Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 114803 |
| ensemblid | ENSG00000162601.12 |
| hgncid | 29401 |
| symbol | MYSM1 |
| name | Myb like, SWIRM and MPN domains 1 |
| refseq_nuc | NM_001085487.3 |
| refseq_prot | NP_001078956.1 |
| ensembl_nuc | ENST00000472487.6 |
| ensembl_prot | ENSP00000418734.1 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 58654743 |
| end | 58700062 |
| strand | - |
| ver | v1.2 |
| region | chr1:58654743-58700062 |
| region5000 | chr1:58649743-58705062 |
| regionname0 | MYSM1_chr1_58654743_58700062 |
| regionname5000 | MYSM1_chr1_58649743_58705062 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 828 | 139 | 21 | 24 | 75 | 5 | 14 | 60 | MYSM1_chr1_58649743_58705062 | MYSM1 | MAAEE others(823): Show |
chr1 | 58649743 | 58705062 |
| a0002 | 1/1 | 828 | 137 | 23 | 19 | 75 | 6 | 12 | 63 | MYSM1_chr1_58649743_58705062 | MYSM1 | MAAEE others(823): Show |
chr1 | 58649743 | 58705062 |
| a0003 | 0/0 | 828 | 59 | 0 | 7 | 42 | 1 | 9 | 28 | MYSM1_chr1_58649743_58705062 | MYSM1 | MAAEE others(823): Show |
chr1 | 58649743 | 58705062 |
| a0004 | 0/0 | 828 | 58 | 39 | 15 | 0 | 0 | 4 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | MAAEE others(823): Show |
chr1 | 58649743 | 58705062 |
| a0005 | 0/0 | 828 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | MAAEE others(823): Show |
chr1 | 58649743 | 58705062 |
| a0006 | 0/0 | 828 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | MAAEE others(823): Show |
chr1 | 58649743 | 58705062 |
| a0007 | 0/0 | 828 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | MAAEE others(823): Show |
chr1 | 58649743 | 58705062 |
| a0008 | 0/0 | 828 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | MAAEE others(823): Show |
chr1 | 58649743 | 58705062 |
| a0009 | 0/0 | 828 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | MAAEE others(823): Show |
chr1 | 58649743 | 58705062 |
| a0010 | 0/0 | 828 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | MAAEE others(823): Show |
chr1 | 58649743 | 58705062 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2484 | 139 | 21 | 24 | 75 | 5 | 14 | MYSM1_chr1_58649743_58705062 | MYSM1 | ATGGC others(2479): Show |
chr1 | 58649743 | 58705062 | ||
| a0002c0002 | 0/1 | 2484 | 97 | 11 | 14 | 58 | 3 | 10 | MYSM1_chr1_58649743_58705062 | MYSM1 | ATGGC others(2479): Show |
chr1 | 58649743 | 58705062 | ||
| a0002c0005 | 1/0 | 2484 | 40 | 12 | 5 | 17 | 3 | 2 | MYSM1_chr1_58649743_58705062 | MYSM1 | ATGGC others(2479): Show |
chr1 | 58649743 | 58705062 | ||
| a0003c0003 | 0/0 | 2484 | 59 | 0 | 7 | 42 | 1 | 9 | MYSM1_chr1_58649743_58705062 | MYSM1 | ATGGC others(2479): Show |
chr1 | 58649743 | 58705062 | ||
| a0004c0004 | 0/0 | 2484 | 58 | 39 | 15 | 0 | 0 | 4 | MYSM1_chr1_58649743_58705062 | MYSM1 | ATGGC others(2479): Show |
chr1 | 58649743 | 58705062 | ||
| a0005c0006 | 0/0 | 2484 | 6 | 6 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | ATGGC others(2479): Show |
chr1 | 58649743 | 58705062 | ||
| a0005c0008 | 0/0 | 2484 | 2 | 2 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | ATGGC others(2479): Show |
chr1 | 58649743 | 58705062 | ||
| a0006c0007 | 0/0 | 2484 | 3 | 3 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | ATGGC others(2479): Show |
chr1 | 58649743 | 58705062 | ||
| a0006c0010 | 0/0 | 2484 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | ATGGC others(2479): Show |
chr1 | 58649743 | 58705062 | ||
| a0007c0009 | 0/0 | 2484 | 2 | 0 | 1 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | ATGGC others(2479): Show |
chr1 | 58649743 | 58705062 | ||
| a0008c0013 | 0/0 | 2484 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | ATGGC others(2479): Show |
chr1 | 58649743 | 58705062 | ||
| a0009c0011 | 0/0 | 2484 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | ATGGC others(2479): Show |
chr1 | 58649743 | 58705062 | ||
| a0010c0012 | 0/0 | 2484 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | ATGGC others(2479): Show |
chr1 | 58649743 | 58705062 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7759 | 56 | 8 | 2 | 39 | 2 | 5 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7754): Show |
chr1 | 58649743 | 58705062 |
| a0001c0001t0004 | 0/0 | 7761 | 27 | 3 | 9 | 9 | 2 | 4 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7756): Show |
chr1 | 58649743 | 58705062 |
| a0001c0001t0008 | 0/0 | 7763 | 11 | 0 | 7 | 4 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7758): Show |
chr1 | 58649743 | 58705062 |
| a0001c0001t0009 | 0/0 | 7757 | 11 | 3 | 0 | 7 | 1 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7752): Show |
chr1 | 58649743 | 58705062 |
| a0001c0001t0017 | 0/0 | 7765 | 4 | 0 | 3 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7760): Show |
chr1 | 58649743 | 58705062 |
| a0001c0001t0018 | 0/0 | 7753 | 4 | 0 | 0 | 2 | 0 | 2 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7748): Show |
chr1 | 58649743 | 58705062 |
| a0001c0001t0019 | 0/0 | 7760 | 4 | 0 | 0 | 4 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7755): Show |
chr1 | 58649743 | 58705062 |
| a0001c0001t0021 | 0/0 | 7755 | 3 | 0 | 0 | 2 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7750): Show |
chr1 | 58649743 | 58705062 |
| a0001c0001t0033 | 0/0 | 7760 | 2 | 0 | 0 | 2 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7755): Show |
chr1 | 58649743 | 58705062 |
| a0001c0001t0034 | 0/0 | 7749 | 2 | 0 | 0 | 1 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7744): Show |
chr1 | 58649743 | 58705062 |
| a0001c0001t0036 | 0/0 | 7755 | 2 | 2 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7750): Show |
chr1 | 58649743 | 58705062 |
| a0001c0001t0037 | 0/0 | 7755 | 2 | 1 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7750): Show |
chr1 | 58649743 | 58705062 |
| a0001c0001t0046 | 0/0 | 7762 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7757): Show |
chr1 | 58649743 | 58705062 |
| a0001c0001t0047 | 0/0 | 7769 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7764): Show |
chr1 | 58649743 | 58705062 |
| a0001c0001t0049 | 0/0 | 7759 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7754): Show |
chr1 | 58649743 | 58705062 |
| a0001c0001t0050 | 0/0 | 7756 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7751): Show |
chr1 | 58649743 | 58705062 |
| a0001c0001t0051 | 0/0 | 7745 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7740): Show |
chr1 | 58649743 | 58705062 |
| a0001c0001t0052 | 0/0 | 7739 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7734): Show |
chr1 | 58649743 | 58705062 |
| a0001c0001t0053 | 0/0 | 7757 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7752): Show |
chr1 | 58649743 | 58705062 |
| a0001c0001t0054 | 0/0 | 7759 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7754): Show |
chr1 | 58649743 | 58705062 |
| a0001c0001t0055 | 0/0 | 7759 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7754): Show |
chr1 | 58649743 | 58705062 |
| a0001c0001t0056 | 0/0 | 7758 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7753): Show |
chr1 | 58649743 | 58705062 |
| a0001c0001t0057 | 0/0 | 7751 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7746): Show |
chr1 | 58649743 | 58705062 |
| a0002c0002t0002 | 0/1 | 7761 | 49 | 2 | 8 | 32 | 3 | 3 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7756): Show |
chr1 | 58649743 | 58705062 |
| a0002c0002t0005 | 0/0 | 7763 | 19 | 1 | 4 | 12 | 0 | 2 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7758): Show |
chr1 | 58649743 | 58705062 |
| a0002c0002t0013 | 0/0 | 7757 | 6 | 1 | 1 | 4 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7752): Show |
chr1 | 58649743 | 58705062 |
| a0002c0002t0014 | 0/0 | 7765 | 5 | 0 | 1 | 3 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7760): Show |
chr1 | 58649743 | 58705062 |
| a0002c0002t0028 | 0/0 | 7757 | 3 | 0 | 0 | 3 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7752): Show |
chr1 | 58649743 | 58705062 |
| a0002c0002t0041 | 0/0 | 7761 | 2 | 0 | 0 | 0 | 0 | 2 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7756): Show |
chr1 | 58649743 | 58705062 |
| a0002c0002t0042 | 0/0 | 7759 | 2 | 0 | 0 | 1 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7754): Show |
chr1 | 58649743 | 58705062 |
| a0002c0002t0044 | 0/0 | 7753 | 2 | 2 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7748): Show |
chr1 | 58649743 | 58705062 |
| a0002c0002t0045 | 0/0 | 7751 | 2 | 2 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7746): Show |
chr1 | 58649743 | 58705062 |
| a0002c0002t0073 | 0/0 | 7769 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7764): Show |
chr1 | 58649743 | 58705062 |
| a0002c0002t0074 | 0/0 | 7765 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7760): Show |
chr1 | 58649743 | 58705062 |
| a0002c0002t0075 | 0/0 | 7759 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7754): Show |
chr1 | 58649743 | 58705062 |
| a0002c0002t0076 | 0/0 | 7755 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7750): Show |
chr1 | 58649743 | 58705062 |
| a0002c0002t0077 | 0/0 | 7749 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7744): Show |
chr1 | 58649743 | 58705062 |
| a0002c0002t0078 | 0/0 | 7753 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7748): Show |
chr1 | 58649743 | 58705062 |
| a0002c0002t0083 | 0/0 | 7761 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7756): Show |
chr1 | 58649743 | 58705062 |
| a0002c0005t0006 | 1/0 | 7751 | 17 | 3 | 1 | 9 | 1 | 2 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7746): Show |
chr1 | 58649743 | 58705062 |
| a0002c0005t0015 | 0/0 | 7778 | 5 | 0 | 0 | 5 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7773): Show |
chr1 | 58649743 | 58705062 |
| a0002c0005t0016 | 0/0 | 7747 | 5 | 1 | 2 | 0 | 2 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7742): Show |
chr1 | 58649743 | 58705062 |
| a0002c0005t0027 | 0/0 | 7758 | 3 | 3 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7753): Show |
chr1 | 58649743 | 58705062 |
| a0002c0005t0029 | 0/0 | 7754 | 3 | 3 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7749): Show |
chr1 | 58649743 | 58705062 |
| a0002c0005t0030 | 0/0 | 7753 | 3 | 0 | 0 | 3 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7748): Show |
chr1 | 58649743 | 58705062 |
| a0002c0005t0043 | 0/0 | 7756 | 2 | 1 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7751): Show |
chr1 | 58649743 | 58705062 |
| a0002c0005t0079 | 0/0 | 7747 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7742): Show |
chr1 | 58649743 | 58705062 |
| a0002c0005t0080 | 0/0 | 7747 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7742): Show |
chr1 | 58649743 | 58705062 |
| a0003c0003t0003 | 0/0 | 7764 | 33 | 0 | 2 | 25 | 1 | 5 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7759): Show |
chr1 | 58649743 | 58705062 |
| a0003c0003t0007 | 0/0 | 7766 | 4 | 0 | 1 | 3 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7761): Show |
chr1 | 58649743 | 58705062 |
| a0003c0003t0010 | 0/0 | 7762 | 5 | 0 | 1 | 2 | 0 | 2 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7757): Show |
chr1 | 58649743 | 58705062 |
| a0003c0003t0011 | 0/0 | 7760 | 3 | 0 | 0 | 2 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7755): Show |
chr1 | 58649743 | 58705062 |
| a0003c0003t0022 | 0/0 | 7768 | 3 | 0 | 0 | 3 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7763): Show |
chr1 | 58649743 | 58705062 |
| a0003c0003t0035 | 0/0 | 7762 | 2 | 0 | 0 | 2 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7757): Show |
chr1 | 58649743 | 58705062 |
| a0003c0003t0038 | 0/0 | 7764 | 2 | 0 | 2 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7759): Show |
chr1 | 58649743 | 58705062 |
| a0003c0003t0058 | 0/0 | 7762 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7757): Show |
chr1 | 58649743 | 58705062 |
| a0003c0003t0059 | 0/0 | 7762 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7757): Show |
chr1 | 58649743 | 58705062 |
| a0003c0003t0062 | 0/0 | 7768 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7763): Show |
chr1 | 58649743 | 58705062 |
| a0003c0003t0064 | 0/0 | 7765 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7760): Show |
chr1 | 58649743 | 58705062 |
| a0003c0003t0065 | 0/0 | 7764 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7759): Show |
chr1 | 58649743 | 58705062 |
| a0003c0003t0067 | 0/0 | 7760 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7755): Show |
chr1 | 58649743 | 58705062 |
| a0003c0003t0082 | 0/0 | 7764 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7759): Show |
chr1 | 58649743 | 58705062 |
| a0004c0004t0003 | 0/0 | 7764 | 11 | 8 | 3 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7759): Show |
chr1 | 58649743 | 58705062 |
| a0004c0004t0007 | 0/0 | 7766 | 8 | 1 | 3 | 0 | 0 | 4 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7761): Show |
chr1 | 58649743 | 58705062 |
| a0004c0004t0010 | 0/0 | 7762 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7757): Show |
chr1 | 58649743 | 58705062 |
| a0004c0004t0012 | 0/0 | 7758 | 6 | 4 | 2 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7753): Show |
chr1 | 58649743 | 58705062 |
| a0004c0004t0020 | 0/0 | 7761 | 4 | 4 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7756): Show |
chr1 | 58649743 | 58705062 |
| a0004c0004t0023 | 0/0 | 7763 | 3 | 2 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7758): Show |
chr1 | 58649743 | 58705062 |
| a0004c0004t0024 | 0/0 | 7753 | 3 | 3 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7748): Show |
chr1 | 58649743 | 58705062 |
| a0004c0004t0026 | 0/0 | 7758 | 2 | 2 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7753): Show |
chr1 | 58649743 | 58705062 |
| a0004c0004t0031 | 0/0 | 7757 | 3 | 1 | 2 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7752): Show |
chr1 | 58649743 | 58705062 |
| a0004c0004t0032 | 0/0 | 7757 | 3 | 3 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7752): Show |
chr1 | 58649743 | 58705062 |
| a0004c0004t0039 | 0/0 | 7764 | 2 | 0 | 2 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7759): Show |
chr1 | 58649743 | 58705062 |
| a0004c0004t0040 | 0/0 | 7759 | 2 | 2 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7754): Show |
chr1 | 58649743 | 58705062 |
| a0004c0004t0060 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7759): Show |
chr1 | 58649743 | 58705062 |
| a0004c0004t0061 | 0/0 | 7765 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7760): Show |
chr1 | 58649743 | 58705062 |
| a0004c0004t0063 | 0/0 | 7766 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7761): Show |
chr1 | 58649743 | 58705062 |
| a0004c0004t0066 | 0/0 | 7751 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7746): Show |
chr1 | 58649743 | 58705062 |
| a0004c0004t0068 | 0/0 | 7760 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7755): Show |
chr1 | 58649743 | 58705062 |
| a0004c0004t0069 | 0/0 | 7760 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7755): Show |
chr1 | 58649743 | 58705062 |
| a0004c0004t0070 | 0/0 | 7757 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7752): Show |
chr1 | 58649743 | 58705062 |
| a0004c0004t0071 | 0/0 | 7749 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7744): Show |
chr1 | 58649743 | 58705062 |
| a0004c0004t0072 | 0/0 | 7758 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7753): Show |
chr1 | 58649743 | 58705062 |
| a0004c0004t0081 | 0/0 | 7763 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7758): Show |
chr1 | 58649743 | 58705062 |
| a0005c0006t0003 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7759): Show |
chr1 | 58649743 | 58705062 |
| a0005c0006t0011 | 0/0 | 7760 | 4 | 4 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7755): Show |
chr1 | 58649743 | 58705062 |
| a0005c0006t0026 | 0/0 | 7758 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7753): Show |
chr1 | 58649743 | 58705062 |
| a0005c0008t0010 | 0/0 | 7762 | 2 | 2 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7757): Show |
chr1 | 58649743 | 58705062 |
| a0006c0007t0025 | 0/0 | 7759 | 3 | 3 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7754): Show |
chr1 | 58649743 | 58705062 |
| a0006c0010t0010 | 0/0 | 7762 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7757): Show |
chr1 | 58649743 | 58705062 |
| a0007c0009t0001 | 0/0 | 7759 | 2 | 0 | 1 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7754): Show |
chr1 | 58649743 | 58705062 |
| a0008c0013t0005 | 0/0 | 7763 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7758): Show |
chr1 | 58649743 | 58705062 |
| a0009c0011t0003 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7759): Show |
chr1 | 58649743 | 58705062 |
| a0010c0012t0048 | 0/0 | 7760 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | AGGTC others(7755): Show |
chr1 | 58649743 | 58705062 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 7 | 5 | 1 | 0 | 1 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0001g0004 | 0/0 | 7 | 0 | 0 | 6 | 1 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0004g0005 | 0/0 | 6 | 2 | 3 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0004g0009 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0004g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0004g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0004g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0004g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0008g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0008g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0008g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0008g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0008g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0008g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0008g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0008g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0008g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0008g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0009g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0009g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0009g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0009g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0009g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0009g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0009g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0009g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0009g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0009g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0009g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0017g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0017g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0017g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0018g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0018g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0018g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0019g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0019g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0019g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0021g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0021g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0021g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0033g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0033g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0034g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0034g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0036g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0036g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0037g0045 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0046g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0047g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0049g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0050g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0051g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0052g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0053g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0054g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0055g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0056g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0001c0001t0057g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0002g0002 | 0/0 | 10 | 0 | 1 | 9 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0002g0006 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0002g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0002g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0002g0019 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0002g0066 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0005g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0005g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0005g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0005g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0005g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0005g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0005g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0005g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0005g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0005g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0005g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0005g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0005g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0005g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0005g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0005g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0013g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0013g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0013g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0013g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0013g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0013g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0014g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0014g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0014g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0014g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0014g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0028g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0028g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0028g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0041g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0042g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0042g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0044g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0045g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0045g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0073g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0074g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0075g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0076g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0077g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0078g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0002t0083g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0005t0006g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0005t0006g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0005t0006g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0005t0006g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0005t0006g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0005t0006g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0005t0006g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0005t0006g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0005t0006g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0005t0006g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0005t0006g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0005t0006g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0005t0006g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0005t0006g0293 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0005t0015g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0005t0015g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0005t0015g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0005t0015g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0005t0015g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0005t0016g0039 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0005t0016g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0005t0016g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0005t0016g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0005t0027g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0005t0027g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0005t0029g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0005t0029g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0005t0030g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0005t0030g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0005t0030g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0005t0043g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0005t0079g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0002c0005t0080g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0003c0003t0003g0001 | 0/0 | 12 | 0 | 1 | 9 | 0 | 2 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0003c0003t0003g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0003c0003t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0003c0003t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0003c0003t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0003c0003t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0003c0003t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0003c0003t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0003c0003t0003g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0003c0003t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0003c0003t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0003c0003t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0003c0003t0003g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0003c0003t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0003c0003t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0003c0003t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0003c0003t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0003c0003t0003g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0003c0003t0003g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0003c0003t0003g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0003c0003t0007g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0003c0003t0007g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0003c0003t0007g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0003c0003t0007g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0003c0003t0010g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0003c0003t0010g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0003c0003t0010g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0003c0003t0010g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0003c0003t0010g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0003c0003t0011g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0003c0003t0011g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0003c0003t0011g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0003c0003t0022g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0003c0003t0022g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0003c0003t0022g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0003c0003t0035g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0003c0003t0035g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0003c0003t0038g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0003c0003t0058g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0003c0003t0059g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0003c0003t0062g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0003c0003t0064g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0003c0003t0065g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0003c0003t0067g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0003c0003t0082g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0003g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0003g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0003g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0003g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0007g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0007g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0007g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0007g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0007g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0007g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0007g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0010g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0012g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0012g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0012g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0012g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0012g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0012g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0020g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0020g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0020g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0020g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0023g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0023g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0023g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0024g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0024g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0026g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0026g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0031g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0031g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0032g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0032g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0032g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0039g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0040g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0040g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0060g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0061g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0063g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0066g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0068g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0069g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0070g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0071g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0072g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0004c0004t0081g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0005c0006t0003g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0005c0006t0011g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0005c0006t0011g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0005c0006t0011g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0005c0006t0026g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0005c0008t0010g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0006c0007t0025g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0006c0007t0025g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0006c0010t0010g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0007c0009t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0007c0009t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0008c0013t0005g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0009c0011t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| a0010c0012t0048g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0096 | EUR | GBR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG00099 | hp2 | a0001 | c0001 | t0009 | g0152 | EUR | GBR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG00140 | hp2 | a0002 | c0005 | t0006 | g0208 | EUR | GBR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG00280 | hp2 | a0003 | c0003 | t0003 | g0285 | EUR | FIN | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG00408 | hp1 | a0003 | c0003 | t0003 | g0001 | EAS | CHS | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG00423 | hp1 | a0002 | c0002 | t0005 | g0016 | EAS | CHS | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG00423 | hp2 | a0001 | c0001 | t0034 | g0137 | EAS | CHS | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG00438 | hp1 | a0002 | c0002 | t0002 | g0069 | EAS | CHS | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG00438 | hp2 | a0003 | c0003 | t0003 | g0001 | EAS | CHS | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG00544 | hp1 | a0002 | c0002 | t0014 | g0090 | EAS | CHS | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG00544 | hp2 | a0002 | c0002 | t0005 | g0125 | EAS | CHS | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG00597 | hp2 | a0003 | c0003 | t0003 | g0001 | EAS | CHS | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG00609 | hp1 | a0003 | c0003 | t0003 | g0001 | EAS | CHS | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG00621 | hp1 | a0008 | c0013 | t0005 | g0114 | EAS | CHS | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG00639 | hp1 | a0002 | c0002 | t0005 | g0017 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG00639 | hp2 | a0004 | c0004 | t0007 | g0298 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG00642 | hp1 | a0002 | c0002 | t0002 | g0105 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0131 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG00673 | hp1 | a0002 | c0005 | t0006 | g0223 | EAS | CHS | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG00673 | hp2 | a0003 | c0003 | t0003 | g0001 | EAS | CHS | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG00735 | hp1 | a0002 | c0002 | t0013 | g0099 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0161 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG00738 | hp1 | a0004 | c0004 | t0023 | g0302 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG00738 | hp2 | a0002 | c0005 | t0080 | g0228 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG00741 | hp1 | a0002 | c0005 | t0016 | g0039 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01070 | hp1 | a0002 | c0002 | t0002 | g0078 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01070 | hp2 | a0001 | c0001 | t0008 | g0058 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01074 | hp1 | a0002 | c0005 | t0043 | g0037 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01074 | hp2 | a0004 | c0004 | t0003 | g0241 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01081 | hp1 | a0004 | c0004 | t0003 | g0247 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01081 | hp2 | a0001 | c0001 | t0008 | g0155 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01099 | hp1 | a0003 | c0003 | t0010 | g0238 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01099 | hp2 | a0001 | c0001 | t0008 | g0147 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01106 | hp1 | a0003 | c0003 | t0003 | g0286 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01106 | hp2 | a0002 | c0002 | t0005 | g0098 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01109 | hp2 | a0004 | c0004 | t0003 | g0307 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01167 | hp1 | a0004 | c0004 | t0012 | g0320 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01167 | hp2 | a0004 | c0004 | t0007 | g0043 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0149 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01169 | hp2 | a0004 | c0004 | t0007 | g0043 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01192 | hp1 | a0001 | c0001 | t0057 | g0060 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0005 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0146 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01243 | hp2 | a0001 | c0001 | t0037 | g0045 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01255 | hp1 | a0002 | c0002 | t0002 | g0077 | AMR | CLM | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01255 | hp2 | a0004 | c0004 | t0012 | g0321 | AMR | CLM | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01256 | hp1 | a0007 | c0009 | t0001 | g0186 | AMR | CLM | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01256 | hp2 | a0004 | c0004 | t0031 | g0044 | AMR | CLM | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01257 | hp1 | a0001 | c0001 | t0008 | g0141 | AMR | CLM | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01257 | hp2 | a0003 | c0003 | t0038 | g0041 | AMR | CLM | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01258 | hp1 | a0004 | c0004 | t0031 | g0044 | AMR | CLM | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01258 | hp2 | a0003 | c0003 | t0038 | g0041 | AMR | CLM | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0025 | AMR | CLM | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01346 | hp2 | a0002 | c0002 | t0014 | g0097 | AMR | CLM | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01361 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01361 | hp2 | a0001 | c0001 | t0017 | g0027 | AMR | CLM | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0025 | AMR | CLM | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01496 | hp2 | a0004 | c0004 | t0069 | g0318 | AMR | CLM | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0009 | EUR | IBS | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01515 | hp2 | a0002 | c0005 | t0016 | g0039 | EUR | IBS | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01516 | hp1 | a0001 | c0001 | t0004 | g0132 | EUR | IBS | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01516 | hp2 | a0002 | c0002 | t0002 | g0019 | EUR | IBS | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01517 | hp1 | a0002 | c0002 | t0002 | g0019 | EUR | IBS | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01517 | hp2 | a0002 | c0005 | t0016 | g0204 | EUR | IBS | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01884 | hp1 | a0006 | c0007 | t0025 | g0063 | AFR | ACB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01884 | hp2 | a0004 | c0004 | t0072 | g0054 | AFR | ACB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01891 | hp2 | a0002 | c0002 | t0044 | g0013 | AFR | ACB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01928 | hp1 | a0002 | c0002 | t0002 | g0006 | AMR | PEL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01928 | hp2 | a0001 | c0001 | t0004 | g0005 | AMR | PEL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01934 | hp1 | a0001 | c0001 | t0047 | g0158 | AMR | PEL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01934 | hp2 | a0002 | c0002 | t0005 | g0112 | AMR | PEL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01952 | hp1 | a0001 | c0001 | t0008 | g0163 | AMR | PEL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01952 | hp2 | a0004 | c0004 | t0063 | g0311 | AMR | PEL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01978 | hp1 | a0002 | c0002 | t0002 | g0006 | AMR | PEL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01978 | hp2 | a0001 | c0001 | t0008 | g0184 | AMR | PEL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01981 | hp1 | a0003 | c0003 | t0067 | g0263 | AMR | PEL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01981 | hp2 | a0002 | c0002 | t0002 | g0117 | AMR | PEL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01993 | hp1 | a0001 | c0001 | t0004 | g0005 | AMR | PEL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01993 | hp2 | a0002 | c0005 | t0016 | g0225 | AMR | PEL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02004 | hp1 | a0003 | c0003 | t0007 | g0249 | AMR | PEL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02004 | hp2 | a0004 | c0004 | t0039 | g0046 | AMR | PEL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02015 | hp1 | a0001 | c0001 | t0008 | g0029 | EAS | KHV | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02015 | hp2 | a0003 | c0003 | t0011 | g0264 | EAS | KHV | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02027 | hp1 | a0001 | c0001 | t0004 | g0023 | EAS | KHV | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02027 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | KHV | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02040 | hp2 | a0003 | c0003 | t0058 | g0267 | EAS | KHV | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02055 | hp1 | a0004 | c0004 | t0024 | g0049 | AFR | ACB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02055 | hp2 | a0002 | c0002 | t0002 | g0088 | AFR | ACB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02074 | hp1 | a0003 | c0003 | t0003 | g0242 | EAS | KHV | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02074 | hp2 | a0001 | c0001 | t0009 | g0156 | EAS | KHV | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02080 | hp1 | a0003 | c0003 | t0022 | g0261 | EAS | KHV | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0177 | EAS | KHV | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02083 | hp1 | a0002 | c0002 | t0028 | g0100 | EAS | KHV | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02083 | hp2 | a0003 | c0003 | t0022 | g0288 | EAS | KHV | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02129 | hp1 | a0002 | c0002 | t0028 | g0094 | EAS | KHV | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02132 | hp2 | a0003 | c0003 | t0022 | g0248 | EAS | KHV | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02135 | hp1 | a0002 | c0002 | t0002 | g0068 | EAS | KHV | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02135 | hp2 | a0001 | c0001 | t0004 | g0023 | EAS | KHV | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02145 | hp1 | a0001 | c0001 | t0009 | g0143 | AFR | ACB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02145 | hp2 | a0006 | c0007 | t0025 | g0014 | AFR | ACB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02148 | hp1 | a0002 | c0002 | t0002 | g0006 | AMR | PEL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02148 | hp2 | a0001 | c0001 | t0017 | g0159 | AMR | PEL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02155 | hp1 | a0003 | c0003 | t0010 | g0262 | EAS | CDX | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02155 | hp2 | a0001 | c0001 | t0051 | g0172 | EAS | CDX | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02257 | hp1 | a0004 | c0004 | t0020 | g0304 | AFR | ACB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02257 | hp2 | a0005 | c0006 | t0003 | g0316 | AFR | ACB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02258 | hp1 | a0001 | c0001 | t0009 | g0313 | AFR | ACB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02258 | hp2 | a0004 | c0004 | t0023 | g0305 | AFR | ACB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02273 | hp1 | a0003 | c0003 | t0003 | g0001 | AMR | PEL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02273 | hp2 | a0004 | c0004 | t0039 | g0046 | AMR | PEL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02280 | hp1 | a0002 | c0005 | t0027 | g0036 | AFR | ACB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02280 | hp2 | a0004 | c0004 | t0020 | g0306 | AFR | ACB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02300 | hp1 | a0001 | c0001 | t0008 | g0160 | AMR | PEL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02300 | hp2 | a0002 | c0002 | t0005 | g0116 | AMR | PEL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02523 | hp1 | a0002 | c0002 | t0083 | g0095 | EAS | KHV | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02523 | hp2 | a0003 | c0003 | t0003 | g0270 | EAS | KHV | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02572 | hp1 | a0005 | c0006 | t0011 | g0314 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02572 | hp2 | a0001 | c0001 | t0050 | g0170 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02602 | hp1 | a0003 | c0003 | t0003 | g0269 | SAS | PJL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02602 | hp2 | a0003 | c0003 | t0003 | g0001 | SAS | PJL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02615 | hp1 | a0002 | c0005 | t0029 | g0312 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02615 | hp2 | a0004 | c0004 | t0024 | g0012 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02622 | hp1 | a0004 | c0004 | t0024 | g0012 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02622 | hp2 | a0002 | c0005 | t0006 | g0227 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02630 | hp1 | a0002 | c0002 | t0013 | g0111 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02683 | hp1 | a0001 | c0001 | t0004 | g0148 | SAS | PJL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02683 | hp2 | a0003 | c0003 | t0010 | g0251 | SAS | PJL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02698 | hp1 | a0003 | c0003 | t0062 | g0255 | SAS | PJL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02698 | hp2 | a0002 | c0002 | t0073 | g0089 | SAS | PJL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02717 | hp1 | a0001 | c0001 | t0053 | g0059 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02717 | hp2 | a0005 | c0006 | t0011 | g0047 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02723 | hp1 | a0002 | c0002 | t0078 | g0057 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02723 | hp2 | a0004 | c0004 | t0081 | g0297 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02735 | hp1 | a0004 | c0004 | t0007 | g0283 | SAS | PJL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02735 | hp2 | a0002 | c0005 | t0006 | g0034 | SAS | PJL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02738 | hp1 | a0002 | c0002 | t0005 | g0108 | SAS | PJL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02738 | hp2 | a0001 | c0001 | t0018 | g0145 | SAS | PJL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02809 | hp1 | a0006 | c0010 | t0010 | g0222 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02809 | hp2 | a0004 | c0004 | t0071 | g0050 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02818 | hp1 | a0002 | c0005 | t0006 | g0213 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02818 | hp2 | a0002 | c0002 | t0005 | g0104 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02886 | hp1 | a0002 | c0002 | t0045 | g0055 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02886 | hp2 | a0004 | c0004 | t0003 | g0042 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02895 | hp1 | a0004 | c0004 | t0012 | g0324 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02895 | hp2 | a0004 | c0004 | t0003 | g0278 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02896 | hp1 | a0004 | c0004 | t0003 | g0252 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02896 | hp2 | a0005 | c0008 | t0010 | g0011 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02897 | hp1 | a0004 | c0004 | t0012 | g0323 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02897 | hp2 | a0005 | c0008 | t0010 | g0011 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02922 | hp1 | a0005 | c0006 | t0011 | g0047 | AFR | ESN | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02922 | hp2 | a0002 | c0005 | t0027 | g0221 | AFR | ESN | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02965 | hp1 | a0004 | c0004 | t0032 | g0292 | AFR | ESN | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02965 | hp2 | a0002 | c0002 | t0076 | g0064 | AFR | ESN | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02970 | hp1 | a0004 | c0004 | t0032 | g0296 | AFR | ESN | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ESN | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02976 | hp2 | a0002 | c0005 | t0029 | g0038 | AFR | ESN | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03041 | hp1 | a0004 | c0004 | t0003 | g0236 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03041 | hp2 | a0002 | c0005 | t0043 | g0037 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03098 | hp1 | a0001 | c0001 | t0036 | g0061 | AFR | MSL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03098 | hp2 | a0004 | c0004 | t0061 | g0277 | AFR | MSL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03130 | hp1 | a0001 | c0001 | t0037 | g0045 | AFR | ESN | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03130 | hp2 | a0004 | c0004 | t0060 | g0246 | AFR | ESN | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03139 | hp1 | a0002 | c0005 | t0027 | g0036 | AFR | ESN | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03139 | hp2 | a0002 | c0005 | t0079 | g0207 | AFR | ESN | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03195 | hp1 | a0005 | c0006 | t0011 | g0315 | AFR | ESN | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03195 | hp2 | a0004 | c0004 | t0003 | g0245 | AFR | ESN | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03209 | hp1 | a0004 | c0004 | t0026 | g0051 | AFR | MSL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03209 | hp2 | a0006 | c0007 | t0025 | g0014 | AFR | MSL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03225 | hp1 | a0002 | c0005 | t0029 | g0038 | AFR | MSL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03225 | hp2 | a0004 | c0004 | t0026 | g0052 | AFR | MSL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03239 | hp1 | a0001 | c0001 | t0021 | g0182 | SAS | PJL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03239 | hp2 | a0002 | c0005 | t0006 | g0224 | SAS | PJL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03453 | hp1 | a0002 | c0002 | t0045 | g0056 | AFR | MSL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03453 | hp2 | a0004 | c0004 | t0007 | g0281 | AFR | MSL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03486 | hp1 | a0004 | c0004 | t0012 | g0322 | AFR | MSL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03486 | hp2 | a0004 | c0004 | t0070 | g0309 | AFR | MSL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03490 | hp1 | a0002 | c0002 | t0041 | g0020 | SAS | PJL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03490 | hp2 | a0001 | c0001 | t0049 | g0187 | SAS | PJL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03491 | hp1 | a0004 | c0004 | t0007 | g0290 | SAS | PJL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03492 | hp1 | a0004 | c0004 | t0007 | g0291 | SAS | PJL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03492 | hp2 | a0002 | c0002 | t0041 | g0020 | SAS | PJL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03516 | hp1 | a0004 | c0004 | t0003 | g0042 | AFR | ESN | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03516 | hp2 | a0004 | c0004 | t0020 | g0308 | AFR | ESN | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03540 | hp2 | a0004 | c0004 | t0010 | g0279 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | MSL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03579 | hp2 | a0004 | c0004 | t0066 | g0048 | AFR | MSL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03654 | hp1 | a0002 | c0002 | t0002 | g0102 | SAS | PJL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03654 | hp2 | a0001 | c0001 | t0034 | g0176 | SAS | PJL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03688 | hp1 | a0003 | c0003 | t0003 | g0001 | SAS | STU | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | STU | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03704 | hp2 | a0002 | c0002 | t0042 | g0106 | SAS | PJL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0005 | SAS | BEB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0129 | SAS | BEB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03927 | hp1 | a0001 | c0001 | t0018 | g0144 | SAS | BEB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03927 | hp2 | a0004 | c0004 | t0007 | g0289 | SAS | BEB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | BEB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03942 | hp2 | a0002 | c0002 | t0002 | g0124 | SAS | BEB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG04115 | hp1 | a0003 | c0003 | t0003 | g0256 | SAS | STU | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG04115 | hp2 | a0002 | c0002 | t0005 | g0080 | SAS | STU | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG04184 | hp1 | a0003 | c0003 | t0010 | g0266 | SAS | BEB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG04184 | hp2 | a0002 | c0002 | t0002 | g0018 | SAS | BEB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG04199 | hp1 | a0007 | c0009 | t0001 | g0183 | SAS | STU | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG04199 | hp2 | a0002 | c0002 | t0014 | g0122 | SAS | STU | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG04228 | hp1 | a0001 | c0001 | t0004 | g0165 | SAS | STU | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG04228 | hp2 | a0003 | c0003 | t0003 | g0287 | SAS | STU | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18522 | hp1 | a0004 | c0004 | t0003 | g0280 | AFR | YRI | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18522 | hp2 | a0004 | c0004 | t0040 | g0310 | AFR | YRI | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18612 | hp1 | a0002 | c0002 | t0005 | g0072 | EAS | CHB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18747 | hp1 | a0002 | c0002 | t0002 | g0082 | EAS | CHB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18747 | hp2 | a0003 | c0003 | t0065 | g0257 | EAS | CHB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18906 | hp1 | a0009 | c0011 | t0003 | g0244 | AFR | YRI | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18906 | hp2 | a0001 | c0001 | t0036 | g0053 | AFR | YRI | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18939 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18940 | hp2 | a0002 | c0002 | t0013 | g0101 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18941 | hp2 | a0002 | c0002 | t0042 | g0083 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18944 | hp1 | a0002 | c0002 | t0005 | g0017 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18945 | hp2 | a0003 | c0003 | t0003 | g0260 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18946 | hp1 | a0002 | c0002 | t0074 | g0091 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18946 | hp2 | a0002 | c0005 | t0006 | g0035 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18947 | hp1 | a0002 | c0002 | t0005 | g0016 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18947 | hp2 | a0003 | c0003 | t0059 | g0268 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18948 | hp1 | a0003 | c0003 | t0003 | g0272 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18948 | hp2 | a0002 | c0002 | t0014 | g0120 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18949 | hp1 | a0002 | c0005 | t0030 | g0212 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18950 | hp2 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18952 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18952 | hp2 | a0001 | c0001 | t0009 | g0198 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18953 | hp1 | a0003 | c0003 | t0003 | g0273 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18953 | hp2 | a0001 | c0001 | t0019 | g0040 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18954 | hp1 | a0001 | c0001 | t0019 | g0040 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18954 | hp2 | a0002 | c0005 | t0006 | g0220 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18957 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18957 | hp2 | a0002 | c0005 | t0030 | g0206 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18959 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18960 | hp1 | a0002 | c0005 | t0015 | g0215 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18960 | hp2 | a0001 | c0001 | t0009 | g0199 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18961 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18961 | hp2 | a0003 | c0003 | t0007 | g0259 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18962 | hp1 | a0002 | c0002 | t0014 | g0067 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18962 | hp2 | a0001 | c0001 | t0052 | g0130 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18965 | hp1 | a0002 | c0005 | t0006 | g0211 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18965 | hp2 | a0003 | c0003 | t0003 | g0010 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18968 | hp2 | a0002 | c0005 | t0006 | g0033 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18969 | hp1 | a0002 | c0002 | t0005 | g0065 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18970 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18970 | hp2 | a0002 | c0005 | t0006 | g0033 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18971 | hp2 | a0002 | c0002 | t0002 | g0119 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18972 | hp1 | a0001 | c0001 | t0004 | g0180 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18972 | hp2 | a0002 | c0002 | t0002 | g0074 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18974 | hp1 | a0002 | c0005 | t0006 | g0210 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18974 | hp2 | a0010 | c0012 | t0048 | g0128 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18977 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18977 | hp2 | a0001 | c0001 | t0004 | g0133 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18978 | hp1 | a0002 | c0002 | t0002 | g0070 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18978 | hp2 | a0003 | c0003 | t0003 | g0271 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18979 | hp1 | a0001 | c0001 | t0046 | g0192 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0135 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18981 | hp1 | a0003 | c0003 | t0003 | g0010 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18981 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18982 | hp2 | a0002 | c0002 | t0002 | g0085 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18983 | hp1 | a0002 | c0002 | t0005 | g0015 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18983 | hp2 | a0001 | c0001 | t0018 | g0022 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18984 | hp1 | a0001 | c0001 | t0021 | g0175 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18984 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18985 | hp1 | a0002 | c0005 | t0015 | g0217 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18985 | hp2 | a0001 | c0001 | t0056 | g0230 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18986 | hp1 | a0003 | c0003 | t0003 | g0235 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18987 | hp1 | a0002 | c0005 | t0006 | g0035 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18987 | hp2 | a0002 | c0002 | t0075 | g0092 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18988 | hp1 | a0002 | c0002 | t0002 | g0071 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18990 | hp1 | a0002 | c0002 | t0002 | g0113 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18990 | hp2 | a0001 | c0001 | t0019 | g0231 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18991 | hp1 | a0003 | c0003 | t0003 | g0010 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18993 | hp2 | a0002 | c0005 | t0006 | g0209 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0118 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18994 | hp2 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18995 | hp1 | a0001 | c0001 | t0009 | g0162 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18995 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18998 | hp1 | a0002 | c0005 | t0015 | g0218 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18998 | hp2 | a0003 | c0003 | t0003 | g0258 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA18999 | hp2 | a0002 | c0005 | t0015 | g0216 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19000 | hp2 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19002 | hp1 | a0002 | c0002 | t0013 | g0093 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19002 | hp2 | a0003 | c0003 | t0003 | g0254 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19004 | hp1 | a0003 | c0003 | t0082 | g0243 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19005 | hp1 | a0002 | c0002 | t0005 | g0073 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19005 | hp2 | a0002 | c0002 | t0005 | g0076 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19007 | hp2 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19009 | hp1 | a0001 | c0001 | t0009 | g0195 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19009 | hp2 | a0003 | c0003 | t0007 | g0253 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19010 | hp2 | a0002 | c0002 | t0002 | g0075 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19011 | hp1 | a0001 | c0001 | t0008 | g0174 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19011 | hp2 | a0002 | c0002 | t0002 | g0084 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19012 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19030 | hp1 | a0004 | c0004 | t0068 | g0282 | AFR | LWK | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19030 | hp2 | a0001 | c0001 | t0054 | g0299 | AFR | LWK | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19043 | hp1 | a0001 | c0001 | t0055 | g0300 | AFR | LWK | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19043 | hp2 | a0002 | c0002 | t0044 | g0013 | AFR | LWK | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19054 | hp1 | a0001 | c0001 | t0021 | g0157 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19054 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19055 | hp1 | a0003 | c0003 | t0003 | g0126 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19055 | hp2 | a0001 | c0001 | t0009 | g0153 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19057 | hp1 | a0001 | c0001 | t0009 | g0171 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19057 | hp2 | a0003 | c0003 | t0011 | g0234 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19058 | hp2 | a0002 | c0002 | t0013 | g0109 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19059 | hp1 | a0003 | c0003 | t0010 | g0276 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19060 | hp1 | a0002 | c0002 | t0005 | g0121 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19060 | hp2 | a0001 | c0001 | t0019 | g0229 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19062 | hp2 | a0002 | c0002 | t0005 | g0015 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19065 | hp1 | a0003 | c0003 | t0003 | g0265 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0086 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19070 | hp1 | a0001 | c0001 | t0033 | g0140 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19070 | hp2 | a0001 | c0001 | t0033 | g0142 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19072 | hp1 | a0002 | c0005 | t0015 | g0219 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19072 | hp2 | a0003 | c0003 | t0003 | g0233 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19075 | hp2 | a0002 | c0005 | t0030 | g0205 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19076 | hp1 | a0002 | c0002 | t0002 | g0103 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19076 | hp2 | a0003 | c0003 | t0064 | g0250 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19077 | hp1 | a0002 | c0002 | t0028 | g0087 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19078 | hp1 | a0002 | c0002 | t0013 | g0107 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19078 | hp2 | a0001 | c0001 | t0008 | g0173 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19080 | hp1 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19080 | hp2 | a0002 | c0002 | t0005 | g0081 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19081 | hp1 | a0002 | c0002 | t0002 | g0123 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19082 | hp1 | a0001 | c0001 | t0017 | g0154 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19082 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19084 | hp1 | a0001 | c0001 | t0018 | g0022 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19084 | hp2 | a0003 | c0003 | t0035 | g0237 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19085 | hp1 | a0001 | c0001 | t0008 | g0029 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19085 | hp2 | a0002 | c0002 | t0002 | g0115 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19087 | hp2 | a0003 | c0003 | t0007 | g0274 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0193 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19088 | hp2 | a0003 | c0003 | t0035 | g0239 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19089 | hp2 | a0003 | c0003 | t0003 | g0240 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19091 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19091 | hp2 | a0002 | c0002 | t0002 | g0079 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | YRI | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA19240 | hp2 | a0004 | c0004 | t0040 | g0301 | AFR | YRI | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA20129 | hp1 | a0004 | c0004 | t0032 | g0295 | AFR | ASW | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA20129 | hp2 | a0004 | c0004 | t0023 | g0232 | AFR | ASW | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | GIH | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA20905 | hp2 | a0003 | c0003 | t0011 | g0275 | SAS | GIH | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01123 | hp1 | a0001 | c0001 | t0017 | g0027 | AMR | CLM | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG01123 | hp2 | a0002 | c0005 | t0006 | g0034 | AMR | CLM | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | ACB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02109 | hp2 | a0004 | c0004 | t0020 | g0303 | AFR | ACB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02486 | hp2 | a0005 | c0006 | t0026 | g0317 | AFR | ACB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02559 | hp1 | a0002 | c0005 | t0016 | g0226 | AFR | ACB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG02559 | hp2 | a0004 | c0004 | t0031 | g0294 | AFR | ACB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG03471 | hp2 | a0002 | c0002 | t0002 | g0110 | AFR | MSL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG06807 | hp1 | a0001 | c0001 | t0009 | g0151 | AFR | USA | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| HG06807 | hp2 | a0002 | c0002 | t0077 | g0062 | AFR | USA | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA20300 | hp1 | a0004 | c0004 | t0003 | g0284 | AFR | USA | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0164 | AFR | USA | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA21309 | hp1 | a0004 | c0004 | t0012 | g0319 | AFR | LWK | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| NA21309 | hp2 | a0002 | c0005 | t0006 | g0214 | AFR | LWK | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0002 | g0066 | REF | REF | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| homoSapiens | grch38p0 | a0002 | c0005 | t0006 | g0293 | REF | REF | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:58660011 | C | T | 5 | a0003 a0004 a0005 others(2): Show |
130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
missense_variant | MODERATE | c.2473G>A | p.Glu825Lys | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 2483/7751 | 2473/2487 | 825/828 | chr1 | 58660011 | |||
| chr1:58660057 | A | T | 1 | a0010 | 1 | NA18974.hp2 | stop_gained | HIGH | c.2427T>A | p.Tyr809* | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 2437/7751 | 2427/2487 | 809/828 | chr1 | 58660057 | |||
| chr1:58660058 | T | A | 1 | a0010 | 1 | NA18974.hp2 | missense_variant | MODERATE | c.2426A>T | p.Tyr809Phe | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 2436/7751 | 2426/2487 | 809/828 | chr1 | 58660058 | |||
| chr1:58660059 | A | T | 1 | a0010 | 1 | NA18974.hp2 | missense_variant | MODERATE | c.2425T>A | p.Tyr809Asn | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 2435/7751 | 2425/2487 | 809/828 | chr1 | 58660059 | |||
| chr1:58671925 | C | G | 1 | a0009 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.1606G>C | p.Glu536Gln | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/20 | 1616/7751 | 1606/2487 | 536/828 | chr1 | 58671925 | |||
| chr1:58682127 | T | G | 1 | a0005 | 8 | HG02257.hp2 HG02486.hp2 HG02572.hp1 others(5): Show |
missense_variant | MODERATE | c.917A>C | p.Lys306Thr | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/20 | 927/7751 | 917/2487 | 306/828 | chr1 | 58682127 | |||
| chr1:58682254 | T | C | 7 | a0001 a0003 a0004 others(4): Show |
268 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(265): Show |
missense_variant | MODERATE | c.790A>G | p.Thr264Ala | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/20 | 800/7751 | 790/2487 | 264/828 | chr1 | 58682254 | |||
| chr1:58682434 | G | A | 1 | a0008 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.610C>T | p.Arg204Cys | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/20 | 620/7751 | 610/2487 | 204/828 | chr1 | 58682434 | |||
| chr1:58682446 | A | T | 1 | a0003 | 59 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(56): Show |
missense_variant | MODERATE | c.598T>A | p.Cys200Ser | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/20 | 608/7751 | 598/2487 | 200/828 | chr1 | 58682446 | |||
| chr1:58682464 | T | C | 1 | a0007 | 2 | HG01256.hp1 HG04199.hp1 |
missense_variant | MODERATE | c.580A>G | p.Lys194Glu | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/20 | 590/7751 | 580/2487 | 194/828 | chr1 | 58682464 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:58661414 | G | A | 2 | a0002c0002 a0008c0013 |
97 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(94): Show |
synonymous_variant | LOW | c.2262C>T | p.Leu754Leu | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 18/20 | 2272/7751 | 2262/2487 | 754/828 | chr1 | 58661414 | |||
| chr1:58676957 | G | A | 1 | a0006c0007 | 3 | HG01884.hp1 HG02145.hp2 HG03209.hp2 |
synonymous_variant | LOW | c.1359C>T | p.Leu453Leu | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 9/20 | 1369/7751 | 1359/2487 | 453/828 | chr1 | 58676957 | |||
| chr1:58677041 | T | C | 9 | a0001c0001 a0003c0003 a0004c0004 others(6): Show |
271 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(268): Show |
synonymous_variant | LOW | c.1275A>G | p.Pro425Pro | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 9/20 | 1285/7751 | 1275/2487 | 425/828 | chr1 | 58677041 | |||
| chr1:58700047 | C | T | 1 | a0005c0008 | 2 | HG02896.hp2 HG02897.hp2 |
synonymous_variant | LOW | c.6G>A | p.Ala2Ala | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/20 | 16/7751 | 6/2487 | 2/828 | chr1 | 58700047 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:58654847 | A | ATTAAGTA others(20): Show |
1 | a0002c0005t0015 | 5 | NA18960.hp1 NA18985.hp1 NA18998.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5123_*5149dupAAAA others(23): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 5149 | chr1 | 58654847 | ||||||
| chr1:58654891 | A | G | 43 | a0003c0003t0003 a0003c0003t0007 a0003c0003t0010 others(40): Show |
130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*5106T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 5106 | chr1 | 58654891 | ||||||
| chr1:58654907 | G | A | 88 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(85): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
3_prime_UTR_variant | MODIFIER | c.*5090C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 5090 | chr1 | 58654907 | ||||||
| chr1:58654917 | C | T | 43 | a0003c0003t0003 a0003c0003t0007 a0003c0003t0010 others(40): Show |
130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*5080G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 5080 | chr1 | 58654917 | ||||||
| chr1:58654978 | C | T | 88 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(85): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
3_prime_UTR_variant | MODIFIER | c.*5019G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 5019 | chr1 | 58654978 | ||||||
| chr1:58655192 | T | G | 2 | a0001c0001t0019 a0001c0001t0056 |
5 | NA18953.hp2 NA18954.hp1 NA18985.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4805A>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 4805 | chr1 | 58655192 | ||||||
| chr1:58655194 | T | C | 1 | a0002c0005t0016 | 5 | HG00741.hp1 HG01515.hp2 HG01517.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4803A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 4803 | chr1 | 58655194 | ||||||
| chr1:58655218 | CAT | C | 3 | a0002c0005t0027 a0002c0005t0029 a0002c0005t0043 |
8 | HG01074.hp1 HG02280.hp1 HG02615.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4777_*4778delAT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 4777 | chr1 | 58655218 | ||||||
| chr1:58655289 | G | A | 43 | a0003c0003t0003 a0003c0003t0007 a0003c0003t0010 others(40): Show |
130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*4708C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 4708 | chr1 | 58655289 | ||||||
| chr1:58655305 | T | C | 1 | a0002c0002t0073 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4692A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 4692 | chr1 | 58655305 | ||||||
| chr1:58655318 | AT | A | 85 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(82): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
3_prime_UTR_variant | MODIFIER | c.*4678delA | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 4678 | chr1 | 58655318 | ||||||
| chr1:58655338 | A | C | 1 | a0002c0005t0079 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4659T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 4659 | chr1 | 58655338 | ||||||
| chr1:58655364 | A | C | 25 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(22): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*4633T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 4633 | chr1 | 58655364 | ||||||
| chr1:58655365 | C | T | 5 | a0001c0001t0036 a0001c0001t0037 a0001c0001t0053 others(2): Show |
7 | HG01192.hp1 HG01243.hp2 HG02717.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4632G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 4632 | chr1 | 58655365 | ||||||
| chr1:58655414 | C | T | 1 | a0002c0002t0075 | 1 | NA18987.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4583G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 4583 | chr1 | 58655414 | ||||||
| chr1:58655415 | T | C | 1 | a0002c0002t0075 | 1 | NA18987.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4582A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 4582 | chr1 | 58655415 | ||||||
| chr1:58655472 | A | AT | 43 | a0003c0003t0003 a0003c0003t0007 a0003c0003t0010 others(40): Show |
130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*4524dupA | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 4524 | chr1 | 58655472 | ||||||
| chr1:58655494 | G | A | 43 | a0003c0003t0003 a0003c0003t0007 a0003c0003t0010 others(40): Show |
130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*4503C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 4503 | chr1 | 58655494 | ||||||
| chr1:58655671 | T | A | 43 | a0003c0003t0003 a0003c0003t0007 a0003c0003t0010 others(40): Show |
130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*4326A>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 4326 | chr1 | 58655671 | ||||||
| chr1:58655971 | G | A | 1 | a0001c0001t0055 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4026C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 4026 | chr1 | 58655971 | ||||||
| chr1:58656019 | T | A | 1 | a0004c0004t0032 | 3 | HG02965.hp1 HG02970.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3978A>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 3978 | chr1 | 58656019 | ||||||
| chr1:58656091 | C | T | 2 | a0004c0004t0012 a0004c0004t0069 |
7 | HG01167.hp1 HG01255.hp2 HG01496.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3906G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 3906 | chr1 | 58656091 | ||||||
| chr1:58656096 | G | C | 43 | a0003c0003t0003 a0003c0003t0007 a0003c0003t0010 others(40): Show |
130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*3901C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 3901 | chr1 | 58656096 | ||||||
| chr1:58656212 | C | T | 1 | a0001c0001t0054 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3785G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 3785 | chr1 | 58656212 | ||||||
| chr1:58656283 | T | A | 1 | a0010c0012t0048 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3714A>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 3714 | chr1 | 58656283 | ||||||
| chr1:58656288 | T | G | 1 | a0001c0001t0049 | 1 | HG03490.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3709A>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 3709 | chr1 | 58656288 | ||||||
| chr1:58656384 | GAAGT | G | 2 | a0002c0002t0044 a0002c0002t0077 |
3 | HG01891.hp2 HG06807.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3609_*3612delACTT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 3609 | chr1 | 58656384 | ||||||
| chr1:58656445 | AAGGTAGT | A | 3 | a0004c0004t0024 a0004c0004t0066 a0004c0004t0071 |
5 | HG02055.hp1 HG02615.hp2 HG02622.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3545_*3551delACTA others(3): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 3545 | chr1 | 58656445 | ||||||
| chr1:58656578 | A | G | 1 | a0006c0007t0025 | 3 | HG01884.hp1 HG02145.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3419T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 3419 | chr1 | 58656578 | ||||||
| chr1:58656599 | G | A | 1 | a0010c0012t0048 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3398C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 3398 | chr1 | 58656599 | ||||||
| chr1:58656617 | T | G | 43 | a0003c0003t0003 a0003c0003t0007 a0003c0003t0010 others(40): Show |
130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*3380A>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 3380 | chr1 | 58656617 | ||||||
| chr1:58656799 | C | A | 1 | a0010c0012t0048 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3198G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 3198 | chr1 | 58656799 | ||||||
| chr1:58656891 | A | C | 1 | a0003c0003t0067 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3106T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 3106 | chr1 | 58656891 | ||||||
| chr1:58657052 | T | G | 1 | a0003c0003t0059 | 1 | NA18947.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2945A>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 2945 | chr1 | 58657052 | ||||||
| chr1:58657120 | G | A | 2 | a0001c0001t0019 a0001c0001t0056 |
5 | NA18953.hp2 NA18954.hp1 NA18985.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2877C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 2877 | chr1 | 58657120 | ||||||
| chr1:58657199 | C | T | 68 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(65): Show |
272 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(269): Show |
3_prime_UTR_variant | MODIFIER | c.*2798G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 2798 | chr1 | 58657199 | ||||||
| chr1:58657203 | G | C | 1 | a0003c0003t0062 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2794C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 2794 | chr1 | 58657203 | ||||||
| chr1:58657238 | G | GA | 82 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(79): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
3_prime_UTR_variant | MODIFIER | c.*2758dupT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 2758 | chr1 | 58657238 | ||||||
| chr1:58657311 | C | T | 1 | a0010c0012t0048 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2686G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 2686 | chr1 | 58657311 | ||||||
| chr1:58657338 | T | G | 1 | a0004c0004t0068 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2659A>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 2659 | chr1 | 58657338 | ||||||
| chr1:58657574 | G | A | 3 | a0002c0002t0028 a0002c0002t0074 a0002c0002t0083 |
5 | HG02083.hp1 HG02129.hp1 HG02523.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2423C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 2423 | chr1 | 58657574 | ||||||
| chr1:58657646 | T | C | 3 | a0002c0005t0027 a0002c0005t0029 a0002c0005t0043 |
8 | HG01074.hp1 HG02280.hp1 HG02615.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2351A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 2351 | chr1 | 58657646 | ||||||
| chr1:58657652 | TTG | T | 3 | a0004c0004t0024 a0004c0004t0066 a0004c0004t0071 |
5 | HG02055.hp1 HG02615.hp2 HG02622.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2343_*2344delCA | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 2343 | chr1 | 58657652 | ||||||
| chr1:58657697 | TTC | T | 2 | a0001c0001t0019 a0001c0001t0056 |
5 | NA18953.hp2 NA18954.hp1 NA18985.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2298_*2299delGA | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 2298 | chr1 | 58657697 | ||||||
| chr1:58657743 | G | A | 1 | a0003c0003t0065 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2254C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 2254 | chr1 | 58657743 | ||||||
| chr1:58657859 | T | C | 6 | a0004c0004t0012 a0004c0004t0031 a0004c0004t0032 others(3): Show |
15 | HG01167.hp1 HG01255.hp2 HG01256.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2138A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 2138 | chr1 | 58657859 | ||||||
| chr1:58657961 | T | C | 3 | a0004c0004t0012 a0004c0004t0069 a0004c0004t0072 |
8 | HG01167.hp1 HG01255.hp2 HG01496.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2036A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 2036 | chr1 | 58657961 | ||||||
| chr1:58657983 | C | T | 15 | a0002c0002t0002 a0002c0002t0005 a0002c0002t0013 others(12): Show |
94 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*2014G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 2014 | chr1 | 58657983 | ||||||
| chr1:58658108 | C | T | 1 | a0006c0007t0025 | 3 | HG01884.hp1 HG02145.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1889G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1889 | chr1 | 58658108 | ||||||
| chr1:58658299 | C | T | 2 | a0004c0004t0039 a0004c0004t0063 |
3 | HG01952.hp2 HG02004.hp2 HG02273.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1698G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1698 | chr1 | 58658299 | ||||||
| chr1:58658323 | A | G | 25 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(22): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*1674T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1674 | chr1 | 58658323 | ||||||
| chr1:58658333 | C | CT | 3 | a0002c0005t0027 a0002c0005t0029 a0002c0005t0043 |
8 | HG01074.hp1 HG02280.hp1 HG02615.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1663dupA | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1663 | chr1 | 58658333 | ||||||
| chr1:58658436 | TGGAA | T | 3 | a0001c0001t0036 a0001c0001t0053 a0001c0001t0057 |
4 | HG01192.hp1 HG02717.hp1 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1557_*1560delTTCC | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1557 | chr1 | 58658436 | ||||||
| chr1:58658551 | G | A | 25 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(22): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*1446C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1446 | chr1 | 58658551 | ||||||
| chr1:58658589 | T | C | 1 | a0002c0005t0015 | 5 | NA18960.hp1 NA18985.hp1 NA18998.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1408A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1408 | chr1 | 58658589 | ||||||
| chr1:58658701 | GA | G | 23 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(20): Show |
137 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*1295delT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1295 | chr1 | 58658701 | ||||||
| chr1:58658801 | G | A | 3 | a0002c0002t0045 a0002c0002t0076 a0002c0002t0078 |
4 | HG02723.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1196C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1196 | chr1 | 58658801 | ||||||
| chr1:58658874 | A | G | 68 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(65): Show |
272 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(269): Show |
3_prime_UTR_variant | MODIFIER | c.*1123T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1123 | chr1 | 58658874 | ||||||
| chr1:58658883 | GAAT | G | 4 | a0004c0004t0020 a0004c0004t0023 a0004c0004t0040 others(1): Show |
10 | HG00738.hp1 HG02109.hp2 HG02257.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1111_*1113delATT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1111 | chr1 | 58658883 | ||||||
| chr1:58658924 | T | A | 1 | a0002c0002t0041 | 2 | HG03490.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1073A>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1073 | chr1 | 58658924 | ||||||
| chr1:58658958 | A | AAC | 3 | a0002c0002t0077 a0002c0002t0078 a0002c0005t0030 |
5 | HG02723.hp1 HG06807.hp2 NA18949.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1037_*1038dupGT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1038 | chr1 | 58658958 | ||||||
| chr1:58658958 | A | AACAC | 3 | a0001c0001t0018 a0002c0002t0076 a0002c0005t0029 |
8 | HG02615.hp1 HG02738.hp2 HG02965.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1035_*1038dupGTGT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1038 | chr1 | 58658958 | ||||||
| chr1:58658958 | A | AACACAC | 14 | a0001c0001t0021 a0001c0001t0037 a0001c0001t0057 others(11): Show |
36 | HG00735.hp1 HG01074.hp1 HG01167.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*1033_*1038dupGTGT others(2): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1038 | chr1 | 58658958 | ||||||
| chr1:58658958 | A | AACACACA others(1): Show |
13 | a0001c0001t0009 a0001c0001t0050 a0002c0002t0042 others(10): Show |
33 | HG00099.hp2 HG01496.hp2 HG01884.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1031_*1038dupGTGT others(4): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1038 | chr1 | 58658958 | ||||||
| chr1:58658958 | A | AACACACA others(3): Show |
19 | a0001c0001t0001 a0001c0001t0036 a0001c0001t0049 others(16): Show |
133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*1029_*1038dupGTGT others(6): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1038 | chr1 | 58658958 | ||||||
| chr1:58658958 | A | AACACACA others(5): Show |
16 | a0001c0001t0004 a0001c0001t0019 a0001c0001t0053 others(13): Show |
110 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*1027_*1038dupGTGT others(8): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1038 | chr1 | 58658958 | ||||||
| chr1:58658958 | A | AACACACA others(7): Show |
8 | a0001c0001t0008 a0002c0002t0014 a0002c0002t0074 others(5): Show |
34 | HG00544.hp1 HG00639.hp2 HG00738.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1025_*1038dupGTGT others(10): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1038 | chr1 | 58658958 | ||||||
| chr1:58658958 | A | AACACACA others(9): Show |
3 | a0001c0001t0017 a0003c0003t0022 a0003c0003t0062 |
8 | HG01123.hp1 HG01361.hp2 HG02080.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1023_*1038dupGTGT others(12): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1038 | chr1 | 58658958 | ||||||
| chr1:58658958 | A | AACACACA others(11): Show |
1 | a0002c0002t0073 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1021_*1038dupGTGT others(14): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1038 | chr1 | 58658958 | ||||||
| chr1:58658958 | A | AACACACA others(13): Show |
1 | a0001c0001t0047 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1019_*1038dupGTGT others(16): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1038 | chr1 | 58658958 | ||||||
| chr1:58658958 | A | ACACACAC others(4): Show |
2 | a0001c0001t0033 a0010c0012t0048 |
3 | NA18974.hp2 NA19070.hp1 NA19070.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1038_*1039insGTGT others(7): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1038 | chr1 | 58658958 | ||||||
| chr1:58658958 | AACAC | A | 4 | a0001c0001t0051 a0002c0005t0016 a0002c0005t0079 others(1): Show |
8 | HG00738.hp2 HG00741.hp1 HG01515.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1035_*1038delGTGT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1035 | chr1 | 58658958 | ||||||
| chr1:58658958 | AACACACA others(3): Show |
A | 1 | a0001c0001t0052 | 1 | NA18962.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1029_*1038delGTGT others(6): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1029 | chr1 | 58658958 | ||||||
| chr1:58658995 | A | ACACACAC others(6): Show |
2 | a0001c0001t0046 a0004c0004t0061 |
2 | HG03098.hp2 NA18979.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1001_*1002insGTGT others(9): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1001 | chr1 | 58658995 | ||||||
| chr1:58659010 | A | G | 1 | a0004c0004t0060 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*987T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 987 | chr1 | 58659010 | ||||||
| chr1:58659119 | CT | C | 25 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(22): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*877delA | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 877 | chr1 | 58659119 | ||||||
| chr1:58659131 | C | T | 68 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(65): Show |
272 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(269): Show |
3_prime_UTR_variant | MODIFIER | c.*866G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 866 | chr1 | 58659131 | ||||||
| chr1:58659145 | CT | C | 3 | a0004c0004t0031 a0004c0004t0032 a0004c0004t0081 |
7 | HG01256.hp2 HG01258.hp1 HG02559.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*851delA | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 851 | chr1 | 58659145 | ||||||
| chr1:58659278 | C | T | 2 | a0003c0003t0058 a0003c0003t0059 |
2 | HG02040.hp2 NA18947.hp2 |
3_prime_UTR_variant | MODIFIER | c.*719G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 719 | chr1 | 58659278 | ||||||
| chr1:58659578 | C | A | 1 | a0003c0003t0082 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*419G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 419 | chr1 | 58659578 | ||||||
| chr1:58659638 | A | G | 1 | a0003c0003t0038 | 2 | HG01257.hp2 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*359T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 359 | chr1 | 58659638 | ||||||
