20/34 | chr12 | 62544250 | |||||||
| chr12:62544258 | A | G | 2 | a0001c0009t0019g0107 a0001c0009t0019g0108 |
2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2467-640A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 20/34 | chr12 | 62544258 | |||||||
| chr12:62544291 | A | G | 1 | a0008c0019t0003g0113 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2467-607A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 20/34 | chr12 | 62544291 | |||||||
| chr12:62544498 | C | G | 1 | a0002c0001t0001g0208 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2467-400C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 20/34 | chr12 | 62544498 | |||||||
| chr12:62544846 | T | G | 1 | a0001c0020t0038g0305 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2467-52T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 20/34 | chr12 | 62544846 | |||||||
| chr12:62544847 | G | A | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2467-51G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 20/34 | chr12 | 62544847 | |||||||
| chr12:62545249 | C | A | 2 | a0002c0001t0001g0223 a0002c0001t0001g0224 |
2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2577+241C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 21/34 | chr12 | 62545249 | |||||||
| chr12:62545275 | T | C | 136 | a0001c0002t0031g0136 a0001c0006t0007g0009 a0001c0006t0007g0010 others(133): Show |
138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.2577+267T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 21/34 | chr12 | 62545275 | |||||||
| chr12:62545612 | G | A | 2 | a0001c0009t0019g0107 a0001c0009t0019g0108 |
2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2577+604G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 21/34 | chr12 | 62545612 | |||||||
| chr12:62545630 | C | G | 1 | a0001c0002t0014g0291 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2577+622C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 21/34 | chr12 | 62545630 | |||||||
| chr12:62545693 | T | TAATAACC others(310): Show |
2 | a0001c0009t0019g0107 a0001c0009t0019g0108 |
2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2577+698_2577+699i others(319): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 21/34 | INFO_REALIGN_3_PRIME | chr12 | 62545693 | ||||||
| chr12:62545777 | C | A | 225 | a0001c0002t0003g0135 a0001c0002t0013g0306 a0001c0002t0013g0308 others(222): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.2577+769C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 21/34 | chr12 | 62545777 | |||||||
| chr12:62545853 | A | G | 1 | a0003c0004t0004g0273 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2577+845A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 21/34 | chr12 | 62545853 | |||||||
| chr12:62545893 | A | G | 1 | a0001c0005t0003g0118 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2577+885A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 21/34 | chr12 | 62545893 | |||||||
| chr12:62546087 | G | T | 2 | a0002c0001t0009g0196 a0002c0001t0009g0197 |
2 | HG00733.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.2578-810G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 21/34 | chr12 | 62546087 | |||||||
| chr12:62546149 | C | T | 1 | a0001c0006t0033g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2578-748C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 21/34 | chr12 | 62546149 | |||||||
| chr12:62546329 | C | T | 1 | a0001c0003t0005g0047 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2578-568C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 21/34 | chr12 | 62546329 | |||||||
| chr12:62546476 | G | A | 6 | a0001c0002t0014g0288 a0001c0002t0014g0289 a0001c0002t0014g0290 others(3): Show |
6 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.2578-421G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 21/34 | chr12 | 62546476 | |||||||
| chr12:62546568 | A | G | 1 | a0002c0001t0001g0156 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2578-329A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 21/34 | chr12 | 62546568 | |||||||
| chr12:62547141 | A | G | 1 | a0001c0003t0050g0078 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2753+69A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | chr12 | 62547141 | |||||||
| chr12:62547289 | G | A | 2 | a0002c0001t0001g0156 a0002c0001t0001g0221 |
2 | NA18956.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.2753+217G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | chr12 | 62547289 | |||||||
| chr12:62547646 | T | C | 136 | a0001c0002t0031g0136 a0001c0006t0007g0009 a0001c0006t0007g0010 others(133): Show |
138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.2753+574T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | chr12 | 62547646 | |||||||
| chr12:62547664 | A | G | 136 | a0001c0002t0031g0136 a0001c0006t0007g0009 a0001c0006t0007g0010 others(133): Show |
138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.2753+592A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | chr12 | 62547664 | |||||||
| chr12:62547718 | A | G | 3 | a0001c0003t0002g0056 a0001c0003t0002g0082 a0001c0003t0002g0095 |
3 | NA18971.hp2 NA18988.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.2753+646A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | chr12 | 62547718 | |||||||
| chr12:62547863 | C | T | 25 | a0001c0005t0003g0109 a0001c0005t0003g0110 a0001c0005t0003g0117 others(22): Show |
25 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.2753+791C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | chr12 | 62547863 | |||||||
| chr12:62548057 | A | G | 136 | a0001c0002t0031g0136 a0001c0006t0007g0009 a0001c0006t0007g0010 others(133): Show |
138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.2753+985A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | chr12 | 62548057 | |||||||
| chr12:62548072 | A | C | 7 | a0001c0003t0005g0050 a0001c0003t0005g0051 a0001c0003t0005g0052 others(4): Show |
7 | NA18941.hp1 NA18946.hp2 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.2753+1000A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | chr12 | 62548072 | |||||||
| chr12:62548149 | A | T | 120 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0111 others(117): Show |
122 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.2753+1077A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | chr12 | 62548149 | |||||||
| chr12:62548223 | C | T | 12 | a0001c0006t0007g0009 a0001c0006t0007g0010 a0001c0006t0007g0011 others(9): Show |
12 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.2753+1151C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | chr12 | 62548223 | |||||||
| chr12:62548292 | T | C | 48 | a0001c0002t0003g0135 a0001c0002t0013g0306 a0001c0002t0013g0308 others(45): Show |
49 | HG00099.hp2 HG00735.hp2 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.2753+1220T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | chr12 | 62548292 | |||||||
| chr12:62548296 | G | C | 1 | a0001c0002t0002g0317 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2753+1224G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | chr12 | 62548296 | |||||||
| chr12:62548418 | G | A | 12 | a0002c0001t0006g0145 a0002c0001t0006g0186 a0002c0001t0006g0190 others(9): Show |
12 | HG01928.hp1 HG02071.hp1 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.2754-1250G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | chr12 | 62548418 | |||||||
| chr12:62548478 | C | T | 120 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0111 others(117): Show |
122 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.2754-1190C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | chr12 | 62548478 | |||||||
| chr12:62548628 | C | T | 1 | a0002c0001t0006g0186 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2754-1040C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | chr12 | 62548628 | |||||||
| chr12:62548883 | A | G | 1 | a0001c0002t0002g0325 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2754-785A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | chr12 | 62548883 | |||||||
| chr12:62548962 | A | C | 1 | a0002c0001t0001g0170 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2754-706A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | chr12 | 62548962 | |||||||
| chr12:62548995 | C | T | 1 | a0002c0001t0001g0180 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2754-673C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | chr12 | 62548995 | |||||||
| chr12:62549095 | A | C | 4 | a0001c0003t0008g0064 a0001c0003t0008g0075 a0001c0003t0008g0076 others(1): Show |
4 | NA18986.hp1 NA18998.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.2754-573A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | chr12 | 62549095 | |||||||
| chr12:62549219 | A | T | 1 | a0003c0004t0004g0260 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2754-449A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | chr12 | 62549219 | |||||||
| chr12:62549401 | C | T | 1 | a0001c0002t0035g0025 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2754-267C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | chr12 | 62549401 | |||||||
| chr12:62549456 | C | CA | 10 | a0001c0002t0002g0348 a0001c0003t0002g0056 a0001c0003t0002g0057 others(7): Show |
10 | HG01192.hp2 HG01361.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.2754-195dupA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | INFO_REALIGN_3_PRIME | chr12 | 62549456 | ||||||
| chr12:62549456 | CA | C | 134 | a0001c0002t0031g0136 a0001c0005t0040g0134 a0001c0006t0007g0009 others(131): Show |
136 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.2754-195delA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | INFO_REALIGN_3_PRIME | chr12 | 62549456 | ||||||
| chr12:62549591 | G | A | 77 | a0001c0002t0003g0135 a0001c0002t0013g0306 a0001c0002t0013g0308 others(74): Show |
77 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.2754-77G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 22/34 | chr12 | 62549591 | |||||||
| chr12:62550045 | G | A | 2 | a0002c0001t0001g0003 a0002c0001t0001g0217 |
3 | HG02886.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2916+215G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62550045 | |||||||
| chr12:62550142 | T | C | 1 | a0001c0002t0022g0294 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2916+312T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62550142 | |||||||
| chr12:62550258 | G | A | 1 | a0002c0001t0001g0185 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2916+428G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62550258 | |||||||
| chr12:62550315 | G | A | 1 | a0002c0001t0001g0243 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2916+485G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62550315 | |||||||
| chr12:62550320 | G | A | 1 | a0003c0004t0004g0260 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2916+490G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62550320 | |||||||
| chr12:62550376 | G | A | 1 | a0002c0001t0001g0215 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2916+546G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62550376 | |||||||
| chr12:62550475 | T | A | 12 | a0002c0001t0001g0002 a0002c0001t0001g0143 a0002c0001t0001g0150 others(9): Show |
13 | HG00544.hp2 HG00597.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.2916+645T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62550475 | |||||||
| chr12:62550562 | A | G | 44 | a0002c0001t0001g0137 a0002c0001t0001g0206 a0002c0001t0001g0207 others(41): Show |
44 | HG00423.hp1 HG00438.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.2916+732A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62550562 | |||||||
| chr12:62550654 | T | C | 1 | a0001c0002t0003g0135 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2916+824T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62550654 | |||||||
| chr12:62550813 | G | C | 12 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(9): Show |
12 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.2916+983G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62550813 | |||||||
| chr12:62550905 | CTTTCTTT others(3): Show |
C | 136 | a0001c0002t0031g0136 a0001c0003t0003g0035 a0001c0003t0003g0036 others(133): Show |
138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.2916+1079_2916+108 others(14): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | INFO_REALIGN_3_PRIME | chr12 | 62550905 | ||||||
| chr12:62550905 | CTTTCTTT others(6): Show |
C | 1 | a0001c0003t0008g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2916+1079_2916+109 others(17): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | INFO_REALIGN_3_PRIME | chr12 | 62550905 | ||||||
| chr12:62550905 | CTTTCTTT others(10): Show |
C | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2916+1079_2916+109 others(21): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | INFO_REALIGN_3_PRIME | chr12 | 62550905 | ||||||
| chr12:62550909 | C | CT | 16 | a0001c0002t0002g0256 a0001c0002t0002g0329 a0001c0002t0002g0342 others(13): Show |
16 | HG00597.hp2 HG00621.hp1 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.2916+1104dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | INFO_REALIGN_3_PRIME | chr12 | 62550909 | ||||||
| chr12:62550909 | CT | C | 24 | a0001c0002t0002g0318 a0001c0002t0003g0135 a0001c0002t0013g0306 others(21): Show |
24 | HG01074.hp1 HG01074.hp2 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.2916+1104delT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | INFO_REALIGN_3_PRIME | chr12 | 62550909 | ||||||
| chr12:62550909 | CTTTTTTT others(4): Show |
C | 1 | a0001c0005t0043g0112 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2916+1094_2916+110 others(15): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | INFO_REALIGN_3_PRIME | chr12 | 62550909 | ||||||
| chr12:62550939 | G | A | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2916+1109G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62550939 | |||||||
| chr12:62550952 | G | A | 2 | a0001c0009t0019g0107 a0001c0009t0019g0108 |
2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2916+1122G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62550952 | |||||||
| chr12:62551022 | T | C | 241 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0003g0135 others(238): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.2916+1192T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62551022 | |||||||
