Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 93432 |
| ensemblid | ENSG00000257743.9 |
| hgncid | 28101 |
| symbol | MGAM2 |
| name | maltase-glucoamylase 2 (putative) |
| refseq_nuc | NM_001293626.2 |
| refseq_prot | NP_001280555.1 |
| ensembl_nuc | ENST00000477922.4 |
| ensembl_prot | ENSP00000420449.3 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 142111718 |
| end | 142222324 |
| strand | + |
| ver | v1.2 |
| region | chr7:142111718-142222324 |
| region5000 | chr7:142106718-142227324 |
| regionname0 | MGAM2_chr7_142111718_142222324 |
| regionname5000 | MGAM2_chr7_142106718_142227324 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 2515 | 85 | 6 | 18 | 50 | 5 | 6 | 39 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0002 | 0/0 | 2515 | 76 | 23 | 11 | 28 | 3 | 11 | 21 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0003 | 0/0 | 2515 | 15 | 0 | 5 | 6 | 1 | 3 | 4 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0004 | 0/0 | 2515 | 13 | 0 | 0 | 12 | 0 | 1 | 9 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0005 | 0/0 | 2515 | 11 | 0 | 0 | 11 | 0 | 0 | 8 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0006 | 0/0 | 2515 | 8 | 0 | 4 | 2 | 1 | 1 | 2 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0007 | 0/0 | 252 | 8 | 1 | 0 | 5 | 0 | 2 | 4 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(247): Show |
chr7 | 142106718 | 142227324 |
| a0008 | 0/0 | 2515 | 7 | 0 | 0 | 7 | 0 | 0 | 5 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0009 | 0/0 | 2515 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0010 | 0/0 | 2515 | 7 | 2 | 3 | 1 | 1 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0011 | 0/0 | 2515 | 6 | 0 | 1 | 3 | 2 | 0 | 3 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0012 | 0/0 | 2515 | 6 | 0 | 5 | 1 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0013 | 0/0 | 2515 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0014 | 0/0 | 2515 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0015 | 0/0 | 2515 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0016 | 0/0 | 2515 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0017 | 0/0 | 2515 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0018 | 0/0 | 2515 | 3 | 0 | 1 | 2 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0019 | 0/0 | 2515 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0020 | 0/0 | 2515 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0021 | 0/0 | 2515 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0022 | 0/0 | 2515 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0023 | 0/0 | 2515 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0024 | 0/0 | 2515 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0025 | 0/0 | 2515 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0026 | 0/0 | 2515 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0027 | 0/0 | 2515 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0028 | 0/0 | 2515 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0029 | 0/0 | 2515 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0030 | 0/0 | 2515 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0031 | 0/0 | 1457 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(1452): Show |
chr7 | 142106718 | 142227324 |
| a0032 | 0/0 | 2515 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0033 | 0/0 | 2515 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0034 | 0/0 | 2515 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0035 | 0/0 | 2515 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0036 | 0/0 | 2515 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0037 | 0/0 | 2515 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0038 | 0/0 | 2515 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0039 | 0/0 | 2515 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0040 | 0/0 | 2515 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0041 | 0/0 | 2515 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0042 | 0/0 | 2515 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0043 | 0/0 | 2515 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0044 | 0/0 | 2515 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0045 | 0/0 | 2515 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0046 | 0/0 | 2515 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0047 | 0/0 | 2515 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0048 | 0/0 | 2515 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0049 | 0/0 | 2515 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0050 | 0/0 | 2515 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0051 | 0/0 | 2515 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0052 | 0/0 | 2515 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0053 | 0/0 | 2515 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0054 | 0/0 | 2515 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0055 | 0/0 | 2515 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0056 | 0/0 | 2515 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0057 | 0/0 | 2515 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0058 | 0/0 | 2515 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0059 | 0/0 | 2515 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0060 | 0/0 | 2515 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0061 | 0/0 | 2515 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0062 | 0/0 | 2515 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0063 | 0/0 | 2515 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| a0064 | 0/1 | 2515 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | MARKL others(2510): Show |
chr7 | 142106718 | 142227324 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 7545 | 54 | 2 | 15 | 32 | 3 | 2 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0001c0004 | 0/0 | 7545 | 29 | 4 | 3 | 16 | 2 | 4 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0001c0038 | 0/0 | 7545 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0001c0052 | 0/0 | 7545 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0002c0002 | 0/0 | 7545 | 38 | 12 | 5 | 13 | 1 | 7 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0002c0003 | 0/0 | 7545 | 36 | 10 | 6 | 14 | 2 | 4 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0002c0058 | 0/0 | 7545 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0002c0072 | 0/0 | 7545 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0003c0007 | 0/0 | 7545 | 8 | 0 | 1 | 4 | 0 | 3 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0003c0009 | 0/0 | 7545 | 7 | 0 | 4 | 2 | 1 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0004c0005 | 0/0 | 7545 | 13 | 0 | 0 | 12 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0005c0006 | 0/0 | 7545 | 11 | 0 | 0 | 11 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0006c0008 | 0/0 | 7545 | 8 | 0 | 4 | 2 | 1 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0007c0033 | 0/0 | 7546 | 2 | 0 | 0 | 2 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7541): Show |
chr7 | 142106718 | 142227324 | ||
| a0007c0034 | 0/0 | 7546 | 2 | 0 | 0 | 1 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7541): Show |
chr7 | 142106718 | 142227324 | ||
| a0007c0080 | 0/0 | 7546 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7541): Show |
chr7 | 142106718 | 142227324 | ||
| a0007c0081 | 0/0 | 7546 | 1 | 0 | 0 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7541): Show |
chr7 | 142106718 | 142227324 | ||
| a0007c0082 | 0/0 | 7546 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7541): Show |
chr7 | 142106718 | 142227324 | ||
| a0007c0083 | 0/0 | 7546 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7541): Show |
chr7 | 142106718 | 142227324 | ||
| a0008c0010 | 0/0 | 7545 | 7 | 0 | 0 | 7 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0009c0011 | 0/0 | 7545 | 7 | 6 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0010c0017 | 0/0 | 7545 | 4 | 2 | 2 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0010c0031 | 0/0 | 7545 | 2 | 0 | 1 | 0 | 1 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0010c0079 | 0/0 | 7545 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0011c0013 | 0/0 | 7545 | 4 | 0 | 0 | 2 | 2 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0011c0022 | 0/0 | 7545 | 2 | 0 | 1 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0012c0012 | 0/0 | 7545 | 6 | 0 | 5 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0013c0016 | 0/0 | 7545 | 4 | 3 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0014c0020 | 0/0 | 7545 | 2 | 2 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0014c0026 | 0/0 | 7545 | 2 | 1 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0015c0015 | 0/0 | 7545 | 4 | 4 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0016c0014 | 0/0 | 7545 | 4 | 4 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0017c0019 | 0/0 | 7545 | 3 | 0 | 0 | 3 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0018c0028 | 0/0 | 7545 | 2 | 0 | 1 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0018c0062 | 0/0 | 7545 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0019c0030 | 0/0 | 7545 | 2 | 2 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0019c0073 | 0/0 | 7545 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0020c0018 | 0/0 | 7545 | 3 | 3 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0021c0023 | 0/0 | 7545 | 2 | 1 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0022c0027 | 0/0 | 7545 | 2 | 2 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0023c0025 | 0/0 | 7545 | 2 | 2 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0024c0074 | 0/0 | 7545 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0024c0075 | 0/0 | 7545 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0025c0032 | 0/0 | 7545 | 2 | 0 | 0 | 0 | 0 | 2 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0026c0029 | 0/0 | 7545 | 2 | 0 | 0 | 0 | 0 | 2 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0027c0021 | 0/0 | 7545 | 2 | 0 | 0 | 2 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0028c0024 | 0/0 | 7545 | 2 | 0 | 0 | 2 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0029c0040 | 0/0 | 7545 | 1 | 0 | 0 | 0 | 1 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0030c0056 | 0/0 | 7545 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0031c0051 | 0/0 | 7545 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0032c0045 | 0/0 | 7545 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0033c0035 | 0/0 | 7545 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0034c0069 | 0/0 | 7545 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0035c0067 | 0/0 | 7545 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0036c0049 | 0/0 | 7545 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0037c0050 | 0/0 | 7545 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0038c0059 | 0/0 | 7545 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0039c0046 | 0/0 | 7545 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0040c0043 | 0/0 | 7545 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0041c0068 | 0/0 | 7545 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0042c0060 | 0/0 | 7545 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0043c0048 | 0/0 | 7545 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0044c0036 | 0/0 | 7545 | 1 | 0 | 0 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0045c0061 | 0/0 | 7545 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0046c0077 | 0/0 | 7545 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0047c0070 | 0/0 | 7545 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0048c0065 | 0/0 | 7545 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0049c0064 | 0/0 | 7545 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0050c0039 | 0/0 | 7545 | 1 | 0 | 0 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0051c0044 | 0/0 | 7545 | 1 | 0 | 0 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0052c0071 | 0/0 | 7545 | 1 | 0 | 0 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0053c0047 | 0/0 | 7545 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0054c0078 | 0/0 | 7545 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0055c0055 | 0/0 | 7545 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0056c0042 | 0/0 | 7545 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0057c0037 | 0/0 | 7545 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0058c0053 | 0/0 | 7545 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0059c0057 | 0/0 | 7545 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0060c0066 | 0/0 | 7545 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0061c0063 | 0/0 | 7545 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0062c0076 | 0/0 | 7545 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0063c0041 | 0/0 | 7545 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 | ||
| a0064c0054 | 0/1 | 7545 | 1 | 0 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | ATGGC others(7540): Show |
chr7 | 142106718 | 142227324 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7903 | 54 | 2 | 15 | 32 | 3 | 2 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0001c0004t0001 | 0/0 | 7903 | 28 | 3 | 3 | 16 | 2 | 4 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0001c0004t0002 | 0/0 | 7903 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0001c0038t0001 | 0/0 | 7903 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0001c0052t0001 | 0/0 | 7903 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0002c0002t0001 | 0/0 | 7903 | 38 | 12 | 5 | 13 | 1 | 7 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0002c0003t0001 | 0/0 | 7903 | 34 | 8 | 6 | 14 | 2 | 4 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0002c0003t0002 | 0/0 | 7903 | 2 | 2 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0002c0058t0001 | 0/0 | 7903 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0002c0072t0001 | 0/0 | 7903 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0003c0007t0001 | 0/0 | 7903 | 8 | 0 | 1 | 4 | 0 | 3 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0003c0009t0001 | 0/0 | 7903 | 7 | 0 | 4 | 2 | 1 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0004c0005t0001 | 0/0 | 7903 | 13 | 0 | 0 | 12 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0005c0006t0001 | 0/0 | 7903 | 11 | 0 | 0 | 11 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0006c0008t0001 | 0/0 | 7903 | 8 | 0 | 4 | 2 | 1 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0007c0033t0001 | 0/0 | 7904 | 2 | 0 | 0 | 2 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7899): Show |
chr7 | 142106718 | 142227324 |
| a0007c0034t0001 | 0/0 | 7904 | 2 | 0 | 0 | 1 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7899): Show |
chr7 | 142106718 | 142227324 |
| a0007c0080t0001 | 0/0 | 7904 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7899): Show |
chr7 | 142106718 | 142227324 |
| a0007c0081t0001 | 0/0 | 7904 | 1 | 0 | 0 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7899): Show |
chr7 | 142106718 | 142227324 |
| a0007c0082t0001 | 0/0 | 7904 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7899): Show |
chr7 | 142106718 | 142227324 |
| a0007c0083t0001 | 0/0 | 7904 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7899): Show |
chr7 | 142106718 | 142227324 |
| a0008c0010t0001 | 0/0 | 7903 | 7 | 0 | 0 | 7 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0009c0011t0001 | 0/0 | 7903 | 6 | 5 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0009c0011t0002 | 0/0 | 7903 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0010c0017t0001 | 0/0 | 7903 | 4 | 2 | 2 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0010c0031t0001 | 0/0 | 7903 | 2 | 0 | 1 | 0 | 1 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0010c0079t0001 | 0/0 | 7903 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0011c0013t0001 | 0/0 | 7903 | 4 | 0 | 0 | 2 | 2 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0011c0022t0001 | 0/0 | 7903 | 2 | 0 | 1 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0012c0012t0001 | 0/0 | 7903 | 6 | 0 | 5 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0013c0016t0001 | 0/0 | 7903 | 4 | 3 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0014c0020t0001 | 0/0 | 7903 | 2 | 2 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0014c0026t0001 | 0/0 | 7903 | 2 | 1 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0015c0015t0001 | 0/0 | 7903 | 4 | 4 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0016c0014t0001 | 0/0 | 7903 | 4 | 4 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0017c0019t0001 | 0/0 | 7903 | 3 | 0 | 0 | 3 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0018c0028t0001 | 0/0 | 7903 | 2 | 0 | 1 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0018c0062t0001 | 0/0 | 7903 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0019c0030t0001 | 0/0 | 7903 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0019c0030t0002 | 0/0 | 7903 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0019c0073t0001 | 0/0 | 7903 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0020c0018t0001 | 0/0 | 7903 | 3 | 3 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0021c0023t0001 | 0/0 | 7903 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0021c0023t0004 | 0/0 | 7903 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0022c0027t0001 | 0/0 | 7903 | 2 | 2 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0023c0025t0001 | 0/0 | 7903 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0023c0025t0002 | 0/0 | 7903 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0024c0074t0001 | 0/0 | 7903 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0024c0075t0001 | 0/0 | 7903 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0025c0032t0001 | 0/0 | 7903 | 2 | 0 | 0 | 0 | 0 | 2 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0026c0029t0001 | 0/0 | 7903 | 2 | 0 | 0 | 0 | 0 | 2 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0027c0021t0001 | 0/0 | 7903 | 2 | 0 | 0 | 2 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0028c0024t0001 | 0/0 | 7903 | 2 | 0 | 0 | 2 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0029c0040t0001 | 0/0 | 7903 | 1 | 0 | 0 | 0 | 1 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0030c0056t0001 | 0/0 | 7903 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0031c0051t0001 | 0/0 | 7903 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0032c0045t0001 | 0/0 | 7903 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0033c0035t0003 | 0/0 | 7903 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0034c0069t0001 | 0/0 | 7903 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0035c0067t0003 | 0/0 | 7903 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0036c0049t0001 | 0/0 | 7903 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0037c0050t0001 | 0/0 | 7903 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0038c0059t0001 | 0/0 | 7903 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0039c0046t0001 | 0/0 | 7903 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0040c0043t0001 | 0/0 | 7903 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0041c0068t0001 | 0/0 | 7903 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0042c0060t0001 | 0/0 | 7903 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0043c0048t0001 | 0/0 | 7903 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0044c0036t0001 | 0/0 | 7903 | 1 | 0 | 0 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0045c0061t0001 | 0/0 | 7903 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0046c0077t0001 | 0/0 | 7903 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0047c0070t0001 | 0/0 | 7903 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0048c0065t0002 | 0/0 | 7903 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0049c0064t0001 | 0/0 | 7903 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0050c0039t0001 | 0/0 | 7903 | 1 | 0 | 0 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0051c0044t0001 | 0/0 | 7903 | 1 | 0 | 0 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0052c0071t0001 | 0/0 | 7903 | 1 | 0 | 0 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0053c0047t0001 | 0/0 | 7903 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0054c0078t0001 | 0/0 | 7903 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0055c0055t0001 | 0/0 | 7903 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0056c0042t0001 | 0/0 | 7903 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0057c0037t0001 | 0/0 | 7903 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0058c0053t0001 | 0/0 | 7903 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0059c0057t0001 | 0/0 | 7903 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0060c0066t0001 | 0/0 | 7903 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0061c0063t0001 | 0/0 | 7903 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0062c0076t0001 | 0/0 | 7903 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0063c0041t0001 | 0/0 | 7903 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| a0064c0054t0001 | 0/1 | 7903 | 1 | 0 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | GCTGG others(7898): Show |
chr7 | 142106718 | 142227324 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0004t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0004t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0004t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0004t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0004t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0004t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0004t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0004t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0004t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0004t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0004t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0004t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0004t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0004t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0004t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0004t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0004t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0004t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0004t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0004t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0004t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0004t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0004t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0004t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0004t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0004t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0004t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0004t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0004t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0038t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0001c0052t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0002t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0002t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0002t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0002t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0002t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0002t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0002t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0002t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0002t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0002t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0002t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0003t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0003t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0003t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0003t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0003t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0003t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0003t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0003t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0003t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0003t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0003t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0003t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0003t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0003t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0003t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0003t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0003t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0003t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0003t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0003t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0003t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0003t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0003t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0003t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0003t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0003t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0003t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0003t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0003t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0003t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0003t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0003t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0003t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0058t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0002c0072t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0003c0007t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0003c0007t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0003c0007t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0003c0007t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0003c0007t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0003c0007t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0003c0007t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0003c0007t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0003c0009t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0003c0009t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0003c0009t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0003c0009t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0003c0009t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0003c0009t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0003c0009t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0004c0005t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0004c0005t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0004c0005t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0004c0005t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0004c0005t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0004c0005t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0004c0005t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0004c0005t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0004c0005t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0004c0005t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0004c0005t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0004c0005t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0004c0005t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0005c0006t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0005c0006t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0005c0006t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0005c0006t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0005c0006t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0005c0006t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0005c0006t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0005c0006t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0005c0006t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0005c0006t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0005c0006t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0006c0008t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0006c0008t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0006c0008t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0006c0008t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0006c0008t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0006c0008t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0006c0008t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0006c0008t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0007c0033t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0007c0033t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0007c0034t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0007c0034t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0007c0080t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0007c0081t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0007c0082t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0007c0083t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0008c0010t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0008c0010t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0008c0010t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0008c0010t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0008c0010t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0008c0010t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0008c0010t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0009c0011t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0009c0011t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0009c0011t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0009c0011t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0009c0011t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0009c0011t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0009c0011t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0010c0017t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0010c0017t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0010c0017t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0010c0017t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0010c0031t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0010c0031t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0010c0079t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0011c0013t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0011c0013t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0011c0013t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0011c0013t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0011c0022t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0011c0022t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0012c0012t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0012c0012t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0012c0012t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0012c0012t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0012c0012t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0012c0012t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0013c0016t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0013c0016t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0013c0016t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0013c0016t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0014c0020t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0014c0026t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0014c0026t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0015c0015t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0015c0015t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0015c0015t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0015c0015t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0016c0014t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0016c0014t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0016c0014t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0016c0014t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0017c0019t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0017c0019t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0017c0019t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0018c0028t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0018c0028t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0018c0062t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0019c0030t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0019c0030t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0019c0073t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0020c0018t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0020c0018t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0020c0018t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0021c0023t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0021c0023t0004g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0022c0027t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0022c0027t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0023c0025t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0023c0025t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0024c0074t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0024c0075t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0025c0032t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0025c0032t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0026c0029t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0026c0029t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0027c0021t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0027c0021t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0028c0024t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0028c0024t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0029c0040t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0030c0056t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0031c0051t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0032c0045t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0033c0035t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0034c0069t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0035c0067t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0036c0049t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0037c0050t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0038c0059t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0039c0046t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0040c0043t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0041c0068t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0042c0060t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0043c0048t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0044c0036t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0045c0061t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0046c0077t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0047c0070t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0048c0065t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0049c0064t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0050c0039t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0051c0044t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0052c0071t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0053c0047t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0054c0078t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0055c0055t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0056c0042t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0057c0037t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0058c0053t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0059c0057t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0060c0066t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0061c0063t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0062c0076t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0063c0041t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| a0064c0054t0001g0159 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0269 | EUR | GBR | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG00099 | hp2 | a0029 | c0040 | t0001 | g0202 | EUR | GBR | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG00140 | hp1 | a0011 | c0013 | t0001 | g0189 | EUR | GBR | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG00140 | hp2 | a0003 | c0009 | t0001 | g0141 | EUR | GBR | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0095 | EUR | FIN | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG00280 | hp2 | a0001 | c0004 | t0001 | g0188 | EUR | FIN | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG00323 | hp1 | a0006 | c0008 | t0001 | g0168 | EUR | FIN | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG00323 | hp2 | a0001 | c0004 | t0001 | g0165 | EUR | FIN | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG00408 | hp1 | a0030 | c0056 | t0001 | g0085 | EAS | CHS | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG00408 | hp2 | a0002 | c0072 | t0001 | g0215 | EAS | CHS | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG00423 | hp1 | a0002 | c0003 | t0001 | g0255 | EAS | CHS | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG00438 | hp1 | a0017 | c0019 | t0001 | g0220 | EAS | CHS | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG00438 | hp2 | a0007 | c0082 | t0001 | g0110 | EAS | CHS | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG00558 | hp1 | a0004 | c0005 | t0001 | g0100 | EAS | CHS | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG00609 | hp1 | a0008 | c0010 | t0001 | g0090 | EAS | CHS | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG00609 | hp2 | a0001 | c0004 | t0001 | g0121 | EAS | CHS | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG00621 | hp2 | a0003 | c0007 | t0001 | g0082 | EAS | CHS | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG00639 | hp2 | a0001 | c0004 | t0001 | g0169 | AMR | PUR | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG00642 | hp1 | a0009 | c0011 | t0001 | g0023 | AMR | PUR | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG00642 | hp2 | a0003 | c0009 | t0001 | g0118 | AMR | PUR | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0253 | AMR | PUR | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG00735 | hp2 | a0013 | c0016 | t0001 | g0283 | AMR | PUR | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG00741 | hp2 | a0002 | c0003 | t0001 | g0010 | AMR | PUR | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01069 | hp2 | a0010 | c0017 | t0001 | g0286 | AMR | PUR | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0318 | AMR | PUR | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01074 | hp1 | a0010 | c0017 | t0001 | g0256 | AMR | PUR | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01074 | hp2 | a0002 | c0003 | t0001 | g0007 | AMR | PUR | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01081 | hp1 | a0002 | c0003 | t0001 | g0258 | AMR | PUR | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0235 | AMR | PUR | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01099 | hp2 | a0003 | c0007 | t0001 | g0142 | AMR | PUR | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0205 | AMR | PUR | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0035 | AMR | PUR | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01167 | hp1 | a0012 | c0012 | t0001 | g0237 | AMR | PUR | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01167 | hp2 | a0011 | c0022 | t0001 | g0279 | AMR | PUR | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01168 | hp1 | a0002 | c0003 | t0001 | g0004 | AMR | PUR | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01168 | hp2 | a0003 | c0009 | t0001 | g0056 | AMR | PUR | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01169 | hp1 | a0012 | c0012 | t0001 | g0236 | AMR | PUR | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01169 | hp2 | a0003 | c0009 | t0001 | g0053 | AMR | PUR | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01192 | hp1 | a0021 | c0023 | t0004 | g0057 | AMR | PUR | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01192 | hp2 | a0018 | c0028 | t0001 | g0231 | AMR | PUR | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01243 | hp1 | a0014 | c0026 | t0001 | g0196 | AMR | PUR | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01243 | hp2 | a0002 | c0003 | t0001 | g0020 | AMR | PUR | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01255 | hp1 | a0010 | c0031 | t0001 | g0234 | AMR | CLM | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01255 | hp2 | a0031 | c0051 | t0001 | g0317 | AMR | CLM | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | CLM | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01261 | hp1 | a0032 | c0045 | t0001 | g0126 | AMR | CLM | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01261 | hp2 | a0002 | c0003 | t0001 | g0197 | AMR | CLM | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01433 | hp1 | a0003 | c0009 | t0001 | g0271 | AMR | CLM | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01496 | hp1 | a0001 | c0004 | t0001 | g0167 | AMR | CLM | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0021 | AMR | CLM | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01516 | hp1 | a0011 | c0013 | t0001 | g0246 | EUR | IBS | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01516 | hp2 | a0002 | c0003 | t0001 | g0003 | EUR | IBS | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01517 | hp1 | a0002 | c0003 | t0001 | g0002 | EUR | IBS | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0074 | EUR | IBS | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01884 | hp1 | a0010 | c0017 | t0001 | g0240 | AFR | ACB | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01884 | hp2 | a0002 | c0003 | t0001 | g0049 | AFR | ACB | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01891 | hp1 | a0022 | c0027 | t0001 | g0038 | AFR | ACB | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01891 | hp2 | a0019 | c0073 | t0001 | g0012 | AFR | ACB | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PEL | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01928 | hp2 | a0012 | c0012 | t0001 | g0322 | AMR | PEL | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01952 | hp1 | a0033 | c0035 | t0003 | g0061 | AMR | PEL | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01952 | hp2 | a0006 | c0008 | t0001 | g0321 | AMR | PEL | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01975 | hp1 | a0001 | c0004 | t0001 | g0280 | AMR | PEL | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01975 | hp2 | a0012 | c0012 | t0001 | g0324 | AMR | PEL | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01978 | hp2 | a0034 | c0069 | t0001 | g0290 | AMR | PEL | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PEL | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02004 | hp2 | a0012 | c0012 | t0001 | g0320 | AMR | PEL | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02015 | hp2 | a0002 | c0003 | t0001 | g0009 | EAS | KHV | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02027 | hp1 | a0001 | c0004 | t0001 | g0160 | EAS | KHV | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02040 | hp1 | a0018 | c0062 | t0001 | g0299 | EAS | KHV | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0249 | EAS | KHV | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02055 | hp1 | a0035 | c0067 | t0003 | g0146 | AFR | ACB | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02055 | hp2 | a0036 | c0049 | t0001 | g0275 | AFR | ACB | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02071 | hp1 | a0008 | c0010 | t0001 | g0091 | EAS | KHV | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02071 | hp2 | a0005 | c0006 | t0001 | g0254 | EAS | KHV | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02080 | hp1 | a0037 | c0050 | t0001 | g0115 | EAS | KHV | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02080 | hp2 | a0002 | c0003 | t0001 | g0228 | EAS | KHV | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0229 | EAS | KHV | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02129 | hp2 | a0005 | c0006 | t0001 | g0248 | EAS | KHV | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | KHV | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02135 | hp2 | a0003 | c0007 | t0001 | g0104 | EAS | KHV | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02145 | hp1 | a0002 | c0003 | t0001 | g0292 | AFR | ACB | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02145 | hp2 | a0038 | c0059 | t0001 | g0026 | AFR | ACB | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02155 | hp1 | a0004 | c0005 | t0001 | g0177 | EAS | CDX | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02155 | hp2 | a0004 | c0005 | t0001 | g0137 | EAS | CDX | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02165 | hp1 | a0001 | c0004 | t0001 | g0089 | EAS | CDX | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | CDX | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0291 | AFR | ACB | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02257 | hp2 | a0015 | c0015 | t0001 | g0014 | AFR | ACB | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0019 | AFR | ACB | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0050 | AFR | ACB | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02293 | hp1 | a0006 | c0008 | t0001 | g0314 | AMR | PEL | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02293 | hp2 | a0006 | c0008 | t0001 | g0315 | AMR | PEL | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0313 | AMR | PEL | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02451 | hp1 | a0039 | c0046 | t0001 | g0102 | AFR | ACB | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0296 | AFR | ACB | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02572 | hp1 | a0041 | c0068 | t0001 | g0022 | AFR | GWD | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02572 | hp2 | a0023 | c0025 | t0002 | g0037 | AFR | GWD | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02615 | hp1 | a0023 | c0025 | t0001 | g0052 | AFR | GWD | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02615 | hp2 | a0016 | c0014 | t0001 | g0079 | AFR | GWD | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02622 | hp1 | a0015 | c0015 | t0001 | g0297 | AFR | GWD | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02622 | hp2 | a0016 | c0014 | t0001 | g0018 | AFR | GWD | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02630 | hp1 | a0024 | c0074 | t0001 | g0031 | AFR | GWD | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02630 | hp2 | a0042 | c0060 | t0001 | g0015 | AFR | GWD | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02647 | hp1 | a0043 | c0048 | t0001 | g0103 | AFR | GWD | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02647 | hp2 | a0002 | c0003 | t0001 | g0033 | AFR | GWD | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0039 | AFR | GWD | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02717 | hp2 | a0002 | c0003 | t0001 | g0073 | AFR | GWD | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0016 | AFR | GWD | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02723 | hp2 | a0014 | c0026 | t0001 | g0327 | AFR | GWD | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0265 | SAS | PJL | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02735 | hp2 | a0044 | c0036 | t0001 | g0184 | SAS | PJL | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02809 | hp1 | a0009 | c0011 | t0001 | g0025 | AFR | GWD | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02809 | hp2 | a0019 | c0030 | t0002 | g0326 | AFR | GWD | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02895 | hp1 | a0010 | c0017 | t0001 | g0302 | AFR | GWD | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02895 | hp2 | a0014 | c0020 | t0001 | g0001 | AFR | GWD | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02896 | hp1 | a0002 | c0003 | t0001 | g0225 | AFR | GWD | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0224 | AFR | GWD | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02897 | hp1 | a0002 | c0003 | t0001 | g0226 | AFR | GWD | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02897 | hp2 | a0014 | c0020 | t0001 | g0001 | AFR | GWD | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02922 | hp1 | a0015 | c0015 | t0001 | g0013 | AFR | ESN | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02922 | hp2 | a0045 | c0061 | t0001 | g0044 | AFR | ESN | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02970 | hp1 | a0002 | c0003 | t0002 | g0230 | AFR | ESN | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02970 | hp2 | a0046 | c0077 | t0001 | g0195 | AFR | ESN | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0043 | AFR | ESN | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02976 | hp2 | a0002 | c0003 | t0002 | g0251 | AFR | ESN | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG03017 | hp1 | a0003 | c0007 | t0001 | g0093 | SAS | PJL | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0151 | SAS | PJL | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG03041 | hp1 | a0020 | c0018 | t0001 | g0148 | AFR | GWD | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG03041 | hp2 | a0013 | c0016 | t0001 | g0042 | AFR | GWD | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG03098 | hp1 | a0024 | c0075 | t0001 | g0185 | AFR | MSL | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0284 | AFR | MSL | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG03130 | hp1 | a0047 | c0070 | t0001 | g0147 | AFR | ESN | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG03130 | hp2 | a0048 | c0065 | t0002 | g0047 | AFR | ESN | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG03195 | hp1 | a0009 | c0011 | t0002 | g0036 | AFR | ESN | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG03195 | hp2 | a0009 | c0011 | t0001 | g0282 | AFR | ESN | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG03209 | hp1 | a0009 | c0011 | t0001 | g0293 | AFR | MSL | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0045 | AFR | MSL | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG03225 | hp1 | a0002 | c0003 | t0001 | g0219 | AFR | MSL | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG03225 | hp2 | a0002 | c0003 | t0001 | g0198 | AFR | MSL | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG03239 | hp1 | a0002 | c0003 | t0001 | g0312 | SAS | PJL | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG03239 | hp2 | a0003 | c0007 | t0001 | g0070 | SAS | PJL | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG03453 | hp1 | a0016 | c0014 | t0001 | g0011 | AFR | MSL | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG03453 | hp2 | a0013 | c0016 | t0001 | g0173 | AFR | MSL | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | MSL | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG03486 | hp2 | a0001 | c0004 | t0001 | g0066 | AFR | MSL | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG03490 | hp1 | a0006 | c0008 | t0001 | g0094 | SAS | PJL | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG03490 | hp2 | a0025 | c0032 | t0001 | g0028 | SAS | PJL | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG03491 | hp1 | a0026 | c0029 | t0001 | g0175 | SAS | PJL | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG03492 | hp1 | a0026 | c0029 | t0001 | g0174 | SAS | PJL | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG03492 | hp2 | a0025 | c0032 | t0001 | g0030 | SAS | PJL | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG03540 | hp2 | a0049 | c0064 | t0001 | g0027 | AFR | GWD | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG03579 | hp1 | a0002 | c0058 | t0001 | g0032 | AFR | MSL | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0199 | AFR | MSL | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG03669 | hp1 | a0001 | c0004 | t0001 | g0072 | SAS | PJL | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG03669 | hp2 | a0050 | c0039 | t0001 | g0048 | SAS | PJL | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0259 | SAS | PJL | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG03704 | hp2 | a0002 | c0003 | t0001 | g0311 | SAS | PJL | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG03710 | hp1 | a0007 | c0034 | t0001 | g0135 | SAS | PJL | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG03710 | hp2 | a0002 | c0003 | t0001 | g0088 | SAS | PJL | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0034 | SAS | BEB | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0310 | SAS | BEB | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG03927 | hp2 | a0007 | c0081 | t0001 | g0129 | SAS | BEB | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG03942 | hp1 | a0001 | c0004 | t0001 | g0278 | SAS | BEB | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0264 | SAS | BEB | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0304 | SAS | BEB | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG04184 | hp2 | a0001 | c0004 | t0001 | g0064 | SAS | BEB | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG04199 | hp1 | a0004 | c0005 | t0001 | g0276 | SAS | STU | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG04199 | hp2 | a0003 | c0007 | t0001 | g0193 | SAS | STU | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG04204 | hp1 | a0051 | c0044 | t0001 | g0005 | SAS | STU | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG04204 | hp2 | a0001 | c0004 | t0001 | g0201 | SAS | STU | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG04228 | hp1 | a0052 | c0071 | t0001 | g0162 | SAS | STU | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG04228 | hp2 | a0002 | c0003 | t0001 | g0250 | SAS | STU | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18522 | hp1 | a0021 | c0023 | t0001 | g0194 | AFR | YRI | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18522 | hp2 | a0019 | c0030 | t0001 | g0200 | AFR | YRI | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0213 | EAS | CHB | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18612 | hp2 | a0053 | c0047 | t0001 | g0092 | EAS | CHB | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18747 | hp1 | a0005 | c0006 | t0001 | g0006 | EAS | CHB | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18747 | hp2 | a0001 | c0004 | t0001 | g0119 | EAS | CHB | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18940 | hp1 | a0005 | c0006 | t0001 | g0243 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18941 | hp1 | a0004 | c0005 | t0001 | g0124 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0298 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18944 | hp1 | a0006 | c0008 | t0001 | g0156 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18944 | hp2 | a0005 | c0006 | t0001 | g0239 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18947 | hp1 | a0002 | c0003 | t0001 | g0244 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18947 | hp2 | a0007 | c0033 | t0001 | g0155 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18948 | hp1 | a0001 | c0004 | t0001 | g0158 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18950 | hp1 | a0008 | c0010 | t0001 | g0081 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18950 | hp2 | a0011 | c0013 | t0001 | g0054 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18951 | hp1 | a0054 | c0078 | t0001 | g0143 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18951 | hp2 | a0055 | c0055 | t0001 | g0083 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18952 | hp1 | a0008 | c0010 | t0001 | g0051 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18952 | hp2 | a0011 | c0013 | t0001 | g0084 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18954 | hp1 | a0005 | c0006 | t0001 | g0295 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18954 | hp2 | a0003 | c0007 | t0001 | g0120 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18956 | hp1 | a0002 | c0003 | t0001 | g0307 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18956 | hp2 | a0007 | c0034 | t0001 | g0186 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18959 | hp1 | a0001 | c0004 | t0001 | g0063 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18960 | hp1 | a0002 | c0003 | t0001 | g0261 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18960 | hp2 | a0004 | c0005 | t0001 | g0111 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18962 | hp2 | a0001 | c0004 | t0001 | g0134 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18963 | hp2 | a0001 | c0004 | t0001 | g0262 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18964 | hp1 | a0002 | c0003 | t0001 | g0208 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18965 | hp1 | a0017 | c0019 | t0001 | g0289 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18965 | hp2 | a0001 | c0004 | t0001 | g0164 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18969 | hp1 | a0004 | c0005 | t0001 | g0058 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18971 | hp1 | a0002 | c0003 | t0001 | g0187 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18971 | hp2 | a0008 | c0010 | t0001 | g0086 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18973 | hp1 | a0004 | c0005 | t0001 | g0114 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18973 | hp2 | a0001 | c0004 | t0001 | g0163 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18974 | hp1 | a0056 | c0042 | t0001 | g0113 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18974 | hp2 | a0002 | c0003 | t0001 | g0323 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18978 | hp1 | a0007 | c0083 | t0001 | g0287 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18978 | hp2 | a0002 | c0003 | t0001 | g0309 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18983 | hp2 | a0004 | c0005 | t0001 | g0123 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18985 | hp1 | a0027 | c0021 | t0001 | g0062 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18986 | hp1 | a0011 | c0022 | t0001 | g0161 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0308 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18988 | hp1 | a0005 | c0006 | t0001 | g0238 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18988 | hp2 | a0057 | c0037 | t0001 | g0144 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18990 | hp2 | a0005 | c0006 | t0001 | g0242 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18992 | hp1 | a0002 | c0003 | t0001 | g0152 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18992 | hp2 | a0012 | c0012 | t0001 | g0214 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18993 | hp1 | a0005 | c0006 | t0001 | g0294 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0288 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0211 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19002 | hp1 | a0058 | c0053 | t0001 | g0182 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19002 | hp2 | a0003 | c0009 | t0001 | g0106 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19004 | hp1 | a0006 | c0008 | t0001 | g0068 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19004 | hp2 | a0059 | c0057 | t0001 | g0206 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19007 | hp1 | a0001 | c0004 | t0001 | g0157 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19007 | hp2 | a0005 | c0006 | t0001 | g0233 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19010 | hp2 | a0001 | c0052 | t0001 | g0109 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19011 | hp1 | a0010 | c0079 | t0001 | g0055 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19012 | hp1 | a0001 | c0004 | t0001 | g0170 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19012 | hp2 | a0001 | c0038 | t0001 | g0099 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19030 | hp1 | a0020 | c0018 | t0001 | g0149 | AFR | LWK | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19030 | hp2 | a0009 | c0011 | t0001 | g0024 | AFR | LWK | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19043 | hp1 | a0022 | c0027 | t0001 | g0040 | AFR | LWK | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19043 | hp2 | a0009 | c0011 | t0001 | g0138 | AFR | LWK | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19058 | hp2 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19062 | hp2 | a0001 | c0004 | t0001 | g0191 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19066 | hp1 | a0001 | c0004 | t0001 | g0128 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19066 | hp2 | a0027 | c0021 | t0001 | g0069 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19068 | hp1 | a0005 | c0006 | t0001 | g0207 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19070 | hp1 | a0060 | c0066 | t0001 | g0305 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19072 | hp1 | a0004 | c0005 | t0001 | g0216 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19072 | hp2 | a0002 | c0003 | t0001 | g0210 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19074 | hp1 | a0003 | c0009 | t0001 | g0098 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19074 | hp2 | a0008 | c0010 | t0001 | g0078 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19078 | hp1 | a0007 | c0033 | t0001 | g0132 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19078 | hp2 | a0002 | c0002 | t0001 | g0319 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19079 | hp1 | a0001 | c0004 | t0001 | g0192 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0209 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19080 | hp1 | a0003 | c0007 | t0001 | g0136 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19080 | hp2 | a0002 | c0003 | t0001 | g0241 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19081 | hp1 | a0061 | c0063 | t0001 | g0252 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19081 | hp2 | a0004 | c0005 | t0001 | g0105 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19082 | hp1 | a0018 | c0028 | t0001 | g0203 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19083 | hp1 | a0017 | c0019 | t0001 | g0232 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19083 | hp2 | a0002 | c0003 | t0001 | g0306 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19087 | hp1 | a0001 | c0004 | t0001 | g0183 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19087 | hp2 | a0004 | c0005 | t0001 | g0270 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19088 | hp1 | a0028 | c0024 | t0001 | g0257 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19088 | hp2 | a0008 | c0010 | t0001 | g0222 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19090 | hp1 | a0028 | c0024 | t0001 | g0204 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0266 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19091 | hp2 | a0004 | c0005 | t0001 | g0133 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19240 | hp1 | a0062 | c0076 | t0001 | g0325 | AFR | YRI | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA19240 | hp2 | a0020 | c0018 | t0001 | g0150 | AFR | YRI | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0285 | AFR | ASW | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA20129 | hp2 | a0016 | c0014 | t0001 | g0017 | AFR | ASW | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA20805 | hp1 | a0010 | c0031 | t0001 | g0263 | EUR | TSI | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0060 | EUR | TSI | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG01123 | hp2 | a0006 | c0008 | t0001 | g0316 | AMR | CLM | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02486 | hp1 | a0040 | c0043 | t0001 | g0059 | AFR | ACB | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG02486 | hp2 | a0013 | c0016 | t0001 | g0041 | AFR | ACB | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG06807 | hp1 | a0001 | c0004 | t0002 | g0065 | AFR | USA | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| HG06807 | hp2 | a0015 | c0015 | t0001 | g0029 | AFR | USA | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0303 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA20300 | hp1 | a0001 | c0004 | t0001 | g0046 | AFR | USA | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA20300 | hp2 | a0001 | c0004 | t0001 | g0145 | AFR | USA | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA21309 | hp1 | a0007 | c0080 | t0001 | g0076 | AFR | LWK | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| NA21309 | hp2 | a0063 | c0041 | t0001 | g0139 | AFR | LWK | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| homoSapiens | chm13v2 | a0064 | c0054 | t0001 | g0159 | REF | REF | MGAM2_chr7_142106718_142227324 | MGAM2 | chr7 | 142106718 | 142227324 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:142131563 | G | A | 1 | a0033 | 1 | HG01952.hp1 | missense_variant | MODERATE | c.356G>A | p.Gly119Glu | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 5/48 | 446/7903 | 356/7548 | 119/2515 | chr7 | 142131563 | |||
| chr7:142132070 | G | A | 1 | a0044 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.560G>A | p.Ser187Asn | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 6/48 | 650/7903 | 560/7548 | 187/2515 | chr7 | 142132070 | |||
| chr7:142134058 | T | C | 1 | a0057 | 1 | NA18988.hp2 | missense_variant | MODERATE | c.653T>C | p.Val218Ala | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 7/48 | 743/7903 | 653/7548 | 218/2515 | chr7 | 142134058 | |||
| chr7:142134141 | A | AC | 1 | a0007 | 8 | HG00438.hp2 HG03710.hp1 HG03927.hp2 others(5): Show |
frameshift_variant | HIGH | c.741dupC | p.Thr248fs | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 7/48 | 832/7903 | 742/7548 | 248/2515 | INFO_REALIGN_3_PRIME | chr7 | 142134141 | ||
| chr7:142138562 | C | G | 37 | a0002 a0005 a0007 others(34): Show |
163 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(160): Show |
missense_variant | MODERATE | c.981C>G | p.Phe327Leu | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 10/48 | 1071/7903 | 981/7548 | 327/2515 | chr7 | 142138562 | |||
| chr7:142140865 | G | A | 1 | a0059 | 1 | NA19004.hp2 | missense_variant | MODERATE | c.1150G>A | p.Ala384Thr | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 11/48 | 1240/7903 | 1150/7548 | 384/2515 | chr7 | 142140865 | |||
| chr7:142143862 | G | A | 2 | a0029 a0050 |
2 | HG00099.hp2 HG03669.hp2 |
missense_variant | MODERATE | c.1411G>A | p.Glu471Lys | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 13/48 | 1501/7903 | 1411/7548 | 471/2515 | chr7 | 142143862 | |||
| chr7:142154151 | C | T | 8 | a0010 a0011 a0021 others(5): Show |
21 | HG00140.hp1 HG00408.hp1 HG01069.hp2 others(18): Show |
missense_variant | MODERATE | c.1768C>T | p.Pro590Ser | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 16/48 | 1858/7903 | 1768/7548 | 590/2515 | chr7 | 142154151 | |||
| chr7:142154739 | A | G | 1 | a0029 | 1 | HG00099.hp2 | missense_variant | MODERATE | c.1817A>G | p.Asn606Ser | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 17/48 | 1907/7903 | 1817/7548 | 606/2515 | chr7 | 142154739 | |||
| chr7:142158013 | C | A | 1 | a0063 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.2000C>A | p.Thr667Asn | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 18/48 | 2090/7903 | 2000/7548 | 667/2515 | chr7 | 142158013 | |||
| chr7:142158058 | G | A | 3 | a0027 a0028 a0056 |
5 | NA18974.hp1 NA18985.hp1 NA19066.hp2 others(2): Show |
missense_variant | MODERATE | c.2045G>A | p.Arg682Gln | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 18/48 | 2135/7903 | 2045/7548 | 682/2515 | chr7 | 142158058 | |||
| chr7:142159288 | G | T | 1 | a0046 | 1 | HG02970.hp2 | missense_variant&splice_region_variant | MODERATE | c.2165G>T | p.Gly722Val | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 20/48 | 2255/7903 | 2165/7548 | 722/2515 | chr7 | 142159288 | |||
| chr7:142160147 | C | T | 1 | a0013 | 4 | HG00735.hp2 HG02486.hp2 HG03041.hp2 others(1): Show |
missense_variant | MODERATE | c.2234C>T | p.Ser745Leu | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 21/48 | 2324/7903 | 2234/7548 | 745/2515 | chr7 | 142160147 | |||
| chr7:142164977 | A | C | 1 | a0058 | 1 | NA19002.hp1 | missense_variant | MODERATE | c.2606A>C | p.Asn869Thr | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 24/48 | 2696/7903 | 2606/7548 | 869/2515 | chr7 | 142164977 | |||
| chr7:142165010 | A | G | 1 | a0062 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.2639A>G | p.Asn880Ser | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 24/48 | 2729/7903 | 2639/7548 | 880/2515 | chr7 | 142165010 | |||
| chr7:142167332 | A | G | 1 | a0024 | 2 | HG02630.hp1 HG03098.hp1 |
missense_variant | MODERATE | c.2873A>G | p.Asp958Gly | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 26/48 | 2963/7903 | 2873/7548 | 958/2515 | chr7 | 142167332 | |||
| chr7:142167406 | G | A | 6 | a0014 a0022 a0023 others(3): Show |
11 | HG01243.hp1 HG01891.hp1 HG02145.hp2 others(8): Show |
missense_variant | MODERATE | c.2947G>A | p.Ala983Thr | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 26/48 | 3037/7903 | 2947/7548 | 983/2515 | chr7 | 142167406 | |||
| chr7:142167474 | G | A | 3 | a0016 a0020 a0024 |
9 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(6): Show |
missense_variant | MODERATE | c.3015G>A | p.Met1005Ile | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 26/48 | 3105/7903 | 3015/7548 | 1005/2515 | chr7 | 142167474 | |||
| chr7:142171322 | T | C | 1 | a0042 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.3233T>C | p.Ile1078Thr | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 28/48 | 3323/7903 | 3233/7548 | 1078/2515 | chr7 | 142171322 | |||
| chr7:142171376 | C | T | 1 | a0019 | 3 | HG01891.hp2 HG02809.hp2 NA18522.hp2 |
missense_variant | MODERATE | c.3287C>T | p.Thr1096Met | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 28/48 | 3377/7903 | 3287/7548 | 1096/2515 | chr7 | 142171376 | |||
| chr7:142172688 | G | A | 1 | a0045 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.3485G>A | p.Arg1162His | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 30/48 | 3575/7903 | 3485/7548 | 1162/2515 | chr7 | 142172688 | |||
| chr7:142172705 | T | A | 1 | a0007 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.3502T>A | p.Leu1168Met | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 30/48 | 3592/7903 | 3502/7548 | 1168/2515 | chr7 | 142172705 | |||
| chr7:142172723 | T | A | 13 | a0003 a0007 a0008 others(10): Show |
45 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(42): Show |
missense_variant | MODERATE | c.3520T>A | p.Leu1174Met | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 30/48 | 3610/7903 | 3520/7548 | 1174/2515 | chr7 | 142172723 | |||
| chr7:142186026 | G | A | 3 | a0054 a0055 a0061 |
3 | NA18951.hp1 NA18951.hp2 NA19081.hp1 |
missense_variant | MODERATE | c.4025G>A | p.Arg1342His | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 35/48 | 4115/7903 | 4025/7548 | 1342/2515 | chr7 | 142186026 | |||
| chr7:142186041 | C | T | 1 | a0052 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.4040C>T | p.Ala1347Val | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 35/48 | 4130/7903 | 4040/7548 | 1347/2515 | chr7 | 142186041 | |||
| chr7:142189444 | C | G | 12 | a0004 a0005 a0008 others(9): Show |
49 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(46): Show |
missense_variant | MODERATE | c.4285C>G | p.Pro1429Ala | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/48 | 4375/7903 | 4285/7548 | 1429/2515 | chr7 | 142189444 | |||
| chr7:142189447 | G | A | 1 | a0032 | 1 | HG01261.hp1 | missense_variant | MODERATE | c.4288G>A | p.Val1430Met | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/48 | 4378/7903 | 4288/7548 | 1430/2515 | chr7 | 142189447 | |||
| chr7:142196179 | C | T | 1 | a0031 | 1 | HG01255.hp2 | stop_gained | HIGH | c.4372C>T | p.Arg1458* | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 38/48 | 4462/7903 | 4372/7548 | 1458/2515 | chr7 | 142196179 | |||
| chr7:142196237 | G | A | 1 | a0049 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.4430G>A | p.Arg1477Gln | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 38/48 | 4520/7903 | 4430/7548 | 1477/2515 | chr7 | 142196237 | |||
| chr7:142196802 | A | G | 4 | a0033 a0035 a0038 others(1): Show |
4 | HG01952.hp1 HG02055.hp1 HG02145.hp2 others(1): Show |
missense_variant | MODERATE | c.4618A>G | p.Asn1540Asp | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 40/48 | 4708/7903 | 4618/7548 | 1540/2515 | chr7 | 142196802 | |||
| chr7:142218394 | T | C | 1 | a0041 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.5221T>C | p.Tyr1741His | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 47/48 | 5311/7903 | 5221/7548 | 1741/2515 | chr7 | 142218394 | |||
| chr7:142218440 | G | T | 1 | a0039 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.5267G>T | p.Trp1756Leu | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 47/48 | 5357/7903 | 5267/7548 | 1756/2515 | chr7 | 142218440 | |||
| chr7:142218515 | G | A | 1 | a0048 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.5342G>A | p.Ser1781Asn | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 47/48 | 5432/7903 | 5342/7548 | 1781/2515 | chr7 | 142218515 | |||
| chr7:142220578 | A | T | 8 | a0004 a0005 a0008 others(5): Show |
38 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(35): Show |
missense_variant | MODERATE | c.6067A>T | p.Thr2023Ser | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 48/48 | 6157/7903 | 6067/7548 | 2023/2515 | chr7 | 142220578 | |||
| chr7:142220659 | A | G | 1 | a0036 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.6148A>G | p.Thr2050Ala | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 48/48 | 6238/7903 | 6148/7548 | 2050/2515 | chr7 | 142220659 | |||
| chr7:142220953 | A | T | 1 | a0034 | 1 | HG01978.hp2 | missense_variant | MODERATE | c.6442A>T | p.Asn2148Tyr | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 48/48 | 6532/7903 | 6442/7548 | 2148/2515 | chr7 | 142220953 | |||
| chr7:142221355 | A | C | 1 | a0060 | 1 | NA19070.hp1 | missense_variant | MODERATE | c.6844A>C | p.Ser2282Arg | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 48/48 | 6934/7903 | 6844/7548 | 2282/2515 | chr7 | 142221355 | |||
| chr7:142221474 | T | G | 1 | a0040 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.6963T>G | p.Ser2321Arg | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 48/48 | 7053/7903 | 6963/7548 | 2321/2515 | chr7 | 142221474 | |||
| chr7:142221661 | A | T | 3 | a0014 a0015 a0043 |
9 | HG01243.hp1 HG02257.hp2 HG02622.hp1 others(6): Show |
missense_variant | MODERATE | c.7150A>T | p.Ile2384Phe | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 48/48 | 7240/7903 | 7150/7548 | 2384/2515 | chr7 | 142221661 | |||
| chr7:142221680 | C | T | 8 | a0006 a0007 a0012 others(5): Show |
23 | HG00323.hp1 HG00438.hp2 HG01123.hp2 others(20): Show |
missense_variant | MODERATE | c.7169C>T | p.Pro2390Leu | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 48/48 | 7259/7903 | 7169/7548 | 2390/2515 | chr7 | 142221680 | |||
| chr7:142221926 | C | T | 1 | a0053 | 1 | NA18612.hp2 | missense_variant | MODERATE | c.7415C>T | p.Thr2472Ile | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 48/48 | 7505/7903 | 7415/7548 | 2472/2515 | chr7 | 142221926 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:142134002 | C | A | 1 | a0014c0020 | 2 | HG02895.hp2 HG02897.hp2 |
synonymous_variant | LOW | c.597C>A | p.Pro199Pro | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 7/48 | 687/7903 | 597/7548 | 199/2515 | chr7 | 142134002 | |||
| chr7:142134146 | C | T | 1 | a0014c0020 | 2 | HG02895.hp2 HG02897.hp2 |
synonymous_variant | LOW | c.741C>T | p.Pro247Pro | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 7/48 | 831/7903 | 741/7548 | 247/2515 | chr7 | 142134146 | |||
| chr7:142137458 | G | A | 1 | a0001c0038 | 1 | NA19012.hp2 | synonymous_variant | LOW | c.873G>A | p.Ala291Ala | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 9/48 | 963/7903 | 873/7548 | 291/2515 | chr7 | 142137458 | |||
| chr7:142137540 | T | C | 1 | a0050c0039 | 1 | HG03669.hp2 | synonymous_variant | LOW | c.955T>C | p.Leu319Leu | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 9/48 | 1045/7903 | 955/7548 | 319/2515 | chr7 | 142137540 | |||
| chr7:142165023 | G | A | 1 | a0002c0058 | 1 | HG03579.hp1 | splice_region_variant&synonymous_variant | LOW | c.2652G>A | p.Lys884Lys | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 24/48 | 2742/7903 | 2652/7548 | 884/2515 | chr7 | 142165023 | |||
| chr7:142186003 | C | T | 2 | a0001c0052 a0002c0072 |
2 | HG00408.hp2 NA19010.hp2 |
synonymous_variant | LOW | c.4002C>T | p.Tyr1334Tyr | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 35/48 | 4092/7903 | 4002/7548 | 1334/2515 | chr7 | 142186003 | |||
| chr7:142189443 | C | T | 1 | a0040c0043 | 1 | HG02486.hp1 | synonymous_variant | LOW | c.4284C>T | p.Ser1428Ser | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/48 | 4374/7903 | 4284/7548 | 1428/2515 | chr7 | 142189443 | |||
| chr7:142196259 | A | G | 42 | a0001c0001 a0001c0038 a0002c0002 others(39): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
synonymous_variant | LOW | c.4452A>G | p.Ala1484Ala | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 38/48 | 4542/7903 | 4452/7548 | 1484/2515 | chr7 | 142196259 | |||
| chr7:142218426 | G | A | 5 | a0033c0035 a0035c0067 a0038c0059 others(2): Show |
5 | HG01952.hp1 HG02055.hp1 HG02145.hp2 others(2): Show |
synonymous_variant | LOW | c.5253G>A | p.Gly1751Gly | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 47/48 | 5343/7903 | 5253/7548 | 1751/2515 | chr7 | 142218426 | |||
| chr7:142220004 | A | G | 5 | a0033c0035 a0035c0067 a0038c0059 others(2): Show |
5 | HG01952.hp1 HG02055.hp1 HG02145.hp2 others(2): Show |
synonymous_variant | LOW | c.5493A>G | p.Pro1831Pro | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 48/48 | 5583/7903 | 5493/7548 | 1831/2515 | chr7 | 142220004 | |||
| chr7:142221582 | G | A | 1 | a0039c0046 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.7071G>A | p.Thr2357Thr | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 48/48 | 7161/7903 | 7071/7548 | 2357/2515 | chr7 | 142221582 | |||
| chr7:142221612 | C | T | 1 | a0010c0079 | 1 | NA19011.hp1 | synonymous_variant | LOW | c.7101C>T | p.Thr2367Thr | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 48/48 | 7191/7903 | 7101/7548 | 2367/2515 | chr7 | 142221612 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:142222100 | C | T | 6 | a0001c0004t0002 a0002c0003t0002 a0009c0011t0002 others(3): Show |
7 | HG02572.hp2 HG02809.hp2 HG02970.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*41C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 48/48 | 41 | chr7 | 142222100 | ||||||
| chr7:142222176 | A | G | 1 | a0021c0023t0004 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*117A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 48/48 | 117 | chr7 | 142222176 | ||||||
| chr7:142222271 | A | G | 2 | a0033c0035t0003 a0035c0067t0003 |
2 | HG01952.hp1 HG02055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*212A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 48/48 | 212 | chr7 | 142222271 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:142111814 | A | T | 1 | a0001c0001t0001g0328 | 1 | NA18955.hp2 | splice_region_variant&intron_variant | LOW | c.-1+7A>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142111814 | |||||||
| chr7:142111893 | T | C | 39 | a0002c0002t0001g0008 a0002c0002t0001g0016 a0002c0002t0001g0019 others(36): Show |
39 | HG00642.hp1 HG00741.hp2 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.-1+86T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142111893 | |||||||
| chr7:142111921 | C | T | 61 | a0001c0001t0001g0313 a0001c0001t0001g0318 a0002c0002t0001g0008 others(58): Show |
61 | HG00642.hp1 HG00741.hp2 HG01071.hp1 others(58): Show |
intron_variant | MODIFIER | c.-1+114C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142111921 | |||||||
| chr7:142111998 | C | CTG | 59 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0221 others(56): Show |
59 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.-1+236_-1+237dupTG | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142111998 | ||||||
| chr7:142111998 | C | CTGTG | 34 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0274 others(31): Show |
34 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.-1+234_-1+237dupTG others(2): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142111998 | ||||||
| chr7:142111998 | C | CTGTGTG | 7 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0002c0002t0001g0303 others(4): Show |
7 | HG01928.hp1 HG02135.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1+232_-1+237dupTG others(4): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142111998 | ||||||
| chr7:142111998 | CTG | C | 76 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0087 others(73): Show |
76 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-1+236_-1+237delTG | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142111998 | ||||||
| chr7:142111998 | CTGTG | C | 32 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(29): Show |
32 | HG00423.hp2 HG00741.hp1 HG01168.hp2 others(29): Show |
intron_variant | MODIFIER | c.-1+234_-1+237delTG others(2): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142111998 | ||||||
| chr7:142111998 | CTGTGTG | C | 7 | a0002c0002t0001g0016 a0015c0015t0001g0013 a0015c0015t0001g0014 others(4): Show |
7 | HG01891.hp2 HG02257.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1+232_-1+237delTG others(4): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142111998 | ||||||
| chr7:142111998 | CTGTGTGT others(1): Show |
C | 3 | a0002c0002t0001g0050 a0002c0003t0001g0049 a0050c0039t0001g0048 |
3 | HG01884.hp2 HG02280.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.-1+230_-1+237delTG others(6): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142111998 | ||||||
| chr7:142111998 | CTGTGTGT others(3): Show |
C | 22 | a0001c0001t0001g0313 a0001c0001t0001g0318 a0002c0002t0001g0008 others(19): Show |
22 | HG00741.hp2 HG01071.hp1 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-1+228_-1+237delTG others(8): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142111998 | ||||||
| chr7:142111998 | CTGTGTGT others(7): Show |
C | 7 | a0002c0002t0001g0308 a0002c0002t0001g0310 a0002c0003t0001g0306 others(4): Show |
7 | HG03239.hp1 HG03704.hp2 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1+224_-1+237delTG others(12): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142111998 | ||||||
| chr7:142111998 | CTGTGTGT others(9): Show |
C | 2 | a0001c0004t0001g0046 a0048c0065t0002g0047 |
2 | HG03130.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-1+222_-1+237delTG others(14): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142111998 | ||||||
| chr7:142111998 | CTGTGTGT others(11): Show |
C | 6 | a0002c0002t0001g0043 a0002c0002t0001g0045 a0013c0016t0001g0041 others(3): Show |
7 | HG02486.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1+220_-1+237delTG others(16): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142111998 | ||||||
| chr7:142112047 | G | T | 1 | a0001c0001t0001g0328 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-1+240G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142112047 | |||||||
| chr7:142112102 | C | T | 61 | a0001c0001t0001g0313 a0001c0001t0001g0318 a0002c0002t0001g0008 others(58): Show |
61 | HG00642.hp1 HG00741.hp2 HG01071.hp1 others(58): Show |
intron_variant | MODIFIER | c.-1+295C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142112102 | |||||||
| chr7:142112128 | C | T | 78 | a0001c0001t0001g0227 a0001c0001t0001g0245 a0001c0001t0001g0247 others(75): Show |
78 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.-1+321C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142112128 | |||||||
| chr7:142112589 | T | C | 62 | a0001c0001t0001g0313 a0001c0001t0001g0318 a0002c0002t0001g0008 others(59): Show |
62 | HG00642.hp1 HG00741.hp2 HG01071.hp1 others(59): Show |
intron_variant | MODIFIER | c.-1+782T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142112589 | |||||||
| chr7:142112624 | G | T | 1 | a0057c0037t0001g0144 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-1+817G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142112624 | |||||||
| chr7:142112681 | C | T | 3 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0029c0040t0001g0202 |
3 | HG00099.hp2 HG00741.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-1+874C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142112681 | |||||||
| chr7:142112709 | C | T | 6 | a0002c0002t0001g0019 a0002c0002t0001g0021 a0002c0002t0001g0034 others(3): Show |
6 | HG01243.hp2 HG01496.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1+902C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142112709 | |||||||
| chr7:142113013 | A | G | 2 | a0003c0007t0001g0142 a0003c0009t0001g0141 |
2 | HG00140.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.-1+1206A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142113013 | |||||||
| chr7:142113119 | G | A | 7 | a0001c0004t0001g0046 a0002c0002t0001g0043 a0002c0002t0001g0045 others(4): Show |
7 | HG02486.hp2 HG02922.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1+1312G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142113119 | |||||||
| chr7:142113210 | C | G | 1 | a0004c0005t0001g0270 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-1+1403C>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142113210 | |||||||
| chr7:142113214 | C | T | 61 | a0001c0001t0001g0313 a0001c0001t0001g0318 a0002c0002t0001g0008 others(58): Show |
61 | HG00642.hp1 HG00741.hp2 HG01071.hp1 others(58): Show |
intron_variant | MODIFIER | c.-1+1407C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142113214 | |||||||
| chr7:142113318 | C | A | 6 | a0001c0004t0001g0145 a0020c0018t0001g0148 a0020c0018t0001g0149 others(3): Show |
6 | HG02055.hp1 HG03041.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1+1511C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142113318 | |||||||
| chr7:142113318 | C | T | 1 | a0014c0020t0001g0001 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-1+1511C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142113318 | |||||||
| chr7:142113350 | A | G | 1 | a0001c0004t0001g0201 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-1+1543A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142113350 | |||||||
| chr7:142113374 | C | G | 3 | a0002c0002t0001g0310 a0002c0003t0001g0311 a0002c0003t0001g0312 |
3 | HG03239.hp1 HG03704.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.-1+1567C>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142113374 | |||||||
| chr7:142113526 | GT | G | 78 | a0001c0001t0001g0227 a0001c0001t0001g0245 a0001c0001t0001g0247 others(75): Show |
78 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.-1+1729delT | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142113526 | ||||||
| chr7:142113556 | C | CA | 3 | a0001c0001t0001g0227 a0002c0002t0001g0229 a0002c0003t0001g0228 |
3 | HG02080.hp2 HG02129.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.-1+1751dupA | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142113556 | ||||||
| chr7:142113612 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-1+1805G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142113612 | |||||||
| chr7:142113799 | A | G | 7 | a0002c0002t0001g0308 a0002c0002t0001g0310 a0002c0003t0001g0306 others(4): Show |
7 | HG03239.hp1 HG03704.hp2 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1+1992A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142113799 | |||||||
| chr7:142113825 | G | C | 61 | a0001c0001t0001g0313 a0001c0001t0001g0318 a0002c0002t0001g0008 others(58): Show |
61 | HG00642.hp1 HG00741.hp2 HG01071.hp1 others(58): Show |
intron_variant | MODIFIER | c.-1+2018G>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142113825 | |||||||
| chr7:142113907 | G | A | 61 | a0001c0001t0001g0313 a0001c0001t0001g0318 a0002c0002t0001g0008 others(58): Show |
61 | HG00642.hp1 HG00741.hp2 HG01071.hp1 others(58): Show |
intron_variant | MODIFIER | c.-1+2100G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142113907 | |||||||
| chr7:142114072 | G | A | 1 | a0014c0020t0001g0001 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-1+2265G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114072 | |||||||
| chr7:142114087 | C | T | 11 | a0002c0002t0001g0199 a0002c0002t0001g0224 a0002c0002t0001g0284 others(8): Show |
11 | HG00735.hp2 HG01261.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.-1+2280C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114087 | |||||||
| chr7:142114130 | C | G | 23 | a0002c0002t0001g0019 a0002c0002t0001g0021 a0002c0002t0001g0034 others(20): Show |
23 | HG00642.hp1 HG01106.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.-1+2323C>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114130 | |||||||
| chr7:142114134 | A | G | 61 | a0001c0001t0001g0313 a0001c0001t0001g0318 a0002c0002t0001g0008 others(58): Show |
61 | HG00642.hp1 HG00741.hp2 HG01071.hp1 others(58): Show |
intron_variant | MODIFIER | c.-1+2327A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114134 | |||||||
| chr7:142114148 | A | G | 15 | a0002c0002t0001g0008 a0002c0002t0001g0016 a0002c0003t0001g0002 others(12): Show |
15 | HG00741.hp2 HG01074.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.-1+2341A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114148 | |||||||
| chr7:142114153 | G | A | 62 | a0001c0001t0001g0313 a0001c0001t0001g0318 a0002c0002t0001g0008 others(59): Show |
62 | HG00642.hp1 HG00741.hp2 HG01071.hp1 others(59): Show |
intron_variant | MODIFIER | c.-1+2346G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114153 | |||||||
| chr7:142114153 | G | GAAAGAAA others(4): Show |
1 | a0002c0002t0001g0151 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-1+2346_-1+2347ins others(11): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114153 | |||||||
| chr7:142114153 | G | GGAAA | 40 | a0001c0001t0001g0060 a0001c0001t0001g0101 a0001c0001t0001g0107 others(37): Show |
40 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.-1+2405_-1+2408dup others(4): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114153 | ||||||
| chr7:142114153 | G | GGAAAGAA others(1): Show |
33 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(30): Show |
33 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.-1+2401_-1+2408dup others(8): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114153 | ||||||
| chr7:142114153 | G | GGAAAGAA others(5): Show |
20 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0087 others(17): Show |
20 | HG00408.hp1 HG00558.hp2 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.-1+2397_-1+2408dup others(12): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114153 | ||||||
| chr7:142114153 | G | GGAAAGAA others(9): Show |
7 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0217 others(4): Show |
7 | HG02615.hp2 NA18947.hp2 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1+2393_-1+2408dup others(16): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114153 | ||||||
| chr7:142114153 | G | GGAAAGAA others(13): Show |
1 | a0002c0003t0001g0152 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-1+2389_-1+2408dup others(20): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114153 | ||||||
| chr7:142114153 | GGAAA | G | 17 | a0001c0001t0001g0071 a0001c0001t0001g0075 a0001c0001t0001g0130 others(14): Show |
17 | HG00639.hp1 HG00741.hp1 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.-1+2405_-1+2408del others(4): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114153 | ||||||
| chr7:142114153 | GGAAAGAA others(1): Show |
G | 3 | a0001c0001t0001g0281 a0035c0067t0003g0146 a0047c0070t0001g0147 |
3 | HG02004.hp1 HG02055.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-1+2401_-1+2408del others(8): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114153 | ||||||
| chr7:142114153 | GGAAAGAA others(5): Show |
G | 5 | a0001c0004t0001g0072 a0002c0003t0001g0073 a0020c0018t0001g0148 others(2): Show |
5 | HG02717.hp2 HG03041.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1+2397_-1+2408del others(12): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114153 | ||||||
| chr7:142114153 | GGAAAGAA others(9): Show |
G | 4 | a0002c0002t0001g0224 a0002c0003t0001g0225 a0002c0003t0001g0226 others(1): Show |
4 | HG02896.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1+2393_-1+2408del others(16): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114153 | ||||||
| chr7:142114153 | GGAAAGAA others(13): Show |
G | 9 | a0002c0002t0001g0199 a0002c0002t0001g0284 a0002c0003t0001g0197 others(6): Show |
9 | HG00735.hp2 HG01243.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.-1+2389_-1+2408del others(20): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114153 | ||||||
| chr7:142114153 | GGAAAGAA others(17): Show |
G | 1 | a0002c0002t0001g0285 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-1+2385_-1+2408del others(24): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114153 | ||||||
| chr7:142114177 | A | G | 1 | a0041c0068t0001g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-1+2370A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114177 | |||||||
| chr7:142114181 | A | G | 1 | a0041c0068t0001g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-1+2374A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114181 | |||||||
| chr7:142114185 | A | G | 2 | a0041c0068t0001g0022 a0062c0076t0001g0325 |
2 | HG02572.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-1+2378A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114185 | |||||||
| chr7:142114187 | A | AAGGAAGG others(12): Show |
1 | a0002c0002t0001g0021 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-1+2381_-1+2382ins others(19): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114187 | ||||||
| chr7:142114189 | A | G | 1 | a0041c0068t0001g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-1+2382A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114189 | |||||||
| chr7:142114191 | A | AAGAAGGA others(23): Show |
1 | a0002c0003t0001g0033 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-1+2385_-1+2386ins others(30): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114191 | ||||||
| chr7:142114191 | A | AAGGAAGG others(8): Show |
1 | a0002c0002t0001g0016 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-1+2385_-1+2386ins others(15): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114191 | ||||||
| chr7:142114191 | A | AAGGAAGG others(12): Show |
2 | a0002c0002t0001g0019 a0062c0076t0001g0325 |
2 | HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-1+2385_-1+2386ins others(19): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114191 | ||||||
| chr7:142114191 | A | AAGGAAGG others(16): Show |
1 | a0002c0003t0001g0010 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-1+2385_-1+2386ins others(23): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114191 | ||||||
| chr7:142114191 | A | AAGGAAGG others(20): Show |
1 | a0002c0003t0001g0020 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-1+2385_-1+2386ins others(27): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114191 | ||||||
| chr7:142114191 | A | G | 1 | a0002c0002t0001g0021 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-1+2384A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114191 | |||||||
| chr7:142114193 | A | G | 3 | a0002c0003t0001g0323 a0012c0012t0001g0324 a0041c0068t0001g0022 |
3 | HG01975.hp2 HG02572.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.-1+2386A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114193 | |||||||
| chr7:142114195 | A | AAGGAAGG others(12): Show |
2 | a0002c0003t0001g0007 a0005c0006t0001g0006 |
2 | HG01074.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.-1+2389_-1+2390ins others(19): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114195 | ||||||
| chr7:142114195 | A | AAGGAAGG others(16): Show |
1 | a0002c0002t0001g0008 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-1+2389_-1+2390ins others(23): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114195 | ||||||
| chr7:142114195 | A | AAGGAAGG others(20): Show |
2 | a0002c0002t0001g0039 a0002c0003t0001g0009 |
2 | HG02015.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-1+2389_-1+2390ins others(27): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114195 | ||||||
| chr7:142114195 | A | AAGGAAGG others(36): Show |
1 | a0019c0030t0002g0326 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-1+2389_-1+2390ins others(43): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114195 | ||||||
| chr7:142114195 | A | G | 7 | a0002c0002t0001g0016 a0002c0002t0001g0019 a0002c0002t0001g0021 others(4): Show |
7 | HG00741.hp2 HG01243.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1+2388A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114195 | |||||||
| chr7:142114196 | A | G | 2 | a0001c0001t0001g0268 a0002c0002t0001g0269 |
2 | HG00099.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.-1+2389A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114196 | |||||||
| chr7:142114197 | A | G | 1 | a0041c0068t0001g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-1+2390A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114197 | |||||||
| chr7:142114198 | GAAAGAAA others(7): Show |
G | 1 | a0001c0001t0001g0140 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-1+2393_-1+2406del others(14): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114198 | ||||||
| chr7:142114199 | A | AAGGAAGG others(16): Show |
4 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0023c0025t0002g0037 others(1): Show |
4 | HG01516.hp2 HG01517.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1+2393_-1+2394ins others(23): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114199 | ||||||
| chr7:142114199 | A | AAGGAAGG others(20): Show |
2 | a0002c0003t0001g0323 a0022c0027t0001g0038 |
2 | HG01891.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.-1+2393_-1+2394ins others(27): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114199 | ||||||
| chr7:142114199 | A | AAGGAAGG others(24): Show |
1 | a0012c0012t0001g0324 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-1+2393_-1+2394ins others(31): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114199 | ||||||
| chr7:142114199 | A | G | 13 | a0002c0002t0001g0008 a0002c0002t0001g0016 a0002c0002t0001g0019 others(10): Show |
13 | HG00741.hp2 HG01074.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.-1+2392A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114199 | |||||||
| chr7:142114200 | A | G | 1 | a0004c0005t0001g0270 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-1+2393A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114200 | |||||||
| chr7:142114200 | AAGAAAGA others(9): Show |
A | 2 | a0001c0001t0001g0268 a0002c0002t0001g0269 |
2 | HG00099.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.-1+2409_-1+2424del others(16): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114200 | ||||||
| chr7:142114201 | A | G | 6 | a0001c0001t0001g0318 a0002c0002t0001g0319 a0006c0008t0001g0316 others(3): Show |
6 | HG01071.hp1 HG01123.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1+2394A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114201 | |||||||
| chr7:142114203 | A | AAGGAAGG others(20): Show |
1 | a0042c0060t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-1+2397_-1+2398ins others(27): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114203 | ||||||
| chr7:142114203 | A | AAGGAAGG others(28): Show |
2 | a0015c0015t0001g0014 a0015c0015t0001g0029 |
2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-1+2397_-1+2398ins others(35): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114203 | ||||||
| chr7:142114203 | A | AAGGAAGG others(32): Show |
1 | a0022c0027t0001g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-1+2397_-1+2398ins others(39): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114203 | ||||||
| chr7:142114203 | A | AAGGAAGG others(36): Show |
1 | a0038c0059t0001g0026 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-1+2397_-1+2398ins others(43): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114203 | ||||||
| chr7:142114203 | A | AAGGAAGG others(52): Show |
1 | a0002c0058t0001g0032 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-1+2397_-1+2398ins others(59): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114203 | ||||||
| chr7:142114203 | A | G | 20 | a0002c0002t0001g0008 a0002c0002t0001g0016 a0002c0002t0001g0019 others(17): Show |
20 | HG00741.hp2 HG01074.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.-1+2396A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114203 | |||||||
| chr7:142114204 | A | G | 3 | a0002c0002t0001g0211 a0002c0002t0001g0298 a0010c0031t0001g0263 |
3 | NA18941.hp2 NA19000.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-1+2397A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114204 | |||||||
| chr7:142114204 | AAGAAAGA others(5): Show |
A | 1 | a0004c0005t0001g0270 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-1+2409_-1+2420del others(12): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114204 | ||||||
| chr7:142114205 | A | G | 3 | a0006c0008t0001g0321 a0012c0012t0001g0322 a0041c0068t0001g0022 |
3 | HG01928.hp2 HG01952.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.-1+2398A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114205 | |||||||
| chr7:142114207 | A | AAGAGAAG others(41): Show |
1 | a0016c0014t0001g0018 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-1+2401_-1+2402ins others(48): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114207 | ||||||
| chr7:142114207 | A | AAGGAAGG others(16): Show |
2 | a0001c0001t0001g0318 a0031c0051t0001g0317 |
2 | HG01071.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.-1+2401_-1+2402ins others(23): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114207 | ||||||
| chr7:142114207 | A | AAGGAAGG others(20): Show |
3 | a0002c0003t0001g0004 a0006c0008t0001g0316 a0012c0012t0001g0320 |
3 | HG01123.hp2 HG01168.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.-1+2401_-1+2402ins others(27): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114207 | ||||||
| chr7:142114207 | A | AAGGAAGG others(24): Show |
2 | a0002c0002t0001g0319 a0015c0015t0001g0013 |
2 | HG02922.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.-1+2401_-1+2402ins others(31): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114207 | ||||||
| chr7:142114207 | A | AAGGAAGG others(32): Show |
1 | a0049c0064t0001g0027 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-1+2401_-1+2402ins others(39): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114207 | ||||||
| chr7:142114207 | A | AAGGAAGG others(36): Show |
1 | a0009c0011t0002g0036 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-1+2401_-1+2402ins others(43): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114207 | ||||||
| chr7:142114207 | A | AAGGAAGG others(44): Show |
1 | a0014c0026t0001g0327 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-1+2401_-1+2402ins others(51): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114207 | ||||||
| chr7:142114207 | A | G | 26 | a0002c0002t0001g0008 a0002c0002t0001g0016 a0002c0002t0001g0019 others(23): Show |
26 | HG00741.hp2 HG01074.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.-1+2400A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114207 | |||||||
| chr7:142114208 | A | G | 13 | a0001c0001t0001g0267 a0001c0004t0001g0262 a0002c0002t0001g0212 others(10): Show |
14 | HG00408.hp2 HG02040.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-1+2401A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114208 | |||||||
| chr7:142114208 | AAGAAAGA others(1): Show |
A | 3 | a0002c0002t0001g0211 a0002c0002t0001g0298 a0010c0031t0001g0263 |
3 | NA18941.hp2 NA19000.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-1+2409_-1+2416del others(8): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114208 | ||||||
| chr7:142114209 | A | G | 3 | a0002c0003t0001g0312 a0006c0008t0001g0315 a0041c0068t0001g0022 |
3 | HG02293.hp2 HG02572.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-1+2402A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114209 | |||||||
| chr7:142114211 | A | AAAGAAAG others(8): Show |
1 | a0001c0004t0001g0191 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-1+2408_-1+2409ins others(15): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114211 | ||||||
| chr7:142114211 | A | AAAGAAAG others(11): Show |
1 | a0001c0001t0001g0328 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-1+2408_-1+2409ins others(18): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114211 | ||||||
| chr7:142114211 | A | AAGGAAGG others(24): Show |
1 | a0012c0012t0001g0322 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-1+2405_-1+2406ins others(31): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114211 | ||||||
| chr7:142114211 | A | AAGGAAGG others(28): Show |
1 | a0006c0008t0001g0321 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-1+2405_-1+2406ins others(35): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114211 | ||||||
| chr7:142114211 | A | G | 37 | a0001c0001t0001g0318 a0002c0002t0001g0008 a0002c0002t0001g0016 others(34): Show |
37 | HG00741.hp2 HG01071.hp1 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.-1+2404A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114211 | |||||||
| chr7:142114212 | A | AAGAAAGA others(3): Show |
1 | a0002c0003t0002g0230 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-1+2408_-1+2409ins others(10): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114212 | ||||||
| chr7:142114212 | A | AAGAAAGA others(17): Show |
1 | a0013c0016t0001g0041 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-1+2408_-1+2409ins others(24): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114212 | ||||||
| chr7:142114212 | A | AAGAAAGA others(5): Show |
5 | a0001c0001t0001g0245 a0001c0004t0001g0121 a0002c0002t0001g0229 others(2): Show |
5 | HG00609.hp2 HG01884.hp1 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1+2408_-1+2409ins others(12): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114212 | ||||||
| chr7:142114212 | A | AAGAAAGA others(1): Show |
19 | a0001c0001t0001g0227 a0002c0002t0001g0291 a0002c0002t0001g0303 others(16): Show |
19 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.-1+2408_-1+2409ins others(8): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114212 | ||||||
| chr7:142114212 | A | AAGAAAGA others(5): Show |
1 | a0013c0016t0001g0042 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-1+2408_-1+2409ins others(12): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114212 | ||||||
| chr7:142114212 | A | AGGAAGGA others(48): Show |
1 | a0009c0011t0001g0025 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-1+2405_-1+2406ins others(55): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114212 | |||||||
| chr7:142114212 | A | G | 17 | a0001c0001t0001g0247 a0001c0004t0001g0046 a0002c0002t0001g0043 others(14): Show |
17 | HG01069.hp2 HG01099.hp1 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.-1+2405A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114212 | |||||||
| chr7:142114212 | AAGAG | A | 13 | a0001c0001t0001g0267 a0001c0004t0001g0262 a0002c0002t0001g0212 others(10): Show |
14 | HG00408.hp2 HG02040.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-1+2409_-1+2412del others(4): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114212 | ||||||
| chr7:142114213 | A | G | 2 | a0002c0003t0001g0309 a0002c0003t0001g0312 |
2 | HG03239.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.-1+2406A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114213 | |||||||