| chr1:58659647 | C | T | 25 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(22): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*350G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 350 | chr1 | 58659647 | ||||||
| chr1:58659707 | C | T | 1 | a0003c0003t0035 | 2 | NA19084.hp2 NA19088.hp2 |
3_prime_UTR_variant | MODIFIER | c.*290G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 290 | chr1 | 58659707 | ||||||
| chr1:58659843 | C | T | 17 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(14): Show |
129 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*154G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 154 | chr1 | 58659843 | ||||||
| chr1:58659860 | T | C | 1 | a0002c0002t0083 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*137A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 137 | chr1 | 58659860 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:58660162 | G | T | 7 | a0004c0004t0012g0319 a0004c0004t0012g0320 a0004c0004t0012g0321 others(4): Show |
7 | HG01167.hp1 HG01255.hp2 HG01496.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.2329-7C>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 19/19 | chr1 | 58660162 | |||||||
| chr1:58660214 | C | G | 1 | a0001c0001t0054g0299 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2329-59G>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 19/19 | chr1 | 58660214 | |||||||
| chr1:58660222 | A | G | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(104): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.2329-67T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 19/19 | chr1 | 58660222 | |||||||
| chr1:58660227 | G | A | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(104): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.2329-72C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 19/19 | chr1 | 58660227 | |||||||
| chr1:58660237 | A | G | 1 | a0001c0001t0001g0188 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.2329-82T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 19/19 | chr1 | 58660237 | |||||||
| chr1:58660346 | G | C | 6 | a0001c0001t0036g0053 a0001c0001t0036g0061 a0001c0001t0037g0045 others(3): Show |
7 | HG01192.hp1 HG01243.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2329-191C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 19/19 | chr1 | 58660346 | |||||||
| chr1:58660435 | C | T | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(104): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.2329-280G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 19/19 | chr1 | 58660435 | |||||||
| chr1:58660617 | C | G | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(104): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.2329-462G>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 19/19 | chr1 | 58660617 | |||||||
| chr1:58660742 | G | A | 2 | a0001c0001t0009g0152 a0001c0001t0021g0182 |
2 | HG00099.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.2328+428C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 19/19 | chr1 | 58660742 | |||||||
| chr1:58660867 | A | G | 1 | a0002c0002t0076g0064 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2328+303T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 19/19 | chr1 | 58660867 | |||||||
| chr1:58660944 | A | G | 295 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(292): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.2328+226T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 19/19 | chr1 | 58660944 | |||||||
| chr1:58661004 | A | C | 295 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(292): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.2328+166T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 19/19 | chr1 | 58661004 | |||||||
| chr1:58661074 | T | C | 3 | a0004c0004t0024g0012 a0004c0004t0024g0049 a0004c0004t0071g0050 |
4 | HG02055.hp1 HG02615.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2328+96A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 19/19 | chr1 | 58661074 | |||||||
| chr1:58661285 | T | A | 2 | a0002c0005t0006g0213 a0002c0005t0006g0214 |
2 | HG02818.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2271-58A>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 18/19 | chr1 | 58661285 | |||||||
| chr1:58661301 | C | T | 7 | a0004c0004t0012g0319 a0004c0004t0012g0320 a0004c0004t0012g0321 others(4): Show |
7 | HG01167.hp1 HG01255.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.2271-74G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 18/19 | chr1 | 58661301 | |||||||
| chr1:58661352 | T | G | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(104): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.2270+54A>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 18/19 | chr1 | 58661352 | |||||||
| chr1:58661521 | C | T | 73 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0007 others(70): Show |
94 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.2165-10G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58661521 | |||||||
| chr1:58661535 | T | C | 108 | a0003c0003t0003g0001 a0003c0003t0003g0010 a0003c0003t0003g0126 others(105): Show |
130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.2165-24A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58661535 | |||||||
| chr1:58661602 | T | A | 1 | a0010c0012t0048g0128 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2165-91A>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58661602 | |||||||
| chr1:58661652 | G | A | 4 | a0004c0004t0007g0043 a0004c0004t0007g0289 a0004c0004t0007g0290 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.2165-141C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58661652 | |||||||
| chr1:58661707 | C | T | 2 | a0003c0003t0003g0260 a0003c0003t0007g0259 |
2 | NA18945.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.2165-196G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58661707 | |||||||
| chr1:58661748 | A | G | 2 | a0003c0003t0003g0260 a0003c0003t0007g0259 |
2 | NA18945.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.2165-237T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58661748 | |||||||
| chr1:58661760 | C | T | 5 | a0002c0005t0027g0036 a0002c0005t0027g0221 a0002c0005t0029g0038 others(2): Show |
8 | HG01074.hp1 HG02280.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.2165-249G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58661760 | |||||||
| chr1:58661827 | A | T | 1 | a0004c0004t0003g0252 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2165-316T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58661827 | |||||||
| chr1:58661878 | C | G | 1 | a0005c0006t0011g0315 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2165-367G>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58661878 | |||||||
| chr1:58661965 | T | G | 215 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(212): Show |
272 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.2165-454A>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58661965 | |||||||
| chr1:58661969 | TG | T | 73 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0007 others(70): Show |
94 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.2165-459delC | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58661969 | |||||||
| chr1:58661970 | G | T | 2 | a0002c0002t0044g0013 a0002c0002t0077g0062 |
3 | HG01891.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2165-459C>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58661970 | |||||||
| chr1:58662032 | G | A | 1 | a0002c0002t0044g0013 | 2 | HG01891.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2165-521C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58662032 | |||||||
| chr1:58662033 | C | G | 104 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(101): Show |
139 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.2165-522G>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58662033 | |||||||
| chr1:58662264 | G | A | 78 | a0003c0003t0003g0001 a0003c0003t0003g0010 a0003c0003t0003g0126 others(75): Show |
95 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.2165-753C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58662264 | |||||||
| chr1:58662303 | C | A | 4 | a0001c0001t0019g0040 a0001c0001t0019g0229 a0001c0001t0019g0231 others(1): Show |
5 | NA18953.hp2 NA18954.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.2165-792G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58662303 | |||||||
| chr1:58662383 | C | A | 1 | a0004c0004t0003g0307 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2165-872G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58662383 | |||||||
| chr1:58662434 | T | C | 1 | a0002c0002t0028g0100 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2165-923A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58662434 | |||||||
| chr1:58662461 | CCT | C | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(103): Show |
141 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.2165-952_2165-951d others(4): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58662461 | |||||||
| chr1:58662462 | C | CT | 161 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0007 others(158): Show |
203 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.2165-952dupA | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58662462 | |||||||
| chr1:58662462 | C | T | 3 | a0002c0002t0002g0078 a0002c0002t0014g0097 a0004c0004t0007g0298 |
3 | HG00639.hp2 HG01070.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.2165-951G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58662462 | |||||||
| chr1:58662493 | A | G | 1 | a0002c0002t0002g0103 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2165-982T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58662493 | |||||||
| chr1:58662521 | A | C | 75 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0007 others(72): Show |
97 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.2165-1010T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58662521 | |||||||
| chr1:58662565 | G | A | 108 | a0003c0003t0003g0001 a0003c0003t0003g0010 a0003c0003t0003g0126 others(105): Show |
130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.2165-1054C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58662565 | |||||||
| chr1:58662598 | C | T | 7 | a0005c0006t0003g0316 a0005c0006t0011g0047 a0005c0006t0011g0314 others(4): Show |
9 | HG02257.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2165-1087G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58662598 | |||||||
| chr1:58662603 | A | T | 4 | a0001c0001t0036g0053 a0001c0001t0036g0061 a0001c0001t0053g0059 others(1): Show |
4 | HG01192.hp1 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2165-1092T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58662603 | |||||||
| chr1:58662659 | G | GA | 6 | a0001c0001t0004g0133 a0001c0001t0019g0040 a0001c0001t0019g0229 others(3): Show |
7 | NA18953.hp2 NA18954.hp1 NA18977.hp2 others(4): Show |
intron_variant | MODIFIER | c.2165-1149dupT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58662659 | |||||||
| chr1:58662659 | GA | G | 5 | a0004c0004t0020g0303 a0004c0004t0020g0304 a0004c0004t0020g0308 others(2): Show |
5 | HG02109.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.2165-1149delT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58662659 | |||||||
| chr1:58662773 | G | A | 2 | a0006c0007t0025g0014 a0006c0007t0025g0063 |
3 | HG01884.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2165-1262C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58662773 | |||||||
| chr1:58662791 | A | C | 1 | a0003c0003t0007g0253 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2165-1280T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58662791 | |||||||
| chr1:58662857 | A | G | 7 | a0005c0006t0003g0316 a0005c0006t0011g0047 a0005c0006t0011g0314 others(4): Show |
9 | HG02257.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2165-1346T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58662857 | |||||||
| chr1:58662972 | A | T | 1 | a0002c0002t0002g0085 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2165-1461T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58662972 | |||||||
| chr1:58663321 | A | G | 5 | a0001c0001t0036g0053 a0001c0001t0036g0061 a0001c0001t0053g0059 others(2): Show |
5 | HG01192.hp1 HG02717.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2165-1810T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58663321 | |||||||
| chr1:58663328 | T | TC | 295 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(292): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.2165-1818dupG | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58663328 | |||||||
| chr1:58663378 | C | G | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(104): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.2165-1867G>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58663378 | |||||||
| chr1:58663435 | T | A | 1 | a0003c0003t0010g0276 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.2165-1924A>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58663435 | |||||||
| chr1:58663518 | G | A | 3 | a0004c0004t0024g0012 a0004c0004t0024g0049 a0004c0004t0071g0050 |
4 | HG02055.hp1 HG02615.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2164+1981C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58663518 | |||||||
| chr1:58663587 | T | C | 4 | a0004c0004t0024g0012 a0004c0004t0024g0049 a0004c0004t0066g0048 others(1): Show |
5 | HG02055.hp1 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2164+1912A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58663587 | |||||||
| chr1:58663670 | T | A | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(104): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.2164+1829A>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58663670 | |||||||
| chr1:58663693 | A | G | 2 | a0004c0004t0039g0046 a0004c0004t0063g0311 |
3 | HG01952.hp2 HG02004.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.2164+1806T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58663693 | |||||||
| chr1:58663844 | G | T | 290 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(287): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.2164+1655C>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58663844 | |||||||
| chr1:58663947 | T | C | 1 | a0002c0002t0076g0064 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2164+1552A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58663947 | |||||||
| chr1:58663972 | A | C | 290 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(287): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.2164+1527T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58663972 | |||||||
| chr1:58663973 | A | C | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(104): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.2164+1526T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58663973 | |||||||
| chr1:58664168 | T | C | 12 | a0002c0002t0002g0079 a0002c0002t0002g0082 a0002c0002t0002g0085 others(9): Show |
14 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.2164+1331A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58664168 | |||||||
| chr1:58664301 | A | G | 108 | a0003c0003t0003g0001 a0003c0003t0003g0010 a0003c0003t0003g0126 others(105): Show |
130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.2164+1198T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58664301 | |||||||
| chr1:58664368 | G | A | 4 | a0001c0001t0019g0040 a0001c0001t0019g0229 a0001c0001t0019g0231 others(1): Show |
5 | NA18953.hp2 NA18954.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.2164+1131C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58664368 | |||||||
| chr1:58664522 | C | T | 4 | a0004c0004t0024g0012 a0004c0004t0024g0049 a0004c0004t0066g0048 others(1): Show |
5 | HG02055.hp1 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2164+977G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58664522 | |||||||
| chr1:58664550 | A | C | 2 | a0006c0007t0025g0014 a0006c0007t0025g0063 |
3 | HG01884.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2164+949T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58664550 | |||||||
| chr1:58664557 | A | C | 111 | a0002c0002t0045g0055 a0002c0002t0045g0056 a0002c0002t0078g0057 others(108): Show |
133 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.2164+942T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58664557 | |||||||
| chr1:58664574 | T | G | 5 | a0005c0006t0003g0316 a0005c0006t0011g0314 a0005c0006t0011g0315 others(2): Show |
6 | HG02257.hp2 HG02572.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2164+925A>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58664574 | |||||||
| chr1:58664686 | C | T | 4 | a0001c0001t0036g0053 a0001c0001t0036g0061 a0001c0001t0053g0059 others(1): Show |
4 | HG01192.hp1 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2164+813G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58664686 | |||||||
| chr1:58664735 | C | T | 108 | a0003c0003t0003g0001 a0003c0003t0003g0010 a0003c0003t0003g0126 others(105): Show |
130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.2164+764G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58664735 | |||||||
| chr1:58664800 | T | C | 3 | a0004c0004t0024g0012 a0004c0004t0024g0049 a0004c0004t0071g0050 |
4 | HG02055.hp1 HG02615.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2164+699A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58664800 | |||||||
| chr1:58664942 | C | T | 290 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(287): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.2164+557G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58664942 | |||||||
| chr1:58664992 | G | A | 108 | a0003c0003t0003g0001 a0003c0003t0003g0010 a0003c0003t0003g0126 others(105): Show |
130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.2164+507C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58664992 | |||||||
| chr1:58665128 | T | C | 4 | a0001c0001t0019g0040 a0001c0001t0019g0229 a0001c0001t0019g0231 others(1): Show |
5 | NA18953.hp2 NA18954.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.2164+371A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58665128 | |||||||
| chr1:58665314 | T | C | 4 | a0002c0002t0045g0055 a0002c0002t0045g0056 a0002c0002t0076g0064 others(1): Show |
4 | HG02723.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2164+185A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58665314 | |||||||
| chr1:58665416 | A | G | 108 | a0003c0003t0003g0001 a0003c0003t0003g0010 a0003c0003t0003g0126 others(105): Show |
130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.2164+83T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58665416 | |||||||
| chr1:58665417 | A | C | 108 | a0003c0003t0003g0001 a0003c0003t0003g0010 a0003c0003t0003g0126 others(105): Show |
130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.2164+82T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58665417 | |||||||
| chr1:58665639 | G | T | 290 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(287): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
splice_region_variant&intron_variant | LOW | c.2032-8C>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58665639 | |||||||
| chr1:58665722 | G | T | 1 | a0001c0001t0057g0060 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2032-91C>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58665722 | |||||||
| chr1:58665782 | C | T | 1 | a0002c0002t0041g0020 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2032-151G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58665782 | |||||||
| chr1:58665809 | C | T | 215 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(212): Show |
272 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.2032-178G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58665809 | |||||||
| chr1:58665851 | G | A | 108 | a0003c0003t0003g0001 a0003c0003t0003g0010 a0003c0003t0003g0126 others(105): Show |
130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.2032-220C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58665851 | |||||||
| chr1:58665927 | C | T | 3 | a0001c0001t0001g0169 a0001c0001t0018g0144 a0001c0001t0018g0145 |
3 | HG02738.hp2 HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.2032-296G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58665927 | |||||||
| chr1:58665928 | G | C | 2 | a0004c0004t0026g0051 a0004c0004t0026g0052 |
2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2032-297C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58665928 | |||||||
| chr1:58666003 | G | A | 4 | a0004c0004t0024g0012 a0004c0004t0024g0049 a0004c0004t0066g0048 others(1): Show |
5 | HG02055.hp1 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2032-372C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666003 | |||||||
| chr1:58666005 | C | T | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(104): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.2032-374G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666005 | |||||||
| chr1:58666012 | C | T | 1 | a0002c0002t0041g0020 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2032-381G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666012 | |||||||
| chr1:58666033 | G | A | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(104): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.2032-402C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666033 | |||||||
| chr1:58666046 | G | C | 1 | a0005c0006t0026g0317 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2032-415C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666046 | |||||||
| chr1:58666057 | TA | T | 8 | a0001c0001t0001g0167 a0001c0001t0001g0200 a0002c0005t0027g0036 others(5): Show |
11 | HG01074.hp1 HG02280.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.2032-427delT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666057 | |||||||
| chr1:58666122 | C | T | 108 | a0003c0003t0003g0001 a0003c0003t0003g0010 a0003c0003t0003g0126 others(105): Show |
130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.2032-491G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666122 | |||||||
| chr1:58666200 | G | C | 2 | a0004c0004t0026g0051 a0004c0004t0026g0052 |
2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2032-569C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666200 | |||||||
| chr1:58666215 | A | G | 5 | a0005c0006t0003g0316 a0005c0006t0011g0314 a0005c0006t0011g0315 others(2): Show |
6 | HG02257.hp2 HG02572.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2032-584T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666215 | |||||||
| chr1:58666332 | CTT | C | 4 | a0001c0001t0001g0008 a0001c0001t0009g0156 a0001c0001t0009g0162 others(1): Show |
6 | HG02074.hp2 NA18982.hp1 NA18995.hp1 others(3): Show |
intron_variant | MODIFIER | c.2032-703_2032-702d others(4): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666332 | |||||||
| chr1:58666526 | G | GA | 215 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(212): Show |
272 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.2031+511dupT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666526 | |||||||
| chr1:58666576 | C | CT | 281 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(278): Show |
360 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(357): Show |
intron_variant | MODIFIER | c.2031+461dupA | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666576 | |||||||
| chr1:58666626 | A | T | 4 | a0001c0001t0019g0040 a0001c0001t0019g0229 a0001c0001t0019g0231 others(1): Show |
5 | NA18953.hp2 NA18954.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.2031+412T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666626 | |||||||
| chr1:58666638 | C | T | 78 | a0003c0003t0003g0001 a0003c0003t0003g0010 a0003c0003t0003g0126 others(75): Show |
95 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.2031+400G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666638 | |||||||
| chr1:58666644 | G | A | 3 | a0002c0002t0002g0068 a0002c0002t0002g0069 a0002c0002t0014g0067 |
3 | HG00438.hp1 HG02135.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.2031+394C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666644 | |||||||
| chr1:58666659 | G | C | 4 | a0001c0001t0019g0040 a0001c0001t0019g0229 a0001c0001t0019g0231 others(1): Show |
5 | NA18953.hp2 NA18954.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.2031+379C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666659 | |||||||
| chr1:58666746 | C | T | 2 | a0004c0004t0003g0245 a0005c0006t0011g0314 |
2 | HG02572.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2031+292G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666746 | |||||||
| chr1:58666883 | A | T | 107 | a0003c0003t0003g0001 a0003c0003t0003g0010 a0003c0003t0003g0126 others(104): Show |
129 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.2031+155T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666883 | |||||||
| chr1:58666884 | A | T | 1 | a0003c0003t0010g0276 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.2031+154T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666884 | |||||||
| chr1:58666885 | T | A | 214 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(211): Show |
271 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.2031+153A>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666885 | |||||||
| chr1:58666887 | A | T | 107 | a0003c0003t0003g0001 a0003c0003t0003g0010 a0003c0003t0003g0126 others(104): Show |
129 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.2031+151T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666887 | |||||||
| chr1:58666888 | T | A | 107 | a0003c0003t0003g0001 a0003c0003t0003g0010 a0003c0003t0003g0126 others(104): Show |
129 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.2031+150A>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666888 | |||||||
| chr1:58666895 | A | T | 108 | a0003c0003t0003g0001 a0003c0003t0003g0010 a0003c0003t0003g0126 others(105): Show |
130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.2031+143T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666895 | |||||||
| chr1:58666897 | T | A | 108 | a0003c0003t0003g0001 a0003c0003t0003g0010 a0003c0003t0003g0126 others(105): Show |
130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.2031+141A>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666897 | |||||||
| chr1:58666964 | AAAGTTT | A | 9 | a0005c0006t0003g0316 a0005c0006t0011g0047 a0005c0006t0011g0314 others(6): Show |
12 | HG01884.hp1 HG02145.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.2031+68_2031+73del others(6): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666964 | |||||||
| chr1:58667234 | C | T | 15 | a0004c0004t0003g0042 a0004c0004t0003g0236 a0004c0004t0003g0241 others(12): Show |
16 | HG01074.hp2 HG01081.hp1 HG02886.hp2 others(13): Show |
splice_region_variant&intron_variant | LOW | c.1843-8G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 15/19 | chr1 | 58667234 | |||||||
| chr1:58667352 | T | G | 108 | a0003c0003t0003g0001 a0003c0003t0003g0010 a0003c0003t0003g0126 others(105): Show |
130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.1843-126A>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 15/19 | chr1 | 58667352 | |||||||
| chr1:58667438 | CATA | C | 6 | a0004c0004t0031g0044 a0004c0004t0031g0294 a0004c0004t0032g0292 others(3): Show |
7 | HG01256.hp2 HG01258.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1843-215_1843-213d others(5): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 15/19 | chr1 | 58667438 | |||||||
| chr1:58667551 | T | C | 1 | a0001c0001t0009g0313 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1842+296A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 15/19 | chr1 | 58667551 | |||||||
| chr1:58667596 | A | G | 108 | a0003c0003t0003g0001 a0003c0003t0003g0010 a0003c0003t0003g0126 others(105): Show |
130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.1842+251T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 15/19 | chr1 | 58667596 | |||||||
| chr1:58667667 | C | T | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(104): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.1842+180G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 15/19 | chr1 | 58667667 | |||||||
| chr1:58667766 | T | C | 1 | a0001c0001t0001g0197 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1842+81A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 15/19 | chr1 | 58667766 | |||||||
| chr1:58667771 | A | G | 1 | a0004c0004t0007g0283 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1842+76T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 15/19 | chr1 | 58667771 | |||||||
| chr1:58667822 | CA | C | 4 | a0004c0004t0020g0303 a0004c0004t0020g0304 a0004c0004t0020g0308 others(1): Show |
4 | HG02109.hp2 HG02257.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1842+24delT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 15/19 | chr1 | 58667822 | |||||||
| chr1:58667966 | C | T | 7 | a0002c0002t0002g0079 a0002c0002t0002g0085 a0002c0002t0005g0015 others(4): Show |
9 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(6): Show |
intron_variant | MODIFIER | c.1768-45G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 14/19 | chr1 | 58667966 | |||||||
| chr1:58668110 | T | C | 4 | a0004c0004t0024g0012 a0004c0004t0024g0049 a0004c0004t0066g0048 others(1): Show |
5 | HG02055.hp1 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1768-189A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 14/19 | chr1 | 58668110 | |||||||
| chr1:58668301 | T | C | 1 | a0001c0001t0001g0030 | 2 | NA18968.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.1767+331A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 14/19 | chr1 | 58668301 | |||||||
| chr1:58668408 | T | C | 7 | a0005c0006t0003g0316 a0005c0006t0011g0047 a0005c0006t0011g0314 others(4): Show |
9 | HG02257.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1767+224A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 14/19 | chr1 | 58668408 | |||||||
| chr1:58668433 | AATTT | A | 3 | a0004c0004t0024g0012 a0004c0004t0024g0049 a0004c0004t0071g0050 |