| chr12:62551077 | G | A | 1 | a0001c0002t0022g0294 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2916+1247G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62551077 | |||||||
| chr12:62551158 | G | T | 6 | a0001c0005t0003g0122 a0001c0005t0003g0123 a0001c0005t0003g0124 others(3): Show |
6 | HG00738.hp2 HG01081.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.2916+1328G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62551158 | |||||||
| chr12:62551312 | T | A | 7 | a0001c0002t0013g0306 a0001c0002t0013g0308 a0001c0002t0013g0309 others(4): Show |
7 | HG01074.hp1 HG01256.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.2916+1482T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62551312 | |||||||
| chr12:62551378 | GGAAACAA others(9): Show |
G | 136 | a0001c0002t0031g0136 a0001c0006t0007g0009 a0001c0006t0007g0010 others(133): Show |
138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.2917-1496_2917-148 others(20): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | INFO_REALIGN_3_PRIME | chr12 | 62551378 | ||||||
| chr12:62551465 | G | A | 148 | a0001c0002t0031g0136 a0001c0006t0003g0005 a0001c0006t0003g0006 others(145): Show |
150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.2917-1416G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62551465 | |||||||
| chr12:62551569 | A | G | 5 | a0002c0001t0001g0147 a0002c0001t0001g0157 a0002c0001t0001g0174 others(2): Show |
5 | HG00280.hp2 HG01257.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.2917-1312A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62551569 | |||||||
| chr12:62551925 | G | T | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2917-956G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62551925 | |||||||
| chr12:62552049 | T | C | 1 | a0001c0006t0003g0008 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2917-832T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62552049 | |||||||
| chr12:62552190 | C | G | 136 | a0001c0002t0031g0136 a0001c0006t0007g0009 a0001c0006t0007g0010 others(133): Show |
138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.2917-691C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62552190 | |||||||
| chr12:62552191 | A | G | 284 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0003g0135 others(281): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.2917-690A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62552191 | |||||||
| chr12:62552347 | C | A | 1 | a0001c0002t0013g0308 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2917-534C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62552347 | |||||||
| chr12:62552430 | TATAAG | T | 10 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(7): Show |
10 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.2917-447_2917-443d others(7): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | INFO_REALIGN_3_PRIME | chr12 | 62552430 | ||||||
| chr12:62552436 | A | G | 4 | a0001c0003t0003g0035 a0001c0003t0003g0036 a0001c0003t0003g0099 others(1): Show |
4 | HG01361.hp2 HG02257.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.2917-445A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62552436 | |||||||
| chr12:62552667 | A | G | 36 | a0001c0003t0005g0045 a0001c0003t0005g0050 a0001c0003t0005g0051 others(33): Show |
36 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.2917-214A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62552667 | |||||||
| chr12:62552752 | T | G | 2 | a0001c0009t0019g0107 a0001c0009t0019g0108 |
2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2917-129T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 23/34 | chr12 | 62552752 | |||||||
| chr12:62553434 | T | G | 1 | a0001c0002t0011g0302 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.3210+260T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 24/34 | chr12 | 62553434 | |||||||
| chr12:62553606 | G | A | 1 | a0002c0001t0001g0243 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3210+432G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 24/34 | chr12 | 62553606 | |||||||
| chr12:62553935 | G | C | 2 | a0002c0001t0001g0210 a0002c0001t0012g0211 |
2 | HG03927.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.3210+761G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 24/34 | chr12 | 62553935 | |||||||
| chr12:62554171 | T | C | 1 | a0001c0003t0005g0092 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.3210+997T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 24/34 | chr12 | 62554171 | |||||||
| chr12:62554497 | CT | C | 38 | a0001c0003t0005g0045 a0001c0003t0005g0046 a0001c0003t0005g0047 others(35): Show |
38 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.3210+1330delT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 24/34 | INFO_REALIGN_3_PRIME | chr12 | 62554497 | ||||||
| chr12:62554510 | T | G | 1 | a0001c0002t0002g0359 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3210+1336T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 24/34 | chr12 | 62554510 | |||||||
| chr12:62554667 | A | T | 3 | a0001c0002t0002g0335 a0006c0010t0002g0336 a0006c0010t0002g0350 |
3 | HG01516.hp2 HG01517.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.3211-1327A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 24/34 | chr12 | 62554667 | |||||||
| chr12:62554688 | G | A | 1 | a0001c0002t0013g0308 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.3211-1306G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 24/34 | chr12 | 62554688 | |||||||
| chr12:62554752 | G | A | 1 | a0003c0004t0004g0277 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.3211-1242G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 24/34 | chr12 | 62554752 | |||||||
| chr12:62554956 | G | A | 120 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0111 others(117): Show |
122 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.3211-1038G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 24/34 | chr12 | 62554956 | |||||||
| chr12:62555042 | C | T | 7 | a0002c0001t0006g0192 a0002c0001t0006g0193 a0002c0001t0006g0204 others(4): Show |
7 | HG01928.hp1 HG02071.hp1 NA18941.hp2 others(4): Show |
intron_variant | MODIFIER | c.3211-952C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 24/34 | chr12 | 62555042 | |||||||
| chr12:62555330 | A | C | 148 | a0001c0002t0031g0136 a0001c0006t0003g0005 a0001c0006t0003g0006 others(145): Show |
150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.3211-664A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 24/34 | chr12 | 62555330 | |||||||
| chr12:62555338 | T | G | 1 | a0001c0003t0005g0071 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.3211-656T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 24/34 | chr12 | 62555338 | |||||||
| chr12:62555353 | G | GT | 12 | a0001c0002t0002g0254 a0001c0002t0013g0306 a0001c0002t0013g0308 others(9): Show |
12 | HG01074.hp1 HG01256.hp1 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.3211-631dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 24/34 | INFO_REALIGN_3_PRIME | chr12 | 62555353 | ||||||
| chr12:62555572 | G | A | 1 | a0002c0001t0001g0170 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.3211-422G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 24/34 | chr12 | 62555572 | |||||||
| chr12:62555657 | A | G | 1 | a0001c0003t0005g0098 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3211-337A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 24/34 | chr12 | 62555657 | |||||||
| chr12:62555807 | T | TA | 59 | a0001c0002t0002g0298 a0001c0002t0002g0317 a0001c0002t0002g0322 others(56): Show |
59 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.3211-168dupA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 24/34 | INFO_REALIGN_3_PRIME | chr12 | 62555807 | ||||||
| chr12:62555807 | TA | T | 118 | a0001c0002t0002g0351 a0001c0002t0011g0300 a0001c0002t0031g0136 others(115): Show |
120 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.3211-168delA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 24/34 | INFO_REALIGN_3_PRIME | chr12 | 62555807 | ||||||
| chr12:62555808 | A | C | 1 | a0002c0001t0006g0190 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.3211-186A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 24/34 | chr12 | 62555808 | |||||||
| chr12:62555825 | A | T | 1 | a0002c0001t0006g0190 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.3211-169A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 24/34 | chr12 | 62555825 | |||||||
| chr12:62555953 | A | G | 1 | a0001c0006t0033g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3211-41A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 24/34 | chr12 | 62555953 | |||||||
| chr12:62556328 | C | T | 3 | a0001c0005t0003g0131 a0001c0005t0003g0132 a0001c0005t0003g0133 |
3 | NA18969.hp2 NA18977.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.3409+136C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62556328 | |||||||
| chr12:62556455 | T | C | 241 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0003g0135 others(238): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.3409+263T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62556455 | |||||||
| chr12:62556487 | G | A | 1 | a0001c0006t0034g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3409+295G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62556487 | |||||||
| chr12:62556593 | A | G | 1 | a0001c0002t0002g0325 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.3409+401A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62556593 | |||||||
| chr12:62556776 | G | C | 136 | a0001c0002t0031g0136 a0001c0006t0007g0009 a0001c0006t0007g0010 others(133): Show |
138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.3409+584G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62556776 | |||||||
| chr12:62556989 | T | A | 59 | a0002c0001t0001g0002 a0002c0001t0001g0111 a0002c0001t0001g0143 others(56): Show |
60 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.3409+797T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62556989 | |||||||
| chr12:62557029 | A | T | 1 | a0001c0002t0003g0135 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3409+837A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557029 | |||||||
| chr12:62557093 | A | G | 1 | a0002c0001t0006g0203 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3409+901A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557093 | |||||||
| chr12:62557331 | G | A | 2 | a0001c0009t0019g0107 a0001c0009t0019g0108 |
2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.3409+1139G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557331 | |||||||
| chr12:62557447 | A | G | 1 | a0002c0001t0001g0221 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.3409+1255A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557447 | |||||||
| chr12:62557475 | A | G | 2 | a0001c0009t0019g0107 a0001c0009t0019g0108 |
2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.3409+1283A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557475 | |||||||
| chr12:62557498 | G | A | 1 | a0002c0001t0009g0196 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3409+1306G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557498 | |||||||
| chr12:62557874 | C | T | 1 | a0001c0005t0003g0121 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3409+1682C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557874 | |||||||
| chr12:62557928 | T | TTA | 7 | a0001c0002t0002g0331 a0001c0003t0002g0057 a0001c0003t0002g0068 others(4): Show |
7 | HG00639.hp2 HG01975.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.3409+1770_3409+177 others(6): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557928 | ||||||
| chr12:62557928 | T | TTATATA | 4 | a0001c0002t0002g0026 a0001c0003t0005g0052 a0001c0003t0005g0087 others(1): Show |
4 | HG00621.hp1 HG02895.hp2 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.3409+1766_3409+177 others(10): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557928 | ||||||
| chr12:62557928 | T | TTATATAT others(3): Show |
1 | a0001c0003t0002g0094 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.3409+1762_3409+177 others(14): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557928 | ||||||
| chr12:62557928 | T | TTATATAT others(7): Show |
2 | a0001c0002t0022g0294 a0001c0003t0005g0101 |
2 | HG00597.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.3409+1758_3409+177 others(18): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557928 | ||||||
| chr12:62557928 | T | TTATATAT others(9): Show |
1 | a0001c0002t0014g0290 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.3409+1756_3409+177 others(20): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557928 | ||||||
| chr12:62557928 | TTA | T | 3 | a0001c0003t0005g0037 a0001c0003t0005g0038 a0001c0003t0005g0039 |
3 | HG02258.hp2 HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3409+1770_3409+177 others(6): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557928 | ||||||
| chr12:62557928 | TTATATAT others(5): Show |
T | 1 | a0001c0003t0021g0001 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.3409+1760_3409+177 others(16): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557928 | ||||||
| chr12:62557928 | TTATATAT others(7): Show |
T | 4 | a0002c0001t0001g0229 a0002c0001t0001g0230 a0002c0001t0001g0244 others(1): Show |
4 | HG02559.hp2 HG02622.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.3409+1758_3409+177 others(18): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557928 | ||||||
| chr12:62557928 | TTATATAT others(9): Show |
T | 24 | a0002c0001t0001g0149 a0002c0001t0001g0150 a0002c0001t0001g0153 others(21): Show |
24 | HG00673.hp1 HG00741.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.3409+1756_3409+177 others(20): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557928 | ||||||
| chr12:62557928 | TTATATAT others(11): Show |
T | 10 | a0002c0001t0001g0003 a0002c0001t0001g0143 a0002c0001t0001g0148 others(7): Show |
11 | HG00423.hp1 HG02015.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.3409+1754_3409+177 others(22): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557928 | ||||||
| chr12:62557928 | TTATATAT others(15): Show |