| chr7:142114215 | A | AAAGAAAG others(6): Show |
1 | a0002c0002t0001g0304 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-1+2408_-1+2409ins others(13): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114215 | |||||||
| chr7:142114215 | A | AAGAAGGA others(51): Show |
1 | a0002c0003t0001g0307 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-1+2408_-1+2409ins others(58): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114215 | |||||||
| chr7:142114215 | A | AAGGAAGG others(28): Show |
1 | a0006c0008t0001g0315 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-1+2408_-1+2409ins others(35): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114215 | |||||||
| chr7:142114215 | A | AAGGAAGG others(32): Show |
2 | a0016c0014t0001g0011 a0019c0073t0001g0012 |
2 | HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-1+2408_-1+2409ins others(39): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114215 | |||||||
| chr7:142114215 | A | AAGGAAGG others(44): Show |
1 | a0024c0074t0001g0031 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-1+2408_-1+2409ins others(51): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114215 | |||||||
| chr7:142114215 | A | AAGGAAGG others(48): Show |
1 | a0002c0002t0001g0308 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-1+2408_-1+2409ins others(55): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114215 | |||||||
| chr7:142114215 | A | AAGGAAGG others(52): Show |
1 | a0009c0011t0001g0024 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-1+2408_-1+2409ins others(59): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114215 | |||||||
| chr7:142114215 | A | G | 40 | a0001c0001t0001g0318 a0002c0002t0001g0008 a0002c0002t0001g0016 others(37): Show |
40 | HG00741.hp2 HG01071.hp1 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.-1+2408A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114215 | |||||||
| chr7:142114216 | G | A | 109 | a0001c0001t0001g0227 a0001c0001t0001g0245 a0001c0001t0001g0247 others(106): Show |
109 | HG00642.hp1 HG00741.hp2 HG01069.hp2 others(106): Show |
intron_variant | MODIFIER | c.-1+2409G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114216 | |||||||
| chr7:142114216 | G | GAGAA | 19 | a0001c0001t0001g0260 a0002c0002t0001g0253 a0002c0002t0001g0259 others(16): Show |
19 | HG00423.hp1 HG00735.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.-1+2423_-1+2426dup others(4): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114216 | ||||||
| chr7:142114217 | A | G | 3 | a0002c0003t0001g0309 a0002c0003t0001g0312 a0006c0008t0001g0314 |
3 | HG02293.hp1 HG03239.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.-1+2410A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114217 | |||||||
| chr7:142114219 | A | AAAGAAAG others(8): Show |
1 | a0006c0008t0001g0156 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-1+2424_-1+2425ins others(15): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114219 | ||||||
| chr7:142114219 | A | AAGGAAGG others(48): Show |
1 | a0002c0003t0001g0306 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-1+2413_-1+2414ins others(55): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114219 | ||||||
| chr7:142114219 | A | AAGGAAGG others(52): Show |
3 | a0002c0002t0001g0034 a0025c0032t0001g0028 a0025c0032t0001g0030 |
3 | HG03490.hp2 HG03492.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.-1+2413_-1+2414ins others(59): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114219 | ||||||
| chr7:142114219 | A | G | 48 | a0001c0001t0001g0318 a0002c0002t0001g0008 a0002c0002t0001g0016 others(45): Show |
48 | HG00741.hp2 HG01071.hp1 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.-1+2412A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114219 | |||||||
| chr7:142114221 | A | G | 2 | a0002c0003t0001g0309 a0002c0003t0001g0312 |
2 | HG03239.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.-1+2414A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114221 | |||||||
| chr7:142114223 | A | AAGGAAGG others(44): Show |
1 | a0006c0008t0001g0314 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-1+2417_-1+2418ins others(51): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114223 | ||||||
| chr7:142114223 | A | AAGGAAGG others(48): Show |
1 | a0002c0002t0001g0035 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-1+2417_-1+2418ins others(55): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114223 | ||||||
| chr7:142114223 | A | AAGGAAGG others(56): Show |
1 | a0002c0003t0001g0311 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-1+2417_-1+2418ins others(63): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114223 | ||||||
| chr7:142114223 | A | AAGGAAGG others(40): Show |
1 | a0002c0003t0001g0312 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-1+2417_-1+2418ins others(47): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114223 | ||||||
| chr7:142114223 | A | AGGAAGGA others(36): Show |
1 | a0002c0003t0001g0309 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-1+2416_-1+2417ins others(43): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114223 | |||||||
| chr7:142114223 | A | G | 52 | a0001c0001t0001g0318 a0002c0002t0001g0008 a0002c0002t0001g0016 others(49): Show |
52 | HG00741.hp2 HG01071.hp1 HG01074.hp2 others(49): Show |
intron_variant | MODIFIER | c.-1+2416A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114223 | |||||||
| chr7:142114224 | A | G | 2 | a0002c0003t0001g0250 a0002c0003t0001g0292 |
2 | HG02145.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-1+2417A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114224 | |||||||
| chr7:142114227 | A | G | 57 | a0001c0001t0001g0318 a0002c0002t0001g0008 a0002c0002t0001g0016 others(54): Show |
57 | HG00741.hp2 HG01071.hp1 HG01074.hp2 others(54): Show |
intron_variant | MODIFIER | c.-1+2420A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114227 | |||||||
| chr7:142114231 | A | AAGGAAGG others(68): Show |
1 | a0009c0011t0001g0023 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-1+2425_-1+2426ins others(75): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142114231 | ||||||
| chr7:142114231 | A | G | 57 | a0001c0001t0001g0318 a0002c0002t0001g0008 a0002c0002t0001g0016 others(54): Show |
57 | HG00741.hp2 HG01071.hp1 HG01074.hp2 others(54): Show |
intron_variant | MODIFIER | c.-1+2424A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114231 | |||||||
| chr7:142114234 | T | G | 61 | a0001c0001t0001g0313 a0001c0001t0001g0318 a0002c0002t0001g0008 others(58): Show |
61 | HG00642.hp1 HG00741.hp2 HG01071.hp1 others(58): Show |
intron_variant | MODIFIER | c.-1+2427T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114234 | |||||||
| chr7:142114235 | A | AAAGAAGG others(60): Show |
1 | a0001c0001t0001g0313 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-1+2428_-1+2429ins others(67): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114235 | |||||||
| chr7:142114235 | A | AAAGAAGG others(72): Show |
1 | a0002c0002t0001g0310 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-1+2428_-1+2429ins others(79): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114235 | |||||||
| chr7:142114235 | A | AAGGAAGG others(60): Show |
1 | a0016c0014t0001g0017 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-1+2428_-1+2429ins others(67): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114235 | |||||||
| chr7:142114235 | A | G | 58 | a0001c0001t0001g0318 a0002c0002t0001g0008 a0002c0002t0001g0016 others(55): Show |
58 | HG00642.hp1 HG00741.hp2 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.-1+2428A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114235 | |||||||
| chr7:142114236 | G | A | 7 | a0002c0002t0001g0308 a0002c0002t0001g0310 a0002c0003t0001g0306 others(4): Show |
7 | HG03239.hp1 HG03704.hp2 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1+2429G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114236 | |||||||
| chr7:142114248 | G | C | 60 | a0001c0001t0001g0313 a0001c0001t0001g0318 a0002c0002t0001g0008 others(57): Show |
60 | HG00642.hp1 HG01071.hp1 HG01074.hp2 others(57): Show |
intron_variant | MODIFIER | c.-1+2441G>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114248 | |||||||
| chr7:142114457 | A | T | 139 | a0001c0001t0001g0227 a0001c0001t0001g0245 a0001c0001t0001g0247 others(136): Show |
139 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.1-2417A>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114457 | |||||||
| chr7:142114588 | A | C | 15 | a0002c0002t0001g0008 a0002c0002t0001g0016 a0002c0003t0001g0002 others(12): Show |
15 | HG00741.hp2 HG01074.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.1-2286A>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114588 | |||||||
| chr7:142114690 | A | G | 139 | a0001c0001t0001g0227 a0001c0001t0001g0245 a0001c0001t0001g0247 others(136): Show |
139 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.1-2184A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114690 | |||||||
| chr7:142114715 | A | G | 1 | a0006c0008t0001g0156 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1-2159A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114715 | |||||||
| chr7:142114834 | A | G | 1 | a0005c0006t0001g0295 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1-2040A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114834 | |||||||
| chr7:142114923 | C | A | 2 | a0002c0003t0001g0033 a0015c0015t0001g0029 |
2 | HG02647.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1-1951C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114923 | |||||||
| chr7:142114987 | A | G | 136 | a0001c0001t0001g0227 a0001c0001t0001g0245 a0001c0001t0001g0247 others(133): Show |
136 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1-1887A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114987 | |||||||
| chr7:142114988 | A | G | 136 | a0001c0001t0001g0227 a0001c0001t0001g0245 a0001c0001t0001g0247 others(133): Show |
136 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1-1886A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114988 | |||||||
| chr7:142114997 | T | C | 136 | a0001c0001t0001g0227 a0001c0001t0001g0245 a0001c0001t0001g0247 others(133): Show |
136 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1-1877T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142114997 | |||||||
| chr7:142115027 | C | T | 1 | a0021c0023t0001g0194 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1-1847C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142115027 | |||||||
| chr7:142115146 | G | A | 136 | a0001c0001t0001g0227 a0001c0001t0001g0245 a0001c0001t0001g0247 others(133): Show |
136 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1-1728G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142115146 | |||||||
| chr7:142115212 | A | G | 136 | a0001c0001t0001g0227 a0001c0001t0001g0245 a0001c0001t0001g0247 others(133): Show |
136 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1-1662A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142115212 | |||||||
| chr7:142115238 | T | A | 2 | a0014c0026t0001g0327 a0019c0030t0002g0326 |
2 | HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1-1636T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142115238 | |||||||
| chr7:142115270 | A | G | 1 | a0002c0002t0001g0291 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1-1604A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142115270 | |||||||
| chr7:142115326 | C | T | 1 | a0045c0061t0001g0044 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1-1548C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142115326 | |||||||
| chr7:142115334 | T | C | 136 | a0001c0001t0001g0227 a0001c0001t0001g0245 a0001c0001t0001g0247 others(133): Show |
136 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1-1540T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142115334 | |||||||
| chr7:142115337 | C | G | 136 | a0001c0001t0001g0227 a0001c0001t0001g0245 a0001c0001t0001g0247 others(133): Show |
136 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1-1537C>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142115337 | |||||||
| chr7:142115407 | A | G | 1 | a0002c0072t0001g0215 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1-1467A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142115407 | |||||||
| chr7:142115408 | G | GGGGGAGG others(24): Show |
1 | a0002c0072t0001g0215 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1-1466_1-1465insGG others(29): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142115408 | |||||||
| chr7:142115409 | C | G | 1 | a0002c0072t0001g0215 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1-1465C>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142115409 | |||||||
| chr7:142115410 | G | A | 135 | a0001c0001t0001g0227 a0001c0001t0001g0245 a0001c0001t0001g0247 others(132): Show |
135 | HG00099.hp1 HG00423.hp1 HG00642.hp1 others(132): Show |
intron_variant | MODIFIER | c.1-1464G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142115410 | |||||||
| chr7:142115521 | T | A | 135 | a0001c0001t0001g0227 a0001c0001t0001g0245 a0001c0001t0001g0247 others(132): Show |
135 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1-1353T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142115521 | |||||||
| chr7:142115547 | T | A | 7 | a0002c0002t0001g0308 a0002c0002t0001g0310 a0002c0003t0001g0306 others(4): Show |
7 | HG03239.hp1 HG03704.hp2 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.1-1327T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142115547 | |||||||
| chr7:142115574 | T | G | 135 | a0001c0001t0001g0227 a0001c0001t0001g0245 a0001c0001t0001g0247 others(132): Show |
135 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1-1300T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142115574 | |||||||
| chr7:142115615 | G | A | 7 | a0002c0002t0001g0308 a0002c0002t0001g0310 a0002c0003t0001g0306 others(4): Show |
7 | HG03239.hp1 HG03704.hp2 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.1-1259G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142115615 | |||||||
| chr7:142115738 | G | A | 3 | a0002c0003t0001g0197 a0014c0026t0001g0327 a0019c0030t0002g0326 |
3 | HG01261.hp2 HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1-1136G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142115738 | |||||||
| chr7:142115780 | T | C | 137 | a0001c0001t0001g0227 a0001c0001t0001g0245 a0001c0001t0001g0247 others(134): Show |
137 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.1-1094T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142115780 | |||||||
| chr7:142115786 | G | A | 1 | a0007c0080t0001g0076 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1-1088G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142115786 | |||||||
| chr7:142115798 | T | A | 24 | a0002c0002t0001g0019 a0002c0002t0001g0021 a0002c0002t0001g0034 others(21): Show |
24 | HG00642.hp1 HG01106.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.1-1076T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142115798 | |||||||
| chr7:142115800 | G | A | 1 | a0010c0079t0001g0055 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1-1074G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142115800 | |||||||
| chr7:142115836 | C | T | 75 | a0001c0001t0001g0227 a0001c0001t0001g0245 a0001c0001t0001g0247 others(72): Show |
75 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.1-1038C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142115836 | |||||||
| chr7:142115851 | T | TATAA | 4 | a0001c0004t0001g0046 a0013c0016t0001g0173 a0045c0061t0001g0044 others(1): Show |
4 | HG02922.hp2 HG03130.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1-1005_1-1002dupTA others(2): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr7 | 142115851 | ||||||
| chr7:142116073 | A | G | 7 | a0002c0002t0001g0308 a0002c0002t0001g0310 a0002c0003t0001g0306 others(4): Show |
7 | HG03239.hp1 HG03704.hp2 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.1-801A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142116073 | |||||||
| chr7:142116115 | T | C | 1 | a0062c0076t0001g0325 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1-759T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142116115 | |||||||
| chr7:142116196 | C | G | 168 | a0001c0001t0001g0227 a0001c0001t0001g0245 a0001c0001t0001g0247 others(165): Show |
169 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.1-678C>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142116196 | |||||||
| chr7:142116226 | C | T | 6 | a0001c0001t0001g0277 a0001c0001t0001g0281 a0001c0001t0001g0300 others(3): Show |
6 | HG01081.hp2 HG01167.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.1-648C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142116226 | |||||||
| chr7:142116308 | G | T | 7 | a0002c0002t0001g0308 a0002c0002t0001g0310 a0002c0003t0001g0306 others(4): Show |
7 | HG03239.hp1 HG03704.hp2 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.1-566G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142116308 | |||||||
| chr7:142116315 | A | G | 7 | a0002c0002t0001g0308 a0002c0002t0001g0310 a0002c0003t0001g0306 others(4): Show |
7 | HG03239.hp1 HG03704.hp2 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.1-559A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142116315 | |||||||
| chr7:142116317 | C | A | 169 | a0001c0001t0001g0140 a0001c0001t0001g0227 a0001c0001t0001g0245 others(166): Show |
170 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.1-557C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142116317 | |||||||
| chr7:142116326 | A | G | 2 | a0002c0003t0001g0033 a0015c0015t0001g0029 |
2 | HG02647.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1-548A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142116326 | |||||||
| chr7:142116358 | T | C | 1 | a0001c0004t0001g0188 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1-516T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142116358 | |||||||
| chr7:142116394 | G | A | 149 | a0001c0001t0001g0227 a0001c0001t0001g0245 a0001c0001t0001g0247 others(146): Show |
150 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.1-480G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142116394 | |||||||
| chr7:142116395 | T | A | 149 | a0001c0001t0001g0227 a0001c0001t0001g0245 a0001c0001t0001g0247 others(146): Show |
150 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.1-479T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 1/47 | chr7 | 142116395 | |||||||
| chr7:142117033 | C | T | 7 | a0001c0004t0001g0046 a0002c0002t0001g0043 a0002c0002t0001g0045 others(4): Show |
7 | HG02486.hp2 HG02976.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.106+54C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 2/47 | chr7 | 142117033 | |||||||
| chr7:142117270 | G | A | 102 | a0001c0001t0001g0227 a0001c0001t0001g0245 a0001c0001t0001g0260 others(99): Show |
102 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.106+291G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 2/47 | chr7 | 142117270 | |||||||
| chr7:142117399 | G | T | 14 | a0002c0002t0001g0019 a0002c0002t0001g0021 a0002c0002t0001g0034 others(11): Show |
14 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.106+420G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 2/47 | chr7 | 142117399 | |||||||
| chr7:142117495 | G | A | 7 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0247 others(4): Show |
7 | HG01257.hp2 HG02165.hp1 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.106+516G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 2/47 | chr7 | 142117495 | |||||||
| chr7:142117556 | C | T | 1 | a0045c0061t0001g0044 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.106+577C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 2/47 | chr7 | 142117556 | |||||||
| chr7:142117696 | T | C | 9 | a0001c0001t0001g0101 a0001c0001t0001g0328 a0001c0004t0001g0163 others(6): Show |
9 | HG00609.hp1 HG00621.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.106+717T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 2/47 | chr7 | 142117696 | |||||||
| chr7:142117783 | C | A | 170 | a0001c0001t0001g0227 a0001c0001t0001g0245 a0001c0001t0001g0260 others(167): Show |
171 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.106+804C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 2/47 | chr7 | 142117783 | |||||||
| chr7:142117931 | G | T | 11 | a0002c0002t0001g0019 a0002c0002t0001g0021 a0002c0002t0001g0034 others(8): Show |
11 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.106+952G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 2/47 | chr7 | 142117931 | |||||||
| chr7:142117931 | GT | G | 15 | a0002c0002t0001g0035 a0002c0003t0001g0033 a0002c0058t0001g0032 others(12): Show |
15 | HG00642.hp1 HG01106.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.106+961delT | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr7 | 142117931 | ||||||
| chr7:142117935 | T | A | 1 | a0062c0076t0001g0325 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.106+956T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 2/47 | chr7 | 142117935 | |||||||
| chr7:142117940 | T | C | 78 | a0001c0001t0001g0227 a0001c0001t0001g0245 a0001c0001t0001g0260 others(75): Show |
78 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.106+961T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 2/47 | chr7 | 142117940 | |||||||
| chr7:142118119 | T | C | 80 | a0001c0001t0001g0227 a0001c0001t0001g0245 a0001c0001t0001g0260 others(77): Show |
80 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.106+1140T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 2/47 | chr7 | 142118119 | |||||||
| chr7:142118126 | C | T | 2 | a0009c0011t0001g0138 a0041c0068t0001g0022 |
2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.106+1147C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 2/47 | chr7 | 142118126 | |||||||
| chr7:142118173 | C | G | 172 | a0001c0001t0001g0227 a0001c0001t0001g0245 a0001c0001t0001g0260 others(169): Show |
173 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.106+1194C>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 2/47 | chr7 | 142118173 | |||||||
| chr7:142118229 | A | C | 77 | a0001c0001t0001g0227 a0001c0001t0001g0245 a0001c0001t0001g0260 others(74): Show |
77 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.106+1250A>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 2/47 | chr7 | 142118229 | |||||||
| chr7:142118230 | T | C | 2 | a0009c0011t0001g0138 a0041c0068t0001g0022 |
2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.106+1251T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 2/47 | chr7 | 142118230 | |||||||
| chr7:142118245 | G | A | 7 | a0002c0002t0001g0291 a0002c0002t0001g0296 a0002c0003t0002g0230 others(4): Show |
7 | HG02257.hp1 HG02451.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.106+1266G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 2/47 | chr7 | 142118245 | |||||||
| chr7:142118370 | A | AAT | 10 | a0002c0002t0001g0308 a0002c0002t0001g0310 a0002c0003t0001g0152 others(7): Show |
10 | HG01261.hp2 HG03225.hp2 HG03239.hp1 others(7): Show |
intron_variant | MODIFIER | c.106+1402_106+1403d others(4): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr7 | 142118370 | ||||||
| chr7:142118482 | A | G | 77 | a0001c0001t0001g0227 a0001c0001t0001g0245 a0001c0001t0001g0260 others(74): Show |
77 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.106+1503A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 2/47 | chr7 | 142118482 | |||||||
| chr7:142118489 | G | A | 2 | a0002c0003t0001g0002 a0002c0003t0001g0003 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.106+1510G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 2/47 | chr7 | 142118489 | |||||||
| chr7:142118538 | A | G | 31 | a0002c0002t0001g0019 a0002c0002t0001g0021 a0002c0002t0001g0034 others(28): Show |
31 | HG00735.hp2 HG01243.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.106+1559A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 2/47 | chr7 | 142118538 | |||||||
| chr7:142118569 | G | A | 2 | a0002c0002t0001g0035 a0009c0011t0002g0036 |
2 | HG01106.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.106+1590G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 2/47 | chr7 | 142118569 | |||||||
| chr7:142118609 | A | G | 1 | a0001c0004t0001g0072 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.106+1630A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 2/47 | chr7 | 142118609 | |||||||
| chr7:142118634 | G | A | 7 | a0001c0004t0001g0046 a0002c0002t0001g0043 a0002c0002t0001g0045 others(4): Show |
7 | HG02486.hp2 HG02976.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.106+1655G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 2/47 | chr7 | 142118634 | |||||||
| chr7:142118797 | C | CA | 29 | a0001c0001t0001g0313 a0001c0001t0001g0318 a0002c0002t0001g0008 others(26): Show |
29 | HG00741.hp2 HG01071.hp1 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.107-1498dupA | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr7 | 142118797 | ||||||
| chr7:142118930 | A | T | 3 | a0014c0026t0001g0327 a0019c0030t0002g0326 a0035c0067t0003g0146 |
3 | HG02055.hp1 HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.107-1372A>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 2/47 | chr7 | 142118930 | |||||||
| chr7:142119190 | A | G | 1 | a0013c0016t0001g0173 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.107-1112A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 2/47 | chr7 | 142119190 | |||||||
| chr7:142119257 | A | G | 28 | a0001c0001t0001g0313 a0001c0001t0001g0318 a0002c0002t0001g0008 others(25): Show |
28 | HG00741.hp2 HG01071.hp1 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.107-1045A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 2/47 | chr7 | 142119257 | |||||||
| chr7:142119272 | A | G | 8 | a0002c0002t0001g0308 a0002c0002t0001g0310 a0002c0003t0001g0152 others(5): Show |
8 | HG03239.hp1 HG03704.hp2 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.107-1030A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 2/47 | chr7 | 142119272 | |||||||
| chr7:142119373 | A | G | 28 | a0001c0001t0001g0313 a0001c0001t0001g0318 a0002c0002t0001g0008 others(25): Show |
28 | HG00741.hp2 HG01071.hp1 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.107-929A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 2/47 | chr7 | 142119373 | |||||||
| chr7:142119478 | T | C | 77 | a0001c0001t0001g0227 a0001c0001t0001g0245 a0001c0001t0001g0260 others(74): Show |
77 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.107-824T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 2/47 | chr7 | 142119478 | |||||||
| chr7:142119502 | A | G | 1 | a0016c0014t0001g0017 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.107-800A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 2/47 | chr7 | 142119502 | |||||||
| chr7:142119532 | C | T | 1 | a0003c0007t0001g0193 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.107-770C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 2/47 | chr7 | 142119532 | |||||||
| chr7:142119536 | C | T | 31 | a0001c0001t0001g0313 a0001c0001t0001g0318 a0002c0002t0001g0008 others(28): Show |
32 | HG00741.hp2 HG01071.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.107-766C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 2/47 | chr7 | 142119536 | |||||||
| chr7:142119658 | T | A | 1 | a0001c0001t0001g0176 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.107-644T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 2/47 | chr7 | 142119658 | |||||||
| chr7:142119674 | T | C | 2 | a0013c0016t0001g0041 a0013c0016t0001g0042 |
2 | HG02486.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.107-628T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 2/47 | chr7 | 142119674 | |||||||
| chr7:142119959 | T | A | 8 | a0002c0002t0001g0308 a0002c0002t0001g0310 a0002c0003t0001g0152 others(5): Show |
8 | HG03239.hp1 HG03704.hp2 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.107-343T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 2/47 | chr7 | 142119959 | |||||||
| chr7:142119972 | C | T | 1 | a0035c0067t0003g0146 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.107-330C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 2/47 | chr7 | 142119972 | |||||||
| chr7:142120108 | G | T | 28 | a0001c0001t0001g0313 a0001c0001t0001g0318 a0002c0002t0001g0008 others(25): Show |
28 | HG00741.hp2 HG01071.hp1 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.107-194G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 2/47 | chr7 | 142120108 | |||||||
| chr7:142120190 | C | T | 7 | a0001c0004t0001g0046 a0002c0002t0001g0043 a0002c0002t0001g0045 others(4): Show |
7 | HG02486.hp2 HG02976.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.107-112C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 2/47 | chr7 | 142120190 | |||||||
| chr7:142120212 | T | C | 1 | a0062c0076t0001g0325 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.107-90T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 2/47 | chr7 | 142120212 | |||||||
| chr7:142120548 | A | G | 1 | a0007c0033t0001g0155 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.186+167A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142120548 | |||||||
| chr7:142120558 | A | C | 1 | a0002c0002t0001g0269 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.186+177A>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142120558 | |||||||
| chr7:142120795 | A | G | 2 | a0001c0001t0001g0172 a0001c0001t0001g0218 |
2 | HG01123.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.186+414A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142120795 | |||||||
| chr7:142120813 | G | A | 3 | a0002c0002t0001g0296 a0009c0011t0001g0293 a0015c0015t0001g0297 |
3 | HG02451.hp2 HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.186+432G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142120813 | |||||||
| chr7:142120963 | A | T | 8 | a0001c0001t0001g0071 a0001c0001t0001g0127 a0001c0004t0001g0063 others(5): Show |
8 | HG00558.hp1 HG02027.hp2 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.186+582A>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142120963 | |||||||
| chr7:142121030 | C | A | 7 | a0001c0004t0001g0046 a0002c0002t0001g0043 a0002c0002t0001g0045 others(4): Show |
7 | HG02486.hp2 HG02976.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.186+649C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142121030 | |||||||
| chr7:142121229 | T | G | 29 | a0001c0001t0001g0313 a0001c0001t0001g0318 a0002c0002t0001g0008 others(26): Show |
29 | HG00741.hp2 HG01071.hp1 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.186+848T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142121229 | |||||||
| chr7:142121233 | G | GTGGCGCG others(42): Show |
1 | a0002c0002t0001g0269 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.186+854_186+902dup others(49): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr7 | 142121233 | ||||||
| chr7:142121394 | C | T | 76 | a0001c0001t0001g0245 a0001c0001t0001g0260 a0002c0002t0001g0205 others(73): Show |
76 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.186+1013C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142121394 | |||||||
| chr7:142121403 | C | T | 2 | a0002c0002t0001g0035 a0009c0011t0002g0036 |
2 | HG01106.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.186+1022C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142121403 | |||||||
| chr7:142121406 | A | G | 8 | a0002c0002t0001g0308 a0002c0002t0001g0310 a0002c0003t0001g0152 others(5): Show |
8 | HG03239.hp1 HG03704.hp2 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.186+1025A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142121406 | |||||||
| chr7:142121527 | G | A | 1 | a0011c0013t0001g0189 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.186+1146G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142121527 | |||||||
| chr7:142121558 | C | A | 1 | a0014c0020t0001g0001 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.186+1177C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142121558 | |||||||
| chr7:142121562 | G | A | 3 | a0001c0001t0001g0221 a0008c0010t0001g0222 a0010c0031t0001g0263 |
3 | NA18983.hp1 NA19088.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.186+1181G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142121562 | |||||||
| chr7:142121699 | C | T | 1 | a0011c0022t0001g0161 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.186+1318C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142121699 | |||||||
| chr7:142121870 | C | T | 9 | a0002c0002t0001g0308 a0002c0002t0001g0310 a0002c0003t0001g0152 others(6): Show |
9 | HG03239.hp1 HG03704.hp2 HG03831.hp2 others(6): Show |
intron_variant | MODIFIER | c.186+1489C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142121870 | |||||||
| chr7:142122137 | C | T | 1 | a0014c0020t0001g0001 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.186+1756C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142122137 | |||||||
| chr7:142122263 | T | G | 1 | a0002c0003t0001g0250 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.186+1882T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142122263 | |||||||
| chr7:142122294 | T | G | 33 | a0001c0001t0001g0313 a0001c0001t0001g0318 a0002c0002t0001g0008 others(30): Show |
34 | HG00741.hp2 HG01071.hp1 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.186+1913T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142122294 | |||||||
| chr7:142122428 | A | G | 1 | a0002c0002t0001g0045 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.186+2047A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142122428 | |||||||
| chr7:142122434 | C | A | 3 | a0001c0001t0001g0176 a0039c0046t0001g0102 a0043c0048t0001g0103 |
3 | HG02451.hp1 HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.186+2053C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142122434 | |||||||
| chr7:142122467 | T | A | 8 | a0002c0002t0001g0308 a0002c0002t0001g0310 a0002c0003t0001g0152 others(5): Show |
8 | HG03239.hp1 HG03704.hp2 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.186+2086T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142122467 | |||||||
| chr7:142122653 | T | G | 2 | a0014c0026t0001g0327 a0019c0030t0002g0326 |
2 | HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.186+2272T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142122653 | |||||||
| chr7:142122783 | A | G | 12 | a0002c0002t0001g0019 a0002c0002t0001g0021 a0002c0002t0001g0034 others(9): Show |
12 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.186+2402A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142122783 | |||||||
| chr7:142122898 | C | T | 3 | a0001c0001t0001g0171 a0001c0004t0001g0192 a0007c0034t0001g0186 |
3 | NA18956.hp2 NA18993.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.186+2517C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142122898 | |||||||
| chr7:142122988 | C | A | 12 | a0002c0002t0001g0019 a0002c0002t0001g0021 a0002c0002t0001g0034 others(9): Show |
12 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.186+2607C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142122988 | |||||||
| chr7:142123076 | C | T | 1 | a0004c0005t0001g0137 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.186+2695C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142123076 | |||||||
| chr7:142123114 | G | C | 12 | a0002c0002t0001g0019 a0002c0002t0001g0021 a0002c0002t0001g0034 others(9): Show |
12 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.186+2733G>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142123114 | |||||||
| chr7:142123171 | C | CT | 15 | a0002c0002t0001g0308 a0002c0002t0001g0310 a0002c0003t0001g0004 others(12): Show |
16 | HG01168.hp1 HG02055.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.186+2802dupT | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr7 | 142123171 | ||||||
| chr7:142123171 | C | CTT | 28 | a0001c0001t0001g0313 a0001c0001t0001g0318 a0002c0002t0001g0008 others(25): Show |
28 | HG00741.hp2 HG01071.hp1 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.186+2801_186+2802d others(4): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr7 | 142123171 | ||||||
| chr7:142123232 | A | AT | 11 | a0001c0001t0001g0245 a0001c0001t0001g0260 a0002c0002t0001g0229 others(8): Show |
11 | HG02040.hp2 HG02129.hp1 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.186+2861dupT | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr7 | 142123232 | ||||||
| chr7:142123261 | A | G | 76 | a0001c0001t0001g0245 a0001c0001t0001g0260 a0002c0002t0001g0205 others(73): Show |
76 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.186+2880A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142123261 | |||||||
| chr7:142123437 | A | T | 1 | a0045c0061t0001g0044 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.186+3056A>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142123437 | |||||||
| chr7:142123590 | G | A | 159 | a0001c0001t0001g0245 a0001c0001t0001g0260 a0001c0001t0001g0313 others(156): Show |
160 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.186+3209G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142123590 | |||||||
| chr7:142123647 | C | T | 40 | a0001c0001t0001g0313 a0001c0001t0001g0318 a0001c0004t0001g0046 others(37): Show |
41 | HG00741.hp2 HG01071.hp1 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.186+3266C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142123647 | |||||||
| chr7:142123709 | A | G | 12 | a0002c0002t0001g0019 a0002c0002t0001g0021 a0002c0002t0001g0034 others(9): Show |
12 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.186+3328A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142123709 | |||||||
| chr7:142123806 | A | G | 1 | a0001c0001t0001g0154 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.186+3425A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142123806 | |||||||
| chr7:142123902 | G | T | 32 | a0001c0001t0001g0313 a0001c0001t0001g0318 a0002c0002t0001g0008 others(29): Show |
32 | HG00741.hp2 HG01071.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.186+3521G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142123902 | |||||||
| chr7:142123940 | G | A | 11 | a0002c0002t0001g0308 a0002c0002t0001g0310 a0002c0003t0001g0152 others(8): Show |
11 | HG02723.hp2 HG02809.hp2 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.186+3559G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142123940 | |||||||
| chr7:142123961 | A | T | 1 | a0024c0075t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.186+3580A>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142123961 | |||||||
| chr7:142123963 | C | CT | 52 | a0001c0001t0001g0127 a0001c0001t0001g0140 a0001c0001t0001g0221 others(49): Show |
53 | HG00621.hp2 HG00642.hp1 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.186+3609dupT | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr7 | 142123963 | ||||||
| chr7:142123963 | C | CTT | 20 | a0001c0001t0001g0171 a0001c0001t0001g0176 a0001c0004t0001g0046 others(17): Show |
20 | HG00735.hp2 HG01106.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.186+3608_186+3609d others(4): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr7 | 142123963 | ||||||
| chr7:142123963 | C | CTTT | 7 | a0002c0002t0001g0019 a0002c0002t0001g0021 a0002c0002t0001g0039 others(4): Show |
7 | HG01496.hp2 HG01891.hp1 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.186+3607_186+3609d others(5): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr7 | 142123963 | ||||||
| chr7:142123963 | CT | C | 7 | a0001c0004t0001g0164 a0002c0002t0001g0043 a0002c0003t0001g0306 others(4): Show |
7 | HG00609.hp1 HG01169.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.186+3609delT | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr7 | 142123963 | ||||||
| chr7:142123963 | CTT | C | 8 | a0002c0002t0001g0308 a0002c0002t0001g0310 a0002c0003t0001g0152 others(5): Show |
8 | HG02723.hp2 HG02809.hp2 HG03239.hp1 others(5): Show |
intron_variant | MODIFIER | c.186+3608_186+3609d others(4): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr7 | 142123963 | ||||||
| chr7:142123963 | CTTTTTTT others(6): Show |
C | 1 | a0011c0013t0001g0246 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.186+3597_186+3609d others(15): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr7 | 142123963 | ||||||
| chr7:142123968 | T | TA | 3 | a0002c0003t0001g0187 a0018c0028t0001g0203 a0057c0037t0001g0144 |
3 | NA18971.hp1 NA18988.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.186+3587_186+3588i others(3): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142123968 | |||||||
| chr7:142123978 | T | A | 5 | a0002c0002t0001g0303 a0002c0003t0001g0187 a0018c0028t0001g0203 others(2): Show |
5 | NA18955.hp1 NA18971.hp1 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.186+3597T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142123978 | |||||||
| chr7:142123978 | T | TA | 71 | a0001c0001t0001g0245 a0001c0001t0001g0260 a0002c0002t0001g0205 others(68): Show |
71 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.186+3597_186+3598i others(3): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142123978 | |||||||
| chr7:142123984 | T | A | 1 | a0018c0028t0001g0231 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.186+3603T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142123984 | |||||||
| chr7:142123985 | T | A | 1 | a0007c0080t0001g0076 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.186+3604T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142123985 | |||||||
| chr7:142124026 | G | A | 8 | a0002c0002t0001g0308 a0002c0002t0001g0310 a0002c0003t0001g0152 others(5): Show |
8 | HG03239.hp1 HG03704.hp2 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.186+3645G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142124026 | |||||||
| chr7:142124045 | T | C | 29 | a0001c0001t0001g0313 a0001c0001t0001g0318 a0002c0002t0001g0008 others(26): Show |
29 | HG00741.hp2 HG01071.hp1 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.186+3664T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142124045 | |||||||
| chr7:142124160 | G | C | 2 | a0013c0016t0001g0041 a0013c0016t0001g0042 |
2 | HG02486.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.186+3779G>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142124160 | |||||||
| chr7:142124194 | G | A | 10 | a0001c0001t0001g0101 a0001c0001t0001g0227 a0001c0001t0001g0328 others(7): Show |
10 | HG00609.hp1 HG00621.hp2 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.186+3813G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142124194 | |||||||
| chr7:142124278 | C | T | 10 | a0002c0002t0001g0308 a0002c0002t0001g0310 a0002c0003t0001g0152 others(7): Show |
10 | HG02723.hp2 HG02809.hp2 HG03239.hp1 others(7): Show |
intron_variant | MODIFIER | c.186+3897C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142124278 | |||||||
| chr7:142124768 | A | T | 11 | a0002c0002t0001g0308 a0002c0002t0001g0310 a0002c0003t0001g0152 others(8): Show |
11 | HG02723.hp2 HG02809.hp2 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.186+4387A>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142124768 | |||||||
| chr7:142125027 | C | T | 26 | a0002c0002t0001g0008 a0002c0002t0001g0016 a0002c0002t0001g0151 others(23): Show |
26 | HG00741.hp2 HG01074.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.186+4646C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142125027 | |||||||
| chr7:142125070 | G | A | 2 | a0002c0002t0001g0043 a0002c0002t0001g0045 |
2 | HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.186+4689G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142125070 | |||||||
| chr7:142125259 | T | A | 7 | a0001c0004t0001g0046 a0002c0002t0001g0043 a0002c0002t0001g0045 others(4): Show |
7 | HG02486.hp2 HG02976.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.186+4878T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142125259 | |||||||
| chr7:142125387 | G | A | 15 | a0001c0001t0001g0154 a0001c0001t0001g0178 a0001c0001t0001g0190 others(12): Show |
15 | HG00323.hp2 HG01071.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.186+5006G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142125387 | |||||||
| chr7:142125521 | T | C | 167 | a0001c0001t0001g0245 a0001c0001t0001g0260 a0001c0004t0001g0046 others(164): Show |
168 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.186+5140T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142125521 | |||||||
| chr7:142125575 | T | C | 1 | a0037c0050t0001g0115 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.186+5194T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142125575 | |||||||
| chr7:142125604 | G | A | 1 | a0002c0003t0001g0020 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.186+5223G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142125604 | |||||||
| chr7:142125605 | T | A | 1 | a0002c0003t0001g0020 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.186+5224T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142125605 | |||||||
| chr7:142125645 | G | T | 9 | a0002c0002t0001g0224 a0002c0002t0001g0284 a0002c0002t0001g0285 others(6): Show |
9 | HG00735.hp2 HG01261.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.186+5264G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142125645 | |||||||
| chr7:142125801 | A | G | 8 | a0002c0002t0001g0308 a0002c0002t0001g0310 a0002c0003t0001g0152 others(5): Show |
8 | HG03239.hp1 HG03704.hp2 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.187-5147A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142125801 | |||||||
| chr7:142125880 | A | G | 1 | a0001c0004t0001g0169 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.187-5068A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142125880 | |||||||
| chr7:142125955 | A | G | 7 | a0001c0004t0001g0046 a0002c0002t0001g0043 a0002c0002t0001g0045 others(4): Show |
7 | HG02486.hp2 HG02976.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.187-4993A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142125955 | |||||||
| chr7:142125976 | C | T | 5 | a0001c0001t0001g0154 a0001c0001t0001g0178 a0001c0001t0001g0190 others(2): Show |
5 | HG00323.hp2 NA18943.hp2 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.187-4972C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142125976 | |||||||
| chr7:142126045 | A | G | 1 | a0018c0028t0001g0231 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.187-4903A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142126045 | |||||||
| chr7:142126074 | T | C | 7 | a0001c0004t0001g0046 a0002c0002t0001g0043 a0002c0002t0001g0045 others(4): Show |
7 | HG02486.hp2 HG02976.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.187-4874T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142126074 | |||||||
| chr7:142126256 | C | T | 151 | a0001c0001t0001g0245 a0001c0001t0001g0260 a0001c0004t0001g0046 others(148): Show |
152 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.187-4692C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142126256 | |||||||
| chr7:142126475 | T | C | 1 | a0001c0001t0001g0190 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.187-4473T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142126475 | |||||||
| chr7:142126486 | A | AT | 7 | a0001c0004t0001g0046 a0002c0002t0001g0043 a0002c0002t0001g0045 others(4): Show |
7 | HG02486.hp2 HG02976.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.187-4450dupT | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr7 | 142126486 | ||||||
| chr7:142126506 | G | A | 1 | a0041c0068t0001g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.187-4442G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142126506 | |||||||
| chr7:142126937 | G | A | 22 | a0002c0002t0001g0008 a0002c0002t0001g0016 a0002c0002t0001g0151 others(19): Show |
22 | HG00741.hp2 HG01074.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.187-4011G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142126937 | |||||||
| chr7:142127025 | T | C | 1 | a0002c0002t0001g0151 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.187-3923T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142127025 | |||||||
| chr7:142127288 | A | G | 5 | a0015c0015t0001g0013 a0015c0015t0001g0014 a0016c0014t0001g0011 others(2): Show |
5 | HG01891.hp2 HG02257.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.187-3660A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142127288 | |||||||
| chr7:142127335 | C | T | 76 | a0001c0001t0001g0245 a0001c0001t0001g0260 a0002c0002t0001g0205 others(73): Show |
76 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.187-3613C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142127335 | |||||||
| chr7:142127358 | AT | A | 11 | a0002c0002t0001g0019 a0002c0002t0001g0021 a0002c0002t0001g0034 others(8): Show |
11 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.187-3582delT | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr7 | 142127358 | ||||||
| chr7:142127388 | G | T | 4 | a0002c0002t0001g0039 a0022c0027t0001g0038 a0022c0027t0001g0040 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.187-3560G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142127388 | |||||||
| chr7:142127417 | C | T | 1 | a0045c0061t0001g0044 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.187-3531C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142127417 | |||||||
| chr7:142127433 | T | G | 20 | a0002c0002t0001g0050 a0002c0002t0001g0199 a0002c0002t0001g0224 others(17): Show |
20 | HG00735.hp2 HG01243.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.187-3515T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142127433 | |||||||
| chr7:142127461 | C | A | 165 | a0001c0001t0001g0245 a0001c0001t0001g0260 a0001c0004t0001g0046 others(162): Show |
166 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.187-3487C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142127461 | |||||||
| chr7:142127676 | T | C | 1 | a0003c0007t0001g0093 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.187-3272T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142127676 | |||||||
| chr7:142127722 | G | A | 8 | a0001c0004t0001g0046 a0001c0004t0001g0157 a0002c0002t0001g0043 others(5): Show |
8 | HG02486.hp2 HG02976.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.187-3226G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142127722 | |||||||
| chr7:142127826 | A | T | 2 | a0002c0003t0001g0225 a0002c0003t0001g0226 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.187-3122A>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142127826 | |||||||
| chr7:142127914 | A | G | 1 | a0045c0061t0001g0044 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.187-3034A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142127914 | |||||||
| chr7:142127936 | G | A | 1 | a0015c0015t0001g0014 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.187-3012G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142127936 | |||||||
| chr7:142128131 | C | A | 1 | a0014c0020t0001g0001 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.187-2817C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142128131 | |||||||
| chr7:142128321 | G | A | 1 | a0001c0001t0001g0301 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.187-2627G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142128321 | |||||||
| chr7:142128508 | A | G | 151 | a0001c0001t0001g0245 a0001c0001t0001g0260 a0001c0004t0001g0046 others(148): Show |
152 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.187-2440A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142128508 | |||||||
| chr7:142128520 | A | T | 4 | a0009c0011t0001g0023 a0009c0011t0001g0024 a0038c0059t0001g0026 others(1): Show |
4 | HG00642.hp1 HG02145.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.187-2428A>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142128520 | |||||||
| chr7:142128622 | A | C | 150 | a0001c0001t0001g0245 a0001c0001t0001g0260 a0001c0004t0001g0046 others(147): Show |
150 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.187-2326A>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142128622 | |||||||
| chr7:142128755 | C | T | 23 | a0001c0001t0001g0087 a0001c0038t0001g0099 a0002c0002t0001g0050 others(20): Show |
23 | HG00558.hp2 HG00735.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.187-2193C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142128755 | |||||||
| chr7:142128834 | G | A | 3 | a0002c0002t0001g0298 a0010c0017t0001g0286 a0028c0024t0001g0204 |
3 | HG01069.hp2 NA18941.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.187-2114G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142128834 | |||||||
| chr7:142128858 | G | A | 2 | a0002c0002t0001g0034 a0006c0008t0001g0316 |
2 | HG01123.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.187-2090G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142128858 | |||||||
| chr7:142128884 | C | T | 151 | a0001c0001t0001g0245 a0001c0001t0001g0260 a0001c0004t0001g0046 others(148): Show |
152 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.187-2064C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142128884 | |||||||
| chr7:142128916 | CT | C | 107 | a0001c0001t0001g0245 a0001c0001t0001g0260 a0002c0002t0001g0019 others(104): Show |
107 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.187-2031delT | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142128916 | |||||||
| chr7:142128979 | G | A | 26 | a0002c0002t0001g0008 a0002c0002t0001g0016 a0002c0002t0001g0151 others(23): Show |
26 | HG00741.hp2 HG01074.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.187-1969G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142128979 | |||||||
| chr7:142128993 | C | A | 2 | a0001c0001t0001g0166 a0001c0004t0001g0164 |
2 | HG00621.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.187-1955C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142128993 | |||||||
| chr7:142129060 | C | T | 11 | a0002c0002t0001g0019 a0002c0002t0001g0021 a0002c0002t0001g0034 others(8): Show |