4 | HG02055.hp1 HG02615.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1767+195_1767+198d others(6): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 14/19 | chr1 | 58668433 | |||||||
| chr1:58668475 | T | C | 4 | a0001c0001t0001g0008 a0001c0001t0009g0156 a0001c0001t0009g0162 others(1): Show |
6 | HG02074.hp2 NA18982.hp1 NA18995.hp1 others(3): Show |
intron_variant | MODIFIER | c.1767+157A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 14/19 | chr1 | 58668475 | |||||||
| chr1:58668623 | T | G | 2 | a0003c0003t0003g0258 a0003c0003t0003g0265 |
2 | NA18998.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1767+9A>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 14/19 | chr1 | 58668623 | |||||||
| chr1:58668698 | C | A | 1 | a0003c0003t0010g0276 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1717-16G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 13/19 | chr1 | 58668698 | |||||||
| chr1:58668699 | A | C | 1 | a0003c0003t0010g0276 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1717-17T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 13/19 | chr1 | 58668699 | |||||||
| chr1:58668914 | G | C | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(104): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.1716+70C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 13/19 | chr1 | 58668914 | |||||||
| chr1:58668935 | C | CAG | 320 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(317): Show |
405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
intron_variant | MODIFIER | c.1716+48_1716+49ins others(2): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 13/19 | chr1 | 58668935 | |||||||
| chr1:58668943 | C | T | 6 | a0004c0004t0031g0044 a0004c0004t0031g0294 a0004c0004t0032g0292 others(3): Show |
7 | HG01256.hp2 HG01258.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1716+41G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 13/19 | chr1 | 58668943 | |||||||
| chr1:58668978 | T | C | 2 | a0004c0004t0012g0320 a0004c0004t0012g0322 |
2 | HG01167.hp1 HG03486.hp1 |
splice_region_variant&intron_variant | LOW | c.1716+6A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 13/19 | chr1 | 58668978 | |||||||
| chr1:58669219 | CA | C | 108 | a0003c0003t0003g0001 a0003c0003t0003g0010 a0003c0003t0003g0126 others(105): Show |
130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.1662-182delT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58669219 | |||||||
| chr1:58669312 | T | C | 2 | a0006c0007t0025g0014 a0006c0007t0025g0063 |
3 | HG01884.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1662-274A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58669312 | |||||||
| chr1:58669439 | C | T | 15 | a0004c0004t0003g0042 a0004c0004t0003g0236 a0004c0004t0003g0241 others(12): Show |
16 | HG01074.hp2 HG01081.hp1 HG02886.hp2 others(13): Show |
intron_variant | MODIFIER | c.1662-401G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58669439 | |||||||
| chr1:58669532 | C | A | 30 | a0004c0004t0003g0307 a0004c0004t0012g0319 a0004c0004t0012g0320 others(27): Show |
35 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(32): Show |
intron_variant | MODIFIER | c.1662-494G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58669532 | |||||||
| chr1:58669657 | C | T | 1 | a0004c0004t0003g0284 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1662-619G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58669657 | |||||||
| chr1:58669825 | G | T | 78 | a0003c0003t0003g0001 a0003c0003t0003g0010 a0003c0003t0003g0126 others(75): Show |
95 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1662-787C>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58669825 | |||||||
| chr1:58669836 | C | CA | 11 | a0002c0005t0006g0208 a0002c0005t0006g0211 a0002c0005t0006g0214 others(8): Show |
14 | HG00140.hp2 HG01074.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1662-799dupT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58669836 | |||||||
| chr1:58669853 | A | C | 3 | a0002c0005t0016g0039 a0002c0005t0016g0204 a0002c0005t0016g0225 |
4 | HG00741.hp1 HG01515.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.1662-815T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58669853 | |||||||
| chr1:58669857 | A | AAAAC | 34 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0134 others(31): Show |
39 | HG00423.hp2 HG00597.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.1662-820_1662-819i others(6): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58669857 | |||||||
| chr1:58669857 | A | AAAC | 93 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(90): Show |
119 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.1662-820_1662-819i others(5): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58669857 | |||||||
| chr1:58669857 | A | AAC | 70 | a0001c0001t0001g0021 a0001c0001t0001g0024 a0001c0001t0001g0026 others(67): Show |
93 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.1662-820_1662-819i others(4): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58669857 | |||||||
| chr1:58669857 | A | AC | 55 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0007 others(52): Show |
73 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.1662-820_1662-819i others(3): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58669857 | |||||||
| chr1:58669857 | A | C | 33 | a0001c0001t0009g0153 a0001c0001t0019g0040 a0001c0001t0019g0229 others(30): Show |
39 | HG00642.hp1 HG01109.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.1662-819T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58669857 | |||||||
| chr1:58669863 | C | A | 1 | a0003c0003t0010g0276 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1662-825G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58669863 | |||||||
| chr1:58669864 | A | C | 1 | a0003c0003t0010g0276 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1662-826T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58669864 | |||||||
| chr1:58669970 | T | C | 75 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0007 others(72): Show |
97 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.1662-932A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58669970 | |||||||
| chr1:58670151 | G | A | 2 | a0003c0003t0058g0267 a0003c0003t0059g0268 |
2 | HG02040.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.1662-1113C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58670151 | |||||||
| chr1:58670162 | A | G | 1 | a0002c0002t0044g0013 | 2 | HG01891.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1662-1124T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58670162 | |||||||
| chr1:58670252 | A | G | 3 | a0004c0004t0032g0292 a0004c0004t0032g0295 a0004c0004t0032g0296 |
3 | HG02965.hp1 HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1662-1214T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58670252 | |||||||
| chr1:58670343 | A | C | 8 | a0004c0004t0012g0319 a0004c0004t0012g0320 a0004c0004t0012g0321 others(5): Show |
8 | HG01167.hp1 HG01255.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1662-1305T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58670343 | |||||||
| chr1:58670639 | C | T | 75 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0007 others(72): Show |
97 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.1661+1231G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58670639 | |||||||
| chr1:58670677 | C | G | 30 | a0004c0004t0003g0307 a0004c0004t0012g0319 a0004c0004t0012g0320 others(27): Show |
35 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(32): Show |
intron_variant | MODIFIER | c.1661+1193G>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58670677 | |||||||
| chr1:58670757 | A | C | 215 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(212): Show |
272 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.1661+1113T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58670757 | |||||||
| chr1:58670759 | T | C | 215 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(212): Show |
272 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.1661+1111A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58670759 | |||||||
| chr1:58670774 | A | T | 9 | a0005c0006t0003g0316 a0005c0006t0011g0047 a0005c0006t0011g0314 others(6): Show |
12 | HG01884.hp1 HG02145.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1661+1096T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58670774 | |||||||
| chr1:58670978 | T | C | 4 | a0001c0001t0019g0040 a0001c0001t0019g0229 a0001c0001t0019g0231 others(1): Show |
5 | NA18953.hp2 NA18954.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.1661+892A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58670978 | |||||||
| chr1:58671166 | C | A | 2 | a0003c0003t0003g0269 a0003c0003t0007g0249 |
2 | HG02004.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.1661+704G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58671166 | |||||||
| chr1:58671203 | C | T | 290 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(287): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.1661+667G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58671203 | |||||||
| chr1:58671232 | G | A | 69 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0007 others(66): Show |
90 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.1661+638C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58671232 | |||||||
| chr1:58671240 | G | C | 30 | a0004c0004t0003g0307 a0004c0004t0012g0319 a0004c0004t0012g0320 others(27): Show |
35 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(32): Show |
intron_variant | MODIFIER | c.1661+630C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58671240 | |||||||
| chr1:58671277 | A | G | 4 | a0004c0004t0024g0012 a0004c0004t0024g0049 a0004c0004t0066g0048 others(1): Show |
5 | HG02055.hp1 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1661+593T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58671277 | |||||||
| chr1:58671439 | T | C | 185 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(182): Show |
237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.1661+431A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58671439 | |||||||
| chr1:58671448 | G | A | 185 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(182): Show |
237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.1661+422C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58671448 | |||||||
| chr1:58671538 | C | T | 185 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(182): Show |
237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.1661+332G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58671538 | |||||||
| chr1:58671601 | C | T | 290 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(287): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.1661+269G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58671601 | |||||||
| chr1:58671628 | C | G | 2 | a0001c0001t0001g0024 a0001c0001t0004g0023 |
4 | HG02027.hp1 HG02135.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.1661+242G>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58671628 | |||||||
| chr1:58671665 | T | C | 1 | a0001c0001t0004g0177 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1661+205A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58671665 | |||||||
| chr1:58671723 | C | T | 5 | a0002c0005t0027g0036 a0002c0005t0027g0221 a0002c0005t0029g0038 others(2): Show |
8 | HG01074.hp1 HG02280.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1661+147G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58671723 | |||||||
| chr1:58671731 | C | CA | 30 | a0004c0004t0003g0307 a0004c0004t0012g0319 a0004c0004t0012g0320 others(27): Show |
35 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(32): Show |
intron_variant | MODIFIER | c.1661+138dupT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58671731 | |||||||
| chr1:58671754 | G | T | 1 | a0002c0002t0044g0013 | 2 | HG01891.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1661+116C>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58671754 | |||||||
| chr1:58671757 | G | C | 30 | a0004c0004t0003g0307 a0004c0004t0012g0319 a0004c0004t0012g0320 others(27): Show |
35 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(32): Show |
intron_variant | MODIFIER | c.1661+113C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58671757 | |||||||
| chr1:58671784 | T | C | 30 | a0004c0004t0003g0307 a0004c0004t0012g0319 a0004c0004t0012g0320 others(27): Show |
35 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(32): Show |
intron_variant | MODIFIER | c.1661+86A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58671784 | |||||||
| chr1:58671792 | A | T | 1 | a0004c0004t0023g0232 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1661+78T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58671792 | |||||||
| chr1:58672072 | T | A | 30 | a0004c0004t0003g0307 a0004c0004t0012g0319 a0004c0004t0012g0320 others(27): Show |
35 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(32): Show |
intron_variant | MODIFIER | c.1573-114A>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 11/19 | chr1 | 58672072 | |||||||
| chr1:58672111 | A | G | 215 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(212): Show |
272 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.1573-153T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 11/19 | chr1 | 58672111 | |||||||
| chr1:58672126 | T | A | 7 | a0002c0002t0002g0079 a0002c0002t0002g0085 a0002c0002t0005g0015 others(4): Show |
9 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(6): Show |
intron_variant | MODIFIER | c.1573-168A>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 11/19 | chr1 | 58672126 | |||||||
| chr1:58672132 | A | C | 6 | a0001c0001t0036g0053 a0001c0001t0036g0061 a0001c0001t0037g0045 others(3): Show |
7 | HG01192.hp1 HG01243.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1573-174T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 11/19 | chr1 | 58672132 | |||||||
| chr1:58672167 | A | C | 1 | a0002c0002t0002g0088 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1573-209T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 11/19 | chr1 | 58672167 | |||||||
| chr1:58672315 | G | A | 185 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(182): Show |
237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.1573-357C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 11/19 | chr1 | 58672315 | |||||||
| chr1:58672500 | C | T | 290 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(287): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.1573-542G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 11/19 | chr1 | 58672500 | |||||||
| chr1:58672553 | A | G | 1 | a0001c0001t0037g0045 | 2 | HG01243.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1573-595T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 11/19 | chr1 | 58672553 | |||||||
| chr1:58672964 | A | G | 30 | a0004c0004t0003g0307 a0004c0004t0012g0319 a0004c0004t0012g0320 others(27): Show |
35 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(32): Show |
intron_variant | MODIFIER | c.1572+609T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 11/19 | chr1 | 58672964 | |||||||
| chr1:58673027 | G | A | 30 | a0004c0004t0003g0307 a0004c0004t0012g0319 a0004c0004t0012g0320 others(27): Show |
35 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(32): Show |
intron_variant | MODIFIER | c.1572+546C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 11/19 | chr1 | 58673027 | |||||||
| chr1:58673143 | C | A | 69 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0007 others(66): Show |
90 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.1572+430G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 11/19 | chr1 | 58673143 | |||||||
| chr1:58673175 | G | A | 1 | a0002c0002t0002g0113 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1572+398C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 11/19 | chr1 | 58673175 | |||||||
| chr1:58673212 | CAT | C | 67 | a0003c0003t0003g0001 a0003c0003t0003g0010 a0003c0003t0003g0126 others(64): Show |
84 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.1572+359_1572+360d others(4): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 11/19 | chr1 | 58673212 | |||||||
| chr1:58673346 | A | G | 1 | a0004c0004t0003g0307 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1572+227T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 11/19 | chr1 | 58673346 | |||||||
| chr1:58673379 | T | C | 1 | a0001c0001t0004g0133 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1572+194A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 11/19 | chr1 | 58673379 | |||||||
| chr1:58673551 | C | G | 185 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(182): Show |
237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.1572+22G>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 11/19 | chr1 | 58673551 | |||||||
| chr1:58673865 | G | A | 185 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(182): Show |
237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.1495-215C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58673865 | |||||||
| chr1:58674053 | G | A | 185 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(182): Show |
237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.1495-403C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58674053 | |||||||
| chr1:58674069 | G | A | 30 | a0004c0004t0003g0307 a0004c0004t0012g0319 a0004c0004t0012g0320 others(27): Show |
35 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(32): Show |
intron_variant | MODIFIER | c.1495-419C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58674069 | |||||||
| chr1:58674092 | T | C | 30 | a0004c0004t0003g0307 a0004c0004t0012g0319 a0004c0004t0012g0320 others(27): Show |
35 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(32): Show |
intron_variant | MODIFIER | c.1495-442A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58674092 | |||||||
| chr1:58674155 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.1495-505C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58674155 | |||||||
| chr1:58674311 | G | A | 1 | a0003c0003t0003g0272 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1495-661C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58674311 | |||||||
| chr1:58674509 | G | C | 5 | a0004c0004t0031g0044 a0004c0004t0031g0294 a0004c0004t0032g0292 others(2): Show |
6 | HG01256.hp2 HG01258.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1495-859C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58674509 | |||||||
| chr1:58674513 | A | G | 1 | a0002c0002t0028g0087 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1495-863T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58674513 | |||||||
| chr1:58674619 | T | C | 50 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0021 others(47): Show |
72 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.1494+858A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58674619 | |||||||
| chr1:58674663 | C | T | 7 | a0005c0006t0003g0316 a0005c0006t0011g0047 a0005c0006t0011g0314 others(4): Show |
9 | HG02257.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1494+814G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58674663 | |||||||
| chr1:58674697 | G | A | 1 | a0002c0002t0005g0116 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1494+780C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58674697 | |||||||
| chr1:58674700 | C | T | 4 | a0001c0001t0036g0053 a0001c0001t0036g0061 a0001c0001t0053g0059 others(1): Show |
4 | HG01192.hp1 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1494+777G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58674700 | |||||||
| chr1:58674701 | G | A | 2 | a0006c0007t0025g0014 a0006c0007t0025g0063 |
3 | HG01884.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1494+776C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58674701 | |||||||
| chr1:58674722 | G | A | 30 | a0002c0002t0045g0055 a0002c0002t0045g0056 a0002c0002t0078g0057 others(27): Show |
34 | HG00140.hp2 HG00673.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1494+755C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58674722 | |||||||
| chr1:58674741 | A | T | 1 | a0002c0002t0005g0073 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1494+736T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58674741 | |||||||
| chr1:58674880 | T | C | 184 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(181): Show |
236 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.1494+597A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58674880 | |||||||
| chr1:58674881 | G | A | 184 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(181): Show |
236 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.1494+596C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58674881 | |||||||
| chr1:58674926 | C | CA | 6 | a0001c0001t0001g0139 a0001c0001t0004g0129 a0001c0001t0009g0143 others(3): Show |
6 | HG02145.hp1 HG02523.hp2 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.1494+550dupT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58674926 | |||||||
| chr1:58674934 | A | AG | 29 | a0004c0004t0003g0307 a0004c0004t0012g0319 a0004c0004t0012g0320 others(26): Show |
34 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.1494+542_1494+543i others(3): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58674934 | |||||||
| chr1:58674990 | C | T | 3 | a0004c0004t0024g0012 a0004c0004t0024g0049 a0004c0004t0071g0050 |
4 | HG02055.hp1 HG02615.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1494+487G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58674990 | |||||||
| chr1:58675016 | G | T | 4 | a0001c0001t0019g0040 a0001c0001t0019g0229 a0001c0001t0019g0231 others(1): Show |
5 | NA18953.hp2 NA18954.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.1494+461C>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58675016 | |||||||
| chr1:58675018 | C | G | 1 | a0003c0003t0003g0258 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1494+459G>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58675018 | |||||||
| chr1:58675051 | A | T | 29 | a0004c0004t0003g0307 a0004c0004t0012g0319 a0004c0004t0012g0320 others(26): Show |
34 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.1494+426T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58675051 | |||||||
| chr1:58675053 | A | G | 1 | a0003c0003t0003g0258 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1494+424T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58675053 | |||||||
| chr1:58675334 | C | T | 2 | a0005c0006t0011g0314 a0005c0008t0010g0011 |
3 | HG02572.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1494+143G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58675334 | |||||||
| chr1:58675353 | A | T | 19 | a0004c0004t0003g0307 a0004c0004t0012g0319 a0004c0004t0012g0320 others(16): Show |
21 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.1494+124T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58675353 | |||||||
| chr1:58675412 | C | T | 4 | a0002c0002t0002g0110 a0002c0002t0013g0111 a0004c0004t0026g0051 others(1): Show |
4 | HG02630.hp1 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1494+65G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58675412 | |||||||
| chr1:58675693 | G | A | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(102): Show |
140 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.1391-113C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 9/19 | chr1 | 58675693 | |||||||
| chr1:58675944 | G | A | 1 | a0002c0002t0044g0013 | 2 | HG01891.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1391-364C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 9/19 | chr1 | 58675944 | |||||||
| chr1:58676146 | C | T | 185 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(182): Show |
237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.1391-566G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 9/19 | chr1 | 58676146 | |||||||
| chr1:58676147 | G | A | 2 | a0002c0002t0002g0019 a0002c0002t0005g0108 |
3 | HG01516.hp2 HG01517.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1391-567C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 9/19 | chr1 | 58676147 | |||||||
| chr1:58676154 | C | G | 29 | a0004c0004t0003g0307 a0004c0004t0012g0319 a0004c0004t0012g0320 others(26): Show |
34 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.1391-574G>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 9/19 | chr1 | 58676154 | |||||||
| chr1:58676241 | A | AC | 29 | a0004c0004t0003g0307 a0004c0004t0012g0319 a0004c0004t0012g0320 others(26): Show |
34 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.1391-662dupG | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 9/19 | chr1 | 58676241 | |||||||
| chr1:58676308 | C | T | 2 | a0003c0003t0003g0235 a0003c0003t0003g0272 |
2 | NA18948.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.1390+618G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 9/19 | chr1 | 58676308 | |||||||
| chr1:58676359 | T | G | 1 | a0004c0004t0072g0054 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1390+567A>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 9/19 | chr1 | 58676359 | |||||||
| chr1:58676372 | C | T | 1 | a0004c0004t0003g0280 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1390+554G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 9/19 | chr1 | 58676372 | |||||||
| chr1:58676402 | C | T | 1 | a0002c0005t0015g0216 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1390+524G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 9/19 | chr1 | 58676402 | |||||||
| chr1:58676405 | G | GA | 7 | a0001c0001t0001g0138 a0001c0001t0004g0180 a0001c0001t0009g0143 others(4): Show |
10 | HG01074.hp1 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1390+520dupT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 9/19 | chr1 | 58676405 | |||||||
| chr1:58676405 | GA | G | 86 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0036g0053 others(83): Show |
109 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1390+520delT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 9/19 | chr1 | 58676405 | |||||||
| chr1:58676527 | G | T | 29 | a0004c0004t0003g0307 a0004c0004t0012g0319 a0004c0004t0012g0320 others(26): Show |
34 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.1390+399C>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 9/19 | chr1 | 58676527 | |||||||
| chr1:58676576 | T | C | 214 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(211): Show |
271 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.1390+350A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 9/19 | chr1 | 58676576 | |||||||
| chr1:58676585 | TAGCATGA others(4): Show |
T | 1 | a0003c0003t0003g0240 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1390+330_1390+340d others(13): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 9/19 | chr1 | 58676585 | |||||||
| chr1:58676710 | C | T | 5 | a0002c0005t0027g0036 a0002c0005t0027g0221 a0002c0005t0029g0038 others(2): Show |
8 | HG01074.hp1 HG02280.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1390+216G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 9/19 | chr1 | 58676710 | |||||||
| chr1:58676892 | C | T | 4 | a0001c0001t0019g0040 a0001c0001t0019g0229 a0001c0001t0019g0231 others(1): Show |
5 | NA18953.hp2 NA18954.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.1390+34G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 9/19 | chr1 | 58676892 | |||||||
| chr1:58677131 | A | G | 1 | a0001c0001t0019g0229 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1260-75T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58677131 | |||||||
| chr1:58677157 | C | T | 29 | a0004c0004t0003g0307 a0004c0004t0012g0319 a0004c0004t0012g0320 others(26): Show |
34 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.1260-101G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58677157 | |||||||
| chr1:58677182 | T | C | 1 | a0003c0003t0003g0271 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1260-126A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58677182 | |||||||
| chr1:58677334 | T | G | 29 | a0004c0004t0003g0307 a0004c0004t0012g0319 a0004c0004t0012g0320 others(26): Show |
34 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.1260-278A>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58677334 | |||||||
| chr1:58677336 | C | T | 29 | a0004c0004t0003g0307 a0004c0004t0012g0319 a0004c0004t0012g0320 others(26): Show |
34 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.1260-280G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58677336 | |||||||
| chr1:58677360 | T | C | 29 | a0004c0004t0003g0307 a0004c0004t0012g0319 a0004c0004t0012g0320 others(26): Show |
34 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.1260-304A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58677360 | |||||||
| chr1:58677428 | T | G | 1 | a0002c0002t0076g0064 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1260-372A>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58677428 | |||||||
| chr1:58677455 | C | T | 29 | a0004c0004t0003g0307 a0004c0004t0012g0319 a0004c0004t0012g0320 others(26): Show |
34 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.1260-399G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58677455 | |||||||
| chr1:58677513 | T | C | 1 | a0002c0002t0014g0122 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1260-457A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58677513 | |||||||
| chr1:58677519 | ATT | A | 4 | a0004c0004t0024g0012 a0004c0004t0024g0049 a0004c0004t0066g0048 others(1): Show |
5 | HG02055.hp1 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1260-465_1260-464d others(4): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58677519 | |||||||
| chr1:58677663 | C | T | 1 | a0001c0001t0055g0300 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1260-607G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58677663 | |||||||
| chr1:58677704 | C | A | 1 | a0002c0005t0027g0036 | 2 | HG02280.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1260-648G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58677704 | |||||||
| chr1:58677716 | C | T | 29 | a0004c0004t0003g0307 a0004c0004t0012g0319 a0004c0004t0012g0320 others(26): Show |