T | 1 | a0001c0003t0005g0081 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3409+1750_3409+177 others(26): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557928 | ||||||
| chr12:62557930 | A | T | 2 | a0001c0016t0032g0252 a0003c0004t0004g0286 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3409+1738A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557930 | |||||||
| chr12:62557941 | TATATATA others(6): Show |
T | 1 | a0002c0001t0001g0226 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3409+1750_3409+176 others(17): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557941 | |||||||
| chr12:62557941 | TATATATA others(8): Show |
T | 1 | a0002c0001t0001g0142 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3409+1750_3409+176 others(19): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557941 | |||||||
| chr12:62557941 | TATATATA others(10): Show |
T | 3 | a0002c0001t0001g0138 a0002c0001t0001g0139 a0002c0001t0001g0219 |
3 | HG02630.hp1 HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.3409+1750_3409+176 others(21): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557941 | |||||||
| chr12:62557942 | ATATATAT others(21): Show |
A | 1 | a0002c0001t0001g0171 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.3409+1752_3409+177 others(32): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557942 | ||||||
| chr12:62557942 | ATATATAT others(25): Show |
A | 1 | a0002c0001t0001g0137 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3409+1752_3409+178 others(36): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557942 | ||||||
| chr12:62557943 | TATATATA others(8): Show |
T | 2 | a0002c0001t0001g0210 a0002c0001t0001g0243 |
2 | NA20129.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.3409+1752_3409+176 others(19): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557943 | |||||||
| chr12:62557943 | TATATATA others(10): Show |
T | 59 | a0002c0001t0001g0002 a0002c0001t0001g0111 a0002c0001t0001g0144 others(56): Show |
60 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.3409+1752_3409+176 others(21): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557943 | |||||||
| chr12:62557945 | TATATATA others(8): Show |
T | 2 | a0002c0001t0001g0218 a0002c0001t0006g0233 |
2 | HG03579.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.3409+1754_3409+176 others(19): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557945 | |||||||
| chr12:62557945 | TATATATA others(10): Show |
T | 12 | a0002c0001t0001g0146 a0002c0001t0001g0155 a0002c0001t0001g0166 others(9): Show |
12 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.3409+1754_3409+177 others(21): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557945 | |||||||
| chr12:62557946 | ATATATAT others(14): Show |
A | 1 | a0003c0004t0004g0279 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.3409+1756_3409+177 others(25): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557946 | ||||||
| chr12:62557948 | ATATATAT others(10): Show |
A | 1 | a0001c0009t0019g0108 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3409+1758_3409+177 others(21): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557948 | ||||||
| chr12:62557948 | ATATATAT others(14): Show |
A | 5 | a0003c0004t0004g0264 a0003c0004t0004g0280 a0003c0004t0004g0281 others(2): Show |
5 | HG02523.hp1 NA18967.hp1 NA19077.hp1 others(2): Show |
intron_variant | MODIFIER | c.3409+1758_3409+177 others(25): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557948 | ||||||
| chr12:62557956 | A | T | 1 | a0002c0001t0001g0226 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3409+1764A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557956 | |||||||
| chr12:62557958 | A | T | 8 | a0001c0018t0002g0299 a0002c0001t0001g0142 a0002c0001t0001g0149 others(5): Show |
8 | HG02055.hp1 HG02145.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.3409+1766A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557958 | |||||||
| chr12:62557959 | TA | T | 4 | a0001c0002t0002g0325 a0001c0002t0002g0330 a0001c0002t0011g0255 others(1): Show |
4 | HG02280.hp1 HG02735.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.3409+1768delA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557959 | |||||||
| chr12:62557960 | A | AT | 9 | a0001c0002t0002g0318 a0001c0002t0002g0353 a0001c0002t0002g0363 others(6): Show |
9 | HG01255.hp2 HG02027.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.3409+1769dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557960 | ||||||
| chr12:62557960 | A | ATT | 3 | a0001c0002t0011g0302 a0005c0008t0002g0334 a0005c0008t0002g0364 |
3 | NA19060.hp1 NA19064.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3409+1769_3409+177 others(6): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557960 | ||||||
| chr12:62557960 | A | T | 41 | a0001c0002t0002g0254 a0001c0002t0002g0321 a0001c0002t0002g0351 others(38): Show |
42 | HG00673.hp1 HG00741.hp1 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.3409+1768A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557960 | |||||||
| chr12:62557960 | ATATTTT | A | 11 | a0001c0005t0003g0118 a0001c0005t0003g0122 a0001c0005t0003g0123 others(8): Show |
11 | HG00738.hp2 HG01081.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.3409+1770_3409+177 others(10): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557960 | ||||||
| chr12:62557961 | TA | T | 4 | a0001c0002t0002g0339 a0001c0002t0015g0314 a0004c0007t0002g0327 others(1): Show |
4 | HG01517.hp1 HG02165.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.3409+1770delA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557961 | |||||||
| chr12:62557962 | A | AT | 8 | a0001c0002t0002g0256 a0001c0002t0002g0298 a0001c0002t0002g0324 others(5): Show |
8 | HG00621.hp2 HG01928.hp2 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.3409+1799dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | ||||||
| chr12:62557962 | A | ATAT | 11 | a0001c0003t0002g0069 a0001c0003t0002g0070 a0001c0003t0002g0077 others(8): Show |
11 | HG00140.hp1 HG02165.hp1 HG03017.hp2 others(8): Show |
intron_variant | MODIFIER | c.3409+1771_3409+177 others(7): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | ||||||
| chr12:62557962 | A | ATATATAT others(4): Show |
1 | a0001c0003t0003g0036 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3409+1771_3409+177 others(15): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | ||||||
| chr12:62557962 | A | ATATATAT others(16): Show |
1 | a0001c0006t0003g0008 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3409+1771_3409+177 others(27): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | ||||||
| chr12:62557962 | A | ATATATAT others(11): Show |
1 | a0001c0006t0003g0106 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3409+1771_3409+177 others(22): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | ||||||
| chr12:62557962 | A | ATATATAT others(17): Show |
1 | a0001c0006t0003g0007 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3409+1771_3409+177 others(28): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | ||||||
| chr12:62557962 | A | ATATATAT others(14): Show |
1 | a0001c0006t0007g0010 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3409+1771_3409+177 others(25): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | ||||||
| chr12:62557962 | A | ATATATAT others(15): Show |
1 | a0001c0006t0003g0006 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3409+1771_3409+177 others(26): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | ||||||
| chr12:62557962 | A | ATATATAT others(8): Show |
1 | a0001c0006t0003g0105 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3409+1771_3409+177 others(19): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | ||||||
| chr12:62557962 | A | ATATATAT others(11): Show |
1 | a0001c0006t0042g0004 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3409+1771_3409+177 others(22): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | ||||||
| chr12:62557962 | A | ATATATAT others(9): Show |
1 | a0001c0006t0007g0021 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3409+1771_3409+177 others(20): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | ||||||
| chr12:62557962 | A | ATATATAT others(11): Show |
2 | a0001c0006t0007g0009 a0001c0006t0007g0015 |
2 | HG01099.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.3409+1771_3409+177 others(22): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | ||||||
| chr12:62557962 | A | ATATATAT others(14): Show |
1 | a0001c0006t0003g0005 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3409+1771_3409+177 others(25): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | ||||||
| chr12:62557962 | A | ATATATAT others(6): Show |
1 | a0001c0006t0034g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3409+1771_3409+177 others(17): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | ||||||
| chr12:62557962 | A | ATATATAT others(7): Show |
3 | a0001c0006t0003g0102 a0001c0006t0003g0103 a0001c0006t0003g0104 |
3 | HG02257.hp2 HG02486.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.3409+1771_3409+177 others(18): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | ||||||
| chr12:62557962 | A | ATATATAT others(9): Show |
2 | a0001c0006t0007g0017 a0001c0006t0007g0019 |
2 | HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.3409+1771_3409+177 others(20): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | ||||||
| chr12:62557962 | A | ATATATAT others(10): Show |
1 | a0001c0006t0007g0016 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3409+1771_3409+177 others(21): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | ||||||
| chr12:62557962 | A | ATATATAT others(5): Show |
1 | a0001c0003t0003g0035 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3409+1771_3409+177 others(16): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | ||||||
| chr12:62557962 | A | ATATATAT others(6): Show |
1 | a0001c0006t0007g0011 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3409+1771_3409+177 others(17): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | ||||||
| chr12:62557962 | A | ATATATTT others(3): Show |
1 | a0001c0003t0003g0042 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.3409+1771_3409+177 others(14): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | ||||||
| chr12:62557962 | A | ATATATTT others(5): Show |
2 | a0001c0006t0007g0014 a0001c0006t0007g0018 |
2 | HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.3409+1771_3409+177 others(16): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | ||||||
| chr12:62557962 | A | ATATATTT others(6): Show |
1 | a0001c0006t0007g0012 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3409+1771_3409+177 others(17): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | ||||||
| chr12:62557962 | A | ATTT | 17 | a0001c0002t0002g0317 a0001c0002t0010g0023 a0001c0002t0010g0031 others(14): Show |
17 | HG02015.hp2 HG02145.hp2 HG02886.hp2 others(14): Show |
intron_variant | MODIFIER | c.3409+1797_3409+179 others(7): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | ||||||
| chr12:62557962 | A | T | 150 | a0001c0002t0002g0254 a0001c0002t0002g0318 a0001c0002t0002g0321 others(147): Show |
153 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.3409+1770A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557962 | |||||||
| chr12:62557962 | ATTTTTTT others(3): Show |
A | 1 | a0001c0002t0048g0320 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3409+1790_3409+179 others(14): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62557962 | ||||||
| chr12:62557963 | T | TA | 3 | a0001c0002t0002g0343 a0001c0002t0014g0291 a0001c0003t0005g0067 |
3 | HG01496.hp2 HG03654.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.3409+1771_3409+177 others(5): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557963 | |||||||
| chr12:62557963 | T | TATA | 7 | a0001c0003t0002g0056 a0001c0003t0002g0082 a0001c0003t0002g0084 others(4): Show |
7 | HG00639.hp1 HG01192.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.3409+1771_3409+177 others(7): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557963 | |||||||
| chr12:62557963 | T | TATATA | 10 | a0001c0002t0002g0304 a0003c0004t0004g0258 a0003c0004t0004g0259 others(7): Show |
10 | HG01069.hp2 HG01074.hp2 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.3409+1771_3409+177 others(9): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557963 | |||||||
| chr12:62557963 | T | TATATATA | 10 | a0001c0002t0013g0306 a0001c0002t0014g0289 a0001c0002t0037g0313 others(7): Show |
10 | HG00673.hp2 HG01074.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.3409+1771_3409+177 others(11): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557963 | |||||||
| chr12:62557963 | T | TATATATA others(4): Show |
7 | a0001c0002t0013g0308 a0001c0002t0026g0310 a0003c0004t0004g0262 others(4): Show |
7 | HG00323.hp2 HG00733.hp2 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.3409+1771_3409+177 others(15): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557963 | |||||||
| chr12:62557963 | T | TATATATA others(10): Show |
1 | a0001c0006t0007g0013 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3409+1771_3409+177 others(21): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557963 | |||||||
| chr12:62557964 | T | A | 9 | a0001c0002t0013g0312 a0001c0002t0014g0290 a0001c0003t0002g0057 others(6): Show |
9 | HG00735.hp2 HG01070.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.3409+1772T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557964 | |||||||
| chr12:62557965 | T | A | 31 | a0001c0002t0002g0343 a0001c0002t0014g0289 a0001c0002t0014g0291 others(28): Show |
31 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.3409+1773T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557965 | |||||||
| chr12:62557966 | T | A | 8 | a0001c0002t0014g0290 a0001c0002t0020g0287 a0001c0002t0020g0292 others(5): Show |
8 | HG00735.hp2 HG01070.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.3409+1774T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557966 | |||||||
| chr12:62557967 | T | A | 21 | a0001c0002t0014g0289 a0001c0002t0014g0291 a0003c0004t0004g0258 others(18): Show |
21 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.3409+1775T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557967 | |||||||
| chr12:62557968 | T | A | 3 | a0001c0002t0014g0290 a0003c0004t0004g0269 a0003c0004t0004g0274 |
