Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 130013 |
| ensemblid | ENSG00000153086.14 |
| hgncid | 19288 |
| symbol | ACMSD |
| name | aminocarboxymuconate semialdehyde decarboxylase |
| refseq_nuc | NM_138326.3 |
| refseq_prot | NP_612199.2 |
| ensembl_nuc | ENST00000356140.10 |
| ensembl_prot | ENSP00000348459.5 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 134838616 |
| end | 134902034 |
| strand | + |
| ver | v1.2 |
| region | chr2:134838616-134902034 |
| region5000 | chr2:134833616-134907034 |
| regionname0 | ACMSD_chr2_134838616_134902034 |
| regionname5000 | ACMSD_chr2_134833616_134907034 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 336 | 369 | 75 | 66 | 178 | 10 | 38 | 145 | ACMSD_chr2_134833616_134907034 | ACMSD | MKIDI others(331): Show |
chr2 | 134833616 | 134907034 |
| a0002 | 0/0 | 336 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | MKIDI others(331): Show |
chr2 | 134833616 | 134907034 |
| a0003 | 0/0 | 49 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | ACMSD_chr2_134833616_134907034 | ACMSD | MKIDI others(44): Show |
chr2 | 134833616 | 134907034 |
| a0004 | 0/0 | 336 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ACMSD_chr2_134833616_134907034 | ACMSD | MKIDI others(331): Show |
chr2 | 134833616 | 134907034 |
| a0005 | 0/0 | 336 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | MKIDI others(331): Show |
chr2 | 134833616 | 134907034 |
| a0006 | 0/0 | 336 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | MKIDI others(331): Show |
chr2 | 134833616 | 134907034 |
| a0007 | 0/0 | 336 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | MKIDI others(331): Show |
chr2 | 134833616 | 134907034 |
| a0008 | 0/0 | 336 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | MKIDI others(331): Show |
chr2 | 134833616 | 134907034 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1008 | 365 | 72 | 66 | 178 | 10 | 37 | ACMSD_chr2_134833616_134907034 | ACMSD | ATGAA others(1003): Show |
chr2 | 134833616 | 134907034 | ||
| a0001c0004 | 0/0 | 1008 | 3 | 3 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | ATGAA others(1003): Show |
chr2 | 134833616 | 134907034 | ||
| a0001c0009 | 0/0 | 1008 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | ATGAA others(1003): Show |
chr2 | 134833616 | 134907034 | ||
| a0002c0002 | 0/0 | 1008 | 4 | 4 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | ATGAA others(1003): Show |
chr2 | 134833616 | 134907034 | ||
| a0003c0003 | 0/0 | 1008 | 3 | 0 | 0 | 3 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | ATGAA others(1003): Show |
chr2 | 134833616 | 134907034 | ||
| a0004c0005 | 0/0 | 1008 | 2 | 0 | 0 | 2 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | ATGAA others(1003): Show |
chr2 | 134833616 | 134907034 | ||
| a0005c0010 | 0/0 | 1008 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | ATGAA others(1003): Show |
chr2 | 134833616 | 134907034 | ||
| a0006c0006 | 0/0 | 1008 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | ATGAA others(1003): Show |
chr2 | 134833616 | 134907034 | ||
| a0007c0007 | 0/0 | 1008 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | ATGAA others(1003): Show |
chr2 | 134833616 | 134907034 | ||
| a0008c0008 | 0/0 | 1008 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | ATGAA others(1003): Show |
chr2 | 134833616 | 134907034 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1252 | 365 | 72 | 66 | 178 | 10 | 37 | ACMSD_chr2_134833616_134907034 | ACMSD | ACAGT others(1247): Show |
chr2 | 134833616 | 134907034 |
| a0001c0004t0001 | 0/0 | 1252 | 3 | 3 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | ACAGT others(1247): Show |
chr2 | 134833616 | 134907034 |
| a0001c0009t0001 | 0/0 | 1252 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | ACAGT others(1247): Show |
chr2 | 134833616 | 134907034 |
| a0002c0002t0001 | 0/0 | 1252 | 4 | 4 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | ACAGT others(1247): Show |
chr2 | 134833616 | 134907034 |
| a0003c0003t0001 | 0/0 | 1252 | 3 | 0 | 0 | 3 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | ACAGT others(1247): Show |
chr2 | 134833616 | 134907034 |
| a0004c0005t0001 | 0/0 | 1252 | 2 | 0 | 0 | 2 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | ACAGT others(1247): Show |
chr2 | 134833616 | 134907034 |
| a0005c0010t0001 | 0/0 | 1252 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | ACAGT others(1247): Show |
chr2 | 134833616 | 134907034 |
| a0006c0006t0001 | 0/0 | 1252 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | ACAGT others(1247): Show |
chr2 | 134833616 | 134907034 |
| a0007c0007t0001 | 0/0 | 1252 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | ACAGT others(1247): Show |
chr2 | 134833616 | 134907034 |
| a0008c0008t0001 | 0/0 | 1252 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | ACAGT others(1247): Show |
chr2 | 134833616 | 134907034 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 9 | 0 | 6 | 0 | 2 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0001t0001g0349 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0004t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0004t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0004t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0001c0009t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0002c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0002c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0002c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0002c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0003c0003t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0003c0003t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0004c0005t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0004c0005t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0005c0010t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0006c0006t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0007c0007t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| a0008c0008t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0088 | EUR | GBR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | CHS | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | CHS | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | CHS | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | CHS | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0322 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0336 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0331 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0302 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0312 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0333 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0347 | AMR | CLM | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | CLM | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0303 | AMR | CLM | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | CLM | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0339 | AMR | CLM | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0348 | AMR | CLM | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0136 | EUR | IBS | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0310 | EUR | IBS | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0118 | EUR | IBS | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PEL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | PEL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02027 | hp2 | a0005 | c0010 | t0001 | g0115 | EAS | KHV | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | KHV | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02040 | hp2 | a0006 | c0006 | t0001 | g0239 | EAS | KHV | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | KHV | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | KHV | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | ACB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0202 | AFR | ACB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02155 | hp2 | a0007 | c0007 | t0001 | g0205 | EAS | CDX | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | CDX | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | CDX | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | ACB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02257 | hp2 | a0001 | c0004 | t0001 | g0171 | AFR | ACB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PEL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0304 | AMR | PEL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | ACB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02572 | hp1 | a0001 | c0004 | t0001 | g0172 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0325 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0342 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02647 | hp2 | a0001 | c0004 | t0001 | g0170 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0334 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02735 | hp2 | a0001 | c0009 | t0001 | g0211 | SAS | PJL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02809 | hp2 | a0008 | c0008 | t0001 | g0327 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0329 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0341 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0338 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0344 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0343 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0345 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0330 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | ESN | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ESN | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0332 | AFR | ESN | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ESN | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | MSL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0337 | AFR | ESN | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ESN | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | ESN | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ESN | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | ESN | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0201 | AFR | MSL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | MSL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | MSL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0197 | AFR | MSL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | MSL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ESN | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0346 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | MSL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | MSL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | STU | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | STU | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0324 | SAS | PJL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | BEB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0323 | SAS | BEB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | BEB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | BEB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | BEB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0326 | SAS | BEB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | BEB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | STU | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | STU | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0300 | SAS | STU | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | STU | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | YRI | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | YRI | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | YRI | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | YRI | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18952 | hp2 | a0004 | c0005 | t0001 | g0222 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18962 | hp2 | a0003 | c0003 | t0001 | g0021 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18988 | hp2 | a0004 | c0005 | t0001 | g0146 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | LWK | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | LWK | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0026 | AFR | LWK | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | LWK | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19070 | hp1 | a0003 | c0003 | t0001 | g0021 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19084 | hp2 | a0003 | c0003 | t0001 | g0268 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ASW | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ASW | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0039 | EUR | TSI | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0096 | EUR | TSI | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0311 | SAS | GIH | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | GIH | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | CLM | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | MSL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | USA | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | USA | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | USA | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | USA | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | LWK | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | LWK | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0349 | REF | REF | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:134845277 | G | T | 1 | a0005 | 1 | HG02027.hp2 | missense_variant&splice_region_variant | MODERATE | c.102G>T | p.Lys34Asn | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/10 | 169/1252 | 102/1011 | 34/336 | chr2 | 134845277 | |||
| chr2:134859306 | C | T | 1 | a0003 | 3 | NA18962.hp2 NA19070.hp1 NA19084.hp2 |
stop_gained | HIGH | c.148C>T | p.Arg50* | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/10 | 215/1252 | 148/1011 | 50/336 | chr2 | 134859306 | |||
| chr2:134859307 | G | A | 1 | a0002 | 4 | HG02145.hp2 HG03225.hp2 HG03486.hp1 others(1): Show |