11 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.187-1888C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142129060 | |||||||
| chr7:142129122 | T | C | 1 | a0006c0008t0001g0094 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.187-1826T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142129122 | |||||||
| chr7:142129208 | C | A | 1 | a0035c0067t0003g0146 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.187-1740C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142129208 | |||||||
| chr7:142129215 | A | C | 1 | a0008c0010t0001g0222 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.187-1733A>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142129215 | |||||||
| chr7:142129593 | G | A | 22 | a0002c0002t0001g0008 a0002c0002t0001g0016 a0002c0002t0001g0151 others(19): Show |
22 | HG00741.hp2 HG01074.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.187-1355G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142129593 | |||||||
| chr7:142129734 | A | G | 4 | a0001c0004t0001g0145 a0020c0018t0001g0148 a0020c0018t0001g0149 others(1): Show |
4 | HG03041.hp1 NA19030.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.187-1214A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142129734 | |||||||
| chr7:142129786 | T | C | 1 | a0014c0020t0001g0001 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.187-1162T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142129786 | |||||||
| chr7:142129817 | C | T | 1 | a0041c0068t0001g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.187-1131C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142129817 | |||||||
| chr7:142129825 | C | CA | 58 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(55): Show |
58 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(55): Show |
intron_variant | MODIFIER | c.187-1083dupA | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr7 | 142129825 | ||||||
| chr7:142129825 | C | CAA | 58 | a0001c0001t0001g0108 a0001c0001t0001g0117 a0001c0001t0001g0127 others(55): Show |
58 | HG00621.hp1 HG00639.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.187-1084_187-1083d others(4): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr7 | 142129825 | ||||||
| chr7:142129825 | C | CAAA | 7 | a0001c0001t0001g0107 a0001c0001t0001g0116 a0001c0001t0001g0223 others(4): Show |
7 | HG01106.hp2 HG01123.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.187-1085_187-1083d others(5): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr7 | 142129825 | ||||||
| chr7:142129825 | CAAAAA | C | 9 | a0001c0001t0001g0125 a0001c0038t0001g0099 a0003c0009t0001g0098 others(6): Show |
9 | HG00408.hp1 NA18941.hp1 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.187-1087_187-1083d others(7): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr7 | 142129825 | ||||||
| chr7:142129825 | CAAAAAAA others(1): Show |
C | 26 | a0002c0002t0001g0034 a0002c0002t0001g0039 a0002c0002t0001g0043 others(23): Show |
26 | HG00423.hp1 HG00735.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.187-1090_187-1083d others(10): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr7 | 142129825 | ||||||
| chr7:142129825 | CAAAAAAA others(2): Show |
C | 76 | a0001c0001t0001g0260 a0002c0002t0001g0019 a0002c0002t0001g0021 others(73): Show |
76 | HG00408.hp2 HG00438.hp1 HG00735.hp2 others(73): Show |
intron_variant | MODIFIER | c.187-1091_187-1083d others(11): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr7 | 142129825 | ||||||
| chr7:142129825 | CAAAAAAA others(3): Show |
C | 17 | a0001c0001t0001g0245 a0002c0002t0001g0199 a0002c0002t0001g0209 others(14): Show |
17 | HG00099.hp1 HG01192.hp2 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.187-1092_187-1083d others(12): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr7 | 142129825 | ||||||
| chr7:142129825 | CAAAAAAA others(4): Show |
C | 6 | a0001c0004t0001g0183 a0002c0003t0001g0226 a0004c0005t0001g0270 others(3): Show |
6 | HG02055.hp1 HG02572.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.187-1093_187-1083d others(13): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr7 | 142129825 | ||||||
| chr7:142129825 | CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0001g0268 a0001c0004t0001g0278 |
2 | HG03942.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.187-1094_187-1083d others(14): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr7 | 142129825 | ||||||
| chr7:142129825 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0176 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.187-1096_187-1083d others(16): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr7 | 142129825 | ||||||
| chr7:142129825 | CAAAAAAA others(11): Show |
C | 2 | a0006c0008t0001g0156 a0063c0041t0001g0139 |
2 | NA18944.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.187-1100_187-1083d others(20): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr7 | 142129825 | ||||||
| chr7:142129825 | CAAAAAAA others(12): Show |
C | 1 | a0001c0001t0001g0075 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.187-1101_187-1083d others(21): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr7 | 142129825 | ||||||
| chr7:142129825 | CAAAAAAA others(15): Show |
C | 22 | a0002c0002t0001g0008 a0002c0002t0001g0016 a0002c0002t0001g0151 others(19): Show |
22 | HG00741.hp2 HG01074.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.187-1104_187-1083d others(24): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr7 | 142129825 | ||||||
| chr7:142129991 | G | A | 107 | a0001c0001t0001g0245 a0001c0001t0001g0260 a0002c0002t0001g0019 others(104): Show |
107 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.187-957G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142129991 | |||||||
| chr7:142130052 | C | T | 11 | a0002c0002t0001g0308 a0002c0002t0001g0310 a0002c0003t0001g0152 others(8): Show |
11 | HG02723.hp2 HG02809.hp2 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.187-896C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142130052 | |||||||
| chr7:142130120 | A | G | 7 | a0001c0004t0001g0046 a0002c0002t0001g0043 a0002c0002t0001g0045 others(4): Show |
7 | HG02486.hp2 HG02976.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.187-828A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142130120 | |||||||
| chr7:142130140 | A | G | 1 | a0005c0006t0001g0242 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.187-808A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142130140 | |||||||
| chr7:142130217 | A | G | 1 | a0006c0008t0001g0094 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.187-731A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142130217 | |||||||
| chr7:142130259 | T | C | 1 | a0045c0061t0001g0044 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.187-689T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142130259 | |||||||
| chr7:142130487 | G | A | 76 | a0001c0001t0001g0245 a0001c0001t0001g0260 a0002c0002t0001g0205 others(73): Show |
76 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.187-461G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142130487 | |||||||
| chr7:142130654 | C | T | 1 | a0007c0080t0001g0076 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.187-294C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142130654 | |||||||
| chr7:142130760 | T | C | 8 | a0002c0002t0001g0308 a0002c0002t0001g0310 a0002c0003t0001g0152 others(5): Show |
8 | HG03239.hp1 HG03704.hp2 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.187-188T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142130760 | |||||||
| chr7:142130931 | C | T | 2 | a0001c0001t0001g0180 a0006c0008t0001g0094 |
2 | HG02015.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.187-17C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142130931 | |||||||
| chr7:142130935 | G | A | 8 | a0002c0002t0001g0308 a0002c0002t0001g0310 a0002c0003t0001g0152 others(5): Show |
8 | HG03239.hp1 HG03704.hp2 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.187-13G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 3/47 | chr7 | 142130935 | |||||||
| chr7:142131236 | A | G | 20 | a0002c0002t0001g0050 a0002c0002t0001g0199 a0002c0002t0001g0224 others(17): Show |
20 | HG00735.hp2 HG01243.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.310+165A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 4/47 | chr7 | 142131236 | |||||||
| chr7:142131370 | G | A | 8 | a0002c0002t0001g0008 a0002c0003t0001g0002 a0002c0003t0001g0003 others(5): Show |
8 | HG00741.hp2 HG01074.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.311-148G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 4/47 | chr7 | 142131370 | |||||||
| chr7:142131395 | G | A | 4 | a0002c0002t0001g0050 a0002c0003t0001g0049 a0002c0003t0001g0073 others(1): Show |
4 | HG01884.hp2 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.311-123G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 4/47 | chr7 | 142131395 | |||||||
| chr7:142131436 | C | CAAAACA | 22 | a0002c0002t0001g0008 a0002c0002t0001g0016 a0002c0002t0001g0151 others(19): Show |
22 | HG00741.hp2 HG01074.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.311-66_311-61dupAC others(4): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr7 | 142131436 | ||||||
| chr7:142131449 | A | C | 1 | a0001c0004t0001g0066 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.311-69A>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 4/47 | chr7 | 142131449 | |||||||
| chr7:142131459 | A | C | 1 | a0041c0068t0001g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.311-59A>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 4/47 | chr7 | 142131459 | |||||||
| chr7:142131761 | T | A | 2 | a0055c0055t0001g0083 a0056c0042t0001g0113 |
2 | NA18951.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.420+134T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 5/47 | chr7 | 142131761 | |||||||
| chr7:142131809 | A | G | 8 | a0002c0002t0001g0308 a0002c0002t0001g0310 a0002c0003t0001g0152 others(5): Show |
8 | HG03239.hp1 HG03704.hp2 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.421-122A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 5/47 | chr7 | 142131809 | |||||||
| chr7:142131828 | G | T | 1 | a0001c0001t0001g0301 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.421-103G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 5/47 | chr7 | 142131828 | |||||||
| chr7:142131861 | A | G | 151 | a0001c0001t0001g0245 a0001c0001t0001g0260 a0001c0004t0001g0046 others(148): Show |
152 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.421-70A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 5/47 | chr7 | 142131861 | |||||||
| chr7:142132156 | G | T | 1 | a0014c0020t0001g0001 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.575+71G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 6/47 | chr7 | 142132156 | |||||||
| chr7:142132222 | G | T | 1 | a0001c0004t0001g0066 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.575+137G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 6/47 | chr7 | 142132222 | |||||||
| chr7:142132346 | A | AATATAAT others(21): Show |
1 | a0001c0001t0001g0153 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.575+287_575+314dup others(28): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr7 | 142132346 | ||||||
| chr7:142132417 | A | G | 1 | a0013c0016t0001g0042 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.575+332A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 6/47 | chr7 | 142132417 | |||||||
| chr7:142132437 | A | C | 20 | a0002c0002t0001g0050 a0002c0002t0001g0199 a0002c0002t0001g0224 others(17): Show |
20 | HG00735.hp2 HG01243.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.575+352A>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 6/47 | chr7 | 142132437 | |||||||
| chr7:142132444 | ATAT | A | 11 | a0002c0002t0001g0019 a0002c0002t0001g0021 a0002c0002t0001g0034 others(8): Show |
11 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.575+363_575+365del others(3): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr7 | 142132444 | ||||||
| chr7:142132507 | TA | T | 4 | a0002c0002t0001g0039 a0022c0027t0001g0038 a0022c0027t0001g0040 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.575+427delA | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr7 | 142132507 | ||||||
| chr7:142132557 | C | T | 149 | a0001c0001t0001g0245 a0001c0001t0001g0260 a0001c0004t0001g0046 others(146): Show |
150 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.575+472C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 6/47 | chr7 | 142132557 | |||||||
| chr7:142132648 | T | C | 8 | a0002c0002t0001g0269 a0002c0003t0001g0088 a0002c0003t0001g0187 others(5): Show |
8 | HG00099.hp1 HG03491.hp1 HG03492.hp1 others(5): Show |
intron_variant | MODIFIER | c.575+563T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 6/47 | chr7 | 142132648 | |||||||
| chr7:142132657 | A | AAATATAA others(16): Show |
1 | a0045c0061t0001g0044 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.575+581_575+603dup others(23): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr7 | 142132657 | ||||||
| chr7:142132688 | T | G | 2 | a0003c0007t0001g0136 a0004c0005t0001g0124 |
2 | NA18941.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.575+603T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 6/47 | chr7 | 142132688 | |||||||
| chr7:142132697 | T | A | 1 | a0001c0004t0001g0201 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.575+612T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 6/47 | chr7 | 142132697 | |||||||
| chr7:142132710 | T | G | 1 | a0011c0013t0001g0246 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.575+625T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 6/47 | chr7 | 142132710 | |||||||
| chr7:142132825 | A | G | 1 | a0008c0010t0001g0081 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.575+740A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 6/47 | chr7 | 142132825 | |||||||
| chr7:142132829 | G | A | 3 | a0002c0002t0001g0050 a0002c0003t0001g0049 a0002c0003t0001g0073 |
3 | HG01884.hp2 HG02280.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.575+744G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 6/47 | chr7 | 142132829 | |||||||
| chr7:142132864 | T | C | 7 | a0001c0004t0001g0046 a0002c0002t0001g0043 a0002c0002t0001g0045 others(4): Show |
7 | HG02486.hp2 HG02976.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.575+779T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 6/47 | chr7 | 142132864 | |||||||
| chr7:142132893 | CAT | C | 10 | a0001c0001t0001g0101 a0001c0001t0001g0227 a0001c0001t0001g0328 others(7): Show |
10 | HG00609.hp1 HG00621.hp2 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.575+811_575+812del others(2): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr7 | 142132893 | ||||||
| chr7:142132929 | C | T | 2 | a0002c0002t0001g0043 a0002c0002t0001g0045 |
2 | HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.575+844C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 6/47 | chr7 | 142132929 | |||||||
| chr7:142132994 | A | G | 1 | a0010c0031t0001g0263 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.575+909A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 6/47 | chr7 | 142132994 | |||||||
| chr7:142133057 | G | A | 151 | a0001c0001t0001g0245 a0001c0001t0001g0260 a0001c0004t0001g0046 others(148): Show |
152 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.576-924G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 6/47 | chr7 | 142133057 | |||||||
| chr7:142133100 | A | ATTAATTT others(36): Show |
1 | a0007c0033t0001g0155 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.576-852_576-810dup others(43): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr7 | 142133100 | ||||||
| chr7:142133112 | T | G | 1 | a0001c0001t0001g0095 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.576-869T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 6/47 | chr7 | 142133112 | |||||||
| chr7:142133177 | G | A | 2 | a0002c0003t0001g0033 a0015c0015t0001g0029 |
2 | HG02647.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.576-804G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 6/47 | chr7 | 142133177 | |||||||
| chr7:142133255 | T | G | 118 | a0001c0001t0001g0245 a0001c0001t0001g0260 a0001c0004t0001g0046 others(115): Show |
119 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.576-726T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 6/47 | chr7 | 142133255 | |||||||
| chr7:142133491 | T | C | 1 | a0013c0016t0001g0042 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.576-490T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 6/47 | chr7 | 142133491 | |||||||
| chr7:142133509 | G | A | 1 | a0001c0001t0001g0117 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.576-472G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 6/47 | chr7 | 142133509 | |||||||
| chr7:142133654 | T | C | 1 | a0041c0068t0001g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.576-327T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 6/47 | chr7 | 142133654 | |||||||
| chr7:142133711 | G | A | 1 | a0063c0041t0001g0139 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.576-270G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 6/47 | chr7 | 142133711 | |||||||
| chr7:142133956 | T | G | 1 | a0009c0011t0001g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.576-25T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 6/47 | chr7 | 142133956 | |||||||
| chr7:142134518 | T | A | 4 | a0002c0002t0001g0050 a0002c0003t0001g0049 a0002c0003t0001g0073 others(1): Show |
4 | HG01884.hp2 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.747+366T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 7/47 | chr7 | 142134518 | |||||||
| chr7:142134658 | T | G | 1 | a0002c0003t0001g0323 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.747+506T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 7/47 | chr7 | 142134658 | |||||||
| chr7:142134749 | C | A | 3 | a0015c0015t0001g0013 a0016c0014t0001g0011 a0019c0073t0001g0012 |
3 | HG01891.hp2 HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.747+597C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 7/47 | chr7 | 142134749 | |||||||
| chr7:142134776 | T | TA | 81 | a0001c0001t0001g0245 a0001c0001t0001g0260 a0001c0004t0001g0145 others(78): Show |
81 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.747+640dupA | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr7 | 142134776 | ||||||
| chr7:142134776 | TA | T | 14 | a0001c0001t0001g0178 a0001c0001t0001g0268 a0001c0004t0001g0119 others(11): Show |
14 | HG02155.hp2 HG03098.hp1 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.747+640delA | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr7 | 142134776 | ||||||
| chr7:142134882 | C | G | 106 | a0001c0001t0001g0245 a0001c0001t0001g0260 a0002c0002t0001g0008 others(103): Show |
107 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.747+730C>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 7/47 | chr7 | 142134882 | |||||||
| chr7:142135130 | G | A | 11 | a0002c0002t0001g0019 a0002c0002t0001g0021 a0002c0002t0001g0034 others(8): Show |
11 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.747+978G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 7/47 | chr7 | 142135130 | |||||||
| chr7:142135183 | A | T | 1 | a0002c0003t0001g0250 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.747+1031A>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 7/47 | chr7 | 142135183 | |||||||
| chr7:142135276 | G | A | 16 | a0002c0002t0001g0199 a0002c0002t0001g0224 a0002c0002t0001g0284 others(13): Show |
16 | HG00735.hp2 HG01243.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.747+1124G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 7/47 | chr7 | 142135276 | |||||||
| chr7:142135329 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.747+1177C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 7/47 | chr7 | 142135329 | |||||||
| chr7:142135330 | G | A | 1 | a0009c0011t0001g0293 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.747+1178G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 7/47 | chr7 | 142135330 | |||||||
| chr7:142135680 | G | A | 106 | a0001c0001t0001g0245 a0001c0001t0001g0260 a0001c0004t0001g0046 others(103): Show |
107 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.748-861G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 7/47 | chr7 | 142135680 | |||||||
| chr7:142135723 | T | TAC | 15 | a0001c0001t0001g0227 a0001c0004t0001g0046 a0002c0002t0001g0035 others(12): Show |
15 | HG01106.hp2 HG01123.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.748-788_748-787dup others(2): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr7 | 142135723 | ||||||
| chr7:142135723 | T | TACAC | 7 | a0009c0011t0001g0023 a0009c0011t0001g0024 a0009c0011t0001g0025 others(4): Show |
7 | HG00642.hp1 HG02055.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.748-790_748-787dup others(4): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr7 | 142135723 | ||||||
| chr7:142135723 | T | TACACAC | 16 | a0002c0002t0001g0043 a0002c0002t0001g0045 a0002c0002t0001g0308 others(13): Show |
17 | HG02486.hp2 HG02895.hp2 HG02897.hp2 others(14): Show |
intron_variant | MODIFIER | c.748-792_748-787dup others(6): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr7 | 142135723 | ||||||
| chr7:142135723 | T | TACACACA others(1): Show |
17 | a0002c0002t0001g0199 a0002c0002t0001g0224 a0002c0002t0001g0284 others(14): Show |
17 | HG00438.hp1 HG00735.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.748-794_748-787dup others(8): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr7 | 142135723 | ||||||
| chr7:142135723 | T | TACACACA others(3): Show |
10 | a0002c0002t0001g0266 a0002c0002t0001g0291 a0002c0003t0001g0219 others(7): Show |
10 | HG00423.hp1 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.748-796_748-787dup others(10): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr7 | 142135723 | ||||||
| chr7:142135723 | T | TACACACA others(5): Show |
31 | a0002c0002t0001g0008 a0002c0002t0001g0151 a0002c0002t0001g0264 others(28): Show |
31 | HG00741.hp2 HG01069.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.748-798_748-787dup others(12): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr7 | 142135723 | ||||||
| chr7:142135723 | T | TACACACA others(7): Show |
47 | a0001c0001t0001g0245 a0002c0002t0001g0016 a0002c0002t0001g0050 others(44): Show |
47 | HG00099.hp1 HG00408.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.748-800_748-787dup others(14): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr7 | 142135723 | ||||||
| chr7:142135723 | T | TACACACA others(9): Show |
7 | a0002c0002t0001g0229 a0002c0003t0001g0073 a0002c0003t0001g0250 others(4): Show |
7 | HG02129.hp1 HG02615.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.748-802_748-787dup others(16): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr7 | 142135723 | ||||||
| chr7:142135723 | T | TACACACA others(11): Show |
4 | a0001c0001t0001g0260 a0002c0002t0001g0205 a0002c0002t0001g0304 others(1): Show |
4 | HG01106.hp1 HG02040.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.748-804_748-787dup others(18): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr7 | 142135723 | ||||||
| chr7:142135723 | T | TACACACA others(13): Show |
1 | a0002c0002t0001g0211 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.748-806_748-787dup others(20): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr7 | 142135723 | ||||||
| chr7:142135723 | TAC | T | 5 | a0002c0002t0001g0034 a0002c0003t0001g0020 a0013c0016t0001g0173 others(2): Show |
5 | HG01243.hp2 HG03453.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.748-788_748-787del others(2): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr7 | 142135723 | ||||||
| chr7:142135743 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.748-798C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 7/47 | chr7 | 142135743 | |||||||
| chr7:142135836 | C | CT | 11 | a0002c0002t0001g0019 a0002c0002t0001g0021 a0002c0002t0001g0034 others(8): Show |
11 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.748-697dupT | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr7 | 142135836 | ||||||
| chr7:142136069 | A | G | 146 | a0001c0001t0001g0245 a0001c0001t0001g0260 a0002c0002t0001g0008 others(143): Show |
147 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.748-472A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 7/47 | chr7 | 142136069 | |||||||
| chr7:142136078 | G | A | 2 | a0014c0026t0001g0327 a0019c0030t0002g0326 |
2 | HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.748-463G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 7/47 | chr7 | 142136078 | |||||||
| chr7:142136393 | T | C | 2 | a0014c0026t0001g0327 a0019c0030t0002g0326 |
2 | HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.748-148T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 7/47 | chr7 | 142136393 | |||||||
| chr7:142136396 | C | A | 1 | a0045c0061t0001g0044 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.748-145C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 7/47 | chr7 | 142136396 | |||||||
| chr7:142136435 | A | G | 1 | a0001c0004t0001g0089 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.748-106A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 7/47 | chr7 | 142136435 | |||||||
| chr7:142136731 | T | C | 1 | a0021c0023t0001g0194 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.847+91T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 8/47 | chr7 | 142136731 | |||||||
| chr7:142136794 | T | C | 41 | a0002c0002t0001g0019 a0002c0002t0001g0021 a0002c0002t0001g0034 others(38): Show |
41 | HG00735.hp2 HG01243.hp1 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.847+154T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 8/47 | chr7 | 142136794 | |||||||
| chr7:142136809 | A | T | 3 | a0026c0029t0001g0174 a0026c0029t0001g0175 a0052c0071t0001g0162 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.847+169A>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 8/47 | chr7 | 142136809 | |||||||
| chr7:142136842 | A | G | 1 | a0001c0004t0001g0163 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.847+202A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 8/47 | chr7 | 142136842 | |||||||
| chr7:142137216 | TA | T | 145 | a0002c0002t0001g0008 a0002c0002t0001g0016 a0002c0002t0001g0019 others(142): Show |
146 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.848-204delA | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 8/47 | INFO_REALIGN_3_PRIME | chr7 | 142137216 | ||||||
| chr7:142137227 | A | C | 18 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0107 others(15): Show |
18 | HG00621.hp1 HG01257.hp2 HG02080.hp1 others(15): Show |
intron_variant | MODIFIER | c.848-206A>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 8/47 | chr7 | 142137227 | |||||||
| chr7:142137251 | T | C | 3 | a0002c0002t0001g0310 a0002c0003t0001g0311 a0002c0003t0001g0312 |
3 | HG03239.hp1 HG03704.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.848-182T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 8/47 | chr7 | 142137251 | |||||||
| chr7:142137346 | C | T | 2 | a0002c0002t0001g0249 a0005c0006t0001g0294 |
2 | HG02040.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.848-87C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 8/47 | chr7 | 142137346 | |||||||
| chr7:142137414 | C | T | 24 | a0002c0002t0001g0019 a0002c0002t0001g0021 a0002c0002t0001g0034 others(21): Show |
24 | HG00735.hp2 HG01243.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.848-19C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 8/47 | chr7 | 142137414 | |||||||
| chr7:142137643 | A | G | 1 | a0001c0004t0001g0063 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.960+98A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 9/47 | chr7 | 142137643 | |||||||
| chr7:142137740 | G | A | 1 | a0007c0081t0001g0129 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.960+195G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 9/47 | chr7 | 142137740 | |||||||
| chr7:142137940 | T | C | 153 | a0002c0002t0001g0008 a0002c0002t0001g0016 a0002c0002t0001g0019 others(150): Show |
154 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.960+395T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 9/47 | chr7 | 142137940 | |||||||
| chr7:142138241 | A | G | 20 | a0002c0002t0001g0008 a0002c0002t0001g0016 a0002c0002t0001g0151 others(17): Show |
20 | HG00741.hp2 HG01074.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.961-301A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 9/47 | chr7 | 142138241 | |||||||
| chr7:142138389 | T | C | 1 | a0048c0065t0002g0047 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.961-153T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 9/47 | chr7 | 142138389 | |||||||
| chr7:142138526 | T | C | 1 | a0002c0002t0001g0266 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.961-16T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 9/47 | chr7 | 142138526 | |||||||
| chr7:142139230 | C | T | 11 | a0002c0003t0001g0033 a0002c0058t0001g0032 a0009c0011t0001g0023 others(8): Show |
11 | HG00642.hp1 HG02145.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1086+563C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 10/47 | chr7 | 142139230 | |||||||
| chr7:142139431 | G | A | 1 | a0045c0061t0001g0044 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1086+764G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 10/47 | chr7 | 142139431 | |||||||
| chr7:142139530 | A | G | 1 | a0021c0023t0004g0057 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1086+863A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 10/47 | chr7 | 142139530 | |||||||
| chr7:142139541 | A | T | 3 | a0002c0003t0001g0244 a0005c0006t0001g0243 a0012c0012t0001g0214 |
3 | NA18940.hp1 NA18947.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.1086+874A>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 10/47 | chr7 | 142139541 | |||||||
| chr7:142139584 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1086+917C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 10/47 | chr7 | 142139584 | |||||||
| chr7:142139659 | C | CA | 25 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0140 others(22): Show |
25 | HG00741.hp1 HG01517.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.1086+1013dupA | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 10/47 | INFO_REALIGN_3_PRIME | chr7 | 142139659 | ||||||
| chr7:142139659 | CA | C | 12 | a0001c0001t0001g0178 a0001c0001t0001g0245 a0002c0002t0001g0319 others(9): Show |
12 | HG00621.hp2 HG02897.hp1 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.1086+1013delA | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 10/47 | INFO_REALIGN_3_PRIME | chr7 | 142139659 | ||||||
| chr7:142139659 | CAAAA | C | 16 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0107 others(13): Show |
16 | HG00621.hp1 HG01257.hp2 HG02165.hp1 others(13): Show |
intron_variant | MODIFIER | c.1086+1010_1086+101 others(8): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 10/47 | INFO_REALIGN_3_PRIME | chr7 | 142139659 | ||||||
| chr7:142139723 | A | G | 1 | a0018c0028t0001g0231 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1086+1056A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 10/47 | chr7 | 142139723 | |||||||
| chr7:142139813 | A | C | 2 | a0014c0026t0001g0196 a0046c0077t0001g0195 |
2 | HG01243.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1087-989A>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 10/47 | chr7 | 142139813 | |||||||
| chr7:142139878 | T | C | 1 | a0014c0020t0001g0001 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1087-924T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 10/47 | chr7 | 142139878 | |||||||
| chr7:142140157 | G | A | 4 | a0001c0001t0001g0127 a0001c0001t0001g0245 a0001c0001t0001g0260 others(1): Show |
4 | HG00558.hp1 HG02027.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.1087-645G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 10/47 | chr7 | 142140157 | |||||||
| chr7:142140170 | A | C | 49 | a0001c0001t0001g0097 a0001c0001t0001g0108 a0001c0001t0001g0154 others(46): Show |
49 | HG00323.hp2 HG00642.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.1087-632A>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 10/47 | chr7 | 142140170 | |||||||
| chr7:142140193 | T | C | 1 | a0004c0005t0001g0137 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1087-609T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 10/47 | chr7 | 142140193 | |||||||
| chr7:142140471 | A | T | 1 | a0010c0017t0001g0302 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1087-331A>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 10/47 | chr7 | 142140471 | |||||||
| chr7:142140736 | G | A | 2 | a0014c0026t0001g0327 a0019c0030t0002g0326 |
2 | HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1087-66G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 10/47 | chr7 | 142140736 | |||||||
| chr7:142140781 | T | C | 65 | a0001c0001t0001g0095 a0001c0001t0001g0108 a0001c0001t0001g0140 others(62): Show |
65 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.1087-21T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 10/47 | chr7 | 142140781 | |||||||
| chr7:142141003 | A | G | 9 | a0002c0002t0001g0284 a0002c0002t0001g0285 a0002c0003t0001g0197 others(6): Show |
9 | HG01261.hp2 HG03098.hp1 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.1219-18A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 11/47 | chr7 | 142141003 | |||||||
| chr7:142141005 | C | T | 2 | a0005c0006t0001g0233 a0005c0006t0001g0239 |
2 | NA18944.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1219-16C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 11/47 | chr7 | 142141005 | |||||||
| chr7:142141160 | G | A | 1 | a0002c0002t0001g0249 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1317+41G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 12/47 | chr7 | 142141160 | |||||||
| chr7:142141241 | T | G | 2 | a0001c0001t0001g0272 a0003c0009t0001g0271 |
2 | HG01257.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1317+122T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 12/47 | chr7 | 142141241 | |||||||
| chr7:142141311 | C | A | 1 | a0002c0002t0001g0151 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1317+192C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 12/47 | chr7 | 142141311 | |||||||
| chr7:142141419 | A | C | 1 | a0011c0022t0001g0161 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1317+300A>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 12/47 | chr7 | 142141419 | |||||||
| chr7:142141443 | A | G | 2 | a0001c0001t0001g0179 a0002c0003t0001g0311 |
2 | HG03491.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1317+324A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 12/47 | chr7 | 142141443 | |||||||
| chr7:142141625 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1317+506G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 12/47 | chr7 | 142141625 | |||||||
| chr7:142141636 | A | T | 129 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0074 others(126): Show |
129 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1317+517A>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 12/47 | chr7 | 142141636 | |||||||
| chr7:142141872 | G | T | 1 | a0001c0004t0001g0064 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1317+753G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 12/47 | chr7 | 142141872 | |||||||
| chr7:142142069 | G | A | 61 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0153 others(58): Show |
61 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.1317+950G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 12/47 | chr7 | 142142069 | |||||||
| chr7:142142148 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1317+1029T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 12/47 | chr7 | 142142148 | |||||||
| chr7:142142161 | C | CT | 322 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0074 others(319): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.1317+1050dupT | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 12/47 | INFO_REALIGN_3_PRIME | chr7 | 142142161 | ||||||
| chr7:142142182 | C | A | 1 | a0035c0067t0003g0146 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1317+1063C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 12/47 | chr7 | 142142182 | |||||||
| chr7:142142198 | A | G | 1 | a0002c0003t0001g0228 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1317+1079A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 12/47 | chr7 | 142142198 | |||||||
| chr7:142142524 | G | GT | 39 | a0001c0001t0001g0096 a0001c0001t0001g0107 a0001c0001t0001g0112 others(36): Show |
39 | HG00642.hp1 HG00735.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.1318-1221dupT | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 12/47 | INFO_REALIGN_3_PRIME | chr7 | 142142524 | ||||||
| chr7:142142524 | G | GTTTTTTT | 42 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0004t0001g0063 others(39): Show |
42 | HG00323.hp2 HG00408.hp2 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.1318-1227_1318-122 others(11): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 12/47 | INFO_REALIGN_3_PRIME | chr7 | 142142524 | ||||||
| chr7:142142524 | G | GTTTTTTT others(1): Show |
18 | a0001c0001t0001g0153 a0001c0001t0001g0166 a0002c0002t0001g0205 others(15): Show |
18 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(15): Show |
intron_variant | MODIFIER | c.1318-1228_1318-122 others(12): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 12/47 | INFO_REALIGN_3_PRIME | chr7 | 142142524 | ||||||
| chr7:142142524 | G | T | 1 | a0010c0017t0001g0302 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1318-1245G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 12/47 | chr7 | 142142524 | |||||||
| chr7:142142524 | GT | G | 8 | a0001c0001t0001g0140 a0002c0003t0001g0088 a0003c0007t0001g0070 others(5): Show |
8 | HG01978.hp2 HG02155.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.1318-1221delT | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 12/47 | INFO_REALIGN_3_PRIME | chr7 | 142142524 | ||||||
| chr7:142142525 | T | G | 2 | a0001c0004t0001g0157 a0003c0007t0001g0120 |
2 | NA18954.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1318-1244T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 12/47 | chr7 | 142142525 | |||||||
| chr7:142142593 | C | T | 1 | a0043c0048t0001g0103 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1318-1176C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 12/47 | chr7 | 142142593 | |||||||
| chr7:142142685 | A | G | 5 | a0002c0002t0001g0284 a0002c0002t0001g0285 a0002c0003t0001g0197 others(2): Show |
5 | HG01261.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1318-1084A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 12/47 | chr7 | 142142685 | |||||||
| chr7:142142732 | T | C | 38 | a0001c0001t0001g0060 a0001c0001t0001g0116 a0001c0001t0001g0178 others(35): Show |
38 | HG00408.hp1 HG00438.hp2 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.1318-1037T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 12/47 | chr7 | 142142732 | |||||||
| chr7:142142902 | T | C | 6 | a0001c0004t0001g0145 a0014c0020t0001g0001 a0020c0018t0001g0148 others(3): Show |
7 | HG02145.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1318-867T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 12/47 | chr7 | 142142902 | |||||||
| chr7:142143030 | G | T | 1 | a0013c0016t0001g0173 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1318-739G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 12/47 | chr7 | 142143030 | |||||||
| chr7:142143103 | T | G | 2 | a0001c0001t0001g0179 a0002c0003t0001g0311 |
2 | HG03491.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1318-666T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 12/47 | chr7 | 142143103 | |||||||
| chr7:142143127 | T | C | 7 | a0014c0026t0001g0196 a0022c0027t0001g0038 a0022c0027t0001g0040 others(4): Show |
7 | HG01243.hp1 HG01891.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1318-642T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 12/47 | chr7 | 142143127 | |||||||
| chr7:142143258 | G | T | 62 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0153 others(59): Show |
62 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.1318-511G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 12/47 | chr7 | 142143258 | |||||||
| chr7:142143259 | C | T | 129 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0074 others(126): Show |
129 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1318-510C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 12/47 | chr7 | 142143259 | |||||||
| chr7:142143356 | TATC | T | 4 | a0002c0003t0001g0219 a0024c0075t0001g0185 a0047c0070t0001g0147 others(1): Show |
4 | HG03098.hp1 HG03130.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1318-411_1318-409d others(5): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 12/47 | INFO_REALIGN_3_PRIME | chr7 | 142143356 | ||||||
| chr7:142143467 | A | T | 6 | a0001c0004t0001g0145 a0014c0020t0001g0001 a0020c0018t0001g0148 others(3): Show |
7 | HG02145.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1318-302A>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 12/47 | chr7 | 142143467 | |||||||
| chr7:142143760 | G | T | 1 | a0033c0035t0003g0061 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1318-9G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 12/47 | chr7 | 142143760 | |||||||
| chr7:142144508 | A | C | 1 | a0045c0061t0001g0044 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1432-353A>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 13/47 | chr7 | 142144508 | |||||||
| chr7:142144614 | A | G | 3 | a0035c0067t0003g0146 a0062c0076t0001g0325 a0063c0041t0001g0139 |
3 | HG02055.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1432-247A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 13/47 | chr7 | 142144614 | |||||||
| chr7:142144710 | G | C | 100 | a0001c0001t0001g0060 a0001c0001t0001g0077 a0001c0001t0001g0080 others(97): Show |
100 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1432-151G>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 13/47 | chr7 | 142144710 | |||||||
| chr7:142144787 | T | C | 1 | a0004c0005t0001g0137 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1432-74T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 13/47 | chr7 | 142144787 | |||||||
| chr7:142144959 | T | G | 1 | a0033c0035t0003g0061 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1516+14T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 14/47 | chr7 | 142144959 | |||||||
| chr7:142145088 | C | G | 102 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0074 others(99): Show |
102 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1516+143C>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 14/47 | chr7 | 142145088 | |||||||
| chr7:142145471 | G | T | 2 | a0001c0001t0001g0179 a0002c0003t0001g0311 |
2 | HG03491.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1516+526G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 14/47 | chr7 | 142145471 | |||||||
| chr7:142145758 | G | GA | 36 | a0001c0001t0001g0060 a0001c0001t0001g0116 a0001c0001t0001g0178 others(33): Show |
36 | HG00408.hp1 HG00438.hp2 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.1516+814dupA | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 14/47 | INFO_REALIGN_3_PRIME | chr7 | 142145758 | ||||||
| chr7:142145917 | C | T | 114 | a0001c0001t0001g0060 a0001c0001t0001g0077 a0001c0001t0001g0080 others(111): Show |
114 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.1516+972C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 14/47 | chr7 | 142145917 | |||||||
| chr7:142146064 | T | C | 67 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0153 others(64): Show |
67 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.1516+1119T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 14/47 | chr7 | 142146064 | |||||||
| chr7:142146142 | G | GT | 7 | a0001c0001t0001g0176 a0009c0011t0001g0023 a0009c0011t0001g0024 others(4): Show |
7 | HG00642.hp1 HG02451.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1516+1215dupT | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 14/47 | INFO_REALIGN_3_PRIME | chr7 | 142146142 | ||||||
| chr7:142146142 | G | GTTT | 13 | a0001c0001t0001g0178 a0001c0001t0001g0190 a0001c0001t0001g0267 others(10): Show |
13 | HG02257.hp1 HG02451.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1516+1213_1516+121 others(7): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 14/47 | INFO_REALIGN_3_PRIME | chr7 | 142146142 | ||||||
| chr7:142146142 | G | GTTTT | 20 | a0001c0001t0001g0060 a0001c0001t0001g0116 a0001c0001t0001g0247 others(17): Show |
20 | HG00408.hp1 HG00438.hp2 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.1516+1212_1516+121 others(8): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 14/47 | INFO_REALIGN_3_PRIME | chr7 | 142146142 | ||||||
| chr7:142146142 | GT | G | 186 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0074 others(183): Show |
186 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.1516+1215delT | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 14/47 | INFO_REALIGN_3_PRIME | chr7 | 142146142 | ||||||
| chr7:142146142 | GTT | G | 12 | a0001c0001t0001g0179 a0002c0002t0001g0284 a0002c0002t0001g0285 others(9): Show |
12 | HG01261.hp2 HG03098.hp1 HG03098.hp2 others(9): Show |
intron_variant | MODIFIER | c.1516+1214_1516+121 others(6): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 14/47 | INFO_REALIGN_3_PRIME | chr7 | 142146142 | ||||||
| chr7:142146142 | GTTT | G | 65 | a0001c0001t0001g0095 a0001c0001t0001g0108 a0001c0001t0001g0140 others(62): Show |
65 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.1516+1213_1516+121 others(7): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 14/47 | INFO_REALIGN_3_PRIME | chr7 | 142146142 | ||||||
| chr7:142146210 | T | G | 7 | a0001c0001t0001g0176 a0009c0011t0001g0023 a0009c0011t0001g0024 others(4): Show |
7 | HG00642.hp1 HG02451.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1517-1246T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 14/47 | chr7 | 142146210 | |||||||
| chr7:142146315 | T | A | 65 | a0001c0001t0001g0095 a0001c0001t0001g0108 a0001c0001t0001g0140 others(62): Show |
65 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.1517-1141T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 14/47 | chr7 | 142146315 | |||||||
| chr7:142146347 | A | C | 1 | a0001c0001t0001g0180 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1517-1109A>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 14/47 | chr7 | 142146347 | |||||||
| chr7:142146731 | AT | A | 62 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0153 others(59): Show |
62 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.1517-711delT | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 14/47 | INFO_REALIGN_3_PRIME | chr7 | 142146731 | ||||||
| chr7:142146804 | T | A | 1 | a0001c0001t0001g0095 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1517-652T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 14/47 | chr7 | 142146804 | |||||||
| chr7:142146806 | C | A | 1 | a0033c0035t0003g0061 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1517-650C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 14/47 | chr7 | 142146806 | |||||||
| chr7:142146814 | G | T | 129 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0074 others(126): Show |
129 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1517-642G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 14/47 | chr7 | 142146814 | |||||||
| chr7:142146820 | C | T | 127 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0074 others(124): Show |
127 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.1517-636C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 14/47 | chr7 | 142146820 | |||||||
| chr7:142146847 | C | A | 3 | a0002c0003t0001g0088 a0006c0008t0001g0094 a0052c0071t0001g0162 |
3 | HG03490.hp1 HG03710.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1517-609C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 14/47 | chr7 | 142146847 | |||||||
| chr7:142146873 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1517-583G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 14/47 | chr7 | 142146873 | |||||||
| chr7:142146916 | C | T | 1 | a0002c0002t0001g0253 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1517-540C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 14/47 | chr7 | 142146916 | |||||||
| chr7:142146932 | T | C | 62 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0153 others(59): Show |
62 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.1517-524T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 14/47 | chr7 | 142146932 | |||||||
| chr7:142147104 | T | C | 67 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0153 others(64): Show |
67 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.1517-352T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 14/47 | chr7 | 142147104 | |||||||
| chr7:142147421 | G | A | 36 | a0001c0001t0001g0060 a0001c0001t0001g0116 a0001c0001t0001g0178 others(33): Show |
36 | HG00408.hp1 HG00438.hp2 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.1517-35G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 14/47 | chr7 | 142147421 | |||||||
| chr7:142147618 | G | A | 3 | a0002c0002t0001g0259 a0002c0003t0001g0258 a0010c0017t0001g0240 |
3 | HG01081.hp1 HG01884.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1634+45G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142147618 | |||||||
| chr7:142147712 | G | A | 57 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0153 others(54): Show |
57 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.1634+139G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142147712 | |||||||
| chr7:142147833 | T | A | 1 | a0004c0005t0001g0270 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1634+260T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142147833 | |||||||
| chr7:142147909 | AT | A | 130 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0095 others(127): Show |
130 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.1634+337delT | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142147909 | |||||||
| chr7:142147914 | G | A | 129 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0074 others(126): Show |
129 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1634+341G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142147914 | |||||||
| chr7:142147928 | A | G | 130 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0095 others(127): Show |
130 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.1634+355A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142147928 | |||||||
| chr7:142147966 | G | T | 1 | a0007c0081t0001g0129 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1634+393G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142147966 | |||||||
| chr7:142147982 | A | G | 131 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0095 others(128): Show |
131 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.1634+409A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142147982 | |||||||
| chr7:142148195 | T | C | 1 | a0001c0004t0001g0201 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1634+622T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142148195 | |||||||
| chr7:142148267 | C | T | 2 | a0016c0014t0001g0017 a0016c0014t0001g0018 |
2 | HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1634+694C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142148267 | |||||||
| chr7:142148271 | C | T | 41 | a0001c0001t0001g0095 a0001c0001t0001g0108 a0001c0001t0001g0218 others(38): Show |
41 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.1634+698C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142148271 | |||||||
| chr7:142148336 | C | T | 6 | a0001c0004t0002g0065 a0002c0002t0001g0050 a0002c0003t0001g0049 others(3): Show |
6 | HG01074.hp1 HG01884.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1634+763C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142148336 | |||||||
| chr7:142148599 | T | C | 3 | a0001c0004t0001g0066 a0002c0002t0001g0199 a0015c0015t0001g0013 |
3 | HG02922.hp1 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1634+1026T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142148599 | |||||||
| chr7:142148603 | G | A | 3 | a0001c0004t0001g0066 a0002c0002t0001g0199 a0015c0015t0001g0013 |
3 | HG02922.hp1 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1634+1030G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142148603 | |||||||
| chr7:142148754 | T | C | 2 | a0001c0001t0001g0179 a0002c0003t0001g0311 |
2 | HG03491.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1634+1181T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142148754 | |||||||
| chr7:142148811 | A | G | 99 | a0001c0001t0001g0067 a0001c0001t0001g0074 a0001c0001t0001g0075 others(96): Show |
99 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1634+1238A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142148811 | |||||||
| chr7:142148955 | G | A | 1 | a0007c0080t0001g0076 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1634+1382G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142148955 | |||||||
| chr7:142149046 | G | A | 2 | a0008c0010t0001g0051 a0018c0062t0001g0299 |
2 | HG02040.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.1634+1473G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142149046 | |||||||
| chr7:142149153 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1634+1580C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142149153 | |||||||
| chr7:142149161 | G | A | 90 | a0001c0001t0001g0067 a0001c0001t0001g0074 a0001c0001t0001g0075 others(87): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1634+1588G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142149161 | |||||||