3 | HG01070.hp2 HG02300.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.3409+1776T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557968 | |||||||
| chr12:62557969 | T | A | 10 | a0001c0002t0014g0289 a0003c0004t0004g0258 a0003c0004t0004g0259 others(7): Show |
10 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(7): Show |
intron_variant | MODIFIER | c.3409+1777T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557969 | |||||||
| chr12:62557970 | T | A | 2 | a0001c0002t0002g0325 a0003c0004t0004g0269 |
2 | HG01070.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.3409+1778T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557970 | |||||||
| chr12:62557971 | T | A | 5 | a0003c0004t0004g0258 a0003c0004t0004g0259 a0003c0004t0004g0273 others(2): Show |
5 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.3409+1779T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557971 | |||||||
| chr12:62557974 | T | A | 1 | a0001c0002t0048g0320 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3409+1782T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557974 | |||||||
| chr12:62557997 | G | C | 2 | a0001c0009t0019g0107 a0001c0009t0019g0108 |
2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.3409+1805G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62557997 | |||||||
| chr12:62558059 | C | G | 1 | a0001c0002t0031g0136 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3409+1867C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62558059 | |||||||
| chr12:62558106 | C | T | 1 | a0002c0001t0001g0178 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.3409+1914C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62558106 | |||||||
| chr12:62558184 | G | A | 1 | a0005c0008t0002g0340 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3409+1992G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62558184 | |||||||
| chr12:62558497 | C | T | 12 | a0001c0006t0007g0009 a0001c0006t0007g0010 a0001c0006t0007g0011 others(9): Show |
12 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.3410-1994C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62558497 | |||||||
| chr12:62558500 | G | A | 1 | a0001c0002t0002g0359 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3410-1991G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62558500 | |||||||
| chr12:62558689 | A | AT | 22 | a0001c0002t0014g0288 a0001c0002t0014g0289 a0001c0002t0014g0290 others(19): Show |
22 | HG00099.hp2 HG01071.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.3410-1785dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62558689 | ||||||
| chr12:62558689 | AT | A | 12 | a0001c0002t0002g0345 a0001c0002t0013g0306 a0001c0002t0013g0308 others(9): Show |
12 | HG01074.hp1 HG01256.hp1 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.3410-1785delT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62558689 | ||||||
| chr12:62558814 | C | T | 1 | a0002c0001t0025g0189 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3410-1677C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62558814 | |||||||
| chr12:62558881 | C | T | 6 | a0001c0002t0014g0288 a0001c0002t0014g0289 a0001c0002t0014g0290 others(3): Show |
6 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.3410-1610C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62558881 | |||||||
| chr12:62558916 | C | T | 148 | a0001c0002t0031g0136 a0001c0006t0003g0005 a0001c0006t0003g0006 others(145): Show |
150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.3410-1575C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62558916 | |||||||
| chr12:62558917 | C | T | 5 | a0001c0006t0003g0102 a0001c0006t0003g0103 a0001c0006t0003g0104 others(2): Show |
5 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.3410-1574C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62558917 | |||||||
| chr12:62559080 | A | T | 4 | a0001c0005t0003g0128 a0001c0005t0003g0129 a0001c0005t0003g0130 others(1): Show |
4 | HG01109.hp1 HG01256.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.3410-1411A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62559080 | |||||||
| chr12:62559121 | A | G | 28 | a0002c0001t0006g0145 a0002c0001t0006g0186 a0002c0001t0006g0190 others(25): Show |
28 | HG00438.hp2 HG00642.hp1 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.3410-1370A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62559121 | |||||||
| chr12:62559130 | C | T | 136 | a0001c0002t0031g0136 a0001c0006t0007g0009 a0001c0006t0007g0010 others(133): Show |
138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.3410-1361C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62559130 | |||||||
| chr12:62559201 | A | G | 2 | a0001c0002t0002g0322 a0001c0002t0002g0331 |
2 | NA18945.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.3410-1290A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62559201 | |||||||
| chr12:62559417 | A | G | 1 | a0002c0001t0001g0150 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.3410-1074A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62559417 | |||||||
| chr12:62559577 | A | G | 1 | a0002c0001t0012g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3410-914A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62559577 | |||||||
| chr12:62559742 | T | C | 1 | a0003c0004t0044g0263 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.3410-749T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62559742 | |||||||
| chr12:62559774 | TA | T | 228 | a0001c0002t0003g0135 a0001c0002t0013g0306 a0001c0002t0013g0308 others(225): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.3410-704delA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62559774 | ||||||
| chr12:62559873 | T | C | 60 | a0002c0001t0001g0002 a0002c0001t0001g0111 a0002c0001t0001g0143 others(57): Show |
61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.3410-618T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62559873 | |||||||
| chr12:62559909 | T | C | 10 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(7): Show |
10 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.3410-582T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62559909 | |||||||
| chr12:62559932 | A | G | 2 | a0001c0002t0013g0309 a0001c0002t0026g0310 |
2 | HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3410-559A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62559932 | |||||||
| chr12:62559993 | A | C | 38 | a0001c0002t0013g0306 a0001c0002t0013g0308 a0001c0002t0013g0309 others(35): Show |
38 | HG00099.hp2 HG00735.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.3410-498A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62559993 | |||||||
| chr12:62560065 | G | A | 1 | a0001c0003t0041g0054 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3410-426G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62560065 | |||||||
| chr12:62560092 | A | G | 33 | a0003c0004t0004g0258 a0003c0004t0004g0259 a0003c0004t0004g0260 others(30): Show |
33 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.3410-399A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62560092 | |||||||
| chr12:62560113 | A | AT | 241 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0003g0135 others(238): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.3410-370dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr12 | 62560113 | ||||||
| chr12:62560436 | A | G | 10 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(7): Show |
10 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.3410-55A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 25/34 | chr12 | 62560436 | |||||||
| chr12:62561210 | A | C | 5 | a0001c0002t0013g0306 a0001c0002t0013g0308 a0001c0002t0013g0312 others(2): Show |
5 | HG01074.hp1 HG01256.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.4032+97A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62561210 | |||||||
| chr12:62561664 | G | A | 1 | a0001c0003t0005g0098 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.4032+551G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62561664 | |||||||
| chr12:62561860 | G | A | 1 | a0003c0004t0004g0279 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.4032+747G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62561860 | |||||||
| chr12:62562233 | C | T | 56 | a0001c0002t0002g0254 a0001c0002t0002g0256 a0001c0002t0002g0298 others(53): Show |
56 | HG00423.hp2 HG00438.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.4032+1120C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62562233 | |||||||
| chr12:62562656 | G | A | 3 | a0002c0001t0001g0138 a0002c0001t0001g0219 a0002c0001t0030g0140 |
3 | HG03098.hp2 HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.4032+1543G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62562656 | |||||||
| chr12:62562711 | G | A | 3 | a0001c0003t0002g0056 a0001c0003t0002g0082 a0001c0003t0002g0095 |
3 | NA18971.hp2 NA18988.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.4032+1598G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62562711 | |||||||
| chr12:62562772 | T | A | 1 | a0002c0001t0001g0235 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.4032+1659T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62562772 | |||||||
| chr12:62562787 | A | G | 1 | a0001c0006t0007g0019 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.4032+1674A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62562787 | |||||||
| chr12:62562829 | T | C | 12 | a0001c0006t0007g0009 a0001c0006t0007g0010 a0001c0006t0007g0011 others(9): Show |
12 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.4032+1716T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62562829 | |||||||
| chr12:62562973 | A | G | 1 | a0001c0003t0050g0078 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.4032+1860A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62562973 | |||||||
| chr12:62563041 | T | C | 5 | a0002c0001t0009g0195 a0002c0001t0009g0196 a0002c0001t0009g0197 others(2): Show |
5 | HG00642.hp1 HG00733.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.4032+1928T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62563041 | |||||||
| chr12:62563046 | T | A | 5 | a0001c0006t0003g0102 a0001c0006t0003g0103 a0001c0006t0003g0104 others(2): Show |
5 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.4032+1933T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62563046 | |||||||
| chr12:62563047 | T | A | 5 | a0001c0006t0003g0102 a0001c0006t0003g0103 a0001c0006t0003g0104 others(2): Show |
5 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.4032+1934T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62563047 | |||||||
| chr12:62563255 | T | G | 45 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(42): Show |
45 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.4033-1982T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62563255 | |||||||
| chr12:62563371 | C | T | 1 | a0001c0006t0033g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4033-1866C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62563371 | |||||||
| chr12:62563505 | T | C | 1 | a0001c0006t0007g0012 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4033-1732T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62563505 | |||||||
| chr12:62563512 | C | T | 5 | a0002c0001t0009g0195 a0002c0001t0009g0196 a0002c0001t0009g0197 others(2): Show |
5 | HG00642.hp1 HG00733.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.4033-1725C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62563512 | |||||||
| chr12:62563650 | G | A | 1 | a0002c0001t0001g0146 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.4033-1587G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62563650 | |||||||
| chr12:62563775 | T | A | 1 | a0001c0003t0023g0066 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.4033-1462T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62563775 | |||||||
| chr12:62563829 | A | G | 2 | a0001c0009t0019g0107 a0001c0009t0019g0108 |
2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.4033-1408A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62563829 | |||||||
| chr12:62563858 | A | G | 7 | a0001c0002t0013g0306 a0001c0002t0013g0308 a0001c0002t0013g0309 others(4): Show |
7 | HG01074.hp1 HG01256.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.4033-1379A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62563858 | |||||||
| chr12:62564108 | A | G | 6 | a0001c0002t0014g0288 a0001c0002t0014g0289 a0001c0002t0014g0290 others(3): Show |
6 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.4033-1129A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62564108 | |||||||
| chr12:62564126 | G | C | 137 | a0001c0002t0031g0136 a0001c0003t0005g0081 a0001c0006t0007g0009 others(134): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.4033-1111G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62564126 | |||||||
| chr12:62564394 | A | T | 1 | a0001c0002t0011g0257 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.4033-843A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62564394 | |||||||
| chr12:62564471 | A | G | 1 | a0002c0001t0001g0226 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4033-766A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62564471 | |||||||
| chr12:62564577 | T | C | 16 | a0001c0003t0002g0055 a0001c0003t0002g0056 a0001c0003t0002g0057 others(13): Show |
16 | HG00544.hp1 HG01192.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.4033-660T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62564577 | |||||||
| chr12:62564627 | A | G | 1 | a0001c0002t0031g0136 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4033-610A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62564627 | |||||||
| chr12:62564789 | C | T | 1 | a0001c0002t0002g0348 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.4033-448C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62564789 | |||||||
| chr12:62564857 | G | C | 10 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(7): Show |
10 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4033-380G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62564857 | |||||||
| chr12:62564945 | T | C | 10 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(7): Show |
10 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4033-292T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 26/34 | chr12 | 62564945 | |||||||