34 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.1260-660G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58677716 | |||||||
| chr1:58677729 | A | G | 76 | a0003c0003t0003g0001 a0003c0003t0003g0010 a0003c0003t0003g0126 others(73): Show |
92 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.1260-673T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58677729 | |||||||
| chr1:58677942 | C | G | 75 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0007 others(72): Show |
97 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.1260-886G>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58677942 | |||||||
| chr1:58678078 | T | C | 1 | a0002c0002t0002g0103 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1260-1022A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58678078 | |||||||
| chr1:58678162 | A | G | 29 | a0004c0004t0003g0307 a0004c0004t0012g0319 a0004c0004t0012g0320 others(26): Show |
34 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.1260-1106T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58678162 | |||||||
| chr1:58678199 | T | C | 29 | a0004c0004t0003g0307 a0004c0004t0012g0319 a0004c0004t0012g0320 others(26): Show |
34 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.1260-1143A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58678199 | |||||||
| chr1:58678252 | C | A | 289 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(286): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.1260-1196G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58678252 | |||||||
| chr1:58678394 | A | G | 1 | a0002c0002t0002g0086 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1260-1338T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58678394 | |||||||
| chr1:58678481 | G | A | 1 | a0003c0003t0003g0272 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1260-1425C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58678481 | |||||||
| chr1:58678674 | A | G | 1 | a0003c0003t0003g0285 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1260-1618T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58678674 | |||||||
| chr1:58678764 | G | A | 65 | a0003c0003t0003g0001 a0003c0003t0003g0010 a0003c0003t0003g0126 others(62): Show |
81 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.1260-1708C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58678764 | |||||||
| chr1:58678793 | C | T | 185 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(182): Show |
237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.1260-1737G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58678793 | |||||||
| chr1:58678806 | A | C | 1 | a0001c0001t0054g0299 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1260-1750T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58678806 | |||||||
| chr1:58678807 | T | C | 213 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(210): Show |
270 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.1260-1751A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58678807 | |||||||
| chr1:58678808 | G | C | 1 | a0003c0003t0003g0273 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1260-1752C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58678808 | |||||||
| chr1:58678821 | C | T | 1 | a0001c0001t0004g0165 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1260-1765G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58678821 | |||||||
| chr1:58678832 | T | G | 1 | a0001c0001t0008g0163 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1260-1776A>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58678832 | |||||||
| chr1:58678916 | G | A | 29 | a0004c0004t0003g0307 a0004c0004t0012g0319 a0004c0004t0012g0320 others(26): Show |
34 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.1260-1860C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58678916 | |||||||
| chr1:58679007 | A | C | 5 | a0004c0004t0020g0303 a0004c0004t0020g0304 a0004c0004t0020g0308 others(2): Show |
5 | HG02109.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1260-1951T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58679007 | |||||||
| chr1:58679009 | G | A | 29 | a0004c0004t0003g0307 a0004c0004t0012g0319 a0004c0004t0012g0320 others(26): Show |
34 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.1260-1953C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58679009 | |||||||
| chr1:58679016 | A | G | 29 | a0004c0004t0003g0307 a0004c0004t0012g0319 a0004c0004t0012g0320 others(26): Show |
34 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.1260-1960T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58679016 | |||||||
| chr1:58679018 | A | G | 1 | a0003c0003t0062g0255 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1260-1962T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58679018 | |||||||
| chr1:58679026 | C | T | 1 | a0002c0005t0029g0312 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1260-1970G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58679026 | |||||||
| chr1:58679115 | A | G | 214 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(211): Show |
271 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.1260-2059T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58679115 | |||||||
| chr1:58679249 | C | A | 29 | a0004c0004t0003g0307 a0004c0004t0012g0319 a0004c0004t0012g0320 others(26): Show |
34 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.1260-2193G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58679249 | |||||||
| chr1:58679387 | C | T | 3 | a0002c0005t0006g0209 a0002c0005t0006g0210 a0002c0005t0006g0211 |
3 | NA18965.hp1 NA18974.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.1260-2331G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58679387 | |||||||
| chr1:58679534 | C | T | 4 | a0004c0004t0003g0236 a0004c0004t0003g0278 a0004c0004t0010g0279 others(1): Show |
4 | HG02895.hp2 HG03041.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1259+2251G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58679534 | |||||||
| chr1:58679679 | G | C | 7 | a0002c0002t0002g0105 a0002c0002t0002g0110 a0002c0002t0005g0104 others(4): Show |
8 | HG00642.hp1 HG02630.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1259+2106C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58679679 | |||||||
| chr1:58679682 | C | A | 1 | a0004c0004t0066g0048 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1259+2103G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58679682 | |||||||
| chr1:58679749 | C | T | 1 | a0003c0003t0065g0257 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1259+2036G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58679749 | |||||||
| chr1:58679780 | A | C | 214 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(211): Show |
271 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.1259+2005T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58679780 | |||||||
| chr1:58679898 | C | G | 1 | a0001c0001t0004g0146 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1259+1887G>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58679898 | |||||||
| chr1:58679971 | G | C | 2 | a0003c0003t0035g0237 a0003c0003t0035g0239 |
2 | NA19084.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1259+1814C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58679971 | |||||||
| chr1:58680006 | G | T | 1 | a0001c0001t0001g0008 | 3 | NA18982.hp1 NA18999.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1259+1779C>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58680006 | |||||||
| chr1:58680026 | C | CAAA | 11 | a0004c0004t0003g0307 a0004c0004t0012g0319 a0004c0004t0012g0320 others(8): Show |
12 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.1259+1756_1259+175 others(7): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58680026 | |||||||
| chr1:58680026 | CA | C | 78 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0007 others(75): Show |
103 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.1259+1758delT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58680026 | |||||||
| chr1:58680026 | CAAAAAAA others(4): Show |
C | 184 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(181): Show |
236 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.1259+1748_1259+175 others(15): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58680026 | |||||||
| chr1:58680026 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0139 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1259+1747_1259+175 others(16): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58680026 | |||||||
| chr1:58680176 | T | C | 3 | a0004c0004t0024g0012 a0004c0004t0024g0049 a0004c0004t0071g0050 |
4 | HG02055.hp1 HG02615.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1259+1609A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58680176 | |||||||
| chr1:58680212 | T | C | 1 | a0003c0003t0007g0274 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1259+1573A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58680212 | |||||||
| chr1:58680277 | T | A | 76 | a0003c0003t0003g0001 a0003c0003t0003g0010 a0003c0003t0003g0126 others(73): Show |
92 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.1259+1508A>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58680277 | |||||||
| chr1:58680286 | C | A | 289 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(286): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.1259+1499G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58680286 | |||||||
| chr1:58680514 | T | C | 190 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(187): Show |
244 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1259+1271A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58680514 | |||||||
| chr1:58680523 | T | C | 97 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(94): Show |
131 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.1259+1262A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58680523 | |||||||
| chr1:58680549 | A | G | 282 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(279): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1259+1236T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58680549 | |||||||
| chr1:58680637 | T | C | 73 | a0001c0001t0001g0190 a0002c0002t0002g0079 a0002c0002t0002g0085 others(70): Show |
91 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.1259+1148A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58680637 | |||||||
| chr1:58680644 | C | T | 1 | a0001c0001t0054g0299 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1259+1141G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58680644 | |||||||
| chr1:58680744 | T | C | 109 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0032 others(106): Show |
129 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(126): Show |
intron_variant | MODIFIER | c.1259+1041A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58680744 | |||||||
| chr1:58680752 | T | C | 1 | a0001c0001t0054g0299 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1259+1033A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58680752 | |||||||
| chr1:58680824 | A | AT | 131 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(128): Show |
170 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.1259+960dupA | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58680824 | |||||||
| chr1:58680824 | AT | A | 15 | a0002c0002t0002g0006 a0002c0002t0002g0070 a0002c0002t0002g0077 others(12): Show |
19 | HG01255.hp1 HG01928.hp1 HG01934.hp2 others(16): Show |
intron_variant | MODIFIER | c.1259+960delA | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58680824 | |||||||
| chr1:58680928 | T | C | 1 | a0002c0005t0006g0227 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1259+857A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58680928 | |||||||
| chr1:58681019 | A | G | 1 | a0003c0003t0062g0255 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1259+766T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58681019 | |||||||
| chr1:58681172 | A | T | 2 | a0004c0004t0026g0051 a0004c0004t0026g0052 |
2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1259+613T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58681172 | |||||||
| chr1:58681335 | T | C | 1 | a0001c0001t0004g0131 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1259+450A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58681335 | |||||||
| chr1:58681339 | A | G | 6 | a0004c0004t0031g0044 a0004c0004t0031g0294 a0004c0004t0032g0292 others(3): Show |
7 | HG01256.hp2 HG01258.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1259+446T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58681339 | |||||||
| chr1:58681409 | C | A | 76 | a0003c0003t0003g0001 a0003c0003t0003g0010 a0003c0003t0003g0126 others(73): Show |
92 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.1259+376G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58681409 | |||||||
| chr1:58681462 | G | A | 2 | a0001c0001t0009g0152 a0001c0001t0021g0182 |
2 | HG00099.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1259+323C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58681462 | |||||||
| chr1:58681748 | G | A | 185 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(182): Show |
237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.1259+37C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58681748 | |||||||
| chr1:58682601 | C | G | 1 | a0001c0001t0009g0152 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.499-56G>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58682601 | |||||||
| chr1:58682650 | A | G | 4 | a0005c0006t0003g0316 a0005c0006t0011g0314 a0005c0006t0011g0315 others(1): Show |
5 | HG02257.hp2 HG02572.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.499-105T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58682650 | |||||||
| chr1:58682679 | G | A | 9 | a0002c0005t0006g0035 a0002c0005t0006g0209 a0002c0005t0006g0210 others(6): Show |
10 | HG00673.hp1 NA18946.hp2 NA18949.hp1 others(7): Show |
intron_variant | MODIFIER | c.499-134C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58682679 | |||||||
| chr1:58682679 | GCTTTTCT others(7): Show |
G | 95 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(92): Show |
129 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.499-148_499-135del others(14): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58682679 | |||||||
| chr1:58682685 | CTTTTTTT others(8): Show |
C | 2 | a0001c0001t0001g0150 a0001c0001t0004g0149 |
2 | HG01169.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.499-155_499-141del others(15): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58682685 | |||||||
| chr1:58682686 | TTTTTTTT others(6): Show |
T | 1 | a0001c0001t0009g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.499-154_499-142del others(13): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58682686 | |||||||
| chr1:58682788 | C | T | 4 | a0005c0006t0003g0316 a0005c0006t0011g0314 a0005c0006t0011g0315 others(1): Show |
5 | HG02257.hp2 HG02572.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.499-243G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58682788 | |||||||
| chr1:58682789 | G | A | 4 | a0001c0001t0036g0053 a0001c0001t0036g0061 a0001c0001t0053g0059 others(1): Show |
4 | HG01192.hp1 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.499-244C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58682789 | |||||||
| chr1:58682807 | T | G | 1 | a0006c0010t0010g0222 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.499-262A>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58682807 | |||||||
| chr1:58682936 | G | C | 296 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(293): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.499-391C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58682936 | |||||||
| chr1:58682946 | C | T | 185 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(182): Show |
237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.499-401G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58682946 | |||||||
| chr1:58683007 | T | C | 2 | a0003c0003t0003g0240 a0003c0003t0010g0276 |
2 | NA19059.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.499-462A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58683007 | |||||||
| chr1:58683038 | G | T | 1 | a0007c0009t0001g0186 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.499-493C>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58683038 | |||||||
| chr1:58683187 | T | C | 1 | a0001c0001t0009g0313 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.499-642A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58683187 | |||||||
| chr1:58683338 | T | C | 1 | a0002c0002t0077g0062 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.499-793A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58683338 | |||||||
| chr1:58683394 | G | A | 1 | a0004c0004t0007g0298 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.499-849C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58683394 | |||||||
| chr1:58683582 | A | AATGAGCA others(3): Show |
1 | a0002c0002t0005g0080 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.499-1047_499-1038d others(12): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58683582 | |||||||
| chr1:58683585 | G | T | 1 | a0002c0005t0027g0036 | 2 | HG02280.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.499-1040C>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58683585 | |||||||
| chr1:58683865 | G | C | 1 | a0002c0005t0006g0035 | 2 | NA18946.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.498+1288C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58683865 | |||||||
| chr1:58683887 | A | T | 4 | a0002c0002t0045g0055 a0002c0002t0045g0056 a0002c0002t0076g0064 others(1): Show |
4 | HG02723.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.498+1266T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58683887 | |||||||
| chr1:58683889 | A | C | 181 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(178): Show |
232 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.498+1264T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58683889 | |||||||
| chr1:58683939 | T | A | 3 | a0001c0001t0009g0143 a0007c0009t0001g0183 a0007c0009t0001g0186 |
3 | HG01256.hp1 HG02145.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.498+1214A>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58683939 | |||||||
| chr1:58683940 | C | G | 181 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(178): Show |
232 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.498+1213G>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58683940 | |||||||
| chr1:58683992 | A | T | 185 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(182): Show |
237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.498+1161T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58683992 | |||||||
| chr1:58684061 | G | T | 76 | a0003c0003t0003g0001 a0003c0003t0003g0010 a0003c0003t0003g0126 others(73): Show |
92 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.498+1092C>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58684061 | |||||||
| chr1:58684152 | G | A | 4 | a0001c0001t0019g0040 a0001c0001t0019g0229 a0001c0001t0019g0231 others(1): Show |
5 | NA18953.hp2 NA18954.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.498+1001C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58684152 | |||||||
| chr1:58684166 | C | A | 294 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(291): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.498+987G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58684166 | |||||||
| chr1:58684293 | C | T | 75 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0007 others(72): Show |
97 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.498+860G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58684293 | |||||||
| chr1:58684326 | G | A | 1 | a0002c0002t0002g0115 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.498+827C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58684326 | |||||||
| chr1:58684355 | G | A | 5 | a0004c0004t0020g0303 a0004c0004t0020g0304 a0004c0004t0020g0308 others(2): Show |
5 | HG02109.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.498+798C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58684355 | |||||||
| chr1:58684382 | G | A | 2 | a0001c0001t0009g0198 a0001c0001t0009g0199 |
2 | NA18952.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.498+771C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58684382 | |||||||
| chr1:58684433 | C | T | 2 | a0002c0002t0002g0075 a0004c0004t0007g0298 |
2 | HG00639.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.498+720G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58684433 | |||||||
| chr1:58684514 | G | A | 76 | a0003c0003t0003g0001 a0003c0003t0003g0010 a0003c0003t0003g0126 others(73): Show |
92 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.498+639C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58684514 | |||||||
| chr1:58684520 | G | A | 76 | a0003c0003t0003g0001 a0003c0003t0003g0010 a0003c0003t0003g0126 others(73): Show |
92 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.498+633C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58684520 | |||||||
| chr1:58684543 | C | A | 181 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(178): Show |
232 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.498+610G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58684543 | |||||||
| chr1:58684564 | C | CA | 10 | a0001c0001t0008g0184 a0001c0001t0036g0053 a0001c0001t0053g0059 others(7): Show |
13 | HG01192.hp1 HG01978.hp2 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.498+588dupT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58684564 | |||||||
| chr1:58684564 | CA | C | 9 | a0003c0003t0003g0254 a0004c0004t0012g0319 a0004c0004t0012g0320 others(6): Show |
9 | HG01167.hp1 HG01255.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.498+588delT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58684564 | |||||||
| chr1:58684608 | C | T | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(102): Show |
140 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.498+545G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58684608 | |||||||
| chr1:58684811 | A | G | 1 | a0002c0005t0079g0207 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.498+342T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58684811 | |||||||
| chr1:58685050 | A | C | 1 | a0003c0003t0007g0253 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.498+103T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58685050 | |||||||
| chr1:58685269 | G | A | 294 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(291): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.400-18C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58685269 | |||||||
| chr1:58685304 | T | C | 2 | a0006c0007t0025g0014 a0006c0007t0025g0063 |
3 | HG01884.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.400-53A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58685304 | |||||||
| chr1:58685325 | T | TA | 32 | a0002c0005t0015g0215 a0002c0005t0015g0216 a0002c0005t0015g0217 others(29): Show |
36 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(33): Show |
intron_variant | MODIFIER | c.400-75dupT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58685325 | |||||||
| chr1:58685325 | TA | T | 184 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(181): Show |
236 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.400-75delT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58685325 | |||||||
| chr1:58685437 | T | C | 1 | a0002c0005t0006g0220 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.400-186A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58685437 | |||||||
| chr1:58685511 | T | C | 1 | a0002c0002t0002g0118 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.400-260A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58685511 | |||||||
| chr1:58685544 | T | C | 4 | a0001c0001t0019g0040 a0001c0001t0019g0229 a0001c0001t0019g0231 others(1): Show |
5 | NA18953.hp2 NA18954.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.400-293A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58685544 | |||||||
| chr1:58685601 | G | C | 181 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(178): Show |
232 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.400-350C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58685601 | |||||||
| chr1:58685699 | A | G | 5 | a0002c0005t0027g0036 a0002c0005t0027g0221 a0002c0005t0029g0038 others(2): Show |
8 | HG01074.hp1 HG02280.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.400-448T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58685699 | |||||||
| chr1:58686067 | A | C | 1 | a0006c0010t0010g0222 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.400-816T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58686067 | |||||||
| chr1:58686165 | A | T | 1 | a0001c0001t0004g0148 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.400-914T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58686165 | |||||||
| chr1:58686216 | A | G | 5 | a0001c0001t0036g0053 a0001c0001t0036g0061 a0001c0001t0053g0059 others(2): Show |
5 | HG01192.hp1 HG02717.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.400-965T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58686216 | |||||||
| chr1:58686286 | A | C | 45 | a0003c0003t0003g0001 a0003c0003t0003g0010 a0003c0003t0003g0126 others(42): Show |
59 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.400-1035T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58686286 | |||||||
| chr1:58686343 | C | T | 185 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(182): Show |
237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.400-1092G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58686343 | |||||||
| chr1:58686383 | G | A | 4 | a0004c0004t0007g0043 a0004c0004t0007g0289 a0004c0004t0007g0290 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.400-1132C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58686383 | |||||||
| chr1:58686462 | T | G | 185 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(182): Show |
237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.400-1211A>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58686462 | |||||||
| chr1:58686596 | A | C | 2 | a0002c0002t0044g0013 a0002c0002t0077g0062 |
3 | HG01891.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.400-1345T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58686596 | |||||||
| chr1:58686795 | G | A | 1 | a0001c0001t0001g0185 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.400-1544C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58686795 | |||||||
| chr1:58686899 | T | C | 1 | a0002c0002t0002g0119 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.400-1648A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58686899 | |||||||
| chr1:58686965 | T | TA | 152 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0007 others(149): Show |
190 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.400-1715dupT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58686965 | |||||||
| chr1:58686981 | A | C | 4 | a0002c0002t0045g0055 a0002c0002t0045g0056 a0002c0002t0076g0064 others(1): Show |
4 | HG02723.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.400-1730T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58686981 | |||||||
| chr1:58687037 | A | C | 1 | a0003c0003t0011g0234 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.400-1786T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58687037 | |||||||
| chr1:58687238 | T | C | 2 | a0002c0002t0005g0121 a0002c0002t0014g0120 |
2 | NA18948.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.399+1800A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58687238 | |||||||
| chr1:58687275 | A | G | 10 | a0004c0004t0020g0303 a0004c0004t0020g0304 a0004c0004t0020g0306 others(7): Show |
10 | HG00738.hp1 HG02109.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.399+1763T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58687275 | |||||||
| chr1:58687338 | G | A | 185 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(182): Show |
237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.399+1700C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58687338 | |||||||
| chr1:58687342 | G | A | 1 | a0007c0009t0001g0186 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.399+1696C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58687342 | |||||||
| chr1:58687351 | T | A | 3 | a0002c0002t0045g0055 a0002c0002t0045g0056 a0002c0002t0078g0057 |
3 | HG02723.hp1 HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.399+1687A>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58687351 | |||||||
| chr1:58687395 | T | C | 185 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(182): Show |
237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.399+1643A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58687395 | |||||||
| chr1:58687505 | A | T | 185 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(182): Show |
237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.399+1533T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58687505 | |||||||
| chr1:58687507 | C | T | 294 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(291): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.399+1531G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58687507 | |||||||
| chr1:58687633 | G | T | 27 | a0004c0004t0003g0307 a0004c0004t0012g0319 a0004c0004t0012g0320 others(24): Show |
31 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.399+1405C>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58687633 | |||||||
| chr1:58687659 | T | C | 15 | a0004c0004t0003g0307 a0004c0004t0012g0319 a0004c0004t0012g0320 others(12): Show |
16 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.399+1379A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58687659 | |||||||
| chr1:58687835 | CTA | C | 27 | a0004c0004t0003g0307 a0004c0004t0012g0319 a0004c0004t0012g0320 others(24): Show |
31 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.399+1201_399+1202d others(4): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58687835 | |||||||