| chr7:142149177 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1634+1604C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142149177 | |||||||
| chr7:142149216 | T | C | 1 | a0002c0002t0001g0205 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1634+1643T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142149216 | |||||||
| chr7:142149229 | C | CA | 28 | a0001c0001t0001g0131 a0001c0001t0001g0172 a0001c0001t0001g0179 others(25): Show |
28 | HG00140.hp2 HG00642.hp2 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.1634+1666dupA | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | INFO_REALIGN_3_PRIME | chr7 | 142149229 | ||||||
| chr7:142149229 | C | CAAA | 158 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0074 others(155): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.1634+1664_1634+166 others(7): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | INFO_REALIGN_3_PRIME | chr7 | 142149229 | ||||||
| chr7:142149246 | A | T | 25 | a0001c0001t0001g0172 a0002c0002t0001g0213 a0002c0003t0001g0088 others(22): Show |
25 | HG00140.hp2 HG00642.hp2 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.1634+1673A>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142149246 | |||||||
| chr7:142149254 | T | G | 164 | a0001c0001t0001g0060 a0001c0001t0001g0095 a0001c0001t0001g0097 others(161): Show |
165 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.1634+1681T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142149254 | |||||||
| chr7:142149264 | G | T | 164 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0074 others(161): Show |
164 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.1634+1691G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142149264 | |||||||
| chr7:142149266 | G | T | 36 | a0001c0001t0001g0178 a0001c0001t0001g0190 a0001c0001t0001g0247 others(33): Show |
36 | HG00408.hp1 HG00438.hp2 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.1634+1693G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142149266 | |||||||
| chr7:142149475 | C | A | 160 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0074 others(157): Show |
160 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.1634+1902C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142149475 | |||||||
| chr7:142149487 | A | C | 301 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(298): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1634+1914A>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142149487 | |||||||
| chr7:142149518 | A | G | 4 | a0001c0001t0001g0116 a0001c0001t0001g0245 a0001c0001t0001g0260 others(1): Show |
4 | NA18962.hp1 NA18985.hp2 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.1634+1945A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142149518 | |||||||
| chr7:142149548 | G | GT | 84 | a0001c0001t0001g0095 a0001c0001t0001g0108 a0001c0001t0001g0140 others(81): Show |
84 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.1634+1985dupT | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | INFO_REALIGN_3_PRIME | chr7 | 142149548 | ||||||
| chr7:142149572 | G | A | 2 | a0001c0001t0001g0131 a0001c0001t0001g0179 |
2 | HG02165.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.1634+1999G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142149572 | |||||||
| chr7:142149601 | T | C | 4 | a0001c0001t0001g0131 a0001c0001t0001g0179 a0019c0030t0002g0326 others(1): Show |
4 | HG02145.hp2 HG02165.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1634+2028T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142149601 | |||||||
| chr7:142149633 | T | C | 46 | a0001c0001t0001g0095 a0001c0001t0001g0108 a0001c0001t0001g0176 others(43): Show |
46 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1634+2060T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142149633 | |||||||
| chr7:142149641 | C | T | 41 | a0001c0001t0001g0095 a0001c0001t0001g0108 a0001c0001t0001g0176 others(38): Show |
41 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.1634+2068C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142149641 | |||||||
| chr7:142149678 | C | T | 1 | a0013c0016t0001g0041 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1634+2105C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142149678 | |||||||
| chr7:142149742 | A | C | 1 | a0002c0002t0001g0253 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1634+2169A>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142149742 | |||||||
| chr7:142149743 | G | A | 1 | a0002c0002t0001g0253 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1634+2170G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142149743 | |||||||
| chr7:142149744 | C | T | 1 | a0002c0002t0001g0253 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1634+2171C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142149744 | |||||||
| chr7:142149763 | C | G | 83 | a0001c0001t0001g0067 a0001c0001t0001g0074 a0001c0001t0001g0075 others(80): Show |
83 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1634+2190C>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142149763 | |||||||
| chr7:142149777 | A | G | 2 | a0008c0010t0001g0078 a0058c0053t0001g0182 |
2 | NA19002.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1634+2204A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142149777 | |||||||
| chr7:142149782 | T | C | 8 | a0001c0001t0001g0060 a0001c0001t0001g0097 a0001c0001t0001g0130 others(5): Show |
8 | HG00639.hp1 HG01074.hp2 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.1634+2209T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142149782 | |||||||
| chr7:142149792 | T | C | 1 | a0054c0078t0001g0143 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1634+2219T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142149792 | |||||||
| chr7:142149821 | G | C | 1 | a0045c0061t0001g0044 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1634+2248G>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142149821 | |||||||
| chr7:142149828 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1634+2255A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142149828 | |||||||
| chr7:142149946 | C | CT | 10 | a0001c0001t0001g0131 a0001c0001t0001g0179 a0001c0004t0001g0066 others(7): Show |
10 | HG02055.hp2 HG02165.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1634+2385dupT | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | INFO_REALIGN_3_PRIME | chr7 | 142149946 | ||||||
| chr7:142150075 | A | G | 256 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0074 others(253): Show |
257 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.1634+2502A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142150075 | |||||||
| chr7:142150100 | C | T | 22 | a0002c0003t0001g0088 a0010c0017t0001g0240 a0010c0017t0001g0256 others(19): Show |
22 | HG00140.hp1 HG00408.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.1634+2527C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142150100 | |||||||
| chr7:142150145 | T | G | 35 | a0001c0001t0001g0140 a0002c0002t0001g0039 a0002c0002t0001g0284 others(32): Show |
35 | HG00140.hp1 HG00408.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.1634+2572T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142150145 | |||||||
| chr7:142150169 | G | A | 8 | a0001c0001t0001g0112 a0001c0004t0001g0119 a0001c0004t0001g0160 others(5): Show |
8 | HG02027.hp1 NA18747.hp2 NA18971.hp1 others(5): Show |
intron_variant | MODIFIER | c.1634+2596G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142150169 | |||||||
| chr7:142150350 | G | A | 8 | a0001c0001t0001g0131 a0001c0001t0001g0179 a0001c0004t0001g0046 others(5): Show |
9 | HG02055.hp2 HG02145.hp2 HG02165.hp2 others(6): Show |
intron_variant | MODIFIER | c.1634+2777G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142150350 | |||||||
| chr7:142150418 | A | G | 12 | a0001c0001t0001g0112 a0001c0001t0001g0178 a0001c0001t0001g0190 others(9): Show |
12 | HG02027.hp1 HG02135.hp1 NA18943.hp2 others(9): Show |
intron_variant | MODIFIER | c.1634+2845A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142150418 | |||||||
| chr7:142150505 | C | T | 81 | a0001c0001t0001g0067 a0001c0001t0001g0074 a0001c0001t0001g0080 others(78): Show |
81 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.1634+2932C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142150505 | |||||||
| chr7:142150524 | C | A | 1 | a0044c0036t0001g0184 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1634+2951C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142150524 | |||||||
| chr7:142150544 | T | A | 1 | a0048c0065t0002g0047 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1634+2971T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142150544 | |||||||
| chr7:142150656 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1634+3083T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142150656 | |||||||
| chr7:142150972 | T | C | 299 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(296): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.1635-3046T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142150972 | |||||||
| chr7:142151096 | G | C | 4 | a0001c0004t0001g0145 a0020c0018t0001g0148 a0020c0018t0001g0149 others(1): Show |
4 | HG03041.hp1 NA19030.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1635-2922G>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142151096 | |||||||
| chr7:142151135 | G | C | 1 | a0001c0001t0001g0101 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1635-2883G>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142151135 | |||||||
| chr7:142151192 | T | C | 12 | a0001c0001t0001g0112 a0001c0001t0001g0178 a0001c0001t0001g0190 others(9): Show |
12 | HG02027.hp1 HG02135.hp1 NA18943.hp2 others(9): Show |
intron_variant | MODIFIER | c.1635-2826T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142151192 | |||||||
| chr7:142151624 | A | G | 1 | a0001c0004t0001g0167 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1635-2394A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142151624 | |||||||
| chr7:142151692 | G | A | 2 | a0001c0001t0001g0127 a0002c0002t0001g0229 |
2 | HG02027.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.1635-2326G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142151692 | |||||||
| chr7:142151740 | G | A | 76 | a0001c0001t0001g0067 a0001c0001t0001g0074 a0001c0001t0001g0080 others(73): Show |
76 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.1635-2278G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142151740 | |||||||
| chr7:142151761 | G | A | 4 | a0001c0004t0001g0145 a0020c0018t0001g0148 a0020c0018t0001g0149 others(1): Show |
4 | HG03041.hp1 NA19030.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1635-2257G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142151761 | |||||||
| chr7:142151788 | GTCTT | G | 42 | a0001c0001t0001g0247 a0001c0001t0001g0267 a0001c0004t0001g0063 others(39): Show |
42 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.1635-2226_1635-222 others(8): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | INFO_REALIGN_3_PRIME | chr7 | 142151788 | ||||||
| chr7:142151810 | G | A | 149 | a0001c0001t0001g0067 a0001c0001t0001g0074 a0001c0001t0001g0080 others(146): Show |
149 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.1635-2208G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142151810 | |||||||
| chr7:142151842 | G | A | 1 | a0001c0004t0001g0072 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1635-2176G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142151842 | |||||||
| chr7:142151898 | A | ACATT | 6 | a0022c0027t0001g0038 a0022c0027t0001g0040 a0023c0025t0001g0052 others(3): Show |
6 | HG01891.hp1 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1635-2119_1635-211 others(8): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | INFO_REALIGN_3_PRIME | chr7 | 142151898 | ||||||
| chr7:142151951 | A | G | 21 | a0010c0017t0001g0240 a0010c0017t0001g0256 a0010c0017t0001g0286 others(18): Show |
21 | HG00140.hp1 HG00408.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.1635-2067A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142151951 | |||||||
| chr7:142152058 | CTT | C | 21 | a0010c0017t0001g0240 a0010c0017t0001g0256 a0010c0017t0001g0286 others(18): Show |
21 | HG00140.hp1 HG00408.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.1635-1958_1635-195 others(6): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | INFO_REALIGN_3_PRIME | chr7 | 142152058 | ||||||
| chr7:142152151 | G | T | 6 | a0022c0027t0001g0038 a0022c0027t0001g0040 a0023c0025t0001g0052 others(3): Show |
6 | HG01891.hp1 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1635-1867G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142152151 | |||||||
| chr7:142152171 | TA | T | 246 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0074 others(243): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.1635-1832delA | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | INFO_REALIGN_3_PRIME | chr7 | 142152171 | ||||||
| chr7:142152173 | A | T | 1 | a0002c0002t0001g0291 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1635-1845A>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142152173 | |||||||
| chr7:142152233 | A | G | 3 | a0002c0003t0001g0073 a0029c0040t0001g0202 a0050c0039t0001g0048 |
3 | HG00099.hp2 HG02717.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1635-1785A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142152233 | |||||||
| chr7:142152450 | G | T | 1 | a0001c0001t0001g0096 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1635-1568G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142152450 | |||||||
| chr7:142152457 | T | C | 44 | a0001c0001t0001g0247 a0001c0001t0001g0267 a0001c0004t0001g0063 others(41): Show |
44 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.1635-1561T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142152457 | |||||||
| chr7:142152460 | A | AGCCCTTT others(339): Show |
1 | a0002c0002t0001g0034 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1635-1543_1635-154 others(350): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | INFO_REALIGN_3_PRIME | chr7 | 142152460 | ||||||
| chr7:142152721 | A | C | 251 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0074 others(248): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.1635-1297A>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142152721 | |||||||
| chr7:142152730 | C | A | 48 | a0001c0001t0001g0060 a0001c0001t0001g0075 a0001c0001t0001g0095 others(45): Show |
48 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.1635-1288C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142152730 | |||||||
| chr7:142152775 | T | C | 77 | a0001c0001t0001g0067 a0001c0001t0001g0074 a0001c0001t0001g0080 others(74): Show |
77 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.1635-1243T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142152775 | |||||||
| chr7:142152818 | A | G | 1 | a0004c0005t0001g0177 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1635-1200A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142152818 | |||||||
| chr7:142152853 | C | T | 7 | a0001c0001t0001g0140 a0002c0002t0001g0039 a0002c0002t0001g0284 others(4): Show |
7 | HG01261.hp2 HG02717.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1635-1165C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142152853 | |||||||
| chr7:142152876 | A | G | 2 | a0054c0078t0001g0143 a0055c0055t0001g0083 |
2 | NA18951.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.1635-1142A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142152876 | |||||||
| chr7:142152909 | G | T | 4 | a0001c0004t0001g0145 a0020c0018t0001g0148 a0020c0018t0001g0149 others(1): Show |
4 | HG03041.hp1 NA19030.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1635-1109G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142152909 | |||||||
| chr7:142152992 | C | CT | 9 | a0001c0001t0001g0140 a0002c0002t0001g0039 a0002c0002t0001g0284 others(6): Show |
9 | HG01261.hp2 HG02055.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1635-1009dupT | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | INFO_REALIGN_3_PRIME | chr7 | 142152992 | ||||||
| chr7:142152992 | CT | C | 223 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(220): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.1635-1009delT | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | INFO_REALIGN_3_PRIME | chr7 | 142152992 | ||||||
| chr7:142152992 | CTT | C | 20 | a0001c0001t0001g0131 a0001c0001t0001g0179 a0001c0001t0001g0227 others(17): Show |
21 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.1635-1010_1635-100 others(6): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | INFO_REALIGN_3_PRIME | chr7 | 142152992 | ||||||
| chr7:142153041 | G | A | 5 | a0009c0011t0001g0025 a0016c0014t0001g0011 a0016c0014t0001g0017 others(2): Show |
5 | HG01891.hp2 HG02622.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1635-977G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142153041 | |||||||
| chr7:142153070 | A | G | 3 | a0001c0004t0001g0066 a0002c0002t0001g0199 a0015c0015t0001g0013 |
3 | HG02922.hp1 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1635-948A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142153070 | |||||||
| chr7:142153146 | C | T | 6 | a0022c0027t0001g0038 a0022c0027t0001g0040 a0023c0025t0001g0052 others(3): Show |
6 | HG01891.hp1 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1635-872C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142153146 | |||||||
| chr7:142153147 | G | A | 7 | a0001c0001t0001g0176 a0009c0011t0001g0023 a0009c0011t0001g0024 others(4): Show |
7 | HG00642.hp1 HG02451.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1635-871G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142153147 | |||||||
| chr7:142153232 | C | A | 7 | a0001c0001t0001g0140 a0002c0002t0001g0039 a0002c0002t0001g0284 others(4): Show |
7 | HG01261.hp2 HG02717.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1635-786C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142153232 | |||||||
| chr7:142153246 | C | T | 4 | a0001c0004t0001g0046 a0014c0020t0001g0001 a0036c0049t0001g0275 others(1): Show |
5 | HG02055.hp2 HG02145.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1635-772C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142153246 | |||||||
| chr7:142153313 | A | G | 21 | a0001c0001t0001g0101 a0001c0001t0001g0112 a0001c0001t0001g0178 others(18): Show |
21 | HG00735.hp2 HG02027.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.1635-705A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142153313 | |||||||
| chr7:142153324 | C | T | 1 | a0001c0004t0001g0170 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1635-694C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142153324 | |||||||
| chr7:142153452 | A | G | 76 | a0001c0001t0001g0067 a0001c0001t0001g0074 a0001c0001t0001g0080 others(73): Show |
76 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.1635-566A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142153452 | |||||||
| chr7:142153584 | G | T | 1 | a0036c0049t0001g0275 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1635-434G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142153584 | |||||||
| chr7:142153808 | G | A | 80 | a0001c0001t0001g0071 a0001c0001t0001g0077 a0001c0001t0001g0097 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.1635-210G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142153808 | |||||||
| chr7:142153909 | C | T | 3 | a0001c0004t0001g0066 a0002c0002t0001g0199 a0015c0015t0001g0013 |
3 | HG02922.hp1 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1635-109C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 15/47 | chr7 | 142153909 | |||||||
| chr7:142154226 | T | A | 2 | a0014c0026t0001g0196 a0014c0026t0001g0327 |
2 | HG01243.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1806+37T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 16/47 | chr7 | 142154226 | |||||||
| chr7:142154252 | A | T | 3 | a0001c0001t0001g0171 a0001c0004t0001g0192 a0007c0034t0001g0186 |
3 | NA18956.hp2 NA18993.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1806+63A>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 16/47 | chr7 | 142154252 | |||||||
| chr7:142154267 | C | G | 1 | a0019c0030t0002g0326 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1806+78C>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 16/47 | chr7 | 142154267 | |||||||
| chr7:142154290 | C | T | 6 | a0022c0027t0001g0038 a0022c0027t0001g0040 a0023c0025t0001g0052 others(3): Show |
6 | HG01891.hp1 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1806+101C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 16/47 | chr7 | 142154290 | |||||||
| chr7:142154355 | T | C | 2 | a0014c0020t0001g0001 a0038c0059t0001g0026 |
3 | HG02145.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1806+166T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 16/47 | chr7 | 142154355 | |||||||
| chr7:142154392 | C | A | 6 | a0022c0027t0001g0038 a0022c0027t0001g0040 a0023c0025t0001g0052 others(3): Show |
6 | HG01891.hp1 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1806+203C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 16/47 | chr7 | 142154392 | |||||||
| chr7:142154495 | G | A | 1 | a0015c0015t0001g0013 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1807-234G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 16/47 | chr7 | 142154495 | |||||||
| chr7:142154510 | G | A | 7 | a0001c0001t0001g0176 a0009c0011t0001g0023 a0009c0011t0001g0024 others(4): Show |
7 | HG00642.hp1 HG02451.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1807-219G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 16/47 | chr7 | 142154510 | |||||||
| chr7:142154582 | G | T | 6 | a0001c0001t0001g0080 a0001c0001t0001g0221 a0001c0004t0001g0157 others(3): Show |
6 | NA18983.hp1 NA18990.hp2 NA19007.hp1 others(3): Show |
intron_variant | MODIFIER | c.1807-147G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 16/47 | chr7 | 142154582 | |||||||
| chr7:142154636 | A | T | 52 | a0001c0001t0001g0060 a0001c0001t0001g0075 a0001c0001t0001g0095 others(49): Show |
52 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.1807-93A>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 16/47 | chr7 | 142154636 | |||||||
| chr7:142154648 | T | C | 5 | a0022c0027t0001g0038 a0022c0027t0001g0040 a0023c0025t0001g0052 others(2): Show |
5 | HG01891.hp1 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1807-81T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 16/47 | chr7 | 142154648 | |||||||
| chr7:142154859 | A | G | 53 | a0001c0001t0001g0060 a0001c0001t0001g0075 a0001c0001t0001g0095 others(50): Show |
53 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.1923+14A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 17/47 | chr7 | 142154859 | |||||||
| chr7:142155134 | T | A | 3 | a0001c0001t0001g0179 a0002c0003t0001g0241 a0017c0019t0001g0289 |
3 | HG03491.hp2 NA18965.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1923+289T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 17/47 | chr7 | 142155134 | |||||||
| chr7:142155393 | G | T | 85 | a0001c0001t0001g0071 a0001c0001t0001g0077 a0001c0001t0001g0097 others(82): Show |
86 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.1923+548G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 17/47 | chr7 | 142155393 | |||||||
| chr7:142155488 | A | G | 1 | a0002c0002t0001g0265 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1923+643A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 17/47 | chr7 | 142155488 | |||||||
| chr7:142155552 | T | C | 52 | a0001c0001t0001g0060 a0001c0001t0001g0075 a0001c0001t0001g0095 others(49): Show |
52 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.1923+707T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 17/47 | chr7 | 142155552 | |||||||
| chr7:142155590 | C | T | 1 | a0001c0004t0001g0046 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1923+745C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 17/47 | chr7 | 142155590 | |||||||
| chr7:142155752 | T | C | 1 | a0046c0077t0001g0195 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1923+907T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 17/47 | chr7 | 142155752 | |||||||
| chr7:142155822 | G | A | 1 | a0036c0049t0001g0275 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1923+977G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 17/47 | chr7 | 142155822 | |||||||
| chr7:142155867 | T | C | 5 | a0022c0027t0001g0038 a0022c0027t0001g0040 a0023c0025t0001g0052 others(2): Show |
5 | HG01891.hp1 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1923+1022T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 17/47 | chr7 | 142155867 | |||||||
| chr7:142155932 | G | A | 157 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0074 others(154): Show |
157 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1923+1087G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 17/47 | chr7 | 142155932 | |||||||
| chr7:142156012 | G | T | 5 | a0022c0027t0001g0038 a0022c0027t0001g0040 a0023c0025t0001g0052 others(2): Show |
5 | HG01891.hp1 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1923+1167G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 17/47 | chr7 | 142156012 | |||||||
| chr7:142156068 | C | T | 1 | a0036c0049t0001g0275 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1923+1223C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 17/47 | chr7 | 142156068 | |||||||
| chr7:142156131 | G | A | 1 | a0021c0023t0004g0057 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1923+1286G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 17/47 | chr7 | 142156131 | |||||||
| chr7:142156141 | G | A | 1 | a0002c0003t0001g0244 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1923+1296G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 17/47 | chr7 | 142156141 | |||||||
| chr7:142156155 | C | CA | 19 | a0001c0004t0001g0145 a0001c0004t0001g0164 a0002c0002t0001g0034 others(16): Show |
19 | HG00099.hp1 HG00735.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.1923+1321dupA | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 17/47 | INFO_REALIGN_3_PRIME | chr7 | 142156155 | ||||||
| chr7:142156157 | A | T | 3 | a0001c0001t0001g0179 a0002c0003t0001g0241 a0017c0019t0001g0289 |
3 | HG03491.hp2 NA18965.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1923+1312A>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 17/47 | chr7 | 142156157 | |||||||
| chr7:142156552 | C | G | 9 | a0001c0004t0001g0145 a0009c0011t0001g0025 a0016c0014t0001g0011 others(6): Show |
9 | HG01891.hp2 HG02622.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1924-1385C>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 17/47 | chr7 | 142156552 | |||||||
| chr7:142156588 | A | G | 5 | a0010c0017t0001g0240 a0011c0013t0001g0246 a0021c0023t0001g0194 others(2): Show |
5 | HG01516.hp1 HG01884.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.1924-1349A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 17/47 | chr7 | 142156588 | |||||||
| chr7:142156595 | A | G | 5 | a0022c0027t0001g0038 a0022c0027t0001g0040 a0023c0025t0001g0052 others(2): Show |
5 | HG01891.hp1 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1924-1342A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 17/47 | chr7 | 142156595 | |||||||
| chr7:142156873 | A | T | 1 | a0013c0016t0001g0173 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1924-1064A>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 17/47 | chr7 | 142156873 | |||||||
| chr7:142156874 | T | C | 138 | a0001c0001t0001g0060 a0001c0001t0001g0075 a0001c0001t0001g0077 others(135): Show |
139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.1924-1063T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 17/47 | chr7 | 142156874 | |||||||
| chr7:142156958 | T | C | 52 | a0001c0001t0001g0060 a0001c0001t0001g0075 a0001c0001t0001g0095 others(49): Show |
52 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.1924-979T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 17/47 | chr7 | 142156958 | |||||||
| chr7:142157044 | G | A | 1 | a0001c0004t0001g0278 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1924-893G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 17/47 | chr7 | 142157044 | |||||||
| chr7:142157085 | A | G | 1 | a0002c0003t0001g0261 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1924-852A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 17/47 | chr7 | 142157085 | |||||||
| chr7:142157210 | A | AT | 13 | a0002c0002t0001g0016 a0002c0002t0001g0043 a0002c0002t0001g0045 others(10): Show |
13 | HG01891.hp1 HG02257.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1924-718dupT | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 17/47 | INFO_REALIGN_3_PRIME | chr7 | 142157210 | ||||||
| chr7:142157237 | T | C | 2 | a0002c0003t0001g0225 a0002c0003t0001g0226 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1924-700T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 17/47 | chr7 | 142157237 | |||||||
| chr7:142157390 | C | A | 3 | a0001c0001t0001g0179 a0002c0003t0001g0241 a0017c0019t0001g0289 |
3 | HG03491.hp2 NA18965.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1924-547C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 17/47 | chr7 | 142157390 | |||||||
| chr7:142157393 | AT | A | 35 | a0001c0001t0001g0176 a0001c0004t0001g0046 a0001c0004t0001g0145 others(32): Show |
36 | HG00099.hp2 HG00642.hp1 HG01255.hp1 others(33): Show |
intron_variant | MODIFIER | c.1924-527delT | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 17/47 | INFO_REALIGN_3_PRIME | chr7 | 142157393 | ||||||
| chr7:142157393 | ATT | A | 76 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0074 others(73): Show |
76 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.1924-528_1924-527d others(4): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 17/47 | INFO_REALIGN_3_PRIME | chr7 | 142157393 | ||||||
| chr7:142157430 | T | A | 1 | a0019c0073t0001g0012 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1924-507T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 17/47 | chr7 | 142157430 | |||||||
| chr7:142157495 | A | G | 53 | a0001c0001t0001g0060 a0001c0001t0001g0075 a0001c0001t0001g0095 others(50): Show |
53 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.1924-442A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 17/47 | chr7 | 142157495 | |||||||
| chr7:142157925 | A | G | 2 | a0001c0004t0001g0201 a0044c0036t0001g0184 |
2 | HG02735.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1924-12A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 17/47 | chr7 | 142157925 | |||||||
| chr7:142157925 | A | T | 13 | a0001c0001t0001g0101 a0001c0001t0001g0112 a0001c0001t0001g0178 others(10): Show |
13 | HG02027.hp1 HG02135.hp1 NA18943.hp2 others(10): Show |
intron_variant | MODIFIER | c.1924-12A>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 17/47 | chr7 | 142157925 | |||||||
| chr7:142158185 | A | G | 86 | a0001c0001t0001g0077 a0001c0001t0001g0097 a0001c0001t0001g0107 others(83): Show |
87 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.2079-63A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 18/47 | chr7 | 142158185 | |||||||
| chr7:142158190 | G | A | 5 | a0022c0027t0001g0038 a0022c0027t0001g0040 a0023c0025t0001g0052 others(2): Show |
5 | HG01891.hp1 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.2079-58G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 18/47 | chr7 | 142158190 | |||||||
| chr7:142158478 | T | A | 2 | a0014c0026t0001g0196 a0014c0026t0001g0327 |
2 | HG01243.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2163+146T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 19/47 | chr7 | 142158478 | |||||||
| chr7:142158645 | T | C | 1 | a0002c0003t0001g0004 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2163+313T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 19/47 | chr7 | 142158645 | |||||||
| chr7:142158888 | G | A | 223 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(220): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.2164-399G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 19/47 | chr7 | 142158888 | |||||||
| chr7:142158960 | C | A | 1 | a0040c0043t0001g0059 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2164-327C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 19/47 | chr7 | 142158960 | |||||||
| chr7:142159011 | C | T | 1 | a0001c0004t0001g0262 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2164-276C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 19/47 | chr7 | 142159011 | |||||||
| chr7:142159267 | C | T | 1 | a0005c0006t0001g0238 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.2164-20C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 19/47 | chr7 | 142159267 | |||||||
| chr7:142159437 | T | C | 5 | a0022c0027t0001g0038 a0022c0027t0001g0040 a0023c0025t0001g0052 others(2): Show |
5 | HG01891.hp1 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.2220+94T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 20/47 | chr7 | 142159437 | |||||||
| chr7:142159635 | C | T | 1 | a0005c0006t0001g0248 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2220+292C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 20/47 | chr7 | 142159635 | |||||||
| chr7:142159650 | C | G | 64 | a0001c0001t0001g0101 a0001c0001t0001g0112 a0001c0001t0001g0178 others(61): Show |
64 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.2220+307C>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 20/47 | chr7 | 142159650 | |||||||
| chr7:142159675 | A | G | 1 | a0046c0077t0001g0195 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2220+332A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 20/47 | chr7 | 142159675 | |||||||
| chr7:142159686 | G | A | 4 | a0001c0004t0001g0046 a0014c0020t0001g0001 a0038c0059t0001g0026 others(1): Show |
5 | HG02145.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.2220+343G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 20/47 | chr7 | 142159686 | |||||||
| chr7:142159690 | C | T | 84 | a0001c0001t0001g0077 a0001c0001t0001g0097 a0001c0001t0001g0107 others(81): Show |
85 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.2220+347C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 20/47 | chr7 | 142159690 | |||||||
| chr7:142159888 | T | C | 1 | a0001c0004t0001g0278 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2221-246T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 20/47 | chr7 | 142159888 | |||||||
| chr7:142159943 | A | T | 1 | a0002c0003t0001g0323 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2221-191A>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 20/47 | chr7 | 142159943 | |||||||
| chr7:142159970 | C | T | 1 | a0002c0003t0001g0010 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2221-164C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 20/47 | chr7 | 142159970 | |||||||
| chr7:142160353 | C | G | 1 | a0002c0003t0001g0311 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2345+95C>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 21/47 | chr7 | 142160353 | |||||||
| chr7:142160391 | C | A | 7 | a0001c0001t0001g0140 a0002c0002t0001g0039 a0002c0002t0001g0284 others(4): Show |
7 | HG01261.hp2 HG02717.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.2345+133C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 21/47 | chr7 | 142160391 | |||||||
| chr7:142160399 | A | G | 47 | a0001c0001t0001g0060 a0001c0001t0001g0075 a0001c0001t0001g0095 others(44): Show |
47 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.2345+141A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 21/47 | chr7 | 142160399 | |||||||
| chr7:142160460 | G | A | 47 | a0001c0001t0001g0060 a0001c0001t0001g0075 a0001c0001t0001g0095 others(44): Show |
47 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.2345+202G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 21/47 | chr7 | 142160460 | |||||||
| chr7:142160566 | C | T | 2 | a0003c0009t0001g0053 a0003c0009t0001g0056 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2345+308C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 21/47 | chr7 | 142160566 | |||||||
| chr7:142160600 | G | T | 84 | a0001c0001t0001g0077 a0001c0001t0001g0097 a0001c0001t0001g0107 others(81): Show |
85 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.2345+342G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 21/47 | chr7 | 142160600 | |||||||
| chr7:142160846 | A | G | 1 | a0013c0016t0001g0173 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2346-279A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 21/47 | chr7 | 142160846 | |||||||
| chr7:142160990 | T | C | 5 | a0022c0027t0001g0038 a0022c0027t0001g0040 a0023c0025t0001g0052 others(2): Show |
5 | HG01891.hp1 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.2346-135T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 21/47 | chr7 | 142160990 | |||||||
| chr7:142161061 | T | C | 67 | a0001c0001t0001g0060 a0001c0001t0001g0075 a0001c0001t0001g0095 others(64): Show |
67 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.2346-64T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 21/47 | chr7 | 142161061 | |||||||
| chr7:142161062 | G | A | 6 | a0001c0004t0002g0065 a0002c0002t0001g0050 a0002c0003t0001g0049 others(3): Show |
6 | HG01884.hp2 HG02280.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.2346-63G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 21/47 | chr7 | 142161062 | |||||||
| chr7:142161258 | C | A | 2 | a0002c0003t0001g0020 a0006c0008t0001g0168 |
2 | HG00323.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.2434+45C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 22/47 | chr7 | 142161258 | |||||||
| chr7:142161272 | C | A | 47 | a0001c0001t0001g0060 a0001c0001t0001g0075 a0001c0001t0001g0095 others(44): Show |
47 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.2434+59C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 22/47 | chr7 | 142161272 | |||||||
| chr7:142161283 | G | T | 1 | a0015c0015t0001g0014 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2434+70G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 22/47 | chr7 | 142161283 | |||||||
| chr7:142161293 | G | A | 5 | a0001c0004t0001g0046 a0014c0020t0001g0001 a0036c0049t0001g0275 others(2): Show |
6 | HG02055.hp2 HG02145.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2434+80G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 22/47 | chr7 | 142161293 | |||||||
| chr7:142161405 | G | C | 1 | a0015c0015t0001g0029 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2434+192G>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 22/47 | chr7 | 142161405 | |||||||
| chr7:142161435 | A | G | 47 | a0001c0001t0001g0060 a0001c0001t0001g0075 a0001c0001t0001g0095 others(44): Show |
47 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.2434+222A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 22/47 | chr7 | 142161435 | |||||||
| chr7:142161451 | T | G | 67 | a0001c0001t0001g0060 a0001c0001t0001g0075 a0001c0001t0001g0095 others(64): Show |
67 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.2434+238T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 22/47 | chr7 | 142161451 | |||||||
| chr7:142161658 | G | A | 36 | a0001c0001t0001g0247 a0001c0001t0001g0267 a0001c0004t0001g0063 others(33): Show |
36 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.2435-297G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 22/47 | chr7 | 142161658 | |||||||
| chr7:142161669 | G | A | 47 | a0001c0001t0001g0060 a0001c0001t0001g0075 a0001c0001t0001g0095 others(44): Show |
47 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.2435-286G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 22/47 | chr7 | 142161669 | |||||||
| chr7:142161707 | G | A | 1 | a0006c0008t0001g0316 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2435-248G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 22/47 | chr7 | 142161707 | |||||||
| chr7:142161716 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2435-239G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 22/47 | chr7 | 142161716 | |||||||
| chr7:142161755 | G | A | 1 | a0050c0039t0001g0048 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2435-200G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 22/47 | chr7 | 142161755 | |||||||
| chr7:142162194 | A | G | 326 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(323): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.2484+190A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 23/47 | chr7 | 142162194 | |||||||
| chr7:142162241 | A | G | 245 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(242): Show |
245 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.2484+237A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 23/47 | chr7 | 142162241 | |||||||
| chr7:142162623 | A | G | 3 | a0001c0004t0001g0066 a0002c0002t0001g0199 a0015c0015t0001g0013 |
3 | HG02922.hp1 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2484+619A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 23/47 | chr7 | 142162623 | |||||||
| chr7:142162681 | T | C | 1 | a0007c0081t0001g0129 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2484+677T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 23/47 | chr7 | 142162681 | |||||||
| chr7:142162849 | G | C | 1 | a0001c0001t0001g0179 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2484+845G>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 23/47 | chr7 | 142162849 | |||||||
| chr7:142162881 | A | G | 207 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0074 others(204): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.2484+877A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 23/47 | chr7 | 142162881 | |||||||
| chr7:142162949 | A | C | 3 | a0002c0002t0001g0308 a0002c0003t0001g0049 a0002c0003t0001g0250 |
3 | HG01884.hp2 HG04228.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.2484+945A>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 23/47 | chr7 | 142162949 | |||||||
| chr7:142163040 | C | T | 76 | a0001c0001t0001g0131 a0001c0001t0001g0247 a0001c0001t0001g0267 others(73): Show |
76 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.2484+1036C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 23/47 | chr7 | 142163040 | |||||||
| chr7:142163172 | T | C | 2 | a0002c0003t0001g0228 a0002c0003t0001g0250 |
2 | HG02080.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.2484+1168T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 23/47 | chr7 | 142163172 | |||||||
| chr7:142163201 | C | G | 2 | a0016c0014t0001g0017 a0016c0014t0001g0018 |
2 | HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2484+1197C>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 23/47 | chr7 | 142163201 | |||||||
| chr7:142163367 | C | T | 32 | a0001c0001t0001g0140 a0002c0002t0001g0019 a0002c0002t0001g0039 others(29): Show |
32 | HG00140.hp1 HG00558.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.2484+1363C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 23/47 | chr7 | 142163367 | |||||||
| chr7:142163502 | G | A | 33 | a0001c0001t0001g0112 a0001c0001t0001g0153 a0001c0001t0001g0301 others(30): Show |
33 | HG00735.hp2 HG01884.hp2 HG02027.hp1 others(30): Show |
intron_variant | MODIFIER | c.2485-1354G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 23/47 | chr7 | 142163502 | |||||||
| chr7:142163584 | G | A | 1 | a0010c0017t0001g0240 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2485-1272G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 23/47 | chr7 | 142163584 | |||||||
| chr7:142163801 | C | T | 56 | a0001c0001t0001g0140 a0001c0001t0001g0176 a0001c0004t0001g0046 others(53): Show |
57 | HG00140.hp1 HG00558.hp1 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.2485-1055C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 23/47 | chr7 | 142163801 | |||||||
| chr7:142163956 | C | T | 48 | a0002c0002t0001g0264 a0002c0002t0001g0310 a0002c0003t0001g0312 others(45): Show |
48 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.2485-900C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 23/47 | chr7 | 142163956 | |||||||
| chr7:142164038 | C | T | 6 | a0014c0020t0001g0001 a0022c0027t0001g0038 a0022c0027t0001g0040 others(3): Show |
7 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2485-818C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 23/47 | chr7 | 142164038 | |||||||
| chr7:142164039 | G | A | 4 | a0001c0001t0001g0071 a0002c0002t0001g0209 a0002c0002t0001g0211 others(1): Show |
4 | NA19000.hp2 NA19004.hp2 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.2485-817G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 23/47 | chr7 | 142164039 | |||||||
| chr7:142164125 | G | A | 1 | a0013c0016t0001g0283 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2485-731G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 23/47 | chr7 | 142164125 | |||||||
| chr7:142164137 | A | C | 2 | a0024c0074t0001g0031 a0024c0075t0001g0185 |
2 | HG02630.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2485-719A>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 23/47 | chr7 | 142164137 | |||||||
| chr7:142164343 | A | G | 1 | a0001c0004t0001g0072 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2485-513A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 23/47 | chr7 | 142164343 | |||||||
| chr7:142164364 | C | T | 140 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(137): Show |
140 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.2485-492C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 23/47 | chr7 | 142164364 | |||||||
| chr7:142164365 | G | A | 2 | a0047c0070t0001g0147 a0048c0065t0002g0047 |
2 | HG03130.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2485-491G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 23/47 | chr7 | 142164365 | |||||||
| chr7:142164406 | A | G | 1 | a0036c0049t0001g0275 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2485-450A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 23/47 | chr7 | 142164406 | |||||||
| chr7:142164537 | G | A | 1 | a0036c0049t0001g0275 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2485-319G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 23/47 | chr7 | 142164537 | |||||||
| chr7:142164684 | T | C | 1 | a0033c0035t0003g0061 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2485-172T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 23/47 | chr7 | 142164684 | |||||||
| chr7:142164703 | C | T | 48 | a0002c0002t0001g0264 a0002c0002t0001g0310 a0002c0003t0001g0312 others(45): Show |
48 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.2485-153C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 23/47 | chr7 | 142164703 | |||||||
| chr7:142164704 | G | A | 1 | a0001c0004t0001g0072 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2485-152G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 23/47 | chr7 | 142164704 | |||||||
| chr7:142165067 | G | A | 1 | a0050c0039t0001g0048 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2652+44G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 24/47 | chr7 | 142165067 | |||||||
| chr7:142165069 | C | T | 9 | a0016c0014t0001g0011 a0016c0014t0001g0017 a0016c0014t0001g0018 others(6): Show |
9 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2652+46C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 24/47 | chr7 | 142165069 | |||||||
| chr7:142165239 | G | A | 48 | a0002c0002t0001g0264 a0002c0002t0001g0310 a0002c0003t0001g0312 others(45): Show |
48 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.2652+216G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 24/47 | chr7 | 142165239 | |||||||
| chr7:142165245 | C | T | 93 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(90): Show |
93 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.2652+222C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 24/47 | chr7 | 142165245 | |||||||
| chr7:142165468 | C | T | 3 | a0001c0004t0001g0066 a0002c0002t0001g0199 a0015c0015t0001g0013 |
3 | HG02922.hp1 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2652+445C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 24/47 | chr7 | 142165468 | |||||||
| chr7:142165758 | G | T | 3 | a0001c0001t0001g0176 a0039c0046t0001g0102 a0043c0048t0001g0103 |
3 | HG02451.hp1 HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2653-340G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 24/47 | chr7 | 142165758 | |||||||
| chr7:142165822 | G | A | 1 | a0002c0003t0001g0004 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2653-276G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 24/47 | chr7 | 142165822 | |||||||
| chr7:142165901 | T | G | 3 | a0001c0001t0001g0172 a0002c0002t0001g0035 a0002c0002t0001g0265 |
3 | HG01106.hp2 HG01123.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.2653-197T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 24/47 | chr7 | 142165901 | |||||||
| chr7:142166088 | C | T | 6 | a0001c0001t0001g0096 a0001c0052t0001g0109 a0002c0003t0001g0208 others(3): Show |
6 | HG00408.hp2 HG02080.hp2 HG04228.hp2 others(3): Show |
intron_variant | MODIFIER | c.2653-10C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 24/47 | chr7 | 142166088 | |||||||
| chr7:142166361 | C | T | 6 | a0001c0001t0001g0176 a0019c0030t0001g0200 a0019c0030t0002g0326 others(3): Show |
6 | HG01891.hp2 HG02451.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2808+108C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 25/47 | chr7 | 142166361 | |||||||
| chr7:142166702 | T | G | 93 | a0001c0001t0001g0112 a0001c0001t0001g0153 a0001c0001t0001g0301 others(90): Show |
94 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.2808+449T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 25/47 | chr7 | 142166702 | |||||||
| chr7:142166704 | T | C | 1 | a0005c0006t0001g0295 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2808+451T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 25/47 | chr7 | 142166704 | |||||||
| chr7:142166762 | T | TA | 6 | a0001c0001t0001g0096 a0001c0052t0001g0109 a0002c0003t0001g0208 others(3): Show |
6 | HG00408.hp2 HG02080.hp2 HG04228.hp2 others(3): Show |
intron_variant | MODIFIER | c.2809-499dupA | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 25/47 | INFO_REALIGN_3_PRIME | chr7 | 142166762 | ||||||
| chr7:142166973 | T | C | 3 | a0001c0001t0001g0117 a0001c0001t0001g0171 a0001c0004t0001g0192 |
3 | NA18993.hp2 NA19011.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.2809-295T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 25/47 | chr7 | 142166973 | |||||||
| chr7:142167005 | A | G | 1 | a0001c0004t0001g0046 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2809-263A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 25/47 | chr7 | 142167005 | |||||||
| chr7:142167072 | G | T | 1 | a0001c0001t0001g0060 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2809-196G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 25/47 | chr7 | 142167072 | |||||||
| chr7:142167497 | T | C | 6 | a0001c0001t0001g0096 a0001c0052t0001g0109 a0002c0003t0001g0208 others(3): Show |
6 | HG00408.hp2 HG02080.hp2 HG04228.hp2 others(3): Show |
intron_variant | MODIFIER | c.3027+11T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 26/47 | chr7 | 142167497 | |||||||
| chr7:142167522 | G | A | 1 | a0001c0004t0001g0167 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3027+36G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 26/47 | chr7 | 142167522 | |||||||
| chr7:142167579 | T | G | 1 | a0002c0003t0001g0258 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3027+93T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 26/47 | chr7 | 142167579 | |||||||
| chr7:142167597 | G | A | 10 | a0014c0020t0001g0001 a0014c0026t0001g0196 a0014c0026t0001g0327 others(7): Show |
11 | HG01243.hp1 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.3027+111G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 26/47 | chr7 | 142167597 | |||||||
| chr7:142167622 | G | C | 93 | a0001c0001t0001g0112 a0001c0001t0001g0153 a0001c0001t0001g0301 others(90): Show |
94 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.3027+136G>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 26/47 | chr7 | 142167622 | |||||||
| chr7:142167632 | G | A | 1 | a0009c0011t0001g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3027+146G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 26/47 | chr7 | 142167632 | |||||||
| chr7:142167722 | T | G | 186 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(183): Show |
187 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.3027+236T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 26/47 | chr7 | 142167722 | |||||||
| chr7:142167762 | G | A | 1 | a0001c0001t0001g0267 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.3027+276G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 26/47 | chr7 | 142167762 | |||||||
| chr7:142167840 | G | A | 1 | a0009c0011t0001g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3027+354G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 26/47 | chr7 | 142167840 | |||||||
| chr7:142167869 | G | A | 38 | a0002c0002t0001g0264 a0002c0002t0001g0310 a0002c0003t0001g0312 others(35): Show |
38 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.3027+383G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 26/47 | chr7 | 142167869 | |||||||
| chr7:142167994 | A | G | 1 | a0008c0010t0001g0051 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.3027+508A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 26/47 | chr7 | 142167994 | |||||||
| chr7:142168271 | C | CT | 7 | a0001c0001t0001g0096 a0001c0004t0001g0169 a0001c0052t0001g0109 others(4): Show |
7 | HG00408.hp2 HG00639.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.3027+800dupT | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr7 | 142168271 | ||||||