| chr12:62565386 | T | G | 2 | a0001c0009t0019g0107 a0001c0009t0019g0108 |
2 | HG02809.hp2 HG03098.hp1 |
splice_region_variant&intron_variant | LOW | c.4176+6T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 27/34 | chr12 | 62565386 | |||||||
| chr12:62565387 | T | A | 2 | a0001c0009t0019g0107 a0001c0009t0019g0108 |
2 | HG02809.hp2 HG03098.hp1 |
splice_region_variant&intron_variant | LOW | c.4176+7T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 27/34 | chr12 | 62565387 | |||||||
| chr12:62565404 | A | T | 1 | a0003c0004t0004g0365 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.4176+24A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 27/34 | chr12 | 62565404 | |||||||
| chr12:62565476 | G | T | 1 | a0002c0001t0029g0151 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.4176+96G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 27/34 | chr12 | 62565476 | |||||||
| chr12:62565641 | C | T | 2 | a0001c0009t0019g0107 a0001c0009t0019g0108 |
2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.4176+261C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 27/34 | chr12 | 62565641 | |||||||
| chr12:62565664 | T | G | 1 | a0001c0002t0002g0325 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.4176+284T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 27/34 | chr12 | 62565664 | |||||||
| chr12:62565665 | C | T | 2 | a0001c0003t0003g0099 a0001c0003t0003g0100 |
2 | HG02615.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.4176+285C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 27/34 | chr12 | 62565665 | |||||||
| chr12:62565684 | G | A | 2 | a0001c0002t0020g0287 a0001c0002t0020g0292 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.4176+304G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 27/34 | chr12 | 62565684 | |||||||
| chr12:62565733 | T | A | 2 | a0001c0005t0003g0109 a0001c0005t0003g0110 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.4177-281T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 27/34 | chr12 | 62565733 | |||||||
| chr12:62566180 | T | G | 10 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(7): Show |
10 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4195-142T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 28/34 | chr12 | 62566180 | |||||||
| chr12:62566237 | G | A | 5 | a0002c0001t0009g0195 a0002c0001t0009g0196 a0002c0001t0009g0197 others(2): Show |
5 | HG00642.hp1 HG00733.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.4195-85G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 28/34 | chr12 | 62566237 | |||||||
| chr12:62566725 | C | T | 1 | a0001c0002t0031g0136 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4323+275C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62566725 | |||||||
| chr12:62566742 | T | TG | 41 | a0001c0002t0002g0254 a0001c0002t0002g0303 a0001c0002t0002g0324 others(38): Show |
41 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.4323+298dupG | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | INFO_REALIGN_3_PRIME | chr12 | 62566742 | ||||||
| chr12:62566832 | A | G | 1 | a0002c0001t0001g0230 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4323+382A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62566832 | |||||||
| chr12:62566866 | C | G | 1 | a0003c0004t0004g0260 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.4323+416C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62566866 | |||||||
| chr12:62566971 | T | C | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4323+521T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62566971 | |||||||
| chr12:62567097 | T | C | 1 | a0002c0001t0001g0219 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4323+647T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62567097 | |||||||
| chr12:62567100 | A | G | 136 | a0001c0002t0031g0136 a0001c0006t0007g0009 a0001c0006t0007g0010 others(133): Show |
138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.4323+650A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62567100 | |||||||
| chr12:62567104 | C | T | 1 | a0001c0003t0005g0067 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.4323+654C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62567104 | |||||||
| chr12:62567204 | A | G | 1 | a0001c0002t0003g0135 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4323+754A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62567204 | |||||||
| chr12:62567491 | C | G | 1 | a0001c0006t0034g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4323+1041C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62567491 | |||||||
| chr12:62567519 | C | T | 120 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0111 others(117): Show |
122 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.4323+1069C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62567519 | |||||||
| chr12:62567619 | G | A | 10 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(7): Show |
10 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4323+1169G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62567619 | |||||||
| chr12:62567714 | C | T | 1 | a0001c0002t0014g0288 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.4323+1264C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62567714 | |||||||
| chr12:62567844 | A | T | 3 | a0001c0003t0002g0057 a0001c0003t0002g0072 a0001c0003t0002g0084 |
3 | HG01192.hp2 HG01496.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.4323+1394A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62567844 | |||||||
| chr12:62568021 | G | A | 120 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0111 others(117): Show |
122 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.4323+1571G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62568021 | |||||||
| chr12:62568064 | C | T | 4 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(1): Show |
4 | HG02976.hp1 HG03195.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.4323+1614C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62568064 | |||||||
| chr12:62568113 | T | A | 7 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0027 others(4): Show |
7 | HG02145.hp2 HG02280.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.4323+1663T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62568113 | |||||||
| chr12:62568297 | A | G | 1 | a0002c0001t0006g0200 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.4323+1847A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62568297 | |||||||
| chr12:62568332 | A | T | 1 | a0001c0003t0005g0034 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4323+1882A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62568332 | |||||||
| chr12:62568417 | C | T | 1 | a0001c0003t0002g0073 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.4323+1967C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62568417 | |||||||
| chr12:62568469 | G | A | 1 | a0001c0002t0002g0321 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.4323+2019G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62568469 | |||||||
| chr12:62568598 | C | T | 1 | a0001c0002t0014g0291 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.4323+2148C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62568598 | |||||||
| chr12:62568608 | G | A | 1 | a0001c0003t0003g0041 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.4323+2158G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62568608 | |||||||
| chr12:62568659 | C | T | 1 | a0002c0001t0001g0161 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.4323+2209C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62568659 | |||||||
| chr12:62569290 | T | C | 10 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(7): Show |
10 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4324-2102T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62569290 | |||||||
| chr12:62569590 | A | G | 1 | a0001c0002t0022g0294 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4324-1802A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62569590 | |||||||
| chr12:62569596 | ATTC | A | 4 | a0002c0001t0001g0226 a0002c0001t0001g0229 a0002c0001t0001g0230 others(1): Show |
4 | HG02559.hp2 HG02622.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.4324-1787_4324-178 others(7): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | INFO_REALIGN_3_PRIME | chr12 | 62569596 | ||||||
| chr12:62569775 | G | A | 1 | a0001c0003t0005g0081 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.4324-1617G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62569775 | |||||||
| chr12:62570115 | G | A | 1 | a0001c0002t0002g0304 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.4324-1277G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62570115 | |||||||
| chr12:62570231 | A | C | 3 | a0002c0001t0001g0206 a0002c0001t0001g0207 a0002c0001t0001g0213 |
3 | HG01884.hp2 HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4324-1161A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62570231 | |||||||
| chr12:62570365 | T | C | 11 | a0003c0004t0004g0258 a0003c0004t0004g0259 a0003c0004t0004g0262 others(8): Show |
11 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.4324-1027T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62570365 | |||||||
| chr12:62570372 | G | A | 3 | a0001c0002t0017g0024 a0001c0002t0017g0032 a0001c0002t0017g0033 |
3 | HG01109.hp2 HG02970.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.4324-1020G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62570372 | |||||||
| chr12:62570416 | A | G | 1 | a0001c0018t0002g0299 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4324-976A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62570416 | |||||||
| chr12:62570568 | C | G | 1 | a0003c0004t0004g0275 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.4324-824C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62570568 | |||||||
| chr12:62570600 | A | G | 1 | a0001c0002t0022g0294 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4324-792A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62570600 | |||||||
| chr12:62570642 | A | G | 1 | a0002c0001t0001g0216 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4324-750A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62570642 | |||||||
| chr12:62570663 | G | A | 15 | a0002c0001t0001g0137 a0002c0001t0001g0206 a0002c0001t0001g0207 others(12): Show |
15 | HG00423.hp1 HG01884.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.4324-729G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62570663 | |||||||
| chr12:62570722 | C | CT | 52 | a0001c0002t0002g0318 a0001c0002t0002g0324 a0001c0002t0002g0342 others(49): Show |
52 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.4324-641dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | INFO_REALIGN_3_PRIME | chr12 | 62570722 | ||||||
| chr12:62570722 | C | CTT | 9 | a0001c0002t0002g0335 a0001c0002t0002g0359 a0001c0002t0013g0306 others(6): Show |
9 | HG01074.hp1 HG01256.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.4324-642_4324-641d others(4): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | INFO_REALIGN_3_PRIME | chr12 | 62570722 | ||||||
| chr12:62570722 | CT | C | 91 | a0001c0002t0002g0325 a0001c0002t0002g0332 a0001c0002t0011g0255 others(88): Show |
91 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.4324-641delT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | INFO_REALIGN_3_PRIME | chr12 | 62570722 | ||||||
| chr12:62570722 | CTT | C | 6 | a0001c0003t0003g0099 a0001c0003t0003g0100 a0001c0005t0003g0109 others(3): Show |
6 | HG01168.hp2 HG01255.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.4324-642_4324-641d others(4): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | INFO_REALIGN_3_PRIME | chr12 | 62570722 | ||||||
| chr12:62570772 | T | C | 148 | a0001c0002t0031g0136 a0001c0006t0003g0005 a0001c0006t0003g0006 others(145): Show |
150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.4324-620T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62570772 | |||||||
| chr12:62570827 | G | A | 16 | a0001c0002t0031g0136 a0001c0006t0007g0009 a0001c0006t0007g0010 others(13): Show |
16 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.4324-565G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62570827 | |||||||
| chr12:62570869 | C | G | 1 | a0001c0003t0005g0067 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.4324-523C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62570869 | |||||||
| chr12:62570880 | T | A | 1 | a0002c0001t0001g0215 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4324-512T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62570880 | |||||||
| chr12:62570916 | G | C | 5 | a0001c0003t0003g0041 a0001c0003t0003g0042 a0001c0003t0003g0043 others(2): Show |
6 | HG01069.hp1 HG01071.hp1 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.4324-476G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62570916 | |||||||
| chr12:62571025 | T | C | 242 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0002g0325 others(239): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.4324-367T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62571025 | |||||||
| chr12:62571195 | A | T | 7 | a0001c0002t0013g0306 a0001c0002t0013g0308 a0001c0002t0013g0309 others(4): Show |
7 | HG01074.hp1 HG01256.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.4324-197A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62571195 | |||||||
| chr12:62571224 | C | T | 2 | a0001c0003t0005g0034 a0001c0003t0005g0040 |
2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.4324-168C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62571224 | |||||||
| chr12:62571369 | T | C | 41 | a0001c0002t0003g0135 a0001c0002t0014g0288 a0001c0002t0014g0289 others(38): Show |
42 | HG00099.hp2 HG00735.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.4324-23T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 29/34 | chr12 | 62571369 | |||||||
| chr12:62571804 | A | G | 3 | a0002c0001t0001g0210 a0002c0001t0001g0235 a0002c0001t0012g0211 |
3 | HG03669.hp2 HG03927.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.4514+222A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62571804 | |||||||
| chr12:62572215 | A | T | 1 | a0001c0006t0003g0104 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4514+633A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62572215 | |||||||