| chr1:58688287 | C | T | 2 | a0001c0001t0004g0146 a0001c0001t0008g0147 |
2 | HG01099.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.399+751G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58688287 | |||||||
| chr1:58688289 | T | C | 2 | a0004c0004t0007g0290 a0004c0004t0007g0291 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.399+749A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58688289 | |||||||
| chr1:58688289 | TA | T | 3 | a0002c0002t0045g0055 a0002c0002t0045g0056 a0002c0002t0078g0057 |
3 | HG02723.hp1 HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.399+748delT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58688289 | |||||||
| chr1:58688421 | TA | T | 27 | a0004c0004t0003g0307 a0004c0004t0012g0319 a0004c0004t0012g0320 others(24): Show |
31 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.399+616delT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58688421 | |||||||
| chr1:58688497 | C | T | 1 | a0004c0004t0031g0294 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.399+541G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58688497 | |||||||
| chr1:58688561 | C | CA | 8 | a0001c0001t0036g0053 a0001c0001t0036g0061 a0001c0001t0053g0059 others(5): Show |
8 | HG00738.hp1 HG01192.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.399+476dupT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58688561 | |||||||
| chr1:58688595 | C | T | 4 | a0002c0002t0045g0055 a0002c0002t0045g0056 a0002c0002t0076g0064 others(1): Show |
4 | HG02723.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.399+443G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58688595 | |||||||
| chr1:58688647 | C | A | 4 | a0001c0001t0019g0040 a0001c0001t0019g0229 a0001c0001t0019g0231 others(1): Show |
5 | NA18953.hp2 NA18954.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.399+391G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58688647 | |||||||
| chr1:58688695 | CA | C | 209 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(206): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.399+342delT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58688695 | |||||||
| chr1:58688695 | CAA | C | 8 | a0001c0001t0001g0191 a0002c0005t0027g0036 a0002c0005t0027g0221 others(5): Show |
11 | HG01074.hp1 HG02280.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.399+341_399+342del others(2): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58688695 | |||||||
| chr1:58688803 | G | A | 1 | a0001c0001t0055g0300 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.399+235C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58688803 | |||||||
| chr1:58688841 | T | C | 1 | a0006c0007t0025g0063 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.399+197A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58688841 | |||||||
| chr1:58689275 | C | T | 1 | a0004c0004t0020g0306 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.321-159G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 5/19 | chr1 | 58689275 | |||||||
| chr1:58689665 | C | A | 2 | a0003c0003t0003g0285 a0003c0003t0003g0286 |
2 | HG00280.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.321-549G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 5/19 | chr1 | 58689665 | |||||||
| chr1:58689765 | A | C | 2 | a0001c0001t0018g0144 a0001c0001t0018g0145 |
2 | HG02738.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.320+461T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 5/19 | chr1 | 58689765 | |||||||
| chr1:58689819 | TA | T | 4 | a0002c0002t0045g0055 a0002c0002t0045g0056 a0002c0002t0076g0064 others(1): Show |
4 | HG02723.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.320+406delT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 5/19 | chr1 | 58689819 | |||||||
| chr1:58689843 | C | G | 4 | a0001c0001t0019g0040 a0001c0001t0019g0229 a0001c0001t0019g0231 others(1): Show |
5 | NA18953.hp2 NA18954.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.320+383G>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 5/19 | chr1 | 58689843 | |||||||
| chr1:58690011 | T | C | 186 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(183): Show |
240 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.320+215A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 5/19 | chr1 | 58690011 | |||||||
| chr1:58690067 | T | C | 4 | a0001c0001t0019g0040 a0001c0001t0019g0229 a0001c0001t0019g0231 others(1): Show |
5 | NA18953.hp2 NA18954.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.320+159A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 5/19 | chr1 | 58690067 | |||||||
| chr1:58690196 | G | T | 1 | a0001c0001t0036g0053 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.320+30C>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 5/19 | chr1 | 58690196 | |||||||
| chr1:58690282 | G | A | 1 | a0001c0001t0049g0187 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.297-33C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 4/19 | chr1 | 58690282 | |||||||
| chr1:58690465 | A | T | 1 | a0002c0002t0002g0077 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.219-48T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58690465 | |||||||
| chr1:58690483 | C | T | 185 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(182): Show |
237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.219-66G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58690483 | |||||||
| chr1:58690568 | ATCAAGCT others(10): Show |
A | 15 | a0004c0004t0003g0307 a0004c0004t0012g0319 a0004c0004t0012g0320 others(12): Show |
16 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.219-168_219-152del others(17): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58690568 | |||||||
| chr1:58690607 | G | A | 1 | a0010c0012t0048g0128 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.219-190C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58690607 | |||||||
| chr1:58690680 | A | AT | 6 | a0001c0001t0056g0230 a0002c0002t0002g0075 a0002c0002t0005g0076 others(3): Show |
7 | HG01891.hp2 HG06807.hp2 NA18985.hp2 others(4): Show |
intron_variant | MODIFIER | c.219-264dupA | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58690680 | |||||||
| chr1:58690680 | AT | A | 189 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(186): Show |
242 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.219-264delA | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58690680 | |||||||
| chr1:58690938 | C | A | 1 | a0003c0003t0003g0287 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.219-521G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58690938 | |||||||
| chr1:58690996 | G | A | 4 | a0004c0004t0024g0012 a0004c0004t0024g0049 a0004c0004t0066g0048 others(1): Show |
5 | HG02055.hp1 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.219-579C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58690996 | |||||||
| chr1:58691005 | C | T | 2 | a0002c0002t0002g0074 a0002c0002t0005g0073 |
2 | NA18972.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.219-588G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58691005 | |||||||
| chr1:58691141 | G | A | 15 | a0004c0004t0003g0307 a0004c0004t0012g0319 a0004c0004t0012g0320 others(12): Show |
16 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.219-724C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58691141 | |||||||
| chr1:58691153 | G | C | 181 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(178): Show |
232 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.219-736C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58691153 | |||||||
| chr1:58691204 | TG | T | 77 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0007 others(74): Show |
100 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.219-788delC | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58691204 | |||||||
| chr1:58691536 | C | G | 1 | a0001c0001t0018g0022 | 2 | NA18983.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.219-1119G>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58691536 | |||||||
| chr1:58691539 | T | C | 1 | a0006c0010t0010g0222 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.219-1122A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58691539 | |||||||
| chr1:58691634 | G | A | 4 | a0001c0001t0019g0040 a0001c0001t0019g0229 a0001c0001t0019g0231 others(1): Show |
5 | NA18953.hp2 NA18954.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-1217C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58691634 | |||||||
| chr1:58691835 | C | G | 27 | a0004c0004t0003g0307 a0004c0004t0012g0319 a0004c0004t0012g0320 others(24): Show |
31 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.218+1026G>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58691835 | |||||||
| chr1:58691978 | A | G | 1 | a0001c0001t0001g0190 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.218+883T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58691978 | |||||||
| chr1:58692023 | G | A | 27 | a0004c0004t0003g0307 a0004c0004t0012g0319 a0004c0004t0012g0320 others(24): Show |
31 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.218+838C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58692023 | |||||||
| chr1:58692081 | A | G | 27 | a0004c0004t0003g0307 a0004c0004t0012g0319 a0004c0004t0012g0320 others(24): Show |
31 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.218+780T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58692081 | |||||||
| chr1:58692356 | C | T | 1 | a0002c0002t0005g0072 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.218+505G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58692356 | |||||||
| chr1:58692419 | T | C | 1 | a0002c0002t0014g0122 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.218+442A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58692419 | |||||||
| chr1:58692431 | T | C | 1 | a0002c0005t0006g0223 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.218+430A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58692431 | |||||||
| chr1:58692450 | C | T | 4 | a0001c0001t0001g0136 a0001c0001t0001g0138 a0001c0001t0004g0135 others(1): Show |
4 | HG00423.hp2 HG00609.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+411G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58692450 | |||||||
| chr1:58692489 | A | G | 212 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(209): Show |
268 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.218+372T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58692489 | |||||||
| chr1:58692502 | G | A | 6 | a0001c0001t0036g0053 a0001c0001t0036g0061 a0001c0001t0037g0045 others(3): Show |
7 | HG01192.hp1 HG01243.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.218+359C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58692502 | |||||||
| chr1:58692695 | G | A | 8 | a0004c0004t0012g0319 a0004c0004t0012g0320 a0004c0004t0012g0321 others(5): Show |
8 | HG01167.hp1 HG01255.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.218+166C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58692695 | |||||||
| chr1:58692960 | T | C | 185 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(182): Show |
237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.148-29A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58692960 | |||||||
| chr1:58693390 | G | T | 185 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(182): Show |
237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.148-459C>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58693390 | |||||||
| chr1:58693413 | C | T | 4 | a0004c0004t0024g0012 a0004c0004t0024g0049 a0004c0004t0066g0048 others(1): Show |
5 | HG02055.hp1 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.148-482G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58693413 | |||||||
| chr1:58693470 | A | G | 1 | a0003c0003t0007g0249 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.148-539T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58693470 | |||||||
| chr1:58693521 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.148-590G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58693521 | |||||||
| chr1:58693630 | T | C | 4 | a0004c0004t0024g0012 a0004c0004t0024g0049 a0004c0004t0066g0048 others(1): Show |
5 | HG02055.hp1 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.148-699A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58693630 | |||||||
| chr1:58693883 | T | G | 1 | a0002c0005t0006g0224 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.148-952A>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58693883 | |||||||
| chr1:58694020 | C | T | 1 | a0001c0001t0004g0133 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.148-1089G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58694020 | |||||||
| chr1:58694135 | G | A | 6 | a0005c0006t0003g0316 a0005c0006t0011g0047 a0005c0006t0011g0314 others(3): Show |
8 | HG02257.hp2 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.147+994C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58694135 | |||||||
| chr1:58694150 | ACT | A | 4 | a0004c0004t0024g0012 a0004c0004t0024g0049 a0004c0004t0066g0048 others(1): Show |
5 | HG02055.hp1 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.147+977_147+978del others(2): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58694150 | |||||||
| chr1:58694164 | T | A | 1 | a0001c0001t0036g0053 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.147+965A>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58694164 | |||||||
| chr1:58694210 | T | C | 1 | a0003c0003t0022g0288 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.147+919A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58694210 | |||||||
| chr1:58694282 | T | C | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(96): Show |
133 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.147+847A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58694282 | |||||||
| chr1:58694514 | G | A | 1 | a0004c0004t0072g0054 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.147+615C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58694514 | |||||||
| chr1:58694611 | G | C | 212 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(209): Show |
268 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.147+518C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58694611 | |||||||
| chr1:58694617 | C | CA | 8 | a0001c0001t0019g0040 a0001c0001t0019g0229 a0001c0001t0019g0231 others(5): Show |
9 | HG03209.hp1 HG03225.hp2 NA18953.hp2 others(6): Show |
intron_variant | MODIFIER | c.147+511dupT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58694617 | |||||||
| chr1:58694617 | CA | C | 9 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0004g0132 others(6): Show |
11 | HG01516.hp1 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.147+511delT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58694617 | |||||||
| chr1:58694692 | C | T | 1 | a0001c0001t0037g0045 | 2 | HG01243.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.147+437G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58694692 | |||||||
| chr1:58694708 | G | C | 185 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(182): Show |
237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.147+421C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58694708 | |||||||
| chr1:58694803 | G | A | 1 | a0002c0002t0002g0124 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.147+326C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58694803 | |||||||
| chr1:58694839 | T | G | 71 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0007 others(68): Show |
93 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.147+290A>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58694839 | |||||||
| chr1:58694868 | C | T | 1 | a0004c0004t0040g0310 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.147+261G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58694868 | |||||||
| chr1:58695045 | C | T | 1 | a0001c0001t0004g0131 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.147+84G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58695045 | |||||||
| chr1:58695052 | TA | T | 186 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(183): Show |
238 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.147+76delT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58695052 | |||||||
| chr1:58695063 | A | AG | 4 | a0002c0002t0045g0055 a0002c0002t0045g0056 a0002c0002t0076g0064 others(1): Show |
4 | HG02723.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.147+65_147+66insC | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58695063 | |||||||
| chr1:58695063 | A | G | 106 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0007 others(103): Show |
136 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.147+66T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58695063 | |||||||
| chr1:58695070 | A | C | 37 | a0002c0002t0045g0055 a0002c0002t0045g0056 a0002c0002t0076g0064 others(34): Show |
44 | HG00140.hp2 HG00673.hp1 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.147+59T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58695070 | |||||||
| chr1:58695213 | A | G | 110 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0007 others(107): Show |
140 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(137): Show |
splice_region_variant&intron_variant | LOW | c.69-6T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58695213 | |||||||
| chr1:58695310 | ATACT | A | 109 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0007 others(106): Show |
139 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.69-107_69-104delAG others(2): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58695310 | |||||||
| chr1:58695313 | C | G | 1 | a0002c0002t0002g0070 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.69-106G>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58695313 | |||||||
| chr1:58695461 | G | A | 4 | a0004c0004t0007g0043 a0004c0004t0007g0289 a0004c0004t0007g0290 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.69-254C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58695461 | |||||||
| chr1:58695597 | A | G | 3 | a0002c0002t0002g0068 a0002c0002t0002g0069 a0002c0002t0014g0067 |
3 | HG00438.hp1 HG02135.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.69-390T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58695597 | |||||||
| chr1:58695643 | C | A | 15 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0189 others(12): Show |
17 | HG00597.hp1 HG02040.hp1 NA18939.hp2 others(14): Show |
intron_variant | MODIFIER | c.69-436G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58695643 | |||||||
| chr1:58695660 | G | GA | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(95): Show |
132 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.69-454dupT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58695660 | |||||||
| chr1:58695663 | A | T | 4 | a0001c0001t0019g0040 a0001c0001t0019g0229 a0001c0001t0019g0231 others(1): Show |
5 | NA18953.hp2 NA18954.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.69-456T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58695663 | |||||||
| chr1:58695836 | G | T | 295 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(292): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.69-629C>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58695836 | |||||||
| chr1:58695907 | T | C | 6 | a0002c0005t0006g0227 a0002c0005t0016g0039 a0002c0005t0016g0204 others(3): Show |
7 | HG00738.hp2 HG00741.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.69-700A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58695907 | |||||||
| chr1:58696006 | C | A | 33 | a0002c0005t0006g0033 a0002c0005t0006g0034 a0002c0005t0006g0035 others(30): Show |
40 | HG00140.hp2 HG00673.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.69-799G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58696006 | |||||||
| chr1:58696039 | C | G | 1 | a0003c0003t0022g0248 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.69-832G>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58696039 | |||||||
| chr1:58696078 | T | C | 1 | a0001c0001t0054g0299 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.69-871A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58696078 | |||||||
| chr1:58696083 | T | G | 1 | a0001c0001t0001g0200 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.69-876A>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58696083 | |||||||
| chr1:58696250 | C | T | 1 | a0001c0001t0004g0129 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.69-1043G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58696250 | |||||||
| chr1:58696268 | T | C | 1 | a0001c0001t0001g0201 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.69-1061A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58696268 | |||||||
| chr1:58696277 | A | G | 316 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(313): Show |
401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.69-1070T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58696277 | |||||||
| chr1:58696434 | T | C | 296 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(293): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.69-1227A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58696434 | |||||||
| chr1:58696476 | T | C | 110 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0007 others(107): Show |
140 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.69-1269A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58696476 | |||||||
| chr1:58696674 | C | G | 4 | a0002c0002t0045g0055 a0002c0002t0045g0056 a0002c0002t0076g0064 others(1): Show |
4 | HG02723.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.69-1467G>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58696674 | |||||||
| chr1:58696821 | A | C | 110 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0007 others(107): Show |
140 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.69-1614T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58696821 | |||||||
| chr1:58696858 | C | T | 2 | a0002c0002t0002g0068 a0002c0002t0014g0067 |
2 | HG02135.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.69-1651G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58696858 | |||||||
| chr1:58697003 | G | A | 126 | a0001c0001t0019g0040 a0001c0001t0019g0229 a0001c0001t0019g0231 others(123): Show |
160 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.69-1796C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58697003 | |||||||
| chr1:58697024 | G | T | 4 | a0001c0001t0019g0040 a0001c0001t0019g0229 a0001c0001t0019g0231 others(1): Show |
5 | NA18953.hp2 NA18954.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.69-1817C>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58697024 | |||||||
| chr1:58697121 | A | G | 110 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0007 others(107): Show |
140 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.69-1914T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58697121 | |||||||
| chr1:58697251 | G | GAGGC | 110 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0007 others(107): Show |
140 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.69-2045_69-2044ins others(4): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58697251 | |||||||
| chr1:58697314 | T | C | 4 | a0001c0001t0019g0040 a0001c0001t0019g0229 a0001c0001t0019g0231 others(1): Show |
5 | NA18953.hp2 NA18954.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.69-2107A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58697314 | |||||||
| chr1:58697349 | TAAG | T | 33 | a0002c0005t0006g0033 a0002c0005t0006g0034 a0002c0005t0006g0035 others(30): Show |
40 | HG00140.hp2 HG00673.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.69-2145_69-2143del others(3): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58697349 | |||||||
| chr1:58697392 | C | T | 4 | a0001c0001t0019g0040 a0001c0001t0019g0229 a0001c0001t0019g0231 others(1): Show |
5 | NA18953.hp2 NA18954.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.69-2185G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58697392 | |||||||
| chr1:58697489 | A | C | 2 | a0002c0002t0044g0013 a0002c0002t0077g0062 |
3 | HG01891.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.69-2282T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58697489 | |||||||
| chr1:58697537 | T | G | 1 | a0002c0002t0005g0125 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.69-2330A>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58697537 | |||||||
| chr1:58697582 | CA | C | 7 | a0001c0001t0019g0040 a0001c0001t0019g0229 a0001c0001t0019g0231 others(4): Show |
8 | HG01517.hp2 NA18953.hp2 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.69-2376delT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58697582 | |||||||
| chr1:58697591 | A | T | 32 | a0002c0005t0006g0033 a0002c0005t0006g0034 a0002c0005t0006g0035 others(29): Show |
39 | HG00140.hp2 HG00673.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.69-2384T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58697591 | |||||||
| chr1:58697591 | AT | A | 6 | a0001c0001t0001g0188 a0001c0001t0001g0200 a0001c0001t0004g0165 others(3): Show |
7 | HG01952.hp2 HG02004.hp2 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.69-2385delA | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58697591 | |||||||
| chr1:58697614 | C | A | 126 | a0001c0001t0019g0040 a0001c0001t0019g0229 a0001c0001t0019g0231 others(123): Show |
160 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.68+2371G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58697614 | |||||||
| chr1:58697651 | G | A | 16 | a0001c0001t0019g0040 a0001c0001t0019g0229 a0001c0001t0019g0231 others(13): Show |
20 | HG02055.hp1 HG02257.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.68+2334C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58697651 | |||||||
| chr1:58697736 | G | C | 120 | a0001c0001t0019g0040 a0001c0001t0019g0229 a0001c0001t0019g0231 others(117): Show |
152 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.68+2249C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58697736 | |||||||
| chr1:58697769 | A | G | 110 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0007 others(107): Show |
140 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.68+2216T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58697769 | |||||||
| chr1:58697790 | T | C | 1 | a0001c0001t0037g0045 | 2 | HG01243.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.68+2195A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58697790 | |||||||
| chr1:58697832 | G | A | 4 | a0001c0001t0019g0040 a0001c0001t0019g0229 a0001c0001t0019g0231 others(1): Show |
5 | NA18953.hp2 NA18954.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.68+2153C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58697832 | |||||||
| chr1:58697835 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.68+2150G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58697835 | |||||||
| chr1:58697868 | C | A | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(96): Show |
133 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.68+2117G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58697868 | |||||||
| chr1:58697881 | A | G | 126 | a0001c0001t0019g0040 a0001c0001t0019g0229 a0001c0001t0019g0231 others(123): Show |
160 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.68+2104T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58697881 | |||||||
| chr1:58698001 | T | G | 6 | a0004c0004t0024g0012 a0004c0004t0024g0049 a0004c0004t0026g0051 others(3): Show |
7 | HG02055.hp1 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.68+1984A>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698001 | |||||||
| chr1:58698045 | C | T | 120 | a0001c0001t0019g0040 a0001c0001t0019g0229 a0001c0001t0019g0231 others(117): Show |
152 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.68+1940G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698045 | |||||||
| chr1:58698084 | C | CTATATAT others(13): Show |
5 | a0004c0004t0012g0319 a0004c0004t0012g0320 a0004c0004t0012g0321 others(2): Show |
5 | HG01167.hp1 HG01255.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.68+1900_68+1901ins others(20): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698084 | |||||||
| chr1:58698084 | C | CTATATAT others(15): Show |
2 | a0004c0004t0012g0323 a0004c0004t0012g0324 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.68+1900_68+1901ins others(22): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698084 | |||||||
| chr1:58698084 | C | CTATATAT others(21): Show |
2 | a0004c0004t0020g0308 a0004c0004t0070g0309 |
2 | HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.68+1900_68+1901ins others(28): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698084 | |||||||
| chr1:58698084 | C | CTATATAT others(23): Show |
1 | a0004c0004t0020g0303 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.68+1900_68+1901ins others(30): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698084 | |||||||
| chr1:58698084 | C | CTATATAT others(31): Show |
2 | a0004c0004t0020g0304 a0004c0004t0023g0305 |
2 | HG02257.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.68+1900_68+1901ins others(38): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698084 | |||||||
| chr1:58698084 | C | CTCTATAT others(13): Show |
1 | a0004c0004t0040g0301 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.68+1900_68+1901ins others(20): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698084 | |||||||
| chr1:58698084 | C | CTCTATAT others(19): Show |
1 | a0004c0004t0023g0302 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.68+1900_68+1901ins others(26): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698084 | |||||||
| chr1:58698084 | C | CTCTATAT others(37): Show |
1 | a0004c0004t0020g0306 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.68+1900_68+1901ins others(44): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698084 | |||||||
| chr1:58698084 | C | CTCTATAT others(49): Show |
1 | a0004c0004t0040g0310 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.68+1900_68+1901ins others(56): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698084 | |||||||