| chr7:142168271 | CT | C | 41 | a0001c0001t0001g0112 a0001c0001t0001g0153 a0001c0001t0001g0301 others(38): Show |
41 | HG00735.hp2 HG01884.hp2 HG02027.hp1 others(38): Show |
intron_variant | MODIFIER | c.3027+800delT | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr7 | 142168271 | ||||||
| chr7:142168373 | G | A | 7 | a0003c0007t0001g0093 a0003c0007t0001g0142 a0003c0009t0001g0118 others(4): Show |
7 | HG00140.hp2 HG00642.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.3027+887G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 26/47 | chr7 | 142168373 | |||||||
| chr7:142168405 | G | T | 1 | a0002c0002t0001g0021 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3027+919G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 26/47 | chr7 | 142168405 | |||||||
| chr7:142168427 | G | A | 1 | a0035c0067t0003g0146 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3027+941G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 26/47 | chr7 | 142168427 | |||||||
| chr7:142168445 | A | G | 2 | a0001c0001t0001g0074 a0006c0008t0001g0094 |
2 | HG01517.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.3027+959A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 26/47 | chr7 | 142168445 | |||||||
| chr7:142168463 | T | C | 1 | a0002c0003t0001g0261 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.3027+977T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 26/47 | chr7 | 142168463 | |||||||
| chr7:142168565 | C | T | 1 | a0009c0011t0001g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3027+1079C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 26/47 | chr7 | 142168565 | |||||||
| chr7:142168578 | C | T | 2 | a0008c0010t0001g0222 a0017c0019t0001g0220 |
2 | HG00438.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.3027+1092C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 26/47 | chr7 | 142168578 | |||||||
| chr7:142168580 | G | T | 3 | a0019c0030t0001g0200 a0019c0030t0002g0326 a0019c0073t0001g0012 |
3 | HG01891.hp2 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.3027+1094G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 26/47 | chr7 | 142168580 | |||||||
| chr7:142168758 | T | C | 1 | a0002c0003t0001g0311 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3027+1272T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 26/47 | chr7 | 142168758 | |||||||
| chr7:142168760 | T | TTTTA | 48 | a0002c0002t0001g0264 a0002c0002t0001g0310 a0002c0003t0001g0312 others(45): Show |
48 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.3027+1275_3027+127 others(8): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr7 | 142168760 | ||||||
| chr7:142168896 | C | G | 2 | a0024c0074t0001g0031 a0024c0075t0001g0185 |
2 | HG02630.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3028-1179C>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 26/47 | chr7 | 142168896 | |||||||
| chr7:142168945 | C | G | 5 | a0001c0004t0002g0065 a0002c0003t0002g0230 a0002c0003t0002g0251 others(2): Show |
5 | HG02055.hp1 HG02970.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.3028-1130C>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 26/47 | chr7 | 142168945 | |||||||
| chr7:142169094 | T | C | 1 | a0001c0004t0001g0046 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3028-981T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 26/47 | chr7 | 142169094 | |||||||
| chr7:142169169 | A | G | 231 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(228): Show |
232 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.3028-906A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 26/47 | chr7 | 142169169 | |||||||
| chr7:142169224 | C | A | 2 | a0014c0020t0001g0001 a0038c0059t0001g0026 |
3 | HG02145.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.3028-851C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 26/47 | chr7 | 142169224 | |||||||
| chr7:142169360 | C | T | 220 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(217): Show |
221 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.3028-715C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 26/47 | chr7 | 142169360 | |||||||
| chr7:142169361 | G | A | 2 | a0001c0001t0001g0108 a0002c0003t0001g0088 |
2 | HG03710.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.3028-714G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 26/47 | chr7 | 142169361 | |||||||
| chr7:142169442 | A | G | 6 | a0001c0001t0001g0112 a0001c0001t0001g0153 a0001c0004t0001g0160 others(3): Show |
6 | HG02027.hp1 NA18947.hp1 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.3028-633A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 26/47 | chr7 | 142169442 | |||||||
| chr7:142169545 | C | T | 33 | a0001c0001t0001g0112 a0001c0001t0001g0153 a0001c0001t0001g0301 others(30): Show |
33 | HG00735.hp2 HG01884.hp2 HG02027.hp1 others(30): Show |
intron_variant | MODIFIER | c.3028-530C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 26/47 | chr7 | 142169545 | |||||||
| chr7:142170056 | T | G | 1 | a0001c0001t0001g0060 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3028-19T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 26/47 | chr7 | 142170056 | |||||||
| chr7:142170334 | G | T | 174 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(171): Show |
174 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.3182+105G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 27/47 | chr7 | 142170334 | |||||||
| chr7:142170519 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.3182+290G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 27/47 | chr7 | 142170519 | |||||||
| chr7:142170700 | C | T | 2 | a0002c0002t0001g0043 a0002c0002t0001g0045 |
2 | HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.3182+471C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 27/47 | chr7 | 142170700 | |||||||
| chr7:142170743 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.3182+514G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 27/47 | chr7 | 142170743 | |||||||
| chr7:142170910 | G | C | 3 | a0001c0001t0001g0176 a0039c0046t0001g0102 a0043c0048t0001g0103 |
3 | HG02451.hp1 HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3183-362G>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 27/47 | chr7 | 142170910 | |||||||
| chr7:142171451 | A | T | 184 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(181): Show |
185 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.3351+11A>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 28/47 | chr7 | 142171451 | |||||||
| chr7:142171506 | C | G | 6 | a0001c0001t0001g0176 a0019c0030t0001g0200 a0019c0030t0002g0326 others(3): Show |
6 | HG01891.hp2 HG02451.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.3351+66C>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 28/47 | chr7 | 142171506 | |||||||
| chr7:142171604 | G | T | 33 | a0001c0001t0001g0112 a0001c0001t0001g0153 a0001c0001t0001g0301 others(30): Show |
33 | HG00735.hp2 HG01884.hp2 HG02027.hp1 others(30): Show |
intron_variant | MODIFIER | c.3351+164G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 28/47 | chr7 | 142171604 | |||||||
| chr7:142171605 | C | CAT | 4 | a0001c0001t0001g0060 a0001c0001t0001g0077 a0001c0004t0001g0072 others(1): Show |
4 | HG01257.hp2 HG01261.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.3351+214_3351+215d others(4): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 28/47 | INFO_REALIGN_3_PRIME | chr7 | 142171605 | ||||||
| chr7:142171605 | C | CATAT | 6 | a0001c0001t0001g0097 a0001c0001t0001g0122 a0001c0001t0001g0313 others(3): Show |
6 | HG01081.hp1 HG02040.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.3351+212_3351+215d others(6): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 28/47 | INFO_REALIGN_3_PRIME | chr7 | 142171605 | ||||||
| chr7:142171605 | CAT | C | 23 | a0001c0001t0001g0181 a0001c0001t0001g0272 a0001c0001t0001g0328 others(20): Show |
23 | HG00642.hp1 HG00735.hp1 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.3351+214_3351+215d others(4): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 28/47 | INFO_REALIGN_3_PRIME | chr7 | 142171605 | ||||||
| chr7:142171605 | CATAT | C | 59 | a0001c0001t0001g0075 a0001c0001t0001g0125 a0001c0001t0001g0154 others(56): Show |
59 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.3351+212_3351+215d others(6): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 28/47 | INFO_REALIGN_3_PRIME | chr7 | 142171605 | ||||||
| chr7:142171605 | CATATAT | C | 35 | a0001c0001t0001g0067 a0001c0001t0001g0080 a0001c0001t0001g0107 others(32): Show |
35 | HG00423.hp2 HG00639.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.3351+210_3351+215d others(8): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 28/47 | INFO_REALIGN_3_PRIME | chr7 | 142171605 | ||||||
| chr7:142171605 | CATATATA others(1): Show |
C | 34 | a0001c0001t0001g0071 a0001c0001t0001g0087 a0001c0001t0001g0101 others(31): Show |
34 | HG00558.hp2 HG00609.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.3351+208_3351+215d others(10): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 28/47 | INFO_REALIGN_3_PRIME | chr7 | 142171605 | ||||||
| chr7:142171605 | CATATATA others(3): Show |
C | 12 | a0001c0001t0001g0074 a0001c0001t0001g0116 a0001c0001t0001g0260 others(9): Show |
12 | HG00280.hp2 HG01168.hp1 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.3351+206_3351+215d others(12): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 28/47 | INFO_REALIGN_3_PRIME | chr7 | 142171605 | ||||||
| chr7:142171605 | CATATATA others(5): Show |
C | 1 | a0015c0015t0001g0014 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3351+204_3351+215d others(14): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 28/47 | INFO_REALIGN_3_PRIME | chr7 | 142171605 | ||||||
| chr7:142171605 | CATATATA others(7): Show |
C | 1 | a0002c0002t0001g0291 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3351+202_3351+215d others(16): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 28/47 | INFO_REALIGN_3_PRIME | chr7 | 142171605 | ||||||
| chr7:142171605 | CATATATA others(9): Show |
C | 4 | a0002c0002t0001g0050 a0002c0003t0001g0049 a0002c0003t0001g0228 others(1): Show |
4 | HG00408.hp2 HG01884.hp2 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.3351+200_3351+215d others(18): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 28/47 | INFO_REALIGN_3_PRIME | chr7 | 142171605 | ||||||
| chr7:142171605 | CATATATA others(11): Show |
C | 12 | a0001c0001t0001g0096 a0001c0001t0001g0176 a0001c0052t0001g0109 others(9): Show |
12 | HG02155.hp1 HG02451.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.3351+198_3351+215d others(20): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 28/47 | INFO_REALIGN_3_PRIME | chr7 | 142171605 | ||||||
| chr7:142171605 | CATATATA others(13): Show |
C | 12 | a0001c0004t0002g0065 a0002c0002t0001g0008 a0002c0003t0002g0230 others(9): Show |
12 | HG02486.hp2 HG02970.hp1 HG02976.hp2 others(9): Show |
intron_variant | MODIFIER | c.3351+196_3351+215d others(22): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 28/47 | INFO_REALIGN_3_PRIME | chr7 | 142171605 | ||||||
| chr7:142171605 | CATATATA others(15): Show |
C | 23 | a0001c0001t0001g0112 a0001c0001t0001g0153 a0001c0001t0001g0301 others(20): Show |
23 | HG00735.hp2 HG02027.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.3351+194_3351+215d others(24): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 28/47 | INFO_REALIGN_3_PRIME | chr7 | 142171605 | ||||||
| chr7:142171605 | CATATATA others(17): Show |
C | 15 | a0001c0001t0001g0117 a0002c0003t0001g0255 a0004c0005t0001g0111 others(12): Show |
16 | HG00423.hp1 HG01243.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.3351+192_3351+215d others(26): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 28/47 | INFO_REALIGN_3_PRIME | chr7 | 142171605 | ||||||
| chr7:142171605 | CATATATA others(19): Show |
C | 20 | a0002c0002t0001g0019 a0002c0002t0001g0021 a0004c0005t0001g0100 others(17): Show |
20 | HG00140.hp1 HG00558.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.3351+190_3351+215d others(28): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 28/47 | INFO_REALIGN_3_PRIME | chr7 | 142171605 | ||||||
| chr7:142171605 | CATATATA others(21): Show |
C | 1 | a0003c0007t0001g0070 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3351+188_3351+215d others(30): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 28/47 | INFO_REALIGN_3_PRIME | chr7 | 142171605 | ||||||
| chr7:142171605 | CATATATA others(23): Show |
C | 44 | a0002c0002t0001g0264 a0002c0002t0001g0310 a0002c0003t0001g0312 others(41): Show |
44 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.3351+186_3351+215d others(32): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 28/47 | INFO_REALIGN_3_PRIME | chr7 | 142171605 | ||||||
| chr7:142171625 | T | TCCACAAC others(35): Show |
2 | a0024c0074t0001g0031 a0024c0075t0001g0185 |
2 | HG02630.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3351+185_3351+186i others(44): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 28/47 | chr7 | 142171625 | |||||||
| chr7:142171627 | T | G | 2 | a0024c0074t0001g0031 a0024c0075t0001g0185 |
2 | HG02630.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3351+187T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 28/47 | chr7 | 142171627 | |||||||
| chr7:142171628 | A | T | 2 | a0024c0074t0001g0031 a0024c0075t0001g0185 |
2 | HG02630.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3351+188A>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 28/47 | chr7 | 142171628 | |||||||
| chr7:142171632 | A | G | 2 | a0024c0074t0001g0031 a0024c0075t0001g0185 |
2 | HG02630.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3351+192A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 28/47 | chr7 | 142171632 | |||||||
| chr7:142171633 | T | G | 2 | a0024c0074t0001g0031 a0024c0075t0001g0185 |
2 | HG02630.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3351+193T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 28/47 | chr7 | 142171633 | |||||||
| chr7:142171654 | A | C | 7 | a0001c0001t0001g0267 a0002c0003t0001g0225 a0002c0003t0001g0226 others(4): Show |
7 | HG01074.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.3351+214A>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 28/47 | chr7 | 142171654 | |||||||
| chr7:142171679 | G | A | 141 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(138): Show |
141 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.3351+239G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 28/47 | chr7 | 142171679 | |||||||
| chr7:142171757 | A | G | 2 | a0002c0003t0001g0007 a0005c0006t0001g0006 |
2 | HG01074.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.3351+317A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 28/47 | chr7 | 142171757 | |||||||
| chr7:142171758 | T | C | 47 | a0002c0002t0001g0264 a0002c0002t0001g0310 a0002c0003t0001g0312 others(44): Show |
47 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.3351+318T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 28/47 | chr7 | 142171758 | |||||||
| chr7:142171761 | C | G | 2 | a0024c0074t0001g0031 a0024c0075t0001g0185 |
2 | HG02630.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3351+321C>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 28/47 | chr7 | 142171761 | |||||||
| chr7:142171819 | G | A | 2 | a0002c0002t0001g0050 a0002c0003t0001g0049 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.3352-279G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 28/47 | chr7 | 142171819 | |||||||
| chr7:142171838 | G | A | 47 | a0002c0002t0001g0264 a0002c0002t0001g0310 a0002c0003t0001g0312 others(44): Show |
47 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.3352-260G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 28/47 | chr7 | 142171838 | |||||||
| chr7:142171986 | G | A | 1 | a0001c0004t0001g0170 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.3352-112G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 28/47 | chr7 | 142171986 | |||||||
| chr7:142172061 | G | A | 4 | a0001c0004t0002g0065 a0002c0003t0002g0230 a0002c0003t0002g0251 others(1): Show |
4 | HG02970.hp1 HG02976.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3352-37G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 28/47 | chr7 | 142172061 | |||||||
| chr7:142172235 | C | T | 1 | a0001c0004t0001g0183 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.3448+41C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 29/47 | chr7 | 142172235 | |||||||
| chr7:142172242 | C | T | 3 | a0009c0011t0001g0023 a0009c0011t0001g0024 a0049c0064t0001g0027 |
3 | HG00642.hp1 HG03540.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3448+48C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 29/47 | chr7 | 142172242 | |||||||
| chr7:142172257 | T | G | 6 | a0001c0001t0001g0096 a0001c0052t0001g0109 a0002c0003t0001g0208 others(3): Show |
6 | HG00408.hp2 HG02080.hp2 HG04228.hp2 others(3): Show |
intron_variant | MODIFIER | c.3448+63T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 29/47 | chr7 | 142172257 | |||||||
| chr7:142172266 | T | C | 1 | a0001c0004t0001g0046 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3448+72T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 29/47 | chr7 | 142172266 | |||||||
| chr7:142172288 | G | T | 1 | a0002c0058t0001g0032 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3448+94G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 29/47 | chr7 | 142172288 | |||||||
| chr7:142172299 | G | A | 1 | a0052c0071t0001g0162 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3448+105G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 29/47 | chr7 | 142172299 | |||||||
| chr7:142172427 | TG | T | 103 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(100): Show |
103 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.3449-224delG | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 29/47 | chr7 | 142172427 | |||||||
| chr7:142172786 | C | A | 1 | a0010c0017t0001g0240 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3561+22C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 30/47 | chr7 | 142172786 | |||||||
| chr7:142173012 | C | T | 1 | a0011c0013t0001g0054 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.3562-217C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 30/47 | chr7 | 142173012 | |||||||
| chr7:142173052 | C | T | 3 | a0001c0001t0001g0176 a0039c0046t0001g0102 a0043c0048t0001g0103 |
3 | HG02451.hp1 HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3562-177C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 30/47 | chr7 | 142173052 | |||||||
| chr7:142173074 | T | C | 206 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(203): Show |
207 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.3562-155T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 30/47 | chr7 | 142173074 | |||||||
| chr7:142173075 | G | A | 6 | a0022c0027t0001g0038 a0022c0027t0001g0040 a0023c0025t0001g0052 others(3): Show |
6 | HG01891.hp1 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.3562-154G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 30/47 | chr7 | 142173075 | |||||||
| chr7:142173092 | G | A | 206 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(203): Show |
207 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.3562-137G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 30/47 | chr7 | 142173092 | |||||||
| chr7:142173106 | T | C | 1 | a0007c0080t0001g0076 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3562-123T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 30/47 | chr7 | 142173106 | |||||||
| chr7:142173196 | A | G | 79 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(76): Show |
80 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.3562-33A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 30/47 | chr7 | 142173196 | |||||||
| chr7:142173200 | T | A | 195 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(192): Show |
196 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.3562-29T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 30/47 | chr7 | 142173200 | |||||||
| chr7:142173682 | G | A | 5 | a0014c0020t0001g0001 a0014c0026t0001g0196 a0014c0026t0001g0327 others(2): Show |
6 | HG01243.hp1 HG02145.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.3687+328G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | chr7 | 142173682 | |||||||
| chr7:142173803 | T | G | 2 | a0024c0074t0001g0031 a0024c0075t0001g0185 |
2 | HG02630.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3687+449T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | chr7 | 142173803 | |||||||
| chr7:142173818 | G | A | 3 | a0001c0001t0001g0176 a0039c0046t0001g0102 a0043c0048t0001g0103 |
3 | HG02451.hp1 HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3687+464G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | chr7 | 142173818 | |||||||
| chr7:142174185 | A | C | 23 | a0002c0002t0001g0008 a0002c0002t0001g0016 a0002c0002t0001g0043 others(20): Show |
23 | HG00735.hp2 HG01884.hp2 HG02155.hp1 others(20): Show |
intron_variant | MODIFIER | c.3687+831A>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | chr7 | 142174185 | |||||||
| chr7:142174647 | A | G | 3 | a0001c0001t0001g0176 a0039c0046t0001g0102 a0043c0048t0001g0103 |
3 | HG02451.hp1 HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3688-1005A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | chr7 | 142174647 | |||||||
| chr7:142174711 | C | T | 3 | a0001c0001t0001g0176 a0039c0046t0001g0102 a0043c0048t0001g0103 |
3 | HG02451.hp1 HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3688-941C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | chr7 | 142174711 | |||||||
| chr7:142174715 | C | CT | 10 | a0001c0001t0001g0074 a0001c0001t0001g0096 a0001c0001t0001g0125 others(7): Show |
10 | HG00280.hp2 HG00735.hp1 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.3688-919dupT | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr7 | 142174715 | ||||||
| chr7:142174715 | C | CTCTTTTT others(3): Show |
6 | a0022c0027t0001g0038 a0022c0027t0001g0040 a0023c0025t0001g0052 others(3): Show |
6 | HG01891.hp1 HG01952.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.3688-936_3688-935i others(12): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr7 | 142174715 | ||||||
| chr7:142174715 | C | CTTTTTTT | 6 | a0001c0001t0001g0176 a0007c0033t0001g0155 a0014c0020t0001g0001 others(3): Show |
7 | HG02145.hp2 HG02451.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.3688-925_3688-919d others(9): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr7 | 142174715 | ||||||
| chr7:142174715 | C | CTTTTTTT others(1): Show |
18 | a0002c0002t0001g0008 a0002c0002t0001g0016 a0002c0002t0001g0043 others(15): Show |
18 | HG00735.hp2 HG01884.hp2 HG02155.hp1 others(15): Show |
intron_variant | MODIFIER | c.3688-926_3688-919d others(10): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr7 | 142174715 | ||||||
| chr7:142174715 | C | CTTTTTTT others(3): Show |
1 | a0063c0041t0001g0139 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3688-928_3688-919d others(12): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr7 | 142174715 | ||||||
| chr7:142174715 | C | CTTTTTTT others(4): Show |
32 | a0003c0007t0001g0070 a0003c0007t0001g0093 a0003c0007t0001g0120 others(29): Show |
32 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.3688-929_3688-919d others(13): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr7 | 142174715 | ||||||
| chr7:142174715 | C | CTTTTTTT others(5): Show |
13 | a0003c0007t0001g0082 a0003c0007t0001g0104 a0003c0007t0001g0136 others(10): Show |
13 | HG00621.hp2 HG02135.hp2 HG03041.hp1 others(10): Show |
intron_variant | MODIFIER | c.3688-930_3688-919d others(14): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr7 | 142174715 | ||||||
| chr7:142174715 | C | CTTTTTTT others(6): Show |
2 | a0011c0022t0001g0279 a0035c0067t0003g0146 |
2 | HG01167.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.3688-931_3688-919d others(15): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr7 | 142174715 | ||||||
| chr7:142174715 | C | CTTTTTTT others(7): Show |
17 | a0002c0002t0001g0019 a0002c0002t0001g0021 a0004c0005t0001g0100 others(14): Show |
17 | HG00140.hp1 HG00558.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.3688-932_3688-919d others(16): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr7 | 142174715 | ||||||
| chr7:142174715 | C | CTTTTTTT others(8): Show |
7 | a0001c0001t0001g0071 a0001c0004t0001g0191 a0002c0003t0001g0004 others(4): Show |
7 | HG01168.hp1 HG02129.hp2 HG04199.hp1 others(4): Show |
intron_variant | MODIFIER | c.3688-933_3688-919d others(17): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr7 | 142174715 | ||||||
| chr7:142174715 | C | CTTTTTTT others(9): Show |
2 | a0010c0017t0001g0256 a0010c0017t0001g0302 |
2 | HG01074.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.3688-934_3688-919d others(18): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr7 | 142174715 | ||||||
| chr7:142174715 | C | CTTTTTTT others(11): Show |
1 | a0009c0011t0001g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3688-936_3688-919d others(20): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr7 | 142174715 | ||||||
| chr7:142174715 | C | CTTTTTTT others(12): Show |
5 | a0001c0001t0001g0140 a0002c0002t0001g0039 a0002c0002t0001g0285 others(2): Show |
5 | HG01261.hp2 HG02717.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.3688-919_3688-918i others(21): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr7 | 142174715 | ||||||
| chr7:142174715 | C | CTTTTTTT others(13): Show |
1 | a0002c0002t0001g0284 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3688-919_3688-918i others(22): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr7 | 142174715 | ||||||
| chr7:142174715 | C | CTTTTTTT others(14): Show |
1 | a0045c0061t0001g0044 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3688-919_3688-918i others(23): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr7 | 142174715 | ||||||
| chr7:142174715 | C | CTTTTTTT others(15): Show |
2 | a0009c0011t0001g0023 a0009c0011t0001g0024 |
2 | HG00642.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3688-919_3688-918i others(24): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr7 | 142174715 | ||||||
| chr7:142174715 | C | CTTTTTTT others(17): Show |
15 | a0001c0001t0001g0179 a0001c0001t0001g0268 a0001c0001t0001g0277 others(12): Show |
15 | HG01081.hp2 HG01255.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.3688-919_3688-918i others(26): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr7 | 142174715 | ||||||
| chr7:142174715 | C | CTTTTTTT others(18): Show |
15 | a0001c0001t0001g0067 a0001c0001t0001g0087 a0001c0001t0001g0117 others(12): Show |
15 | HG00423.hp2 HG00558.hp2 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.3688-919_3688-918i others(27): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr7 | 142174715 | ||||||
| chr7:142174715 | C | CTTTTTTT others(19): Show |
9 | a0001c0004t0001g0170 a0002c0002t0001g0151 a0002c0002t0001g0304 others(6): Show |
9 | HG02015.hp2 HG03017.hp2 HG04184.hp1 others(6): Show |
intron_variant | MODIFIER | c.3688-919_3688-918i others(28): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr7 | 142174715 | ||||||
| chr7:142174715 | C | CTTTTTTT others(20): Show |
4 | a0001c0001t0001g0180 a0002c0003t0001g0002 a0002c0003t0001g0003 others(1): Show |
4 | HG01516.hp2 HG01517.hp1 HG02015.hp1 others(1): Show |
intron_variant | MODIFIER | c.3688-919_3688-918i others(29): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr7 | 142174715 | ||||||
| chr7:142174715 | C | CTTTTTTT others(21): Show |
5 | a0001c0001t0001g0080 a0001c0001t0001g0218 a0001c0004t0001g0157 others(2): Show |
5 | HG01433.hp2 HG02735.hp2 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.3688-919_3688-918i others(30): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr7 | 142174715 | ||||||
| chr7:142174715 | C | CTTTTTTT others(22): Show |
2 | a0001c0001t0001g0171 a0059c0057t0001g0206 |
2 | NA18993.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.3688-919_3688-918i others(31): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr7 | 142174715 | ||||||
| chr7:142174715 | C | CTTTTTTT others(23): Show |
4 | a0001c0004t0001g0134 a0001c0004t0001g0158 a0001c0004t0001g0192 others(1): Show |
4 | NA18948.hp1 NA18962.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.3688-919_3688-918i others(32): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr7 | 142174715 | ||||||
| chr7:142174715 | C | CTTTTTTT others(24): Show |
2 | a0001c0004t0001g0163 a0002c0002t0001g0211 |
2 | NA18973.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.3688-919_3688-918i others(33): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr7 | 142174715 | ||||||
| chr7:142174715 | C | CTTTTTTT others(25): Show |
2 | a0001c0001t0001g0154 a0002c0002t0001g0288 |
2 | NA18998.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.3688-919_3688-918i others(34): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr7 | 142174715 | ||||||
| chr7:142174715 | CT | C | 7 | a0001c0001t0001g0060 a0001c0001t0001g0131 a0001c0004t0001g0089 others(4): Show |
7 | HG02165.hp1 HG02165.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.3688-919delT | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr7 | 142174715 | ||||||
| chr7:142174737 | T | A | 196 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(193): Show |
197 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.3688-915T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | chr7 | 142174737 | |||||||
| chr7:142174823 | C | G | 2 | a0001c0001t0001g0074 a0006c0008t0001g0094 |
2 | HG01517.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.3688-829C>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | chr7 | 142174823 | |||||||
| chr7:142174855 | A | G | 2 | a0047c0070t0001g0147 a0048c0065t0002g0047 |
2 | HG03130.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.3688-797A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | chr7 | 142174855 | |||||||
| chr7:142174872 | A | C | 80 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(77): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.3688-780A>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | chr7 | 142174872 | |||||||
| chr7:142174893 | A | G | 33 | a0001c0001t0001g0140 a0002c0002t0001g0019 a0002c0002t0001g0021 others(30): Show |
33 | HG00140.hp1 HG00558.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.3688-759A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | chr7 | 142174893 | |||||||
| chr7:142174970 | C | T | 1 | a0001c0004t0001g0046 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3688-682C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | chr7 | 142174970 | |||||||
| chr7:142175034 | C | T | 1 | a0002c0003t0001g0208 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.3688-618C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | chr7 | 142175034 | |||||||
| chr7:142175071 | A | G | 80 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(77): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.3688-581A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | chr7 | 142175071 | |||||||
| chr7:142175103 | G | T | 77 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(74): Show |
77 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.3688-549G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | chr7 | 142175103 | |||||||
| chr7:142175236 | T | A | 71 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(68): Show |
71 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.3688-416T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | chr7 | 142175236 | |||||||
| chr7:142175283 | C | G | 23 | a0002c0002t0001g0008 a0002c0002t0001g0016 a0002c0002t0001g0043 others(20): Show |
23 | HG00735.hp2 HG01884.hp2 HG02155.hp1 others(20): Show |
intron_variant | MODIFIER | c.3688-369C>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | chr7 | 142175283 | |||||||
| chr7:142175427 | CAGA | C | 32 | a0001c0001t0001g0140 a0002c0002t0001g0019 a0002c0002t0001g0021 others(29): Show |
32 | HG00140.hp1 HG00558.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.3688-222_3688-220d others(5): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr7 | 142175427 | ||||||
| chr7:142175429 | G | C | 1 | a0012c0012t0001g0324 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.3688-223G>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | chr7 | 142175429 | |||||||
| chr7:142175467 | C | A | 80 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(77): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.3688-185C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | chr7 | 142175467 | |||||||
| chr7:142175602 | G | T | 1 | a0024c0075t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3688-50G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | chr7 | 142175602 | |||||||
| chr7:142175631 | C | T | 80 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(77): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.3688-21C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 31/47 | chr7 | 142175631 | |||||||
| chr7:142175794 | C | A | 80 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(77): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.3816+14C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142175794 | |||||||
| chr7:142175870 | C | T | 3 | a0001c0001t0001g0328 a0001c0004t0001g0134 a0002c0002t0001g0298 |
3 | NA18941.hp2 NA18955.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.3816+90C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142175870 | |||||||
| chr7:142175871 | C | G | 80 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(77): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.3816+91C>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142175871 | |||||||
| chr7:142175918 | T | C | 1 | a0005c0006t0001g0254 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3816+138T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142175918 | |||||||
| chr7:142176095 | C | CAAAA | 9 | a0001c0001t0001g0096 a0001c0052t0001g0109 a0002c0003t0001g0208 others(6): Show |
9 | HG00408.hp2 HG01891.hp2 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.3816+325_3816+328d others(6): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | INFO_REALIGN_3_PRIME | chr7 | 142176095 | ||||||
| chr7:142176095 | C | CAAAAAA | 67 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(64): Show |
67 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.3816+323_3816+328d others(8): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | INFO_REALIGN_3_PRIME | chr7 | 142176095 | ||||||
| chr7:142176095 | CA | C | 62 | a0001c0001t0001g0140 a0002c0002t0001g0008 a0002c0002t0001g0016 others(59): Show |
62 | HG00140.hp1 HG00558.hp1 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.3816+328delA | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | INFO_REALIGN_3_PRIME | chr7 | 142176095 | ||||||
| chr7:142176107 | AAG | A | 48 | a0003c0007t0001g0070 a0003c0007t0001g0082 a0003c0007t0001g0093 others(45): Show |
48 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.3816+328_3816+329d others(4): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142176107 | |||||||
| chr7:142176110 | G | T | 80 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(77): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.3816+330G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142176110 | |||||||
| chr7:142176173 | T | C | 1 | a0001c0001t0001g0101 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.3816+393T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142176173 | |||||||
| chr7:142176185 | G | T | 1 | a0001c0001t0001g0077 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.3816+405G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142176185 | |||||||
| chr7:142176319 | C | T | 209 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(206): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.3816+539C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142176319 | |||||||
| chr7:142176398 | C | T | 33 | a0001c0001t0001g0140 a0002c0002t0001g0019 a0002c0002t0001g0021 others(30): Show |
33 | HG00140.hp1 HG00558.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.3816+618C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142176398 | |||||||
| chr7:142176412 | C | T | 1 | a0047c0070t0001g0147 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3816+632C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142176412 | |||||||
| chr7:142176413 | G | A | 80 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(77): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.3816+633G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142176413 | |||||||
| chr7:142176466 | TGTGTGAG others(1): Show |
T | 80 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(77): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.3816+690_3816+697d others(10): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | INFO_REALIGN_3_PRIME | chr7 | 142176466 | ||||||
| chr7:142176623 | G | T | 30 | a0001c0001t0001g0140 a0002c0002t0001g0019 a0002c0002t0001g0021 others(27): Show |
30 | HG00140.hp1 HG00558.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.3816+843G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142176623 | |||||||
| chr7:142176676 | TAGAC | T | 80 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(77): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.3816+900_3816+903d others(6): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | INFO_REALIGN_3_PRIME | chr7 | 142176676 | ||||||
| chr7:142176702 | T | C | 52 | a0003c0007t0001g0070 a0003c0007t0001g0082 a0003c0007t0001g0093 others(49): Show |
52 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.3816+922T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142176702 | |||||||
| chr7:142176827 | T | C | 1 | a0002c0003t0001g0208 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.3816+1047T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142176827 | |||||||
| chr7:142176866 | A | G | 80 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(77): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.3816+1086A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142176866 | |||||||
| chr7:142176885 | C | T | 4 | a0004c0005t0001g0100 a0010c0017t0001g0286 a0011c0022t0001g0161 others(1): Show |
4 | HG00558.hp1 HG01069.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.3816+1105C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142176885 | |||||||
| chr7:142177001 | G | T | 80 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(77): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.3816+1221G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142177001 | |||||||
| chr7:142177026 | T | C | 6 | a0001c0001t0001g0096 a0001c0052t0001g0109 a0002c0003t0001g0208 others(3): Show |
6 | HG00408.hp2 HG02080.hp2 HG04228.hp2 others(3): Show |
intron_variant | MODIFIER | c.3816+1246T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142177026 | |||||||
| chr7:142177070 | G | T | 6 | a0001c0001t0001g0180 a0001c0001t0001g0218 a0002c0002t0001g0304 others(3): Show |
6 | HG01168.hp1 HG01433.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.3816+1290G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142177070 | |||||||
| chr7:142177224 | G | T | 1 | a0004c0005t0001g0124 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.3816+1444G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142177224 | |||||||
| chr7:142177273 | C | T | 2 | a0003c0007t0001g0142 a0003c0009t0001g0141 |
2 | HG00140.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.3816+1493C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142177273 | |||||||
| chr7:142177277 | C | T | 2 | a0012c0012t0001g0236 a0012c0012t0001g0237 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.3816+1497C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142177277 | |||||||
| chr7:142177295 | A | C | 3 | a0001c0001t0001g0272 a0002c0002t0001g0205 a0002c0002t0001g0235 |
3 | HG01099.hp1 HG01106.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.3816+1515A>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142177295 | |||||||
| chr7:142177338 | A | G | 1 | a0012c0012t0001g0322 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.3816+1558A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142177338 | |||||||
| chr7:142177348 | G | A | 1 | a0001c0004t0001g0046 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3816+1568G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142177348 | |||||||
| chr7:142177491 | C | A | 2 | a0014c0020t0001g0001 a0038c0059t0001g0026 |
3 | HG02145.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.3816+1711C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142177491 | |||||||
| chr7:142177639 | G | T | 80 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(77): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.3816+1859G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142177639 | |||||||
| chr7:142177745 | C | T | 4 | a0009c0011t0001g0023 a0009c0011t0001g0024 a0045c0061t0001g0044 others(1): Show |
4 | HG00642.hp1 HG02922.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.3816+1965C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142177745 | |||||||
| chr7:142177810 | A | G | 80 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(77): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.3816+2030A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142177810 | |||||||
| chr7:142177893 | G | C | 1 | a0006c0008t0001g0094 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3816+2113G>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142177893 | |||||||
| chr7:142178247 | T | C | 30 | a0001c0001t0001g0140 a0002c0002t0001g0019 a0002c0002t0001g0021 others(27): Show |
30 | HG00140.hp1 HG00558.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.3816+2467T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142178247 | |||||||
| chr7:142178475 | TAATAATT others(2): Show |
T | 3 | a0019c0030t0001g0200 a0019c0030t0002g0326 a0019c0073t0001g0012 |
3 | HG01891.hp2 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.3816+2698_3816+270 others(13): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | INFO_REALIGN_3_PRIME | chr7 | 142178475 | ||||||
| chr7:142178540 | A | G | 17 | a0001c0001t0001g0101 a0001c0001t0001g0107 a0001c0001t0001g0116 others(14): Show |
17 | HG00408.hp1 HG02027.hp2 HG02129.hp1 others(14): Show |
intron_variant | MODIFIER | c.3816+2760A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142178540 | |||||||
| chr7:142178790 | C | T | 1 | a0002c0003t0001g0210 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.3816+3010C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142178790 | |||||||
| chr7:142178893 | C | A | 6 | a0001c0001t0001g0096 a0001c0052t0001g0109 a0002c0003t0001g0208 others(3): Show |
6 | HG00408.hp2 HG02080.hp2 HG04228.hp2 others(3): Show |
intron_variant | MODIFIER | c.3816+3113C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142178893 | |||||||
| chr7:142178899 | G | T | 45 | a0003c0007t0001g0070 a0003c0007t0001g0082 a0003c0007t0001g0093 others(42): Show |
45 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.3816+3119G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142178899 | |||||||
| chr7:142178901 | A | G | 1 | a0011c0013t0001g0246 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.3816+3121A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142178901 | |||||||
| chr7:142178946 | A | C | 7 | a0002c0002t0001g0008 a0004c0005t0001g0177 a0005c0006t0001g0242 others(4): Show |
7 | HG02155.hp1 HG04228.hp1 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.3816+3166A>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142178946 | |||||||
| chr7:142178996 | T | A | 170 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(167): Show |
171 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.3816+3216T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142178996 | |||||||
| chr7:142179321 | T | C | 1 | a0062c0076t0001g0325 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3816+3541T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142179321 | |||||||
| chr7:142179562 | T | C | 80 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(77): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.3817-3704T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142179562 | |||||||
| chr7:142179672 | T | G | 3 | a0014c0026t0001g0196 a0014c0026t0001g0327 a0062c0076t0001g0325 |
3 | HG01243.hp1 HG02723.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3817-3594T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142179672 | |||||||
| chr7:142179840 | G | A | 1 | a0007c0083t0001g0287 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.3817-3426G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142179840 | |||||||
| chr7:142179851 | A | G | 80 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(77): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.3817-3415A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142179851 | |||||||
| chr7:142179858 | G | A | 1 | a0002c0003t0001g0073 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3817-3408G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142179858 | |||||||
| chr7:142179877 | A | G | 71 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(68): Show |
71 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.3817-3389A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142179877 | |||||||
| chr7:142179967 | T | G | 60 | a0002c0002t0001g0264 a0002c0002t0001g0310 a0002c0003t0001g0312 others(57): Show |
61 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.3817-3299T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142179967 | |||||||
| chr7:142180072 | G | A | 1 | a0009c0011t0001g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3817-3194G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142180072 | |||||||
| chr7:142180100 | T | C | 2 | a0005c0006t0001g0233 a0005c0006t0001g0239 |
2 | NA18944.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.3817-3166T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142180100 | |||||||
| chr7:142180113 | A | G | 83 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(80): Show |
83 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.3817-3153A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142180113 | |||||||
| chr7:142180147 | A | G | 83 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(80): Show |
83 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.3817-3119A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142180147 | |||||||
| chr7:142180249 | T | C | 48 | a0002c0002t0001g0264 a0002c0002t0001g0310 a0002c0003t0001g0312 others(45): Show |
48 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.3817-3017T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142180249 | |||||||
| chr7:142180261 | A | C | 2 | a0002c0003t0001g0225 a0002c0003t0001g0226 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3817-3005A>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142180261 | |||||||
| chr7:142180272 | A | C | 2 | a0014c0026t0001g0196 a0014c0026t0001g0327 |
2 | HG01243.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.3817-2994A>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142180272 | |||||||
| chr7:142180292 | A | T | 80 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(77): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.3817-2974A>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142180292 | |||||||
| chr7:142180300 | C | G | 1 | a0035c0067t0003g0146 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3817-2966C>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142180300 | |||||||
| chr7:142180386 | G | C | 4 | a0004c0005t0001g0100 a0010c0017t0001g0286 a0011c0022t0001g0161 others(1): Show |
4 | HG00558.hp1 HG01069.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.3817-2880G>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142180386 | |||||||
| chr7:142180394 | TG | T | 80 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(77): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.3817-2868delG | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | INFO_REALIGN_3_PRIME | chr7 | 142180394 | ||||||
| chr7:142180474 | A | G | 1 | a0001c0038t0001g0099 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.3817-2792A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142180474 | |||||||
| chr7:142180492 | A | G | 59 | a0002c0002t0001g0264 a0002c0002t0001g0310 a0002c0003t0001g0312 others(56): Show |
60 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.3817-2774A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142180492 | |||||||
| chr7:142180523 | T | C | 200 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(197): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.3817-2743T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142180523 | |||||||
| chr7:142180532 | T | A | 1 | a0063c0041t0001g0139 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3817-2734T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142180532 | |||||||
| chr7:142180592 | A | T | 80 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(77): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.3817-2674A>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142180592 | |||||||
| chr7:142180602 | T | A | 1 | a0063c0041t0001g0139 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3817-2664T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142180602 | |||||||
| chr7:142180754 | T | A | 83 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(80): Show |
83 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.3817-2512T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142180754 | |||||||
| chr7:142180815 | G | T | 1 | a0002c0003t0001g0004 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.3817-2451G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142180815 | |||||||
| chr7:142180876 | A | G | 3 | a0001c0001t0001g0176 a0039c0046t0001g0102 a0043c0048t0001g0103 |
3 | HG02451.hp1 HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3817-2390A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142180876 | |||||||
| chr7:142181260 | G | A | 71 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(68): Show |
71 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.3817-2006G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142181260 | |||||||
| chr7:142181294 | C | T | 2 | a0014c0020t0001g0001 a0038c0059t0001g0026 |
3 | HG02145.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.3817-1972C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142181294 | |||||||
| chr7:142181407 | A | G | 80 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(77): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.3817-1859A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142181407 | |||||||
| chr7:142181445 | T | C | 80 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(77): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.3817-1821T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142181445 | |||||||
| chr7:142181532 | C | G | 80 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(77): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.3817-1734C>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142181532 | |||||||
| chr7:142181637 | T | C | 80 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(77): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.3817-1629T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142181637 | |||||||
| chr7:142181754 | C | T | 80 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(77): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.3817-1512C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142181754 | |||||||
| chr7:142181803 | G | A | 8 | a0002c0002t0001g0008 a0004c0005t0001g0177 a0005c0006t0001g0242 others(5): Show |
8 | HG02155.hp1 HG02257.hp2 HG04228.hp1 others(5): Show |
intron_variant | MODIFIER | c.3817-1463G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142181803 | |||||||
| chr7:142181840 | C | T | 3 | a0001c0001t0001g0176 a0039c0046t0001g0102 a0043c0048t0001g0103 |
3 | HG02451.hp1 HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3817-1426C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142181840 | |||||||
| chr7:142181863 | C | A | 80 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(77): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.3817-1403C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142181863 | |||||||
| chr7:142181872 | C | T | 80 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(77): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.3817-1394C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142181872 | |||||||
| chr7:142181878 | C | G | 80 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(77): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.3817-1388C>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142181878 | |||||||
| chr7:142181946 | A | G | 83 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(80): Show |
83 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.3817-1320A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142181946 | |||||||
| chr7:142182140 | A | G | 199 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(196): Show |
200 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.3817-1126A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142182140 | |||||||
| chr7:142182148 | C | T | 48 | a0002c0002t0001g0264 a0002c0002t0001g0310 a0002c0003t0001g0312 others(45): Show |
48 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.3817-1118C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142182148 | |||||||
| chr7:142182155 | G | A | 2 | a0002c0003t0001g0225 a0002c0003t0001g0226 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3817-1111G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142182155 | |||||||