| chr12:62572415 | T | C | 5 | a0001c0003t0003g0041 a0001c0003t0003g0042 a0001c0003t0003g0043 others(2): Show |
6 | HG01069.hp1 HG01071.hp1 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.4514+833T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62572415 | |||||||
| chr12:62572804 | C | T | 25 | a0001c0005t0003g0109 a0001c0005t0003g0110 a0001c0005t0003g0117 others(22): Show |
25 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.4514+1222C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62572804 | |||||||
| chr12:62572815 | A | T | 2 | a0001c0003t0003g0099 a0001c0003t0003g0100 |
2 | HG02615.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.4514+1233A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62572815 | |||||||
| chr12:62572886 | A | G | 1 | a0001c0006t0007g0012 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4514+1304A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62572886 | |||||||
| chr12:62573171 | G | C | 5 | a0003c0004t0004g0264 a0003c0004t0004g0280 a0003c0004t0004g0281 others(2): Show |
5 | HG02523.hp1 NA18967.hp1 NA19077.hp1 others(2): Show |
intron_variant | MODIFIER | c.4514+1589G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62573171 | |||||||
| chr12:62573189 | G | A | 1 | a0002c0001t0001g0180 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.4514+1607G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62573189 | |||||||
| chr12:62573315 | T | C | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4514+1733T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62573315 | |||||||
| chr12:62573394 | C | CT | 8 | a0001c0003t0005g0101 a0001c0003t0008g0076 a0001c0005t0003g0120 others(5): Show |
8 | HG00597.hp2 HG01255.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.4514+1827dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr12 | 62573394 | ||||||
| chr12:62573517 | A | G | 2 | a0001c0009t0019g0107 a0001c0009t0019g0108 |
2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.4514+1935A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62573517 | |||||||
| chr12:62573526 | A | G | 4 | a0001c0003t0003g0035 a0001c0003t0003g0036 a0001c0003t0003g0099 others(1): Show |
4 | HG01361.hp2 HG02257.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.4514+1944A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62573526 | |||||||
| chr12:62573650 | C | T | 25 | a0001c0005t0003g0109 a0001c0005t0003g0110 a0001c0005t0003g0117 others(22): Show |
25 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.4514+2068C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62573650 | |||||||
| chr12:62573665 | T | G | 3 | a0001c0003t0002g0068 a0001c0006t0003g0008 a0002c0001t0001g0246 |
3 | HG01891.hp1 NA18962.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.4514+2083T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62573665 | |||||||
| chr12:62573668 | T | C | 7 | a0001c0002t0013g0306 a0001c0002t0013g0308 a0001c0002t0013g0309 others(4): Show |
7 | HG01074.hp1 HG01256.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.4514+2086T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62573668 | |||||||
| chr12:62574225 | A | G | 1 | a0001c0003t0005g0040 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4514+2643A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62574225 | |||||||
| chr12:62574343 | CTTGGAAA others(13): Show |
C | 3 | a0003c0004t0004g0258 a0003c0004t0004g0259 a0003c0004t0004g0296 |
3 | HG01167.hp1 HG01169.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.4514+2767_4514+278 others(24): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr12 | 62574343 | ||||||
| chr12:62574407 | C | T | 10 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(7): Show |
10 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4514+2825C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62574407 | |||||||
| chr12:62574436 | G | A | 9 | a0002c0001t0001g0163 a0002c0001t0001g0166 a0002c0001t0001g0172 others(6): Show |
9 | HG02027.hp2 HG02135.hp1 NA18943.hp1 others(6): Show |
intron_variant | MODIFIER | c.4514+2854G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62574436 | |||||||
| chr12:62574500 | T | C | 136 | a0001c0002t0031g0136 a0001c0006t0007g0009 a0001c0006t0007g0010 others(133): Show |
138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.4514+2918T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62574500 | |||||||
| chr12:62574596 | A | T | 1 | a0001c0002t0048g0320 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4514+3014A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62574596 | |||||||
| chr12:62574677 | T | C | 1 | a0001c0002t0002g0325 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.4514+3095T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62574677 | |||||||
| chr12:62574825 | T | C | 1 | a0002c0001t0001g0205 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.4514+3243T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62574825 | |||||||
| chr12:62574960 | CA | C | 148 | a0001c0002t0031g0136 a0001c0006t0003g0005 a0001c0006t0003g0006 others(145): Show |
150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.4514+3386delA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr12 | 62574960 | ||||||
| chr12:62575225 | G | T | 1 | a0001c0003t0005g0045 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4515-3220G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62575225 | |||||||
| chr12:62575291 | G | A | 1 | a0002c0001t0012g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4515-3154G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62575291 | |||||||
| chr12:62575888 | T | C | 45 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(42): Show |
45 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.4515-2557T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62575888 | |||||||
| chr12:62575924 | C | T | 60 | a0002c0001t0001g0003 a0002c0001t0001g0137 a0002c0001t0001g0138 others(57): Show |
61 | HG00423.hp1 HG00438.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.4515-2521C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62575924 | |||||||
| chr12:62576006 | G | A | 2 | a0002c0001t0001g0003 a0002c0001t0001g0217 |
3 | HG02886.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4515-2439G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62576006 | |||||||
| chr12:62576073 | T | C | 1 | a0003c0004t0004g0286 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4515-2372T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62576073 | |||||||
| chr12:62576172 | G | A | 54 | a0002c0001t0001g0002 a0002c0001t0001g0111 a0002c0001t0001g0143 others(51): Show |
55 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.4515-2273G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62576172 | |||||||
| chr12:62576358 | G | T | 7 | a0001c0002t0013g0306 a0001c0002t0013g0308 a0001c0002t0013g0309 others(4): Show |
7 | HG01074.hp1 HG01256.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.4515-2087G>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62576358 | |||||||
| chr12:62576526 | C | T | 3 | a0001c0003t0003g0041 a0001c0003t0003g0042 a0001c0003t0003g0043 |
3 | NA19004.hp2 NA19070.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.4515-1919C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62576526 | |||||||
| chr12:62576657 | C | T | 25 | a0001c0005t0003g0109 a0001c0005t0003g0110 a0001c0005t0003g0117 others(22): Show |
25 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.4515-1788C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62576657 | |||||||
| chr12:62576678 | A | G | 10 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(7): Show |
10 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4515-1767A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62576678 | |||||||
| chr12:62576702 | A | G | 135 | a0001c0002t0031g0136 a0001c0006t0007g0009 a0001c0006t0007g0010 others(132): Show |
137 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.4515-1743A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62576702 | |||||||
| chr12:62576728 | T | C | 1 | a0002c0001t0001g0215 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4515-1717T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62576728 | |||||||
| chr12:62577045 | A | T | 2 | a0001c0005t0003g0122 a0001c0005t0003g0124 |
2 | HG00738.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.4515-1400A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62577045 | |||||||
| chr12:62577052 | C | T | 1 | a0001c0002t0002g0321 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.4515-1393C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62577052 | |||||||
| chr12:62577154 | G | A | 1 | a0002c0001t0001g0221 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.4515-1291G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62577154 | |||||||
| chr12:62577598 | T | C | 2 | a0001c0002t0035g0025 a0002c0001t0001g0172 |
2 | HG02280.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.4515-847T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62577598 | |||||||
| chr12:62577672 | T | C | 4 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(1): Show |
4 | HG02976.hp1 HG03195.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.4515-773T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62577672 | |||||||
| chr12:62578082 | A | T | 1 | a0002c0001t0001g0149 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.4515-363A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62578082 | |||||||
| chr12:62578114 | C | T | 1 | a0001c0002t0002g0324 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.4515-331C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62578114 | |||||||
| chr12:62578123 | T | C | 2 | a0003c0004t0004g0258 a0003c0004t0004g0259 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.4515-322T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62578123 | |||||||
| chr12:62578162 | C | T | 1 | a0002c0001t0001g0163 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.4515-283C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | chr12 | 62578162 | |||||||
| chr12:62578430 | G | GT | 146 | a0001c0002t0031g0136 a0001c0006t0003g0005 a0001c0006t0003g0006 others(143): Show |
148 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(145): Show |
splice_acceptor_variant&intron_variant | HIGH | c.4515-3dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr12 | 62578430 | ||||||
| chr12:62578646 | C | T | 1 | a0001c0002t0011g0257 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.4575+141C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 31/34 | chr12 | 62578646 | |||||||
| chr12:62578765 | T | G | 6 | a0001c0002t0014g0288 a0001c0002t0014g0289 a0001c0002t0014g0290 others(3): Show |
6 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.4575+260T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 31/34 | chr12 | 62578765 | |||||||
| chr12:62578810 | A | G | 1 | a0001c0002t0002g0304 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.4575+305A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 31/34 | chr12 | 62578810 | |||||||
| chr12:62579072 | C | CA | 11 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(8): Show |
11 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.4575+579dupA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 31/34 | INFO_REALIGN_3_PRIME | chr12 | 62579072 | ||||||
| chr12:62579446 | G | A | 1 | a0001c0002t0003g0135 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4576-851G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 31/34 | chr12 | 62579446 | |||||||
| chr12:62579450 | G | A | 2 | a0003c0004t0004g0267 a0003c0004t0004g0271 |
2 | NA19062.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.4576-847G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 31/34 | chr12 | 62579450 | |||||||
| chr12:62579550 | C | T | 1 | a0003c0004t0004g0271 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.4576-747C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 31/34 | chr12 | 62579550 | |||||||
| chr12:62579559 | T | TA | 134 | a0001c0002t0031g0136 a0001c0003t0005g0091 a0001c0003t0008g0075 others(131): Show |
136 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.4576-721dupA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 31/34 | INFO_REALIGN_3_PRIME | chr12 | 62579559 | ||||||
| chr12:62580469 | A | C | 1 | a0001c0003t0005g0098 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.4699+49A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62580469 | |||||||
| chr12:62580601 | A | G | 7 | a0001c0002t0013g0306 a0001c0002t0013g0308 a0001c0002t0013g0309 others(4): Show |
7 | HG01074.hp1 HG01256.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.4699+181A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62580601 | |||||||
| chr12:62580688 | A | G | 1 | a0003c0004t0004g0277 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.4699+268A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62580688 | |||||||
| chr12:62580958 | G | A | 2 | a0001c0002t0002g0322 a0001c0002t0002g0331 |
2 | NA18945.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.4699+538G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62580958 | |||||||
| chr12:62581189 | A | G | 1 | a0001c0006t0007g0021 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4699+769A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62581189 | |||||||
| chr12:62581256 | C | T | 2 | a0001c0002t0013g0309 a0001c0002t0026g0310 |
2 | HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.4699+836C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62581256 | |||||||
| chr12:62581385 | G | A | 10 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(7): Show |
10 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4699+965G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62581385 | |||||||
| chr12:62581459 | A | G | 1 | a0001c0003t0005g0034 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4699+1039A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62581459 | |||||||
| chr12:62581485 | C | G | 1 | a0001c0002t0013g0308 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.4699+1065C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62581485 | |||||||
| chr12:62581527 | C | T | 136 | a0001c0002t0031g0136 a0001c0006t0007g0009 a0001c0006t0007g0010 others(133): Show |