| chr1:58698084 | CTA | C | 50 | a0003c0003t0003g0001 a0003c0003t0003g0010 a0003c0003t0003g0126 others(47): Show |
66 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.68+1899_68+1900del others(2): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698084 | |||||||
| chr1:58698086 | A | C | 17 | a0003c0003t0003g0233 a0003c0003t0003g0235 a0003c0003t0003g0240 others(14): Show |
17 | HG00639.hp2 HG01074.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.68+1899T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698086 | |||||||
| chr1:58698088 | A | C | 50 | a0003c0003t0003g0001 a0003c0003t0003g0010 a0003c0003t0003g0126 others(47): Show |
66 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.68+1897T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698088 | |||||||
| chr1:58698098 | A | ATTTTTTT others(7): Show |
2 | a0002c0002t0045g0055 a0002c0002t0045g0056 |
2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.68+1886_68+1887ins others(14): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698098 | |||||||
| chr1:58698099 | TA | T | 8 | a0003c0003t0003g0240 a0003c0003t0003g0242 a0003c0003t0082g0243 others(5): Show |
8 | HG01074.hp2 HG01081.hp1 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.68+1885delT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698099 | |||||||
| chr1:58698099 | TATA | T | 4 | a0003c0003t0003g0233 a0003c0003t0003g0235 a0003c0003t0011g0234 others(1): Show |
4 | HG03041.hp1 NA18986.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.68+1883_68+1885del others(3): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698099 | |||||||
| chr1:58698100 | A | ATATATAT others(27): Show |
1 | a0001c0001t0019g0040 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.68+1884_68+1885ins others(34): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698100 | |||||||
| chr1:58698100 | A | ATTTTTTT others(5): Show |
2 | a0002c0005t0027g0036 a0002c0005t0029g0312 |
3 | HG02280.hp1 HG02615.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.68+1884_68+1885ins others(12): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698100 | |||||||
| chr1:58698100 | A | ATTTTTTT others(9): Show |
1 | a0002c0002t0078g0057 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.68+1884_68+1885ins others(16): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698100 | |||||||
| chr1:58698100 | A | T | 2 | a0002c0002t0045g0055 a0002c0002t0045g0056 |
2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.68+1885T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698100 | |||||||
| chr1:58698101 | TA | T | 3 | a0003c0003t0010g0238 a0003c0003t0035g0237 a0003c0003t0035g0239 |
3 | HG01099.hp1 NA19084.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.68+1883delT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698101 | |||||||
| chr1:58698102 | A | ATATATAT others(16): Show |
1 | a0005c0006t0011g0047 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(23): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(22): Show |
1 | a0004c0004t0007g0298 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(29): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(45): Show |
1 | a0001c0001t0037g0045 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(52): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(46): Show |
1 | a0002c0005t0080g0228 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(53): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(41): Show |
1 | a0002c0005t0006g0035 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(48): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(42): Show |
1 | a0002c0005t0016g0226 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(49): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(29): Show |
1 | a0001c0001t0054g0299 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(36): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(46): Show |
1 | a0006c0007t0025g0014 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(53): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(39): Show |
1 | a0002c0002t0041g0020 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(46): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(31): Show |
1 | a0006c0010t0010g0222 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(38): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(36): Show |
2 | a0002c0005t0006g0209 a0002c0005t0015g0219 |
2 | NA18993.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(43): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(37): Show |
1 | a0002c0002t0014g0090 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(44): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(39): Show |
1 | a0002c0002t0002g0105 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(46): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(41): Show |
2 | a0002c0002t0005g0112 a0006c0007t0025g0014 |
2 | HG01934.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(48): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(42): Show |
1 | a0002c0002t0002g0006 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(49): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(31): Show |
1 | a0002c0005t0006g0210 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(38): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(32): Show |
1 | a0002c0005t0030g0212 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(39): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(35): Show |
1 | a0002c0002t0002g0071 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(42): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(36): Show |
1 | a0002c0002t0005g0104 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(43): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(38): Show |
1 | a0002c0002t0002g0007 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(45): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(27): Show |
1 | a0001c0001t0037g0045 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(34): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(31): Show |
1 | a0002c0005t0030g0206 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(38): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(32): Show |
4 | a0002c0005t0006g0211 a0002c0005t0006g0220 a0002c0005t0015g0217 others(1): Show |
4 | NA18954.hp2 NA18965.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(39): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(33): Show |
2 | a0002c0005t0015g0216 a0002c0005t0030g0205 |
2 | NA18999.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(40): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(34): Show |
2 | a0002c0002t0002g0002 a0004c0004t0024g0012 |
2 | HG02615.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(41): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(35): Show |
1 | a0002c0002t0002g0103 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(42): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(36): Show |
3 | a0002c0002t0002g0086 a0002c0002t0002g0117 a0002c0002t0013g0109 |
3 | HG01981.hp2 NA19058.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(43): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(37): Show |
3 | a0002c0002t0002g0006 a0002c0002t0002g0018 a0002c0002t0002g0075 |
3 | HG01928.hp1 NA19007.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(44): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(19): Show |
2 | a0005c0006t0011g0047 a0005c0006t0026g0317 |
2 | HG02486.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(26): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(34): Show |
2 | a0001c0001t0019g0040 a0001c0001t0019g0231 |
2 | NA18953.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(41): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(22): Show |
2 | a0004c0004t0023g0232 a0005c0006t0011g0315 |
2 | HG03195.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(29): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(24): Show |
1 | a0005c0008t0010g0011 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(31): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(29): Show |
1 | a0004c0004t0071g0050 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(36): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(30): Show |
1 | a0002c0005t0015g0215 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(37): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(32): Show |
1 | a0002c0002t0002g0002 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(39): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(33): Show |
1 | a0002c0002t0028g0087 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(40): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(34): Show |
1 | a0002c0002t0002g0006 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(41): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(35): Show |
5 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0113 others(2): Show |
5 | NA18939.hp1 NA18940.hp2 NA18987.hp2 others(2): Show |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(42): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(36): Show |
1 | a0002c0002t0005g0017 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(43): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(37): Show |
2 | a0002c0002t0002g0002 a0002c0002t0002g0006 |
2 | HG02148.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(44): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(38): Show |
1 | a0002c0002t0002g0115 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(45): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(17): Show |
1 | a0004c0004t0072g0054 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(24): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(32): Show |
1 | a0001c0001t0019g0229 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(39): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(25): Show |
2 | a0001c0001t0009g0152 a0002c0005t0006g0223 |
2 | HG00099.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(32): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(28): Show |
1 | a0002c0005t0006g0033 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(35): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(29): Show |
1 | a0004c0004t0024g0012 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(36): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(30): Show |
1 | a0002c0002t0002g0019 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(37): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(31): Show |
1 | a0002c0002t0002g0119 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(38): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(32): Show |
1 | a0002c0002t0005g0108 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(39): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(30): Show |
1 | a0001c0001t0056g0230 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(37): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(20): Show |
2 | a0005c0006t0003g0316 a0005c0006t0011g0314 |
2 | HG02257.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(27): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(23): Show |
1 | a0002c0005t0016g0204 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(30): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(24): Show |
3 | a0001c0001t0001g0004 a0002c0005t0006g0208 a0002c0005t0016g0039 |
3 | HG00140.hp2 HG01515.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(31): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(27): Show |
2 | a0002c0002t0002g0002 a0002c0002t0002g0124 |
2 | HG03942.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(34): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(28): Show |
9 | a0002c0002t0002g0002 a0002c0002t0002g0102 a0002c0002t0005g0073 others(6): Show |
10 | HG03654.hp1 HG03704.hp2 HG04115.hp2 others(7): Show |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(35): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(29): Show |
2 | a0002c0002t0014g0122 a0004c0004t0024g0049 |
2 | HG02055.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(36): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(30): Show |
2 | a0002c0002t0002g0078 a0002c0002t0002g0123 |
2 | HG01070.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(37): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(31): Show |
3 | a0002c0002t0002g0070 a0002c0002t0028g0094 a0002c0002t0028g0100 |
3 | HG02083.hp1 HG02129.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(38): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(33): Show |
2 | a0002c0002t0002g0007 a0002c0002t0005g0072 |
2 | HG02027.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(40): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(20): Show |
1 | a0002c0005t0006g0214 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(27): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(22): Show |
2 | a0002c0005t0016g0039 a0002c0005t0016g0225 |
2 | HG00741.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(29): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(24): Show |
1 | a0002c0002t0005g0116 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(31): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(25): Show |
1 | a0002c0005t0006g0034 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(32): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(27): Show |
1 | a0004c0004t0066g0048 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(34): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(28): Show |
2 | a0002c0002t0002g0074 a0002c0002t0014g0097 |
2 | HG01346.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(35): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(29): Show |
3 | a0002c0002t0002g0118 a0002c0002t0005g0016 a0006c0007t0025g0063 |
3 | HG01884.hp1 NA18947.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(36): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(30): Show |
4 | a0002c0002t0005g0065 a0002c0002t0005g0125 a0002c0002t0083g0095 others(1): Show |
4 | HG00544.hp2 HG00621.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(37): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(12): Show |
1 | a0002c0002t0013g0099 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(19): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(20): Show |
6 | a0001c0001t0001g0032 a0001c0001t0001g0189 a0001c0001t0001g0196 others(3): Show |
6 | HG01243.hp1 HG03927.hp1 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(27): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(22): Show |
1 | a0001c0001t0050g0170 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(29): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(24): Show |
1 | a0002c0005t0006g0034 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(31): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(26): Show |
1 | a0002c0002t0002g0002 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(33): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(27): Show |
8 | a0002c0002t0002g0079 a0002c0002t0002g0085 a0002c0002t0002g0096 others(5): Show |
8 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(5): Show |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(34): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(28): Show |
7 | a0002c0002t0002g0007 a0002c0002t0002g0084 a0002c0002t0002g0088 others(4): Show |
8 | HG02055.hp2 NA18981.hp2 NA18983.hp1 others(5): Show |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(35): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(29): Show |
3 | a0002c0002t0002g0002 a0002c0002t0014g0120 a0002c0002t0074g0091 |
3 | HG01361.hp1 NA18946.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(36): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(30): Show |
1 | a0002c0002t0002g0018 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(37): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(17): Show |
6 | a0001c0001t0001g0004 a0001c0001t0001g0166 a0001c0001t0001g0191 others(3): Show |
6 | HG00140.hp1 HG01256.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(24): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(18): Show |
12 | a0001c0001t0001g0031 a0001c0001t0001g0127 a0001c0001t0001g0134 others(9): Show |
13 | HG02040.hp1 HG02738.hp2 HG03490.hp2 others(10): Show |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(25): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(19): Show |
3 | a0001c0001t0001g0003 a0001c0001t0001g0181 a0001c0001t0004g0180 |
4 | HG01891.hp1 HG02486.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(26): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(20): Show |
3 | a0001c0001t0004g0129 a0001c0001t0008g0029 a0001c0001t0008g0147 |
3 | HG01099.hp2 HG02015.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(27): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(21): Show |
1 | a0001c0001t0009g0143 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(28): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(22): Show |
1 | a0001c0001t0004g0005 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(29): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(26): Show |
1 | a0002c0002t0002g0082 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(33): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(27): Show |
3 | a0002c0002t0002g0068 a0002c0002t0002g0069 a0002c0002t0014g0067 |
3 | HG00438.hp1 HG02135.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(34): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(11): Show |
1 | a0001c0001t0055g0300 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(18): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(13): Show |
1 | a0001c0001t0004g0177 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(20): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(14): Show |
1 | a0002c0005t0079g0207 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(21): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(17): Show |
1 | a0001c0001t0004g0133 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(24): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(18): Show |
16 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0032 others(13): Show |
18 | HG00597.hp1 HG01070.hp2 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(25): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(19): Show |
9 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0024 others(6): Show |
10 | HG00621.hp2 HG01934.hp1 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(26): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(20): Show |
4 | a0001c0001t0001g0024 a0001c0001t0004g0149 a0001c0001t0008g0141 others(1): Show |
4 | HG01169.hp1 HG01257.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(27): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(21): Show |
1 | a0004c0004t0039g0046 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(28): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(35): Show |
1 | a0002c0005t0006g0224 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(42): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(14): Show |
1 | a0002c0005t0006g0035 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(21): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(16): Show |
1 | a0001c0001t0009g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(23): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(17): Show |
9 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(6): Show |
9 | HG02129.hp2 HG02148.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(24): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(18): Show |
26 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0026 others(23): Show |
36 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(25): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(19): Show |
6 | a0001c0001t0001g0004 a0001c0001t0004g0005 a0001c0001t0004g0023 others(3): Show |
6 | HG01978.hp2 HG02004.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(26): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(20): Show |
1 | a0001c0001t0009g0156 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(27): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(21): Show |
1 | a0004c0004t0063g0311 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(28): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(11): Show |
2 | a0001c0001t0036g0053 a0001c0001t0053g0059 |
2 | HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(18): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(13): Show |
2 | a0004c0004t0026g0051 a0004c0004t0026g0052 |
2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(20): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(15): Show |
2 | a0002c0002t0002g0110 a0002c0002t0013g0111 |
2 | HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(22): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(16): Show |
1 | a0001c0001t0004g0164 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(23): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(18): Show |
2 | a0001c0001t0004g0009 a0001c0001t0009g0313 |
2 | HG02258.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(25): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0021 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(26): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(21): Show |
1 | a0002c0002t0042g0083 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(28): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(10): Show |
2 | a0001c0001t0036g0061 a0001c0001t0057g0060 |
2 | HG01192.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(17): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATAT others(18): Show |
1 | a0002c0002t0002g0077 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(25): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATATTT others(9): Show |
1 | a0002c0005t0006g0213 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(16): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATATTTTT others(6): Show |
3 | a0002c0005t0006g0227 a0002c0005t0027g0221 a0002c0005t0043g0037 |
4 | HG01074.hp1 HG02622.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(13): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATTTTTTT others(5): Show |
1 | a0002c0005t0029g0038 | 2 | HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.68+1871_68+1882dup others(12): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATTTTTTT others(7): Show |
1 | a0002c0002t0044g0013 | 2 | HG01891.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.68+1869_68+1882dup others(14): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATTTTTTT others(11): Show |
1 | a0002c0002t0077g0062 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(18): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | ATTTTTTT others(12): Show |
1 | a0002c0002t0002g0002 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(19): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698102 | A | T | 63 | a0002c0002t0045g0055 a0002c0002t0045g0056 a0002c0002t0078g0057 others(60): Show |
78 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.68+1883T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | |||||||
| chr1:58698103 | T | TATATATA others(6): Show |
1 | a0001c0001t0001g0202 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.68+1881_68+1882ins others(13): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698103 | |||||||
| chr1:58698103 | T | TATATATA others(16): Show |
1 | a0004c0004t0003g0307 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.68+1881_68+1882ins others(23): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698103 | |||||||
| chr1:58698104 | T | A | 9 | a0004c0004t0012g0319 a0004c0004t0012g0320 a0004c0004t0012g0321 others(6): Show |
9 | HG01167.hp1 HG01255.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.68+1881A>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698104 | |||||||
| chr1:58698105 | T | A | 1 | a0001c0001t0019g0231 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.68+1880A>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698105 | |||||||
| chr1:58698315 | T | C | 1 | a0001c0001t0036g0061 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.68+1670A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698315 | |||||||
| chr1:58698351 | C | T | 1 | a0002c0002t0005g0065 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.68+1634G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698351 | |||||||
| chr1:58698468 | A | G | 110 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0007 others(107): Show |
140 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.68+1517T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698468 | |||||||
| chr1:58698515 | C | G | 1 | a0004c0004t0023g0232 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.68+1470G>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698515 | |||||||
| chr1:58698548 | A | AG | 116 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0007 others(113): Show |
147 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.68+1436dupC | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698548 | |||||||
| chr1:58698572 | A | AAAAATT | 120 | a0001c0001t0019g0040 a0001c0001t0019g0229 a0001c0001t0019g0231 others(117): Show |
152 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.68+1412_68+1413ins others(6): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698572 | |||||||
| chr1:58698585 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.68+1400A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698585 | |||||||
| chr1:58698741 | T | C | 6 | a0005c0006t0003g0316 a0005c0006t0011g0047 a0005c0006t0011g0314 others(3): Show |
8 | HG02257.hp2 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.68+1244A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698741 | |||||||
| chr1:58698797 | T | A | 1 | a0004c0004t0040g0310 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.68+1188A>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698797 | |||||||
| chr1:58698825 | C | A | 4 | a0002c0002t0045g0055 a0002c0002t0045g0056 a0002c0002t0076g0064 others(1): Show |
4 | HG02723.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.68+1160G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698825 | |||||||
| chr1:58698840 | C | T | 110 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0007 others(107): Show |
140 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.68+1145G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698840 | |||||||
| chr1:58698855 | T | C | 69 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0007 others(66): Show |
90 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.68+1130A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698855 | |||||||
| chr1:58698911 | C | T | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(95): Show |
132 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.68+1074G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698911 | |||||||
| chr1:58699038 | T | C | 2 | a0004c0004t0039g0046 a0004c0004t0063g0311 |
3 | HG01952.hp2 HG02004.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.68+947A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58699038 | |||||||
| chr1:58699047 | A | C | 1 | a0003c0003t0003g0126 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.68+938T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58699047 | |||||||
| chr1:58699178 | G | C | 1 | a0004c0004t0072g0054 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.68+807C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58699178 | |||||||
| chr1:58699320 | G | A | 1 | a0001c0001t0001g0021 | 2 | HG03942.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.68+665C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58699320 | |||||||
| chr1:58699370 | A | C | 78 | a0001c0001t0001g0021 a0002c0002t0002g0002 a0002c0002t0002g0006 others(75): Show |
102 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.68+615T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58699370 | |||||||
| chr1:58699528 | C | T | 4 | a0001c0001t0036g0053 a0001c0001t0036g0061 a0001c0001t0053g0059 others(1): Show |
4 | HG01192.hp1 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.68+457G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58699528 | |||||||
| chr1:58699593 | C | T | 1 | a0001c0001t0008g0058 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.68+392G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58699593 | |||||||
| chr1:58699616 | C | T | 3 | a0002c0002t0045g0055 a0002c0002t0045g0056 a0002c0002t0078g0057 |
3 | HG02723.hp1 HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.68+369G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58699616 | |||||||
| chr1:58699697 | G | C | 1 | a0002c0005t0029g0312 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.68+288C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58699697 | |||||||
| chr1:58699727 | T | C | 1 | a0001c0001t0009g0313 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.68+258A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58699727 | |||||||
| chr1:58699829 | C | A | 6 | a0005c0006t0003g0316 a0005c0006t0011g0047 a0005c0006t0011g0314 others(3): Show |
8 | HG02257.hp2 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.68+156G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58699829 | |||||||
| chr1:58699836 | C | T | 1 | a0004c0004t0072g0054 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.68+149G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58699836 | |||||||
| chr1:58699871 | C | T | 1 | a0001c0001t0036g0053 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.68+114G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58699871 | |||||||
| chr1:58699923 | G | A | 7 | a0004c0004t0012g0319 a0004c0004t0012g0320 a0004c0004t0012g0321 others(4): Show |
7 | HG01167.hp1 HG01255.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.68+62C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58699923 | |||||||
| chr1:58699944 | TC | T | 6 | a0004c0004t0024g0012 a0004c0004t0024g0049 a0004c0004t0026g0051 others(3): Show |
7 | HG02055.hp1 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.68+40delG | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58699944 |