| chr7:142182185 | G | C | 2 | a0024c0074t0001g0031 a0024c0075t0001g0185 |
2 | HG02630.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3817-1081G>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142182185 | |||||||
| chr7:142182222 | C | T | 1 | a0028c0024t0001g0257 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.3817-1044C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142182222 | |||||||
| chr7:142182303 | G | A | 23 | a0002c0002t0001g0008 a0002c0002t0001g0016 a0002c0002t0001g0043 others(20): Show |
23 | HG00735.hp2 HG01884.hp2 HG02155.hp1 others(20): Show |
intron_variant | MODIFIER | c.3817-963G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142182303 | |||||||
| chr7:142182493 | C | T | 3 | a0019c0030t0001g0200 a0019c0030t0002g0326 a0019c0073t0001g0012 |
3 | HG01891.hp2 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.3817-773C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142182493 | |||||||
| chr7:142182496 | A | G | 1 | a0001c0004t0001g0046 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3817-770A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142182496 | |||||||
| chr7:142182556 | G | A | 3 | a0001c0001t0001g0176 a0039c0046t0001g0102 a0043c0048t0001g0103 |
3 | HG02451.hp1 HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3817-710G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142182556 | |||||||
| chr7:142182583 | A | G | 4 | a0001c0004t0002g0065 a0002c0003t0002g0230 a0002c0003t0002g0251 others(1): Show |
4 | HG02970.hp1 HG02976.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3817-683A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142182583 | |||||||
| chr7:142182655 | A | G | 80 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(77): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.3817-611A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142182655 | |||||||
| chr7:142182683 | C | A | 1 | a0017c0019t0001g0289 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.3817-583C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142182683 | |||||||
| chr7:142182726 | C | T | 2 | a0014c0020t0001g0001 a0038c0059t0001g0026 |
3 | HG02145.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.3817-540C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142182726 | |||||||
| chr7:142182838 | T | C | 80 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(77): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.3817-428T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142182838 | |||||||
| chr7:142182866 | T | A | 3 | a0001c0001t0001g0176 a0039c0046t0001g0102 a0043c0048t0001g0103 |
3 | HG02451.hp1 HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3817-400T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142182866 | |||||||
| chr7:142182875 | G | A | 1 | a0035c0067t0003g0146 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3817-391G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142182875 | |||||||
| chr7:142182947 | G | T | 80 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(77): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.3817-319G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142182947 | |||||||
| chr7:142183099 | G | A | 2 | a0014c0020t0001g0001 a0038c0059t0001g0026 |
3 | HG02145.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.3817-167G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142183099 | |||||||
| chr7:142183114 | G | A | 2 | a0047c0070t0001g0147 a0048c0065t0002g0047 |
2 | HG03130.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.3817-152G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142183114 | |||||||
| chr7:142183129 | TTTTTA | T | 33 | a0001c0001t0001g0140 a0002c0002t0001g0019 a0002c0002t0001g0021 others(30): Show |
33 | HG00140.hp1 HG00558.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.3817-128_3817-124d others(7): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | INFO_REALIGN_3_PRIME | chr7 | 142183129 | ||||||
| chr7:142183141 | T | G | 3 | a0001c0001t0001g0176 a0039c0046t0001g0102 a0043c0048t0001g0103 |
3 | HG02451.hp1 HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3817-125T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 32/47 | chr7 | 142183141 | |||||||
| chr7:142183658 | A | G | 1 | a0001c0004t0001g0046 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3924+285A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 33/47 | chr7 | 142183658 | |||||||
| chr7:142183823 | T | C | 1 | a0008c0010t0001g0086 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.3924+450T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 33/47 | chr7 | 142183823 | |||||||
| chr7:142183870 | T | C | 2 | a0025c0032t0001g0028 a0025c0032t0001g0030 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.3924+497T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 33/47 | chr7 | 142183870 | |||||||
| chr7:142183950 | C | CT | 42 | a0001c0001t0001g0060 a0001c0001t0001g0074 a0001c0001t0001g0077 others(39): Show |
42 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(39): Show |
intron_variant | MODIFIER | c.3924+617dupT | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 33/47 | INFO_REALIGN_3_PRIME | chr7 | 142183950 | ||||||
| chr7:142183950 | C | CTT | 42 | a0001c0001t0001g0075 a0001c0001t0001g0101 a0001c0001t0001g0112 others(39): Show |
42 | HG00408.hp1 HG00639.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.3924+616_3924+617d others(4): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 33/47 | INFO_REALIGN_3_PRIME | chr7 | 142183950 | ||||||
| chr7:142183950 | C | CTTT | 15 | a0001c0001t0001g0166 a0001c0001t0001g0181 a0001c0001t0001g0190 others(12): Show |
15 | HG00423.hp1 HG00621.hp1 HG01928.hp1 others(12): Show |
intron_variant | MODIFIER | c.3924+615_3924+617d others(5): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 33/47 | INFO_REALIGN_3_PRIME | chr7 | 142183950 | ||||||
| chr7:142183950 | CTTTT | C | 5 | a0002c0003t0001g0007 a0014c0020t0001g0001 a0015c0015t0001g0029 others(2): Show |
6 | HG01074.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.3924+614_3924+617d others(6): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 33/47 | INFO_REALIGN_3_PRIME | chr7 | 142183950 | ||||||
| chr7:142183950 | CTTTTTTT others(2): Show |
C | 9 | a0001c0001t0001g0096 a0001c0001t0001g0107 a0001c0052t0001g0109 others(6): Show |
9 | HG02135.hp2 HG03491.hp1 HG03492.hp1 others(6): Show |
intron_variant | MODIFIER | c.3924+609_3924+617d others(11): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 33/47 | INFO_REALIGN_3_PRIME | chr7 | 142183950 | ||||||
| chr7:142183950 | CTTTTTTT others(3): Show |
C | 36 | a0001c0004t0001g0278 a0002c0003t0001g0208 a0002c0003t0001g0228 others(33): Show |
36 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.3924+608_3924+617d others(12): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 33/47 | INFO_REALIGN_3_PRIME | chr7 | 142183950 | ||||||
| chr7:142183950 | CTTTTTTT others(4): Show |
C | 34 | a0001c0001t0001g0067 a0001c0001t0001g0117 a0001c0001t0001g0154 others(31): Show |
34 | HG00423.hp2 HG01167.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.3924+607_3924+617d others(13): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 33/47 | INFO_REALIGN_3_PRIME | chr7 | 142183950 | ||||||
| chr7:142183950 | CTTTTTTT others(5): Show |
C | 70 | a0001c0001t0001g0071 a0001c0001t0001g0080 a0001c0001t0001g0087 others(67): Show |
70 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.3924+606_3924+617d others(14): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 33/47 | INFO_REALIGN_3_PRIME | chr7 | 142183950 | ||||||
| chr7:142183950 | CTTTTTTT others(6): Show |
C | 9 | a0001c0001t0001g0140 a0002c0003t0001g0004 a0002c0003t0001g0292 others(6): Show |
9 | HG01167.hp2 HG01168.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.3924+605_3924+617d others(15): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 33/47 | INFO_REALIGN_3_PRIME | chr7 | 142183950 | ||||||
| chr7:142183950 | CTTTTTTT others(8): Show |
C | 2 | a0033c0035t0003g0061 a0035c0067t0003g0146 |
2 | HG01952.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.3924+603_3924+617d others(17): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 33/47 | INFO_REALIGN_3_PRIME | chr7 | 142183950 | ||||||
| chr7:142183950 | CTTTTTTT others(9): Show |
C | 9 | a0001c0001t0001g0116 a0001c0001t0001g0245 a0001c0001t0001g0260 others(6): Show |
9 | HG01891.hp1 HG02486.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.3924+602_3924+617d others(18): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 33/47 | INFO_REALIGN_3_PRIME | chr7 | 142183950 | ||||||
| chr7:142183950 | CTTTTTTT others(10): Show |
C | 1 | a0010c0017t0001g0240 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3924+601_3924+617d others(19): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 33/47 | INFO_REALIGN_3_PRIME | chr7 | 142183950 | ||||||
| chr7:142183950 | CTTTTTTT others(11): Show |
C | 1 | a0046c0077t0001g0195 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3924+600_3924+617d others(20): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 33/47 | INFO_REALIGN_3_PRIME | chr7 | 142183950 | ||||||
| chr7:142183950 | CTTTTTTT others(14): Show |
C | 1 | a0001c0004t0001g0046 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3924+597_3924+617d others(23): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 33/47 | INFO_REALIGN_3_PRIME | chr7 | 142183950 | ||||||
| chr7:142183950 | CTTTTTTT others(19): Show |
C | 26 | a0001c0001t0001g0176 a0002c0002t0001g0008 a0002c0002t0001g0016 others(23): Show |
26 | HG00735.hp2 HG01884.hp2 HG02155.hp1 others(23): Show |
intron_variant | MODIFIER | c.3924+592_3924+617d others(28): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 33/47 | INFO_REALIGN_3_PRIME | chr7 | 142183950 | ||||||
| chr7:142183950 | CTTTTTTT others(20): Show |
C | 1 | a0001c0001t0001g0277 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3924+591_3924+617d others(29): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 33/47 | INFO_REALIGN_3_PRIME | chr7 | 142183950 | ||||||
| chr7:142184066 | A | G | 1 | a0035c0067t0003g0146 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3924+693A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 33/47 | chr7 | 142184066 | |||||||
| chr7:142184075 | C | T | 1 | a0001c0004t0001g0046 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3924+702C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 33/47 | chr7 | 142184075 | |||||||
| chr7:142184192 | C | T | 34 | a0001c0001t0001g0140 a0002c0002t0001g0019 a0002c0002t0001g0021 others(31): Show |
34 | HG00140.hp1 HG00558.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.3924+819C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 33/47 | chr7 | 142184192 | |||||||
| chr7:142184238 | G | A | 53 | a0003c0007t0001g0070 a0003c0007t0001g0082 a0003c0007t0001g0093 others(50): Show |
54 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.3925-839G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 33/47 | chr7 | 142184238 | |||||||
| chr7:142184341 | A | G | 79 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(76): Show |
79 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.3925-736A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 33/47 | chr7 | 142184341 | |||||||
| chr7:142184697 | A | G | 1 | a0034c0069t0001g0290 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.3925-380A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 33/47 | chr7 | 142184697 | |||||||
| chr7:142184777 | C | G | 3 | a0001c0001t0001g0176 a0039c0046t0001g0102 a0043c0048t0001g0103 |
3 | HG02451.hp1 HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3925-300C>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 33/47 | chr7 | 142184777 | |||||||
| chr7:142184882 | CAT | C | 79 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(76): Show |
79 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.3925-193_3925-192d others(4): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 33/47 | INFO_REALIGN_3_PRIME | chr7 | 142184882 | ||||||
| chr7:142185245 | C | T | 3 | a0002c0003t0001g0152 a0002c0003t0001g0306 a0002c0003t0001g0309 |
3 | NA18978.hp2 NA18992.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.3987+106C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 34/47 | chr7 | 142185245 | |||||||
| chr7:142185403 | A | G | 79 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(76): Show |
79 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.3987+264A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 34/47 | chr7 | 142185403 | |||||||
| chr7:142185404 | C | T | 1 | a0046c0077t0001g0195 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3987+265C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 34/47 | chr7 | 142185404 | |||||||
| chr7:142185661 | T | TA | 7 | a0001c0001t0001g0096 a0001c0001t0001g0179 a0001c0052t0001g0109 others(4): Show |
7 | HG00408.hp2 HG02080.hp2 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.3988-316dupA | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 34/47 | INFO_REALIGN_3_PRIME | chr7 | 142185661 | ||||||
| chr7:142185831 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.3988-158C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 34/47 | chr7 | 142185831 | |||||||
| chr7:142186144 | CT | C | 130 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0080 others(127): Show |
131 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.4122+35delT | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 35/47 | INFO_REALIGN_3_PRIME | chr7 | 142186144 | ||||||
| chr7:142186355 | C | G | 134 | a0001c0001t0001g0122 a0001c0001t0001g0140 a0001c0001t0001g0154 others(131): Show |
135 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.4122+232C>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 35/47 | chr7 | 142186355 | |||||||
| chr7:142186413 | C | A | 2 | a0001c0001t0001g0154 a0007c0083t0001g0287 |
2 | NA18978.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.4122+290C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 35/47 | chr7 | 142186413 | |||||||
| chr7:142186515 | C | T | 3 | a0002c0002t0001g0034 a0002c0002t0001g0269 a0010c0017t0001g0240 |
3 | HG00099.hp1 HG01884.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.4122+392C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 35/47 | chr7 | 142186515 | |||||||
| chr7:142186532 | G | A | 5 | a0022c0027t0001g0040 a0023c0025t0001g0052 a0023c0025t0002g0037 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.4122+409G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 35/47 | chr7 | 142186532 | |||||||
| chr7:142186585 | A | T | 3 | a0001c0001t0001g0176 a0016c0014t0001g0079 a0043c0048t0001g0103 |
3 | HG02615.hp2 HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.4122+462A>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 35/47 | chr7 | 142186585 | |||||||
| chr7:142186958 | AT | A | 226 | a0001c0001t0001g0060 a0001c0001t0001g0071 a0001c0001t0001g0075 others(223): Show |
227 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.4123-778delT | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 35/47 | INFO_REALIGN_3_PRIME | chr7 | 142186958 | ||||||
| chr7:142187187 | G | C | 1 | a0037c0050t0001g0115 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.4123-563G>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 35/47 | chr7 | 142187187 | |||||||
| chr7:142187242 | A | C | 2 | a0001c0001t0001g0131 a0058c0053t0001g0182 |
2 | HG02165.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.4123-508A>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 35/47 | chr7 | 142187242 | |||||||
| chr7:142187392 | G | T | 12 | a0009c0011t0001g0023 a0009c0011t0001g0024 a0009c0011t0001g0025 others(9): Show |
12 | HG00642.hp1 HG02486.hp1 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.4123-358G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 35/47 | chr7 | 142187392 | |||||||
| chr7:142187395 | G | C | 128 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(125): Show |
128 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.4123-355G>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 35/47 | chr7 | 142187395 | |||||||
| chr7:142187407 | G | A | 3 | a0002c0003t0001g0197 a0002c0003t0001g0198 a0024c0074t0001g0031 |
3 | HG01261.hp2 HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.4123-343G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 35/47 | chr7 | 142187407 | |||||||
| chr7:142187455 | A | G | 1 | a0013c0016t0001g0283 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.4123-295A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 35/47 | chr7 | 142187455 | |||||||
| chr7:142187666 | T | G | 1 | a0009c0011t0002g0036 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4123-84T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 35/47 | chr7 | 142187666 | |||||||
| chr7:142187716 | C | A | 1 | a0049c0064t0001g0027 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4123-34C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 35/47 | chr7 | 142187716 | |||||||
| chr7:142187848 | T | C | 19 | a0001c0001t0001g0080 a0001c0001t0001g0096 a0001c0001t0001g0131 others(16): Show |
19 | HG00621.hp2 HG02040.hp2 HG02165.hp2 others(16): Show |
intron_variant | MODIFIER | c.4207+14T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 36/47 | chr7 | 142187848 | |||||||
| chr7:142187913 | G | T | 1 | a0004c0005t0001g0058 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.4207+79G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 36/47 | chr7 | 142187913 | |||||||
| chr7:142187925 | A | G | 7 | a0001c0004t0001g0046 a0002c0003t0001g0219 a0019c0030t0002g0326 others(4): Show |
7 | HG01891.hp2 HG01952.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.4207+91A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 36/47 | chr7 | 142187925 | |||||||
| chr7:142188076 | G | T | 3 | a0001c0004t0002g0065 a0002c0003t0002g0230 a0002c0003t0002g0251 |
3 | HG02970.hp1 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.4207+242G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 36/47 | chr7 | 142188076 | |||||||
| chr7:142188109 | A | AAC | 29 | a0001c0001t0001g0223 a0001c0004t0001g0046 a0001c0004t0001g0063 others(26): Show |
29 | HG00140.hp1 HG00609.hp2 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.4207+316_4207+317d others(4): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 36/47 | INFO_REALIGN_3_PRIME | chr7 | 142188109 | ||||||
| chr7:142188109 | A | AACAC | 18 | a0001c0001t0001g0108 a0001c0004t0001g0145 a0001c0004t0001g0163 others(15): Show |
18 | HG01884.hp1 HG02055.hp1 HG02809.hp1 others(15): Show |
intron_variant | MODIFIER | c.4207+314_4207+317d others(6): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 36/47 | INFO_REALIGN_3_PRIME | chr7 | 142188109 | ||||||
| chr7:142188109 | A | AACACAC | 46 | a0001c0004t0001g0064 a0001c0004t0001g0066 a0001c0004t0001g0072 others(43): Show |
46 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(43): Show |
intron_variant | MODIFIER | c.4207+312_4207+317d others(8): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 36/47 | INFO_REALIGN_3_PRIME | chr7 | 142188109 | ||||||
| chr7:142188109 | A | AACACACA others(1): Show |
18 | a0001c0004t0001g0201 a0002c0003t0001g0004 a0002c0003t0001g0088 others(15): Show |
19 | HG00558.hp1 HG00642.hp2 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.4207+310_4207+317d others(10): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 36/47 | INFO_REALIGN_3_PRIME | chr7 | 142188109 | ||||||
| chr7:142188109 | A | AACACACA others(3): Show |
17 | a0001c0004t0001g0089 a0001c0004t0001g0119 a0001c0004t0001g0280 others(14): Show |
17 | HG01952.hp1 HG01975.hp1 HG02015.hp2 others(14): Show |
intron_variant | MODIFIER | c.4207+308_4207+317d others(12): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 36/47 | INFO_REALIGN_3_PRIME | chr7 | 142188109 | ||||||
| chr7:142188109 | A | AACACACA others(5): Show |
19 | a0004c0005t0001g0111 a0004c0005t0001g0123 a0005c0006t0001g0006 others(16): Show |
19 | HG00438.hp1 HG00609.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.4207+306_4207+317d others(14): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 36/47 | INFO_REALIGN_3_PRIME | chr7 | 142188109 | ||||||
| chr7:142188109 | A | AACACACA others(7): Show |
4 | a0005c0006t0001g0238 a0005c0006t0001g0248 a0005c0006t0001g0295 others(1): Show |
4 | HG02129.hp2 NA18954.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.4207+304_4207+317d others(16): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 36/47 | INFO_REALIGN_3_PRIME | chr7 | 142188109 | ||||||
| chr7:142188109 | A | AACACACA others(9): Show |
1 | a0005c0006t0001g0254 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.4207+302_4207+317d others(18): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 36/47 | INFO_REALIGN_3_PRIME | chr7 | 142188109 | ||||||
| chr7:142188109 | A | AACACACA others(11): Show |
1 | a0009c0011t0001g0023 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.4207+300_4207+317d others(20): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 36/47 | INFO_REALIGN_3_PRIME | chr7 | 142188109 | ||||||
| chr7:142188109 | A | ACACACAC others(4): Show |
1 | a0002c0003t0001g0210 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.4207+275_4207+276i others(13): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 36/47 | chr7 | 142188109 | |||||||
| chr7:142188109 | AAC | A | 22 | a0001c0001t0001g0140 a0002c0002t0001g0008 a0002c0002t0001g0039 others(19): Show |
22 | HG00099.hp2 HG00140.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.4207+316_4207+317d others(4): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 36/47 | INFO_REALIGN_3_PRIME | chr7 | 142188109 | ||||||
| chr7:142188109 | AACAC | A | 126 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(123): Show |
126 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.4207+314_4207+317d others(6): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 36/47 | INFO_REALIGN_3_PRIME | chr7 | 142188109 | ||||||
| chr7:142188109 | AACACAC | A | 4 | a0002c0002t0001g0291 a0002c0002t0001g0310 a0002c0058t0001g0032 others(1): Show |
4 | HG02257.hp1 HG03579.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.4207+312_4207+317d others(8): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 36/47 | INFO_REALIGN_3_PRIME | chr7 | 142188109 | ||||||
| chr7:142188109 | AACACACA others(3): Show |
A | 3 | a0001c0001t0001g0300 a0004c0005t0001g0177 a0039c0046t0001g0102 |
3 | HG01928.hp1 HG02155.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.4207+308_4207+317d others(12): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 36/47 | INFO_REALIGN_3_PRIME | chr7 | 142188109 | ||||||
| chr7:142188280 | T | G | 118 | a0001c0001t0001g0097 a0001c0001t0001g0108 a0001c0001t0001g0130 others(115): Show |
119 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.4207+446T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 36/47 | chr7 | 142188280 | |||||||
| chr7:142188324 | A | C | 49 | a0004c0005t0001g0058 a0004c0005t0001g0100 a0004c0005t0001g0105 others(46): Show |
49 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.4207+490A>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 36/47 | chr7 | 142188324 | |||||||
| chr7:142188365 | A | G | 1 | a0039c0046t0001g0102 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4207+531A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 36/47 | chr7 | 142188365 | |||||||
| chr7:142188441 | TA | T | 10 | a0001c0004t0001g0157 a0001c0004t0001g0160 a0001c0052t0001g0109 others(7): Show |
10 | HG00423.hp1 HG01074.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.4207+616delA | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 36/47 | INFO_REALIGN_3_PRIME | chr7 | 142188441 | ||||||
| chr7:142188483 | C | T | 22 | a0006c0008t0001g0068 a0006c0008t0001g0094 a0006c0008t0001g0156 others(19): Show |
22 | HG00323.hp1 HG00438.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.4207+649C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 36/47 | chr7 | 142188483 | |||||||
| chr7:142188942 | A | G | 119 | a0001c0001t0001g0097 a0001c0001t0001g0108 a0001c0001t0001g0130 others(116): Show |
120 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.4208-425A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 36/47 | chr7 | 142188942 | |||||||
| chr7:142189323 | T | G | 1 | a0005c0006t0001g0243 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.4208-44T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 36/47 | chr7 | 142189323 | |||||||
| chr7:142189646 | A | G | 1 | a0008c0010t0001g0091 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.4346+141A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142189646 | |||||||
| chr7:142189780 | G | A | 5 | a0014c0020t0001g0001 a0014c0026t0001g0196 a0014c0026t0001g0327 others(2): Show |
6 | HG01243.hp1 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.4346+275G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142189780 | |||||||
| chr7:142189914 | A | G | 5 | a0001c0004t0002g0065 a0002c0003t0002g0230 a0002c0003t0002g0251 others(2): Show |
5 | HG02970.hp1 HG02976.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.4346+409A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142189914 | |||||||
| chr7:142190033 | A | T | 3 | a0015c0015t0001g0013 a0015c0015t0001g0014 a0015c0015t0001g0297 |
3 | HG02257.hp2 HG02622.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.4346+528A>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142190033 | |||||||
| chr7:142190075 | A | G | 1 | a0019c0030t0002g0326 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4346+570A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142190075 | |||||||
| chr7:142190084 | AT | A | 26 | a0001c0004t0001g0046 a0001c0004t0001g0066 a0002c0003t0001g0049 others(23): Show |
27 | HG01074.hp1 HG01243.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.4346+589delT | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | INFO_REALIGN_3_PRIME | chr7 | 142190084 | ||||||
| chr7:142190240 | G | A | 48 | a0004c0005t0001g0058 a0004c0005t0001g0100 a0004c0005t0001g0105 others(45): Show |
48 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.4346+735G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142190240 | |||||||
| chr7:142190267 | C | CT | 25 | a0001c0001t0001g0087 a0001c0001t0001g0112 a0001c0001t0001g0166 others(22): Show |
25 | HG00558.hp2 HG00621.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.4346+786dupT | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | INFO_REALIGN_3_PRIME | chr7 | 142190267 | ||||||
| chr7:142190267 | CT | C | 25 | a0001c0004t0001g0262 a0002c0002t0001g0249 a0002c0002t0001g0303 others(22): Show |
26 | HG00621.hp2 HG01074.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.4346+786delT | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | INFO_REALIGN_3_PRIME | chr7 | 142190267 | ||||||
| chr7:142190267 | CTTTT | C | 38 | a0001c0001t0001g0097 a0001c0001t0001g0108 a0001c0001t0001g0130 others(35): Show |
38 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.4346+783_4346+786d others(6): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | INFO_REALIGN_3_PRIME | chr7 | 142190267 | ||||||
| chr7:142190267 | CTTTTTTT | C | 40 | a0001c0001t0001g0221 a0001c0004t0001g0158 a0002c0002t0001g0213 others(37): Show |
40 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.4346+780_4346+786d others(9): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | INFO_REALIGN_3_PRIME | chr7 | 142190267 | ||||||
| chr7:142190278 | T | C | 1 | a0012c0012t0001g0236 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.4346+773T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142190278 | |||||||
| chr7:142190341 | G | A | 5 | a0002c0003t0001g0197 a0002c0003t0001g0198 a0010c0017t0001g0256 others(2): Show |
5 | HG01074.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.4346+836G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142190341 | |||||||
| chr7:142190390 | G | A | 1 | a0001c0004t0001g0119 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.4346+885G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142190390 | |||||||
| chr7:142190396 | C | T | 37 | a0004c0005t0001g0058 a0004c0005t0001g0100 a0004c0005t0001g0105 others(34): Show |
37 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.4346+891C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142190396 | |||||||
| chr7:142190414 | G | A | 1 | a0001c0052t0001g0109 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.4346+909G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142190414 | |||||||
| chr7:142190493 | C | T | 1 | a0007c0033t0001g0155 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.4346+988C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142190493 | |||||||
| chr7:142190597 | A | G | 1 | a0039c0046t0001g0102 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4346+1092A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142190597 | |||||||
| chr7:142190623 | C | T | 6 | a0001c0004t0001g0066 a0002c0003t0001g0225 a0002c0003t0001g0226 others(3): Show |
6 | HG02572.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.4346+1118C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142190623 | |||||||
| chr7:142190835 | T | A | 2 | a0001c0004t0001g0046 a0047c0070t0001g0147 |
2 | HG03130.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.4346+1330T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142190835 | |||||||
| chr7:142190910 | G | A | 38 | a0004c0005t0001g0058 a0004c0005t0001g0100 a0004c0005t0001g0105 others(35): Show |
38 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.4346+1405G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142190910 | |||||||
| chr7:142190936 | G | A | 1 | a0002c0003t0001g0049 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.4346+1431G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142190936 | |||||||
| chr7:142190946 | G | A | 1 | a0032c0045t0001g0126 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.4346+1441G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142190946 | |||||||
| chr7:142190971 | C | CA | 11 | a0004c0005t0001g0111 a0004c0005t0001g0123 a0004c0005t0001g0124 others(8): Show |
11 | NA18941.hp1 NA18950.hp1 NA18951.hp1 others(8): Show |
intron_variant | MODIFIER | c.4346+1472dupA | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | INFO_REALIGN_3_PRIME | chr7 | 142190971 | ||||||
| chr7:142190992 | A | G | 3 | a0001c0004t0001g0167 a0003c0009t0001g0271 a0010c0017t0001g0240 |
3 | HG01433.hp1 HG01496.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.4346+1487A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142190992 | |||||||
| chr7:142191134 | GA | G | 239 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(236): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.4346+1640delA | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | INFO_REALIGN_3_PRIME | chr7 | 142191134 | ||||||
| chr7:142191156 | G | A | 1 | a0039c0046t0001g0102 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4346+1651G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142191156 | |||||||
| chr7:142191256 | C | T | 1 | a0002c0003t0001g0187 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.4346+1751C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142191256 | |||||||
| chr7:142191302 | C | G | 1 | a0001c0001t0001g0172 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.4346+1797C>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142191302 | |||||||
| chr7:142191338 | G | A | 5 | a0002c0003t0001g0197 a0002c0003t0001g0198 a0010c0017t0001g0256 others(2): Show |
5 | HG01074.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.4346+1833G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142191338 | |||||||
| chr7:142191420 | T | C | 1 | a0024c0075t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4346+1915T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142191420 | |||||||
| chr7:142191572 | C | T | 48 | a0004c0005t0001g0058 a0004c0005t0001g0100 a0004c0005t0001g0105 others(45): Show |
48 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.4346+2067C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142191572 | |||||||
| chr7:142191577 | C | T | 116 | a0001c0001t0001g0097 a0001c0001t0001g0108 a0001c0001t0001g0130 others(113): Show |
117 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.4346+2072C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142191577 | |||||||
| chr7:142191602 | C | A | 2 | a0009c0011t0001g0025 a0033c0035t0003g0061 |
2 | HG01952.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.4346+2097C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142191602 | |||||||
| chr7:142191604 | A | C | 286 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(283): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.4346+2099A>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142191604 | |||||||
| chr7:142191606 | A | C | 59 | a0001c0001t0001g0087 a0001c0001t0001g0101 a0001c0001t0001g0116 others(56): Show |
60 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.4346+2101A>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142191606 | |||||||
| chr7:142191608 | A | C | 1 | a0001c0004t0001g0046 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.4346+2103A>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142191608 | |||||||
| chr7:142191614 | A | G | 1 | a0003c0007t0001g0120 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.4346+2109A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142191614 | |||||||
| chr7:142191728 | A | G | 1 | a0049c0064t0001g0027 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4346+2223A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142191728 | |||||||
| chr7:142191733 | T | C | 6 | a0001c0004t0001g0066 a0002c0003t0001g0225 a0002c0003t0001g0226 others(3): Show |
6 | HG02572.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.4346+2228T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142191733 | |||||||
| chr7:142191816 | G | C | 173 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(170): Show |
173 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.4346+2311G>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142191816 | |||||||
| chr7:142191915 | A | T | 5 | a0001c0001t0001g0080 a0001c0001t0001g0247 a0001c0001t0001g0267 others(2): Show |
5 | NA18940.hp2 NA18941.hp2 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.4346+2410A>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142191915 | |||||||
| chr7:142192031 | G | T | 1 | a0047c0070t0001g0147 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4346+2526G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142192031 | |||||||
| chr7:142192175 | G | T | 1 | a0020c0018t0001g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4346+2670G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142192175 | |||||||
| chr7:142192192 | A | C | 1 | a0048c0065t0002g0047 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.4346+2687A>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142192192 | |||||||
| chr7:142192222 | A | G | 2 | a0013c0016t0001g0041 a0013c0016t0001g0042 |
2 | HG02486.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.4346+2717A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142192222 | |||||||
| chr7:142192257 | A | G | 1 | a0049c0064t0001g0027 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4346+2752A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142192257 | |||||||
| chr7:142192302 | G | T | 1 | a0015c0015t0001g0013 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.4346+2797G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142192302 | |||||||
| chr7:142192580 | A | G | 1 | a0016c0014t0001g0079 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4346+3075A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142192580 | |||||||
| chr7:142192649 | A | C | 1 | a0005c0006t0001g0248 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.4346+3144A>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142192649 | |||||||
| chr7:142192664 | A | C | 4 | a0033c0035t0003g0061 a0035c0067t0003g0146 a0038c0059t0001g0026 others(1): Show |
4 | HG01952.hp1 HG02055.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.4346+3159A>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142192664 | |||||||
| chr7:142192666 | C | T | 1 | a0001c0004t0001g0158 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.4346+3161C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142192666 | |||||||
| chr7:142192726 | C | A | 9 | a0001c0001t0001g0067 a0001c0001t0001g0107 a0001c0001t0001g0122 others(6): Show |
9 | HG00423.hp2 HG00621.hp1 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.4346+3221C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142192726 | |||||||
| chr7:142192775 | A | T | 1 | a0049c0064t0001g0027 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4346+3270A>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142192775 | |||||||
| chr7:142192795 | G | A | 1 | a0039c0046t0001g0102 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4346+3290G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142192795 | |||||||
| chr7:142192854 | T | C | 48 | a0004c0005t0001g0058 a0004c0005t0001g0100 a0004c0005t0001g0105 others(45): Show |
48 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.4347-3300T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142192854 | |||||||
| chr7:142192907 | A | G | 127 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(124): Show |
127 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.4347-3247A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142192907 | |||||||
| chr7:142192939 | A | G | 1 | a0006c0008t0001g0094 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.4347-3215A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142192939 | |||||||
| chr7:142192991 | G | T | 190 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(187): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.4347-3163G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142192991 | |||||||
| chr7:142192996 | AT | A | 3 | a0015c0015t0001g0013 a0015c0015t0001g0014 a0015c0015t0001g0297 |
3 | HG02257.hp2 HG02622.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.4347-3152delT | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | INFO_REALIGN_3_PRIME | chr7 | 142192996 | ||||||
| chr7:142193019 | T | C | 48 | a0004c0005t0001g0058 a0004c0005t0001g0100 a0004c0005t0001g0105 others(45): Show |
48 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.4347-3135T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142193019 | |||||||
| chr7:142193105 | G | T | 1 | a0001c0004t0001g0046 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.4347-3049G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142193105 | |||||||
| chr7:142193159 | C | T | 1 | a0047c0070t0001g0147 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4347-2995C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142193159 | |||||||
| chr7:142193225 | C | G | 48 | a0004c0005t0001g0058 a0004c0005t0001g0100 a0004c0005t0001g0105 others(45): Show |
48 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.4347-2929C>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142193225 | |||||||
| chr7:142193253 | T | A | 3 | a0006c0008t0001g0094 a0026c0029t0001g0174 a0026c0029t0001g0175 |
3 | HG03490.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.4347-2901T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142193253 | |||||||
| chr7:142193500 | G | A | 1 | a0009c0011t0001g0024 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4347-2654G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142193500 | |||||||
| chr7:142193528 | T | C | 2 | a0008c0010t0001g0090 a0008c0010t0001g0091 |
2 | HG00609.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.4347-2626T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142193528 | |||||||
| chr7:142193630 | A | G | 1 | a0039c0046t0001g0102 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4347-2524A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142193630 | |||||||
| chr7:142193671 | A | G | 48 | a0004c0005t0001g0058 a0004c0005t0001g0100 a0004c0005t0001g0105 others(45): Show |
48 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.4347-2483A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142193671 | |||||||
| chr7:142194003 | A | G | 9 | a0002c0003t0001g0049 a0014c0020t0001g0001 a0014c0026t0001g0196 others(6): Show |
10 | HG01243.hp1 HG01884.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.4347-2151A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142194003 | |||||||
| chr7:142194032 | T | C | 1 | a0009c0011t0001g0282 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4347-2122T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142194032 | |||||||
| chr7:142194036 | C | CT | 10 | a0009c0011t0001g0023 a0009c0011t0001g0024 a0009c0011t0001g0025 others(7): Show |
10 | HG00642.hp1 HG01891.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.4347-2104dupT | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | INFO_REALIGN_3_PRIME | chr7 | 142194036 | ||||||
| chr7:142194036 | CT | C | 66 | a0001c0001t0001g0097 a0001c0001t0001g0108 a0001c0001t0001g0130 others(63): Show |
67 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.4347-2104delT | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | INFO_REALIGN_3_PRIME | chr7 | 142194036 | ||||||
| chr7:142194101 | C | G | 172 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(169): Show |
172 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.4347-2053C>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142194101 | |||||||
| chr7:142194137 | A | G | 1 | a0006c0008t0001g0314 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.4347-2017A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142194137 | |||||||
| chr7:142194167 | C | T | 67 | a0001c0001t0001g0097 a0001c0001t0001g0108 a0001c0001t0001g0130 others(64): Show |
68 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.4347-1987C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142194167 | |||||||
| chr7:142194168 | A | G | 239 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(236): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.4347-1986A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142194168 | |||||||
| chr7:142194379 | A | T | 7 | a0001c0001t0001g0108 a0002c0002t0001g0019 a0002c0002t0001g0021 others(4): Show |
7 | HG00140.hp1 HG01192.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.4347-1775A>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142194379 | |||||||
| chr7:142194454 | A | G | 1 | a0010c0079t0001g0055 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.4347-1700A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142194454 | |||||||
| chr7:142194497 | C | G | 6 | a0001c0004t0001g0066 a0002c0003t0001g0225 a0002c0003t0001g0226 others(3): Show |
6 | HG02572.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.4347-1657C>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142194497 | |||||||
| chr7:142194529 | AT | A | 41 | a0001c0001t0001g0097 a0001c0001t0001g0108 a0001c0001t0001g0130 others(38): Show |
41 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.4347-1622delT | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | INFO_REALIGN_3_PRIME | chr7 | 142194529 | ||||||
| chr7:142194530 | T | A | 1 | a0009c0011t0001g0293 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.4347-1624T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142194530 | |||||||
| chr7:142194533 | C | G | 221 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(218): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.4347-1621C>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142194533 | |||||||
| chr7:142194543 | C | T | 3 | a0001c0004t0002g0065 a0002c0003t0002g0230 a0002c0003t0002g0251 |
3 | HG02970.hp1 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.4347-1611C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142194543 | |||||||
| chr7:142194687 | C | CGT | 79 | a0001c0001t0001g0060 a0001c0001t0001g0074 a0001c0001t0001g0075 others(76): Show |
79 | HG00099.hp1 HG00621.hp2 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.4347-1467_4347-146 others(6): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142194687 | |||||||
| chr7:142194687 | C | CGTGT | 22 | a0001c0001t0001g0107 a0001c0001t0001g0122 a0001c0001t0001g0125 others(19): Show |
22 | HG00438.hp2 HG01099.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.4347-1467_4347-146 others(8): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142194687 | |||||||
| chr7:142194687 | CATGT | C | 5 | a0001c0001t0001g0071 a0001c0001t0001g0095 a0001c0001t0001g0153 others(2): Show |
5 | HG00280.hp1 HG01891.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.4347-1466_4347-146 others(8): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142194687 | |||||||
| chr7:142194687 | CATGTGTG others(5): Show |
C | 1 | a0001c0001t0001g0077 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.4347-1466_4347-145 others(16): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142194687 | |||||||
| chr7:142194688 | A | G | 117 | a0001c0001t0001g0060 a0001c0001t0001g0074 a0001c0001t0001g0075 others(114): Show |
117 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.4347-1466A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142194688 | |||||||
| chr7:142194690 | GTGTGTA | G | 3 | a0013c0016t0001g0041 a0013c0016t0001g0042 a0046c0077t0001g0195 |
3 | HG02486.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.4347-1458_4347-145 others(10): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | INFO_REALIGN_3_PRIME | chr7 | 142194690 | ||||||
| chr7:142194692 | GTGTA | G | 43 | a0001c0001t0001g0097 a0001c0001t0001g0108 a0001c0001t0001g0130 others(40): Show |
43 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.4347-1458_4347-145 others(8): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | INFO_REALIGN_3_PRIME | chr7 | 142194692 | ||||||
| chr7:142194694 | GTA | G | 4 | a0002c0002t0001g0285 a0021c0023t0004g0057 a0022c0027t0001g0040 others(1): Show |
4 | HG01192.hp1 HG02572.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.4347-1458_4347-145 others(6): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | INFO_REALIGN_3_PRIME | chr7 | 142194694 | ||||||
| chr7:142194696 | A | ATGTG | 36 | a0004c0005t0001g0058 a0004c0005t0001g0100 a0004c0005t0001g0105 others(33): Show |
36 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.4347-1428_4347-142 others(8): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | INFO_REALIGN_3_PRIME | chr7 | 142194696 | ||||||
| chr7:142194696 | A | ATGTGTGT others(3): Show |
2 | a0014c0020t0001g0001 a0014c0026t0001g0327 |
3 | HG02723.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4347-1434_4347-142 others(14): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | INFO_REALIGN_3_PRIME | chr7 | 142194696 | ||||||
| chr7:142194696 | A | ATGTGTGT others(5): Show |
1 | a0043c0048t0001g0103 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.4347-1436_4347-142 others(16): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | INFO_REALIGN_3_PRIME | chr7 | 142194696 | ||||||
| chr7:142194696 | A | ATGTGTGT others(7): Show |
2 | a0015c0015t0001g0013 a0015c0015t0001g0297 |
2 | HG02622.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.4347-1438_4347-142 others(18): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | INFO_REALIGN_3_PRIME | chr7 | 142194696 | ||||||
| chr7:142194696 | A | ATGTGTGT others(9): Show |
1 | a0015c0015t0001g0014 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4347-1440_4347-142 others(20): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | INFO_REALIGN_3_PRIME | chr7 | 142194696 | ||||||
| chr7:142194696 | A | G | 129 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(126): Show |
129 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.4347-1458A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142194696 | |||||||
| chr7:142194696 | ATG | A | 92 | a0001c0004t0001g0046 a0001c0004t0001g0063 a0001c0004t0001g0064 others(89): Show |
92 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.4347-1426_4347-142 others(6): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | INFO_REALIGN_3_PRIME | chr7 | 142194696 | ||||||
| chr7:142194696 | ATGTG | A | 6 | a0001c0004t0001g0145 a0003c0009t0001g0053 a0003c0009t0001g0056 others(3): Show |
6 | HG01074.hp1 HG01168.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.4347-1428_4347-142 others(8): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | INFO_REALIGN_3_PRIME | chr7 | 142194696 | ||||||
| chr7:142194744 | T | A | 1 | a0001c0001t0001g0301 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.4347-1410T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142194744 | |||||||
| chr7:142195178 | C | T | 214 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(211): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.4347-976C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142195178 | |||||||
| chr7:142195179 | A | G | 222 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(219): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.4347-975A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142195179 | |||||||
| chr7:142195189 | C | T | 7 | a0009c0011t0001g0023 a0009c0011t0001g0024 a0009c0011t0001g0025 others(4): Show |
7 | HG00642.hp1 HG02809.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.4347-965C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142195189 | |||||||
| chr7:142195279 | C | T | 37 | a0004c0005t0001g0058 a0004c0005t0001g0100 a0004c0005t0001g0105 others(34): Show |
37 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.4347-875C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142195279 | |||||||
| chr7:142195319 | T | C | 1 | a0001c0001t0001g0247 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.4347-835T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142195319 | |||||||
| chr7:142195345 | C | CT | 21 | a0001c0001t0001g0127 a0001c0001t0001g0172 a0002c0002t0001g0034 others(18): Show |
22 | HG00558.hp1 HG00621.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.4347-781dupT | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | INFO_REALIGN_3_PRIME | chr7 | 142195345 | ||||||
| chr7:142195345 | C | CTT | 38 | a0001c0001t0001g0140 a0002c0002t0001g0264 a0002c0002t0001g0284 others(35): Show |
38 | HG00408.hp1 HG00438.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.4347-782_4347-781d others(4): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | INFO_REALIGN_3_PRIME | chr7 | 142195345 | ||||||
| chr7:142195345 | CT | C | 23 | a0001c0001t0001g0080 a0001c0001t0001g0217 a0001c0001t0001g0247 others(20): Show |
23 | HG00323.hp1 HG00408.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.4347-781delT | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | INFO_REALIGN_3_PRIME | chr7 | 142195345 | ||||||
| chr7:142195345 | CTT | C | 76 | a0001c0004t0001g0046 a0001c0004t0001g0063 a0001c0004t0001g0064 others(73): Show |
76 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.4347-782_4347-781d others(4): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | INFO_REALIGN_3_PRIME | chr7 | 142195345 | ||||||
| chr7:142195345 | CTTT | C | 13 | a0001c0004t0001g0167 a0001c0004t0001g0188 a0002c0003t0001g0004 others(10): Show |
13 | HG00280.hp2 HG01069.hp2 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.4347-783_4347-781d others(5): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | INFO_REALIGN_3_PRIME | chr7 | 142195345 | ||||||
| chr7:142195345 | CTTTTTTT others(4): Show |
C | 2 | a0009c0011t0001g0138 a0022c0027t0001g0038 |
2 | HG01891.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.4347-791_4347-781d others(13): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | INFO_REALIGN_3_PRIME | chr7 | 142195345 | ||||||
| chr7:142195418 | C | T | 72 | a0001c0001t0001g0060 a0001c0001t0001g0071 a0001c0001t0001g0074 others(69): Show |
72 | HG00099.hp1 HG00280.hp1 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.4347-736C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142195418 | |||||||
| chr7:142195516 | C | T | 2 | a0001c0004t0001g0201 a0044c0036t0001g0184 |
2 | HG02735.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.4347-638C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142195516 | |||||||
| chr7:142195522 | A | AT | 175 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(172): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.4347-618dupT | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | INFO_REALIGN_3_PRIME | chr7 | 142195522 | ||||||
| chr7:142195558 | T | C | 73 | a0001c0001t0001g0060 a0001c0001t0001g0071 a0001c0001t0001g0074 others(70): Show |
73 | HG00099.hp1 HG00280.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.4347-596T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142195558 | |||||||
| chr7:142195563 | G | A | 1 | a0019c0030t0002g0326 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4347-591G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142195563 | |||||||
| chr7:142195581 | T | C | 1 | a0017c0019t0001g0220 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4347-573T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142195581 | |||||||
| chr7:142195718 | C | G | 5 | a0001c0004t0001g0066 a0002c0003t0001g0225 a0002c0003t0001g0226 others(2): Show |
5 | HG02615.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4347-436C>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142195718 | |||||||
| chr7:142195723 | T | G | 220 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(217): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.4347-431T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142195723 | |||||||
| chr7:142195756 | T | C | 221 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(218): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.4347-398T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142195756 | |||||||