138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.4699+1107C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62581527 | |||||||
| chr12:62581606 | C | G | 10 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(7): Show |
10 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4699+1186C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62581606 | |||||||
| chr12:62581625 | C | T | 2 | a0001c0002t0011g0300 a0001c0002t0011g0302 |
2 | NA18939.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.4699+1205C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62581625 | |||||||
| chr12:62581852 | T | G | 12 | a0001c0006t0007g0009 a0001c0006t0007g0010 a0001c0006t0007g0011 others(9): Show |
12 | HG01099.hp1 HG01891.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.4699+1432T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62581852 | |||||||
| chr12:62581855 | A | C | 1 | a0001c0003t0005g0038 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4699+1435A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62581855 | |||||||
| chr12:62581905 | C | G | 6 | a0001c0002t0014g0288 a0001c0002t0014g0289 a0001c0002t0014g0290 others(3): Show |
6 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.4699+1485C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62581905 | |||||||
| chr12:62582180 | C | G | 1 | a0002c0001t0001g0161 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.4699+1760C>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62582180 | |||||||
| chr12:62582509 | CTCTTTTT others(4): Show |
C | 2 | a0002c0001t0001g0139 a0002c0001t0012g0141 |
2 | HG02145.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.4699+2101_4699+211 others(15): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62582509 | ||||||
| chr12:62582658 | C | T | 1 | a0001c0003t0005g0067 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.4699+2238C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62582658 | |||||||
| chr12:62582722 | T | TA | 93 | a0002c0001t0001g0002 a0002c0001t0001g0111 a0002c0001t0001g0143 others(90): Show |
94 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.4699+2314dupA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62582722 | ||||||
| chr12:62583361 | A | G | 1 | a0001c0002t0031g0136 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4700-1933A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62583361 | |||||||
| chr12:62583374 | A | G | 3 | a0003c0004t0004g0268 a0003c0004t0004g0269 a0003c0004t0004g0270 |
3 | HG00280.hp1 HG00733.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.4700-1920A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62583374 | |||||||
| chr12:62583382 | A | G | 136 | a0001c0002t0031g0136 a0001c0006t0007g0009 a0001c0006t0007g0010 others(133): Show |
138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.4700-1912A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62583382 | |||||||
| chr12:62583383 | G | A | 148 | a0001c0002t0031g0136 a0001c0006t0003g0005 a0001c0006t0003g0006 others(145): Show |
150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.4700-1911G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62583383 | |||||||
| chr12:62583395 | AG | A | 136 | a0001c0002t0031g0136 a0001c0006t0007g0009 a0001c0006t0007g0010 others(133): Show |
138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.4700-1897delG | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62583395 | ||||||
| chr12:62583447 | A | G | 284 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0003g0135 others(281): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.4700-1847A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62583447 | |||||||
| chr12:62583675 | A | G | 1 | a0001c0003t0005g0040 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4700-1619A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62583675 | |||||||
| chr12:62583786 | T | TA | 11 | a0001c0003t0003g0041 a0001c0003t0003g0042 a0001c0003t0003g0043 others(8): Show |
12 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.4700-1492dupA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62583786 | ||||||
| chr12:62583911 | G | A | 20 | a0001c0002t0002g0303 a0001c0002t0002g0329 a0001c0002t0002g0332 others(17): Show |
20 | HG00642.hp2 HG00735.hp1 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.4700-1383G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62583911 | |||||||
| chr12:62583960 | C | CA | 10 | a0001c0002t0002g0346 a0001c0002t0003g0135 a0001c0003t0003g0041 others(7): Show |
11 | HG00642.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.4700-1320dupA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62583960 | ||||||
| chr12:62583968 | A | C | 1 | a0001c0003t0008g0061 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.4700-1326A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62583968 | |||||||
| chr12:62583975 | C | A | 2 | a0002c0001t0001g0226 a0002c0001t0001g0229 |
2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4700-1319C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62583975 | |||||||
| chr12:62583975 | C | CA | 21 | a0001c0002t0014g0290 a0001c0006t0003g0005 a0001c0006t0003g0006 others(18): Show |
21 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.4700-1307dupA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62583975 | ||||||
| chr12:62583980 | A | C | 1 | a0002c0001t0001g0215 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4700-1314A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62583980 | |||||||
| chr12:62583987 | A | C | 2 | a0002c0001t0009g0195 a0007c0014t0009g0237 |
2 | HG00642.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.4700-1307A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62583987 | |||||||
| chr12:62584009 | G | A | 16 | a0003c0004t0004g0260 a0003c0004t0004g0264 a0003c0004t0004g0265 others(13): Show |
16 | HG00673.hp2 HG02523.hp1 NA18944.hp2 others(13): Show |
intron_variant | MODIFIER | c.4700-1285G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62584009 | |||||||
| chr12:62584112 | A | T | 1 | a0001c0002t0013g0312 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.4700-1182A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62584112 | |||||||
| chr12:62584221 | G | C | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4700-1073G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62584221 | |||||||
| chr12:62584479 | G | A | 1 | a0001c0002t0010g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4700-815G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62584479 | |||||||
| chr12:62584485 | C | T | 1 | a0002c0001t0001g0208 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4700-809C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62584485 | |||||||
| chr12:62584705 | C | CA | 100 | a0001c0002t0002g0254 a0001c0002t0002g0304 a0001c0002t0002g0331 others(97): Show |
100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.4700-566dupA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62584705 | ||||||
| chr12:62584705 | C | CAA | 21 | a0001c0002t0013g0306 a0001c0002t0013g0308 a0001c0002t0013g0309 others(18): Show |
21 | HG00741.hp2 HG01074.hp1 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.4700-567_4700-566d others(4): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62584705 | ||||||
| chr12:62584705 | CA | C | 23 | a0001c0003t0003g0043 a0001c0005t0003g0117 a0001c0005t0003g0119 others(20): Show |
23 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.4700-566delA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62584705 | ||||||
| chr12:62584775 | C | T | 1 | a0005c0008t0002g0340 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.4700-519C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62584775 | |||||||
| chr12:62584839 | G | A | 1 | a0001c0002t0003g0135 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4700-455G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62584839 | |||||||
| chr12:62585065 | GCA | G | 14 | a0001c0002t0002g0254 a0001c0002t0002g0256 a0001c0002t0002g0338 others(11): Show |
14 | HG00099.hp2 HG00621.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.4700-184_4700-183d others(4): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62585065 | ||||||
| chr12:62585065 | GCACA | G | 94 | a0001c0002t0002g0298 a0001c0002t0002g0304 a0001c0002t0002g0317 others(91): Show |
94 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.4700-186_4700-183d others(6): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62585065 | ||||||
| chr12:62585065 | GCACACA | G | 28 | a0001c0002t0002g0322 a0001c0002t0002g0331 a0001c0002t0002g0335 others(25): Show |
28 | HG00597.hp2 HG01074.hp1 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.4700-188_4700-183d others(8): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62585065 | ||||||
| chr12:62585065 | GCACACAC others(1): Show |
G | 54 | a0001c0002t0002g0321 a0001c0002t0002g0352 a0001c0002t0005g0362 others(51): Show |
55 | HG00140.hp1 HG00621.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.4700-190_4700-183d others(10): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62585065 | ||||||
| chr12:62585065 | GCACACAC others(3): Show |
G | 9 | a0001c0002t0002g0324 a0001c0003t0003g0048 a0001c0003t0005g0034 others(6): Show |
9 | HG02258.hp2 HG03471.hp2 HG03654.hp1 others(6): Show |
intron_variant | MODIFIER | c.4700-192_4700-183d others(12): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62585065 | ||||||
| chr12:62585065 | GCACACAC others(5): Show |
G | 17 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0010g0023 others(14): Show |
17 | HG01109.hp2 HG02109.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.4700-194_4700-183d others(14): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62585065 | ||||||
| chr12:62585065 | GCACACAC others(7): Show |
G | 11 | a0001c0006t0003g0006 a0001c0006t0003g0007 a0001c0006t0003g0103 others(8): Show |
11 | HG01891.hp2 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.4700-196_4700-183d others(16): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62585065 | ||||||
| chr12:62585065 | GCACACAC others(11): Show |
G | 1 | a0001c0002t0003g0135 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4700-200_4700-183d others(20): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62585065 | ||||||
| chr12:62585093 | ACACACAC others(10): Show |
A | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4700-200_4700-184d others(19): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62585093 | |||||||
| chr12:62585094 | CACACACA others(12): Show |
C | 34 | a0001c0006t0033g0022 a0002c0001t0001g0147 a0002c0001t0001g0148 others(31): Show |
34 | HG00733.hp1 HG01257.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.4700-196_4700-178d others(21): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62585094 | ||||||
| chr12:62585096 | CACACACA others(8): Show |
C | 7 | a0001c0006t0007g0009 a0001c0006t0007g0010 a0001c0006t0007g0012 others(4): Show |
7 | HG02572.hp1 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.4700-196_4700-182d others(17): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62585096 | ||||||
| chr12:62585096 | CACACACA others(10): Show |
C | 9 | a0002c0001t0001g0218 a0002c0001t0006g0145 a0002c0001t0006g0202 others(6): Show |
9 | HG00438.hp2 HG02647.hp2 HG03579.hp2 others(6): Show |
intron_variant | MODIFIER | c.4700-194_4700-178d others(19): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62585096 | ||||||
| chr12:62585096 | CACACACA others(13): Show |
C | 2 | a0002c0001t0001g0171 a0002c0001t0001g0182 |
2 | HG01106.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.4700-196_4700-177d others(22): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62585096 | ||||||
| chr12:62585097 | ACACACAC others(6): Show |
A | 1 | a0001c0006t0007g0015 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.4700-196_4700-184d others(15): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62585097 | |||||||
| chr12:62585097 | ACACACAC others(11): Show |
A | 11 | a0002c0001t0001g0149 a0002c0001t0001g0176 a0002c0001t0001g0178 others(8): Show |
11 | HG00642.hp1 HG02895.hp1 HG03927.hp1 others(8): Show |
intron_variant | MODIFIER | c.4700-196_4700-179d others(20): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62585097 | |||||||
| chr12:62585098 | CACACACA others(8): Show |
C | 3 | a0002c0001t0001g0139 a0002c0001t0006g0201 a0002c0001t0006g0222 |
3 | HG01261.hp2 HG02074.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.4700-192_4700-178d others(17): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62585098 | ||||||
| chr12:62585098 | CACACACA others(11): Show |
C | 9 | a0002c0001t0001g0003 a0002c0001t0001g0160 a0002c0001t0001g0168 others(6): Show |
10 | HG00673.hp1 HG00738.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.4700-194_4700-177d others(20): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62585098 | ||||||
| chr12:62585098 | CACACACA others(12): Show |
C | 42 | a0002c0001t0001g0002 a0002c0001t0001g0111 a0002c0001t0001g0137 others(39): Show |
43 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(40): Show |
intron_variant | MODIFIER | c.4700-194_4700-176d others(21): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62585098 | ||||||
| chr12:62585098 | CACACACA others(13): Show |
C | 1 | a0002c0001t0001g0175 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.4700-194_4700-175d others(22): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62585098 | ||||||
| chr12:62585100 | CACACACA others(10): Show |
C | 6 | a0002c0001t0001g0138 a0002c0001t0001g0153 a0002c0001t0001g0219 others(3): Show |
6 | HG03098.hp2 HG03139.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.4700-192_4700-176d others(19): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62585100 | ||||||
| chr12:62585100 | CACACACA others(11): Show |
C | 1 | a0002c0001t0001g0142 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4700-192_4700-175d others(20): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62585100 | ||||||
| chr12:62585101 | ACACACAC others(7): Show |
A | 1 | a0002c0001t0012g0141 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4700-192_4700-179d others(16): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62585101 | |||||||
| chr12:62585102 | CACACACA others(10): Show |
C | 1 | a0002c0001t0001g0167 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.4700-190_4700-174d others(19): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62585102 | ||||||