| chr7:142195822 | G | A | 1 | a0002c0003t0001g0049 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.4347-332G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142195822 | |||||||
| chr7:142195969 | T | C | 125 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(122): Show |
125 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.4347-185T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142195969 | |||||||
| chr7:142196005 | T | C | 1 | a0001c0001t0001g0318 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.4347-149T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142196005 | |||||||
| chr7:142196116 | T | C | 1 | a0005c0006t0001g0238 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.4347-38T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 37/47 | chr7 | 142196116 | |||||||
| chr7:142196303 | C | T | 1 | a0047c0070t0001g0147 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4480+16C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 38/47 | chr7 | 142196303 | |||||||
| chr7:142196308 | G | A | 1 | a0001c0001t0001g0116 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.4480+21G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 38/47 | chr7 | 142196308 | |||||||
| chr7:142196912 | C | A | 1 | a0004c0005t0001g0177 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.4632+96C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 40/47 | chr7 | 142196912 | |||||||
| chr7:142197131 | G | A | 38 | a0004c0005t0001g0058 a0004c0005t0001g0100 a0004c0005t0001g0105 others(35): Show |
38 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.4633-269G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 40/47 | chr7 | 142197131 | |||||||
| chr7:142197167 | T | C | 38 | a0004c0005t0001g0058 a0004c0005t0001g0100 a0004c0005t0001g0105 others(35): Show |
38 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.4633-233T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 40/47 | chr7 | 142197167 | |||||||
| chr7:142197766 | C | T | 1 | a0009c0011t0002g0036 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4866+38C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 42/47 | chr7 | 142197766 | |||||||
| chr7:142197795 | T | C | 226 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(223): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.4866+67T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 42/47 | chr7 | 142197795 | |||||||
| chr7:142197932 | T | A | 6 | a0001c0004t0001g0066 a0002c0003t0001g0225 a0002c0003t0001g0226 others(3): Show |
6 | HG02615.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.4866+204T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 42/47 | chr7 | 142197932 | |||||||
| chr7:142197961 | A | AC | 231 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(228): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.4867-178_4867-177i others(3): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 42/47 | chr7 | 142197961 | |||||||
| chr7:142198223 | C | A | 124 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(121): Show |
124 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.4923+28C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 43/47 | chr7 | 142198223 | |||||||
| chr7:142198347 | G | C | 1 | a0024c0075t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4923+152G>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 43/47 | chr7 | 142198347 | |||||||
| chr7:142198356 | C | T | 5 | a0033c0035t0003g0061 a0035c0067t0003g0146 a0038c0059t0001g0026 others(2): Show |
5 | HG01952.hp1 HG02055.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.4923+161C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 43/47 | chr7 | 142198356 | |||||||
| chr7:142198480 | A | T | 1 | a0002c0002t0001g0266 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.4924-135A>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 43/47 | chr7 | 142198480 | |||||||
| chr7:142198577 | T | C | 4 | a0033c0035t0003g0061 a0035c0067t0003g0146 a0038c0059t0001g0026 others(1): Show |
4 | HG01952.hp1 HG02055.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.4924-38T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 43/47 | chr7 | 142198577 | |||||||
| chr7:142198758 | G | A | 1 | a0002c0003t0001g0255 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.5048+19G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 44/47 | chr7 | 142198758 | |||||||
| chr7:142198817 | C | T | 1 | a0030c0056t0001g0085 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.5048+78C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 44/47 | chr7 | 142198817 | |||||||
| chr7:142198880 | T | C | 223 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(220): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.5048+141T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 44/47 | chr7 | 142198880 | |||||||
| chr7:142198897 | T | C | 223 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(220): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.5048+158T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 44/47 | chr7 | 142198897 | |||||||
| chr7:142199159 | G | A | 9 | a0002c0003t0001g0152 a0002c0003t0001g0244 a0002c0003t0001g0306 others(6): Show |
9 | HG01069.hp2 HG01167.hp2 NA18947.hp1 others(6): Show |
intron_variant | MODIFIER | c.5048+420G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 44/47 | chr7 | 142199159 | |||||||
| chr7:142199231 | T | A | 38 | a0004c0005t0001g0058 a0004c0005t0001g0100 a0004c0005t0001g0105 others(35): Show |
38 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.5048+492T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 44/47 | chr7 | 142199231 | |||||||
| chr7:142199320 | A | G | 1 | a0002c0003t0001g0049 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.5049-560A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 44/47 | chr7 | 142199320 | |||||||
| chr7:142199480 | TA | T | 237 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.5049-395delA | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 44/47 | INFO_REALIGN_3_PRIME | chr7 | 142199480 | ||||||
| chr7:142199701 | T | C | 3 | a0015c0015t0001g0013 a0015c0015t0001g0014 a0015c0015t0001g0297 |
3 | HG02257.hp2 HG02622.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.5049-179T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 44/47 | chr7 | 142199701 | |||||||
| chr7:142199710 | A | G | 2 | a0009c0011t0001g0138 a0022c0027t0001g0038 |
2 | HG01891.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.5049-170A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 44/47 | chr7 | 142199710 | |||||||
| chr7:142199719 | A | G | 226 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(223): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.5049-161A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 44/47 | chr7 | 142199719 | |||||||
| chr7:142199822 | C | T | 2 | a0046c0077t0001g0195 a0062c0076t0001g0325 |
2 | HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.5049-58C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 44/47 | chr7 | 142199822 | |||||||
| chr7:142199860 | C | CT | 204 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(201): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
splice_region_variant&intron_variant | LOW | c.5049-6dupT | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 44/47 | INFO_REALIGN_3_PRIME | chr7 | 142199860 | ||||||
| chr7:142199860 | C | CTT | 20 | a0001c0001t0001g0074 a0002c0002t0001g0016 a0002c0002t0001g0043 others(17): Show |
20 | HG01099.hp1 HG01099.hp2 HG01517.hp2 others(17): Show |
splice_region_variant&intron_variant | LOW | c.5049-7_5049-6dupTT | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 44/47 | INFO_REALIGN_3_PRIME | chr7 | 142199860 | ||||||
| chr7:142200088 | C | A | 1 | a0002c0003t0001g0292 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5137+120C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142200088 | |||||||
| chr7:142200278 | G | A | 124 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(121): Show |
124 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.5137+310G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142200278 | |||||||
| chr7:142200298 | G | A | 2 | a0002c0002t0001g0035 a0002c0002t0001g0265 |
2 | HG01106.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.5137+330G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142200298 | |||||||
| chr7:142200389 | T | A | 1 | a0039c0046t0001g0102 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.5137+421T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142200389 | |||||||
| chr7:142200454 | T | C | 1 | a0004c0005t0001g0105 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.5137+486T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142200454 | |||||||
| chr7:142200561 | A | C | 227 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(224): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.5137+593A>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142200561 | |||||||
| chr7:142200884 | T | C | 5 | a0014c0020t0001g0001 a0014c0026t0001g0196 a0014c0026t0001g0327 others(2): Show |
6 | HG01243.hp1 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.5137+916T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142200884 | |||||||
| chr7:142200975 | T | G | 6 | a0001c0004t0001g0066 a0002c0003t0001g0225 a0002c0003t0001g0226 others(3): Show |
6 | HG02615.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.5137+1007T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142200975 | |||||||
| chr7:142200987 | C | T | 1 | a0019c0030t0002g0326 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.5137+1019C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142200987 | |||||||
| chr7:142200990 | TTATG | T | 218 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(215): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.5137+1027_5137+103 others(8): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | INFO_REALIGN_3_PRIME | chr7 | 142200990 | ||||||
| chr7:142201071 | C | CT | 14 | a0001c0001t0001g0273 a0002c0002t0001g0043 a0002c0002t0001g0304 others(11): Show |
14 | HG00323.hp1 HG00642.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.5137+1113dupT | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | INFO_REALIGN_3_PRIME | chr7 | 142201071 | ||||||
| chr7:142201071 | C | CTT | 70 | a0001c0001t0001g0087 a0001c0001t0001g0101 a0001c0001t0001g0108 others(67): Show |
70 | HG00140.hp1 HG00558.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.5137+1112_5137+111 others(6): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | INFO_REALIGN_3_PRIME | chr7 | 142201071 | ||||||
| chr7:142201071 | C | CTTT | 118 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(115): Show |
118 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.5137+1111_5137+111 others(7): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | INFO_REALIGN_3_PRIME | chr7 | 142201071 | ||||||
| chr7:142201071 | C | CTTTT | 11 | a0001c0001t0001g0112 a0001c0001t0001g0178 a0001c0001t0001g0300 others(8): Show |
11 | HG01928.hp1 HG02080.hp1 HG03831.hp1 others(8): Show |
intron_variant | MODIFIER | c.5137+1110_5137+111 others(8): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | INFO_REALIGN_3_PRIME | chr7 | 142201071 | ||||||
| chr7:142201077 | T | C | 2 | a0002c0003t0001g0004 a0002c0003t0001g0088 |
2 | HG01168.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.5137+1109T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142201077 | |||||||
| chr7:142201081 | TC | T | 14 | a0001c0004t0001g0066 a0002c0003t0001g0049 a0002c0003t0001g0225 others(11): Show |
15 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.5137+1114delC | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142201081 | |||||||
| chr7:142201082 | C | T | 219 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.5137+1114C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142201082 | |||||||
| chr7:142201132 | C | T | 172 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(169): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.5137+1164C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142201132 | |||||||
| chr7:142201266 | C | T | 10 | a0002c0003t0001g0197 a0002c0003t0001g0198 a0009c0011t0001g0023 others(7): Show |
10 | HG00642.hp1 HG01261.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.5137+1298C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142201266 | |||||||
| chr7:142201320 | T | C | 1 | a0010c0017t0001g0256 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.5137+1352T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142201320 | |||||||
| chr7:142201321 | C | T | 1 | a0048c0065t0002g0047 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.5137+1353C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142201321 | |||||||
| chr7:142201322 | G | A | 218 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(215): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.5137+1354G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142201322 | |||||||
| chr7:142201359 | C | T | 1 | a0023c0025t0001g0052 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.5137+1391C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142201359 | |||||||
| chr7:142201360 | G | A | 2 | a0001c0004t0001g0046 a0021c0023t0001g0194 |
2 | NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.5137+1392G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142201360 | |||||||
| chr7:142201418 | G | A | 1 | a0005c0006t0001g0248 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.5137+1450G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142201418 | |||||||
| chr7:142201522 | G | A | 218 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(215): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.5137+1554G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142201522 | |||||||
| chr7:142201657 | A | G | 1 | a0038c0059t0001g0026 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.5137+1689A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142201657 | |||||||
| chr7:142201706 | C | T | 240 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(237): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.5137+1738C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142201706 | |||||||
| chr7:142201742 | A | G | 1 | a0001c0004t0001g0089 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.5137+1774A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142201742 | |||||||
| chr7:142201776 | C | A | 1 | a0001c0004t0001g0046 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.5137+1808C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142201776 | |||||||
| chr7:142201981 | AAAAGCAA others(2): Show |
A | 231 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(228): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.5137+2025_5137+203 others(13): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | INFO_REALIGN_3_PRIME | chr7 | 142201981 | ||||||
| chr7:142202346 | G | A | 226 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(223): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.5137+2378G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142202346 | |||||||
| chr7:142202503 | G | A | 1 | a0007c0080t0001g0076 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.5137+2535G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142202503 | |||||||
| chr7:142202508 | C | T | 9 | a0001c0001t0001g0101 a0001c0001t0001g0117 a0001c0001t0001g0154 others(6): Show |
9 | HG02135.hp1 NA18943.hp1 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.5137+2540C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142202508 | |||||||
| chr7:142202838 | T | A | 4 | a0001c0004t0002g0065 a0002c0003t0002g0230 a0002c0003t0002g0251 others(1): Show |
4 | HG02572.hp2 HG02970.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.5137+2870T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142202838 | |||||||
| chr7:142203100 | C | T | 5 | a0033c0035t0003g0061 a0035c0067t0003g0146 a0038c0059t0001g0026 others(2): Show |
5 | HG01952.hp1 HG02055.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.5137+3132C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142203100 | |||||||
| chr7:142203104 | T | A | 4 | a0033c0035t0003g0061 a0035c0067t0003g0146 a0038c0059t0001g0026 others(1): Show |
4 | HG01952.hp1 HG02055.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.5137+3136T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142203104 | |||||||
| chr7:142203143 | T | C | 4 | a0033c0035t0003g0061 a0035c0067t0003g0146 a0038c0059t0001g0026 others(1): Show |
4 | HG01952.hp1 HG02055.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.5137+3175T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142203143 | |||||||
| chr7:142203163 | T | C | 10 | a0001c0001t0001g0125 a0001c0001t0001g0178 a0001c0001t0001g0190 others(7): Show |
10 | HG01071.hp1 HG01928.hp1 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.5137+3195T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142203163 | |||||||
| chr7:142203222 | T | C | 4 | a0033c0035t0003g0061 a0035c0067t0003g0146 a0038c0059t0001g0026 others(1): Show |
4 | HG01952.hp1 HG02055.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.5137+3254T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142203222 | |||||||
| chr7:142203275 | T | C | 1 | a0017c0019t0001g0232 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.5137+3307T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142203275 | |||||||
| chr7:142203523 | A | G | 1 | a0019c0030t0002g0326 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.5137+3555A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142203523 | |||||||
| chr7:142203632 | G | T | 1 | a0002c0003t0001g0049 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.5137+3664G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142203632 | |||||||
| chr7:142203808 | C | G | 1 | a0039c0046t0001g0102 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.5137+3840C>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142203808 | |||||||
| chr7:142203831 | TA | T | 39 | a0001c0004t0001g0046 a0004c0005t0001g0058 a0004c0005t0001g0100 others(36): Show |
39 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.5137+3870delA | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | INFO_REALIGN_3_PRIME | chr7 | 142203831 | ||||||
| chr7:142204043 | T | C | 14 | a0001c0004t0001g0066 a0002c0003t0001g0225 a0002c0003t0001g0226 others(11): Show |
15 | HG01243.hp1 HG02257.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.5137+4075T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142204043 | |||||||
| chr7:142204089 | A | T | 1 | a0039c0046t0001g0102 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.5137+4121A>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142204089 | |||||||
| chr7:142204765 | T | C | 80 | a0001c0004t0001g0063 a0001c0004t0001g0064 a0001c0004t0001g0072 others(77): Show |
80 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.5138-3808T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142204765 | |||||||
| chr7:142204885 | A | G | 5 | a0033c0035t0003g0061 a0035c0067t0003g0146 a0038c0059t0001g0026 others(2): Show |
5 | HG01952.hp1 HG02055.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.5138-3688A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142204885 | |||||||
| chr7:142204930 | G | A | 5 | a0033c0035t0003g0061 a0035c0067t0003g0146 a0038c0059t0001g0026 others(2): Show |
5 | HG01952.hp1 HG02055.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.5138-3643G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142204930 | |||||||
| chr7:142204963 | T | C | 10 | a0001c0001t0001g0125 a0001c0001t0001g0178 a0001c0001t0001g0190 others(7): Show |
10 | HG01071.hp1 HG01928.hp1 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.5138-3610T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142204963 | |||||||
| chr7:142204979 | A | G | 1 | a0042c0060t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.5138-3594A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142204979 | |||||||
| chr7:142205040 | G | A | 5 | a0001c0004t0001g0066 a0002c0003t0001g0225 a0002c0003t0001g0226 others(2): Show |
5 | HG02615.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.5138-3533G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142205040 | |||||||
| chr7:142205102 | T | C | 1 | a0063c0041t0001g0139 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.5138-3471T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142205102 | |||||||
| chr7:142205145 | G | A | 1 | a0019c0030t0002g0326 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.5138-3428G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142205145 | |||||||
| chr7:142205172 | C | T | 1 | a0001c0004t0001g0046 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.5138-3401C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142205172 | |||||||
| chr7:142205209 | A | G | 6 | a0002c0003t0001g0197 a0002c0003t0001g0198 a0010c0017t0001g0256 others(3): Show |
6 | HG01074.hp1 HG01261.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.5138-3364A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142205209 | |||||||
| chr7:142205487 | TA | T | 212 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(209): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.5138-3084delA | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | INFO_REALIGN_3_PRIME | chr7 | 142205487 | ||||||
| chr7:142205488 | A | T | 27 | a0001c0004t0001g0066 a0002c0003t0001g0049 a0002c0003t0001g0197 others(24): Show |
28 | HG01074.hp1 HG01243.hp1 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.5138-3085A>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142205488 | |||||||
| chr7:142205629 | T | C | 1 | a0006c0008t0001g0321 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.5138-2944T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142205629 | |||||||
| chr7:142205717 | C | T | 4 | a0033c0035t0003g0061 a0035c0067t0003g0146 a0038c0059t0001g0026 others(1): Show |
4 | HG01952.hp1 HG02055.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.5138-2856C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142205717 | |||||||
| chr7:142205718 | G | A | 5 | a0014c0020t0001g0001 a0014c0026t0001g0196 a0014c0026t0001g0327 others(2): Show |
6 | HG01243.hp1 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.5138-2855G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142205718 | |||||||
| chr7:142206013 | A | C | 7 | a0002c0003t0001g0049 a0002c0003t0001g0197 a0002c0003t0001g0198 others(4): Show |
7 | HG01074.hp1 HG01261.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.5138-2560A>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142206013 | |||||||
| chr7:142206072 | T | G | 1 | a0013c0016t0001g0173 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5138-2501T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142206072 | |||||||
| chr7:142206186 | G | C | 3 | a0001c0001t0001g0071 a0001c0001t0001g0112 a0001c0001t0001g0153 |
3 | NA19062.hp1 NA19068.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.5138-2387G>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142206186 | |||||||
| chr7:142206239 | C | T | 1 | a0002c0002t0001g0235 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.5138-2334C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142206239 | |||||||
| chr7:142206351 | T | C | 1 | a0035c0067t0003g0146 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.5138-2222T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142206351 | |||||||
| chr7:142206361 | T | C | 1 | a0002c0002t0001g0151 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.5138-2212T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142206361 | |||||||
| chr7:142206402 | T | G | 3 | a0015c0015t0001g0013 a0015c0015t0001g0014 a0015c0015t0001g0297 |
3 | HG02257.hp2 HG02622.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.5138-2171T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142206402 | |||||||
| chr7:142206481 | T | A | 38 | a0004c0005t0001g0058 a0004c0005t0001g0100 a0004c0005t0001g0105 others(35): Show |
38 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.5138-2092T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142206481 | |||||||
| chr7:142206615 | A | C | 2 | a0004c0005t0001g0058 a0004c0005t0001g0270 |
2 | NA18969.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.5138-1958A>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142206615 | |||||||
| chr7:142206694 | A | G | 1 | a0007c0034t0001g0135 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.5138-1879A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142206694 | |||||||
| chr7:142206817 | T | C | 3 | a0006c0008t0001g0094 a0026c0029t0001g0174 a0026c0029t0001g0175 |
3 | HG03490.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.5138-1756T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142206817 | |||||||
| chr7:142206818 | A | G | 7 | a0001c0004t0001g0066 a0002c0003t0001g0219 a0002c0003t0001g0225 others(4): Show |
7 | HG02615.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.5138-1755A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142206818 | |||||||
| chr7:142206859 | A | C | 1 | a0063c0041t0001g0139 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.5138-1714A>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142206859 | |||||||
| chr7:142206861 | G | C | 1 | a0001c0004t0001g0121 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.5138-1712G>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142206861 | |||||||
| chr7:142206878 | C | G | 43 | a0001c0001t0001g0087 a0001c0001t0001g0171 a0002c0002t0001g0016 others(40): Show |
43 | HG00323.hp1 HG00438.hp2 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.5138-1695C>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142206878 | |||||||
| chr7:142206883 | A | T | 125 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(122): Show |
125 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.5138-1690A>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142206883 | |||||||
| chr7:142207056 | G | C | 3 | a0009c0011t0001g0138 a0022c0027t0001g0038 a0040c0043t0001g0059 |
3 | HG01891.hp1 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.5138-1517G>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142207056 | |||||||
| chr7:142207156 | C | T | 2 | a0001c0001t0001g0328 a0001c0004t0001g0165 |
2 | HG00323.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.5138-1417C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142207156 | |||||||
| chr7:142207401 | C | CATTT | 10 | a0002c0002t0001g0043 a0002c0002t0001g0045 a0002c0002t0001g0050 others(7): Show |
10 | HG01261.hp2 HG02280.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.5138-1147_5138-114 others(8): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | INFO_REALIGN_3_PRIME | chr7 | 142207401 | ||||||
| chr7:142207401 | CATTT | C | 5 | a0033c0035t0003g0061 a0035c0067t0003g0146 a0038c0059t0001g0026 others(2): Show |
5 | HG01952.hp1 HG02055.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.5138-1147_5138-114 others(8): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | INFO_REALIGN_3_PRIME | chr7 | 142207401 | ||||||
| chr7:142207487 | G | A | 4 | a0033c0035t0003g0061 a0035c0067t0003g0146 a0038c0059t0001g0026 others(1): Show |
4 | HG01952.hp1 HG02055.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.5138-1086G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142207487 | |||||||
| chr7:142207488 | C | T | 5 | a0033c0035t0003g0061 a0035c0067t0003g0146 a0038c0059t0001g0026 others(2): Show |
5 | HG01952.hp1 HG02055.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.5138-1085C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142207488 | |||||||
| chr7:142207511 | C | T | 38 | a0004c0005t0001g0058 a0004c0005t0001g0100 a0004c0005t0001g0105 others(35): Show |
38 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.5138-1062C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142207511 | |||||||
| chr7:142207570 | C | T | 1 | a0001c0001t0001g0125 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.5138-1003C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142207570 | |||||||
| chr7:142207587 | G | A | 1 | a0039c0046t0001g0102 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.5138-986G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142207587 | |||||||
| chr7:142207757 | G | C | 1 | a0007c0082t0001g0110 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.5138-816G>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142207757 | |||||||
| chr7:142207852 | A | T | 3 | a0015c0015t0001g0013 a0015c0015t0001g0014 a0015c0015t0001g0297 |
3 | HG02257.hp2 HG02622.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.5138-721A>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142207852 | |||||||
| chr7:142207987 | A | G | 3 | a0001c0004t0001g0191 a0002c0003t0001g0210 a0059c0057t0001g0206 |
3 | NA19004.hp2 NA19062.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.5138-586A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142207987 | |||||||
| chr7:142208286 | A | G | 8 | a0004c0005t0001g0100 a0004c0005t0001g0105 a0004c0005t0001g0133 others(5): Show |
8 | HG00408.hp1 HG00558.hp1 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.5138-287A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 45/47 | chr7 | 142208286 | |||||||
| chr7:142208701 | T | C | 1 | a0019c0030t0002g0326 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.5187+79T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142208701 | |||||||
| chr7:142208854 | G | T | 1 | a0038c0059t0001g0026 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.5187+232G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142208854 | |||||||
| chr7:142208874 | T | C | 1 | a0049c0064t0001g0027 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.5187+252T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142208874 | |||||||
| chr7:142208959 | T | G | 1 | a0001c0004t0001g0119 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.5187+337T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142208959 | |||||||
| chr7:142209120 | G | A | 246 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(243): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.5187+498G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142209120 | |||||||
| chr7:142209267 | A | T | 2 | a0008c0010t0001g0090 a0008c0010t0001g0091 |
2 | HG00609.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.5187+645A>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142209267 | |||||||
| chr7:142209282 | C | G | 7 | a0001c0004t0001g0066 a0002c0003t0001g0219 a0002c0003t0001g0225 others(4): Show |
7 | HG02615.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.5187+660C>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142209282 | |||||||
| chr7:142209340 | G | A | 38 | a0001c0001t0001g0097 a0001c0001t0001g0108 a0001c0001t0001g0130 others(35): Show |
38 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.5187+718G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142209340 | |||||||
| chr7:142209760 | T | C | 1 | a0048c0065t0002g0047 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.5187+1138T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142209760 | |||||||
| chr7:142209840 | T | C | 1 | a0038c0059t0001g0026 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.5187+1218T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142209840 | |||||||
| chr7:142209848 | T | C | 1 | a0005c0006t0001g0242 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.5187+1226T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142209848 | |||||||
| chr7:142209876 | G | T | 1 | a0001c0001t0001g0180 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.5187+1254G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142209876 | |||||||
| chr7:142210026 | G | A | 7 | a0001c0004t0001g0066 a0002c0003t0001g0219 a0002c0003t0001g0225 others(4): Show |
7 | HG02615.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.5187+1404G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142210026 | |||||||
| chr7:142210199 | C | T | 227 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(224): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.5187+1577C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142210199 | |||||||
| chr7:142210222 | G | A | 1 | a0018c0028t0001g0203 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.5187+1600G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142210222 | |||||||
| chr7:142210299 | GT | G | 222 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(219): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.5187+1689delT | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | INFO_REALIGN_3_PRIME | chr7 | 142210299 | ||||||
| chr7:142210300 | T | G | 1 | a0001c0001t0001g0218 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.5187+1678T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142210300 | |||||||
| chr7:142210321 | G | A | 5 | a0033c0035t0003g0061 a0035c0067t0003g0146 a0038c0059t0001g0026 others(2): Show |
5 | HG01952.hp1 HG02055.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.5187+1699G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142210321 | |||||||
| chr7:142210357 | C | G | 1 | a0002c0058t0001g0032 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.5187+1735C>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142210357 | |||||||
| chr7:142210396 | C | T | 2 | a0002c0003t0001g0004 a0002c0003t0001g0088 |
2 | HG01168.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.5187+1774C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142210396 | |||||||
| chr7:142210492 | G | A | 1 | a0012c0012t0001g0322 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.5187+1870G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142210492 | |||||||
| chr7:142210518 | A | G | 2 | a0002c0003t0001g0033 a0002c0003t0001g0073 |
2 | HG02647.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.5187+1896A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142210518 | |||||||
| chr7:142210772 | T | C | 1 | a0039c0046t0001g0102 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.5187+2150T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142210772 | |||||||
| chr7:142210825 | T | C | 3 | a0009c0011t0001g0138 a0022c0027t0001g0038 a0040c0043t0001g0059 |
3 | HG01891.hp1 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.5187+2203T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142210825 | |||||||
| chr7:142211099 | C | T | 4 | a0001c0004t0002g0065 a0002c0003t0002g0230 a0002c0003t0002g0251 others(1): Show |
4 | HG02572.hp2 HG02970.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.5187+2477C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142211099 | |||||||
| chr7:142211127 | A | G | 173 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(170): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.5187+2505A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142211127 | |||||||
| chr7:142211585 | G | C | 4 | a0002c0002t0001g0212 a0002c0002t0001g0266 a0002c0002t0001g0288 others(1): Show |
4 | HG02572.hp1 NA18998.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.5187+2963G>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142211585 | |||||||
| chr7:142211744 | T | C | 38 | a0001c0001t0001g0097 a0001c0001t0001g0108 a0001c0001t0001g0130 others(35): Show |
38 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.5187+3122T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142211744 | |||||||
| chr7:142211757 | T | G | 5 | a0033c0035t0003g0061 a0035c0067t0003g0146 a0038c0059t0001g0026 others(2): Show |
5 | HG01952.hp1 HG02055.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.5187+3135T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142211757 | |||||||
| chr7:142211873 | C | G | 15 | a0002c0003t0001g0049 a0002c0003t0001g0197 a0002c0003t0001g0198 others(12): Show |
16 | HG01074.hp1 HG01243.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.5187+3251C>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142211873 | |||||||
| chr7:142211876 | C | T | 1 | a0005c0006t0001g0233 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.5187+3254C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142211876 | |||||||
| chr7:142211949 | G | A | 1 | a0009c0011t0001g0293 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.5187+3327G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142211949 | |||||||
| chr7:142212028 | G | A | 1 | a0039c0046t0001g0102 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.5187+3406G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142212028 | |||||||
| chr7:142212068 | A | G | 1 | a0003c0007t0001g0070 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.5187+3446A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142212068 | |||||||
| chr7:142212070 | A | G | 3 | a0002c0003t0001g0197 a0002c0003t0001g0198 a0024c0074t0001g0031 |
3 | HG01261.hp2 HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.5187+3448A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142212070 | |||||||
| chr7:142212074 | T | C | 1 | a0047c0070t0001g0147 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.5187+3452T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142212074 | |||||||
| chr7:142212099 | T | C | 6 | a0002c0003t0001g0197 a0002c0003t0001g0198 a0010c0017t0001g0256 others(3): Show |
6 | HG01074.hp1 HG01261.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.5187+3477T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142212099 | |||||||
| chr7:142212144 | G | A | 1 | a0002c0003t0001g0219 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.5187+3522G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142212144 | |||||||
| chr7:142212350 | A | G | 227 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(224): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.5187+3728A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142212350 | |||||||
| chr7:142212545 | G | A | 1 | a0002c0003t0001g0311 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.5187+3923G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142212545 | |||||||
| chr7:142212583 | C | T | 1 | a0039c0046t0001g0102 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.5187+3961C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142212583 | |||||||
| chr7:142212640 | C | T | 2 | a0026c0029t0001g0174 a0026c0029t0001g0175 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.5187+4018C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142212640 | |||||||
| chr7:142212643 | A | G | 1 | a0001c0004t0001g0160 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.5187+4021A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142212643 | |||||||
| chr7:142212663 | C | A | 3 | a0001c0001t0001g0217 a0001c0001t0001g0268 a0028c0024t0001g0204 |
3 | NA18964.hp2 NA18984.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.5187+4041C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142212663 | |||||||
| chr7:142212721 | C | T | 173 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(170): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.5187+4099C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142212721 | |||||||
| chr7:142212767 | A | G | 1 | a0006c0008t0001g0315 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.5187+4145A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142212767 | |||||||
| chr7:142212772 | T | C | 173 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(170): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.5187+4150T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142212772 | |||||||
| chr7:142212927 | A | G | 1 | a0002c0002t0001g0021 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.5187+4305A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142212927 | |||||||
| chr7:142213137 | A | G | 5 | a0033c0035t0003g0061 a0035c0067t0003g0146 a0038c0059t0001g0026 others(2): Show |
5 | HG01952.hp1 HG02055.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.5187+4515A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142213137 | |||||||
| chr7:142213245 | CA | C | 5 | a0033c0035t0003g0061 a0035c0067t0003g0146 a0038c0059t0001g0026 others(2): Show |
5 | HG01952.hp1 HG02055.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.5187+4624delA | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142213245 | |||||||
| chr7:142213263 | T | G | 8 | a0014c0020t0001g0001 a0014c0026t0001g0196 a0014c0026t0001g0327 others(5): Show |
9 | HG01243.hp1 HG02257.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.5187+4641T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142213263 | |||||||
| chr7:142213281 | C | A | 174 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(171): Show |
174 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.5187+4659C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142213281 | |||||||
| chr7:142213421 | G | A | 1 | a0003c0007t0001g0120 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.5187+4799G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142213421 | |||||||
| chr7:142213443 | A | G | 80 | a0001c0004t0001g0063 a0001c0004t0001g0064 a0001c0004t0001g0072 others(77): Show |
80 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.5187+4821A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142213443 | |||||||
| chr7:142213496 | C | A | 4 | a0001c0004t0002g0065 a0002c0003t0002g0230 a0002c0003t0002g0251 others(1): Show |
4 | HG02572.hp2 HG02970.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.5188-4865C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142213496 | |||||||
| chr7:142213535 | C | CTATAAAA others(1): Show |
3 | a0002c0002t0001g0264 a0002c0002t0001g0310 a0052c0071t0001g0162 |
3 | HG03831.hp2 HG03942.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.5188-4820_5188-481 others(12): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | INFO_REALIGN_3_PRIME | chr7 | 142213535 | ||||||
| chr7:142213535 | C | CTATAAAC others(1): Show |
170 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(167): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.5188-4825_5188-481 others(12): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | INFO_REALIGN_3_PRIME | chr7 | 142213535 | ||||||
| chr7:142213738 | A | G | 1 | a0002c0002t0001g0016 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.5188-4623A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142213738 | |||||||
| chr7:142213963 | C | T | 241 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(238): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.5188-4398C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142213963 | |||||||
| chr7:142214059 | C | T | 5 | a0033c0035t0003g0061 a0035c0067t0003g0146 a0038c0059t0001g0026 others(2): Show |
5 | HG01952.hp1 HG02055.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.5188-4302C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142214059 | |||||||
| chr7:142214168 | T | C | 1 | a0040c0043t0001g0059 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5188-4193T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142214168 | |||||||
| chr7:142214288 | G | A | 1 | a0007c0033t0001g0155 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.5188-4073G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142214288 | |||||||
| chr7:142214318 | A | C | 240 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(237): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.5188-4043A>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142214318 | |||||||
| chr7:142214395 | A | G | 1 | a0002c0003t0001g0007 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.5188-3966A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142214395 | |||||||
| chr7:142214471 | A | G | 1 | a0054c0078t0001g0143 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.5188-3890A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142214471 | |||||||
| chr7:142214474 | A | C | 2 | a0001c0001t0001g0171 a0002c0002t0001g0209 |
2 | NA18993.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.5188-3887A>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142214474 | |||||||
| chr7:142214515 | T | C | 1 | a0001c0004t0001g0046 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.5188-3846T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142214515 | |||||||
| chr7:142214838 | T | A | 10 | a0001c0001t0001g0067 a0001c0001t0001g0107 a0001c0001t0001g0116 others(7): Show |
10 | HG00423.hp2 HG00621.hp1 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.5188-3523T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142214838 | |||||||
| chr7:142214965 | G | T | 1 | a0019c0030t0002g0326 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.5188-3396G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142214965 | |||||||
| chr7:142215095 | T | C | 1 | a0014c0020t0001g0001 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.5188-3266T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142215095 | |||||||
| chr7:142215355 | C | T | 1 | a0040c0043t0001g0059 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5188-3006C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142215355 | |||||||
| chr7:142215376 | G | T | 2 | a0009c0011t0001g0138 a0022c0027t0001g0038 |
2 | HG01891.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.5188-2985G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142215376 | |||||||
| chr7:142215458 | TA | T | 10 | a0001c0001t0001g0080 a0001c0001t0001g0096 a0001c0001t0001g0247 others(7): Show |
10 | HG01074.hp1 HG01516.hp2 HG03540.hp2 others(7): Show |
intron_variant | MODIFIER | c.5188-2888delA | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | INFO_REALIGN_3_PRIME | chr7 | 142215458 | ||||||
| chr7:142215556 | T | A | 3 | a0002c0002t0001g0249 a0002c0002t0001g0303 a0003c0007t0001g0082 |
3 | HG00621.hp2 HG02040.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.5188-2805T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142215556 | |||||||
| chr7:142215632 | C | T | 5 | a0001c0004t0001g0066 a0002c0003t0001g0225 a0002c0003t0001g0226 others(2): Show |
5 | HG02615.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.5188-2729C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142215632 | |||||||
| chr7:142215745 | C | T | 1 | a0002c0003t0001g0219 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.5188-2616C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142215745 | |||||||
| chr7:142215758 | C | CAA | 7 | a0001c0004t0001g0066 a0002c0003t0001g0219 a0002c0003t0001g0225 others(4): Show |
7 | HG02615.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.5188-2585_5188-258 others(6): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | INFO_REALIGN_3_PRIME | chr7 | 142215758 | ||||||
| chr7:142215758 | CA | C | 168 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(165): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.5188-2584delA | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | INFO_REALIGN_3_PRIME | chr7 | 142215758 | ||||||
| chr7:142215758 | CAA | C | 7 | a0001c0001t0001g0273 a0003c0007t0001g0120 a0035c0067t0003g0146 others(4): Show |
7 | HG01069.hp1 HG02055.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.5188-2585_5188-258 others(6): Show |
MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | INFO_REALIGN_3_PRIME | chr7 | 142215758 | ||||||
| chr7:142215773 | A | C | 1 | a0009c0011t0001g0293 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.5188-2588A>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142215773 | |||||||
| chr7:142215790 | T | C | 135 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(132): Show |
135 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.5188-2571T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142215790 | |||||||
| chr7:142215909 | G | A | 232 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(229): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.5188-2452G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142215909 | |||||||
| chr7:142216041 | T | C | 2 | a0002c0003t0001g0225 a0002c0003t0001g0226 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.5188-2320T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142216041 | |||||||
| chr7:142216218 | T | C | 1 | a0011c0013t0001g0246 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5188-2143T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142216218 | |||||||
| chr7:142216225 | C | T | 39 | a0001c0004t0001g0046 a0004c0005t0001g0058 a0004c0005t0001g0100 others(36): Show |
39 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.5188-2136C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142216225 | |||||||
| chr7:142216241 | C | T | 3 | a0002c0002t0001g0264 a0002c0002t0001g0310 a0052c0071t0001g0162 |
3 | HG03831.hp2 HG03942.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.5188-2120C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142216241 | |||||||
| chr7:142216491 | A | C | 1 | a0002c0003t0001g0049 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.5188-1870A>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142216491 | |||||||
| chr7:142216492 | A | G | 7 | a0001c0004t0001g0066 a0002c0003t0001g0219 a0002c0003t0001g0225 others(4): Show |
7 | HG02615.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.5188-1869A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142216492 | |||||||
| chr7:142216564 | G | A | 7 | a0001c0004t0001g0066 a0002c0003t0001g0219 a0002c0003t0001g0225 others(4): Show |
7 | HG02615.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.5188-1797G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142216564 | |||||||
| chr7:142216879 | G | T | 10 | a0001c0001t0001g0067 a0001c0001t0001g0107 a0001c0001t0001g0116 others(7): Show |
10 | HG00423.hp2 HG00621.hp1 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.5188-1482G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142216879 | |||||||
| chr7:142216964 | C | G | 7 | a0009c0011t0001g0023 a0009c0011t0001g0024 a0009c0011t0001g0025 others(4): Show |
7 | HG00642.hp1 HG02809.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.5188-1397C>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142216964 | |||||||
| chr7:142217028 | T | G | 1 | a0041c0068t0001g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.5188-1333T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142217028 | |||||||
| chr7:142217039 | C | A | 135 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(132): Show |
135 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.5188-1322C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142217039 | |||||||
| chr7:142217140 | C | T | 8 | a0002c0003t0001g0152 a0002c0003t0001g0244 a0002c0003t0001g0306 others(5): Show |
8 | HG01069.hp2 HG01167.hp2 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.5188-1221C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142217140 | |||||||
| chr7:142217237 | G | A | 1 | a0009c0011t0002g0036 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.5188-1124G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142217237 | |||||||
| chr7:142217481 | T | C | 7 | a0001c0004t0001g0066 a0002c0003t0001g0219 a0002c0003t0001g0225 others(4): Show |
7 | HG02615.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.5188-880T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142217481 | |||||||
| chr7:142217706 | T | A | 38 | a0001c0001t0001g0097 a0001c0001t0001g0108 a0001c0001t0001g0130 others(35): Show |
38 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.5188-655T>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142217706 | |||||||
| chr7:142217808 | A | T | 240 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(237): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.5188-553A>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142217808 | |||||||
| chr7:142217913 | G | A | 8 | a0014c0020t0001g0001 a0014c0026t0001g0196 a0014c0026t0001g0327 others(5): Show |
9 | HG01243.hp1 HG02257.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.5188-448G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142217913 | |||||||
| chr7:142217938 | G | T | 3 | a0015c0015t0001g0013 a0015c0015t0001g0014 a0015c0015t0001g0297 |
3 | HG02257.hp2 HG02622.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.5188-423G>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142217938 | |||||||
| chr7:142218016 | G | A | 1 | a0009c0011t0002g0036 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.5188-345G>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142218016 | |||||||
| chr7:142218331 | T | C | 1 | a0001c0004t0001g0046 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.5188-30T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 46/47 | chr7 | 142218331 | |||||||
| chr7:142218597 | T | C | 1 | a0063c0041t0001g0139 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.5358+66T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 47/47 | chr7 | 142218597 | |||||||
| chr7:142219132 | C | A | 1 | a0002c0003t0001g0219 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.5358+601C>A | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 47/47 | chr7 | 142219132 | |||||||
| chr7:142219190 | C | T | 1 | a0001c0052t0001g0109 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.5358+659C>T | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 47/47 | chr7 | 142219190 | |||||||
| chr7:142219256 | T | G | 1 | a0001c0004t0002g0065 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.5359-614T>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 47/47 | chr7 | 142219256 | |||||||
| chr7:142219467 | A | G | 1 | a0001c0004t0001g0063 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.5359-403A>G | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 47/47 | chr7 | 142219467 | |||||||
| chr7:142219532 | T | C | 240 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0071 others(237): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.5359-338T>C | MGAM2 | ENSG00000257743.9 | transcript | ENST00000477922.4 | protein_coding | 47/47 | chr7 | 142219532 |