| chr12:62585102 | CACACACA others(12): Show |
C | 1 | a0002c0001t0001g0246 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4700-190_4700-172d others(21): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62585102 | ||||||
| chr12:62585104 | CACACACA others(5): Show |
C | 1 | a0001c0006t0034g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4700-188_4700-177d others(14): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr12 | 62585104 | ||||||
| chr12:62585114 | A | C | 1 | a0001c0002t0002g0353 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.4700-180A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62585114 | |||||||
| chr12:62585115 | C | A | 25 | a0001c0002t0002g0353 a0001c0006t0007g0009 a0001c0006t0007g0010 others(22): Show |
25 | HG01099.hp1 HG01884.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.4700-179C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62585115 | |||||||
| chr12:62585125 | C | A | 140 | a0001c0002t0013g0306 a0001c0002t0013g0308 a0001c0002t0013g0312 others(137): Show |
142 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.4700-169C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62585125 | |||||||
| chr12:62585131 | A | C | 1 | a0002c0001t0001g0161 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.4700-163A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62585131 | |||||||
| chr12:62585154 | A | G | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4700-140A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62585154 | |||||||
| chr12:62585183 | C | T | 1 | a0002c0001t0001g0241 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.4700-111C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 32/34 | chr12 | 62585183 | |||||||
| chr12:62585566 | ACT | A | 10 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(7): Show |
10 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4907+68_4907+69del others(2): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 33/34 | INFO_REALIGN_3_PRIME | chr12 | 62585566 | ||||||
| chr12:62586037 | G | A | 1 | a0001c0002t0002g0325 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.4907+536G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 33/34 | chr12 | 62586037 | |||||||
| chr12:62586149 | T | G | 1 | a0001c0018t0002g0299 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4907+648T>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 33/34 | chr12 | 62586149 | |||||||
| chr12:62586232 | C | T | 3 | a0001c0003t0005g0037 a0001c0003t0005g0038 a0001c0003t0005g0039 |
3 | HG02258.hp2 HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.4907+731C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 33/34 | chr12 | 62586232 | |||||||
| chr12:62586333 | G | A | 10 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(7): Show |
10 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4907+832G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 33/34 | chr12 | 62586333 | |||||||
| chr12:62586390 | C | T | 1 | a0002c0001t0001g0223 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.4907+889C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 33/34 | chr12 | 62586390 | |||||||
| chr12:62586597 | A | T | 1 | a0001c0002t0002g0339 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.4907+1096A>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 33/34 | chr12 | 62586597 | |||||||
| chr12:62586800 | T | A | 148 | a0001c0002t0002g0298 a0001c0006t0003g0005 a0001c0006t0003g0006 others(145): Show |
150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.4908-1274T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 33/34 | chr12 | 62586800 | |||||||
| chr12:62587069 | C | T | 1 | a0001c0002t0002g0329 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.4908-1005C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 33/34 | chr12 | 62587069 | |||||||
| chr12:62587175 | A | G | 5 | a0001c0003t0003g0041 a0001c0003t0003g0042 a0001c0003t0003g0043 others(2): Show |
6 | HG01069.hp1 HG01071.hp1 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.4908-899A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 33/34 | chr12 | 62587175 | |||||||
| chr12:62587259 | A | G | 1 | a0001c0006t0007g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4908-815A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 33/34 | chr12 | 62587259 | |||||||
| chr12:62587379 | T | TA | 26 | a0001c0003t0005g0050 a0001c0005t0003g0109 a0001c0005t0003g0110 others(23): Show |
26 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.4908-682dupA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 33/34 | INFO_REALIGN_3_PRIME | chr12 | 62587379 | ||||||
| chr12:62587379 | TA | T | 53 | a0001c0002t0022g0294 a0001c0002t0031g0136 a0001c0003t0003g0099 others(50): Show |
53 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.4908-682delA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 33/34 | INFO_REALIGN_3_PRIME | chr12 | 62587379 | ||||||
| chr12:62587486 | AGGCAGGA others(9): Show |
A | 1 | a0001c0006t0033g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4908-581_4908-566d others(18): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 33/34 | INFO_REALIGN_3_PRIME | chr12 | 62587486 | ||||||
| chr12:62587647 | T | A | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4908-427T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 33/34 | chr12 | 62587647 | |||||||
| chr12:62587664 | C | T | 7 | a0002c0001t0006g0192 a0002c0001t0006g0193 a0002c0001t0006g0204 others(4): Show |
7 | HG01928.hp1 HG02071.hp1 NA18941.hp2 others(4): Show |
intron_variant | MODIFIER | c.4908-410C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 33/34 | chr12 | 62587664 | |||||||
| chr12:62587779 | T | C | 1 | a0002c0001t0001g0246 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4908-295T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 33/34 | chr12 | 62587779 | |||||||
| chr12:62587848 | TGATAA | T | 3 | a0002c0001t0001g0147 a0002c0001t0001g0244 a0002c0001t0001g0245 |
3 | NA18968.hp2 NA19009.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.4908-224_4908-220d others(7): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 33/34 | INFO_REALIGN_3_PRIME | chr12 | 62587848 | ||||||
| chr12:62587956 | T | C | 1 | a0001c0016t0032g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4908-118T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 33/34 | chr12 | 62587956 | |||||||
| chr12:62588213 | G | A | 2 | a0001c0002t0014g0289 a0001c0002t0014g0290 |
2 | HG02300.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.4990+57G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62588213 | |||||||
| chr12:62588242 | A | G | 2 | a0001c0003t0005g0052 a0010c0011t0005g0093 |
2 | NA18941.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.4990+86A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62588242 | |||||||
| chr12:62588258 | C | A | 1 | a0001c0006t0034g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4990+102C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62588258 | |||||||
| chr12:62588372 | C | CT | 134 | a0001c0002t0031g0136 a0001c0006t0007g0009 a0001c0006t0007g0010 others(131): Show |
136 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.4990+228dupT | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr12 | 62588372 | ||||||
| chr12:62588482 | A | G | 1 | a0002c0001t0001g0240 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.4990+326A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62588482 | |||||||
| chr12:62588508 | T | A | 5 | a0001c0003t0003g0041 a0001c0003t0003g0042 a0001c0003t0003g0043 others(2): Show |
6 | HG01069.hp1 HG01071.hp1 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.4990+352T>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62588508 | |||||||
| chr12:62588821 | A | C | 1 | a0001c0002t0002g0331 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.4990+665A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62588821 | |||||||
| chr12:62588861 | A | G | 1 | a0001c0006t0034g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4990+705A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62588861 | |||||||
| chr12:62589089 | T | C | 1 | a0001c0002t0002g0318 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.4990+933T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62589089 | |||||||
| chr12:62589255 | A | G | 2 | a0001c0009t0019g0107 a0001c0009t0019g0108 |
2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.4990+1099A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62589255 | |||||||
| chr12:62589363 | C | T | 93 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0003g0135 others(90): Show |
94 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.4990+1207C>T | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62589363 | |||||||
| chr12:62589629 | G | A | 7 | a0001c0002t0013g0306 a0001c0002t0013g0308 a0001c0002t0013g0309 others(4): Show |
7 | HG01074.hp1 HG01256.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.4990+1473G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62589629 | |||||||
| chr12:62589744 | T | TA | 18 | a0001c0003t0005g0046 a0001c0003t0005g0047 a0001c0003t0005g0086 others(15): Show |
18 | HG01884.hp1 HG02055.hp2 HG02083.hp2 others(15): Show |
intron_variant | MODIFIER | c.4990+1609dupA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr12 | 62589744 | ||||||
| chr12:62589744 | TA | T | 132 | a0001c0002t0002g0030 a0001c0002t0002g0331 a0001c0002t0002g0351 others(129): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.4990+1609delA | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr12 | 62589744 | ||||||
| chr12:62589744 | TAA | T | 12 | a0001c0016t0032g0252 a0002c0001t0001g0138 a0002c0001t0001g0143 others(9): Show |
12 | HG02083.hp1 HG02895.hp1 HG03139.hp1 others(9): Show |
intron_variant | MODIFIER | c.4990+1608_4990+160 others(6): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr12 | 62589744 | ||||||
| chr12:62589844 | A | G | 7 | a0001c0002t0013g0306 a0001c0002t0013g0308 a0001c0002t0013g0309 others(4): Show |
7 | HG01074.hp1 HG01256.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.4990+1688A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62589844 | |||||||
| chr12:62590121 | T | C | 241 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0003g0135 others(238): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.4990+1965T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62590121 | |||||||
| chr12:62590226 | G | A | 1 | a0002c0001t0001g0249 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.4990+2070G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62590226 | |||||||
| chr12:62590238 | G | A | 9 | a0001c0002t0013g0306 a0001c0002t0013g0308 a0001c0002t0013g0309 others(6): Show |
9 | HG01074.hp1 HG01256.hp1 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.4990+2082G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62590238 | |||||||
| chr12:62590312 | G | C | 241 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0003g0135 others(238): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.4990+2156G>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62590312 | |||||||
| chr12:62590318 | T | C | 241 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0003g0135 others(238): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.4990+2162T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62590318 | |||||||
| chr12:62590352 | G | A | 10 | a0001c0006t0003g0005 a0001c0006t0003g0006 a0001c0006t0003g0007 others(7): Show |
10 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4990+2196G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62590352 | |||||||
| chr12:62590706 | A | G | 13 | a0002c0001t0001g0003 a0002c0001t0001g0138 a0002c0001t0001g0139 others(10): Show |
14 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.4991-1880A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62590706 | |||||||
| chr12:62591035 | G | A | 3 | a0002c0001t0001g0209 a0002c0001t0001g0212 a0002c0001t0012g0220 |
3 | HG00423.hp1 NA18955.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.4991-1551G>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62591035 | |||||||
| chr12:62591147 | CAACTG | C | 7 | a0001c0002t0013g0306 a0001c0002t0013g0308 a0001c0002t0013g0309 others(4): Show |
7 | HG01074.hp1 HG01256.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.4991-1436_4991-143 others(9): Show |
MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chr12 | 62591147 | ||||||
| chr12:62591343 | T | C | 1 | a0001c0006t0033g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4991-1243T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62591343 | |||||||
| chr12:62591554 | A | C | 1 | a0001c0002t0002g0323 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.4991-1032A>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62591554 | |||||||
| chr12:62591788 | A | G | 3 | a0002c0001t0001g0147 a0002c0001t0001g0244 a0002c0001t0001g0245 |
3 | NA18968.hp2 NA19009.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.4991-798A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62591788 | |||||||
| chr12:62591826 | A | G | 1 | a0001c0003t0005g0051 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.4991-760A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62591826 | |||||||
| chr12:62592064 | A | G | 4 | a0001c0005t0003g0118 a0001c0005t0003g0120 a0001c0005t0003g0121 others(1): Show |
4 | HG01255.hp1 HG02602.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.4991-522A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62592064 | |||||||
| chr12:62592091 | C | A | 135 | a0001c0006t0007g0009 a0001c0006t0007g0010 a0001c0006t0007g0011 others(132): Show |
137 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.4991-495C>A | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62592091 | |||||||
| chr12:62592301 | T | C | 4 | a0002c0001t0001g0240 a0002c0001t0001g0241 a0002c0001t0001g0242 others(1): Show |
4 | HG01934.hp1 HG01975.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.4991-285T>C | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62592301 | |||||||
| chr12:62592381 | A | G | 1 | a0002c0001t0001g0248 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.4991-205A>G | MON2 | ENSG00000061987.16 | transcript | ENST00000393630.8 | protein_coding | 34/34 | chr12 | 62592381 |