missense_variant | MODERATE | c.149G>A | p.Arg50Gln | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/10 | 216/1252 | 149/1011 | 50/336 | chr2 | 134859307 | |||
| chr2:134859321 | G | C | 1 | a0004 | 2 | NA18952.hp2 NA18988.hp2 |
missense_variant | MODERATE | c.163G>C | p.Asp55His | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/10 | 230/1252 | 163/1011 | 55/336 | chr2 | 134859321 | |||
| chr2:134870986 | T | C | 1 | a0006 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.602T>C | p.Ile201Thr | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/10 | 669/1252 | 602/1011 | 201/336 | chr2 | 134870986 | |||
| chr2:134871015 | G | A | 1 | a0007 | 1 | HG02155.hp2 | missense_variant | MODERATE | c.631G>A | p.Val211Ile | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/10 | 698/1252 | 631/1011 | 211/336 | chr2 | 134871015 | |||
| chr2:134901813 | G | A | 1 | a0008 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.964G>A | p.Gly322Ser | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 10/10 | 1031/1252 | 964/1011 | 322/336 | chr2 | 134901813 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:134838715 | A | T | 1 | a0001c0004 | 3 | HG02257.hp2 HG02572.hp1 HG02647.hp2 |
synonymous_variant | LOW | c.33A>T | p.Pro11Pro | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/10 | 100/1252 | 33/1011 | 11/336 | chr2 | 134838715 | |||
| chr2:134871050 | C | T | 1 | a0001c0009 | 1 | HG02735.hp2 | synonymous_variant | LOW | c.666C>T | p.Phe222Phe | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/10 | 733/1252 | 666/1011 | 222/336 | chr2 | 134871050 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:134838838 | T | C | 1 | a0001c0001t0001g0022 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.57+99T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134838838 | |||||||
| chr2:134839032 | A | C | 3 | a0001c0001t0001g0346 a0001c0001t0001g0347 a0001c0001t0001g0348 |
3 | HG01255.hp1 HG01361.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.57+293A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134839032 | |||||||
| chr2:134839120 | G | A | 1 | a0001c0001t0001g0023 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.57+381G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134839120 | |||||||
| chr2:134839170 | A | G | 3 | a0001c0001t0001g0023 a0001c0001t0001g0344 a0001c0001t0001g0345 |
3 | HG02896.hp1 HG02897.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.57+431A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134839170 | |||||||
| chr2:134839206 | T | A | 1 | a0001c0001t0001g0024 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.57+467T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134839206 | |||||||
| chr2:134839396 | T | G | 1 | a0001c0001t0001g0025 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.57+657T>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134839396 | |||||||
| chr2:134839407 | A | T | 3 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 |
3 | HG02630.hp2 HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.57+668A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134839407 | |||||||
| chr2:134839693 | G | A | 1 | a0002c0002t0001g0026 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.57+954G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134839693 | |||||||
| chr2:134839694 | T | C | 1 | a0002c0002t0001g0026 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.57+955T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134839694 | |||||||
| chr2:134839695 | A | C | 1 | a0002c0002t0001g0026 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.57+956A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134839695 | |||||||
| chr2:134839696 | T | C | 1 | a0002c0002t0001g0026 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.57+957T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134839696 | |||||||
| chr2:134839756 | C | G | 2 | a0001c0001t0001g0344 a0001c0001t0001g0345 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.57+1017C>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134839756 | |||||||
| chr2:134839863 | A | G | 1 | a0001c0001t0001g0340 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.57+1124A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134839863 | |||||||
| chr2:134839918 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.57+1179G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134839918 | |||||||
| chr2:134840058 | T | G | 221 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(218): Show |
236 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(233): Show |
intron_variant | MODIFIER | c.57+1319T>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840058 | |||||||
| chr2:134840087 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0230 |
2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.57+1348T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840087 | |||||||
| chr2:134840166 | G | GAAAAAAA others(3): Show |
1 | a0001c0001t0001g0231 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.57+1427_57+1428ins others(10): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840166 | |||||||
| chr2:134840167 | C | A | 3 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
3 | HG02486.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.57+1428C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840167 | |||||||
| chr2:134840167 | C | CA | 23 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
27 | HG00558.hp2 HG01123.hp1 HG01952.hp1 others(24): Show |
intron_variant | MODIFIER | c.57+1454dupA | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840167 | ||||||
| chr2:134840167 | C | CAA | 6 | a0001c0001t0001g0141 a0001c0001t0001g0273 a0001c0001t0001g0274 others(3): Show |
6 | HG00438.hp1 HG02040.hp1 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.57+1453_57+1454dup others(2): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840167 | ||||||
| chr2:134840167 | C | CAAAAAAA | 12 | a0001c0001t0001g0139 a0001c0001t0001g0262 a0001c0001t0001g0263 others(9): Show |
12 | HG01346.hp1 NA18951.hp1 NA18965.hp2 others(9): Show |
intron_variant | MODIFIER | c.57+1448_57+1454dup others(7): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840167 | ||||||
| chr2:134840167 | C | CAAAAAAA others(1): Show |
18 | a0001c0001t0001g0027 a0001c0001t0001g0138 a0001c0001t0001g0246 others(15): Show |
18 | HG00741.hp1 HG01168.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.57+1447_57+1454dup others(8): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840167 | ||||||
| chr2:134840167 | C | CAAAAAAA others(2): Show |
13 | a0001c0001t0001g0024 a0001c0001t0001g0136 a0001c0001t0001g0137 others(10): Show |
13 | HG00438.hp2 HG00597.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.57+1446_57+1454dup others(9): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840167 | ||||||
| chr2:134840167 | C | CAAAAAAA others(3): Show |
11 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0128 others(8): Show |
13 | HG00609.hp1 HG01069.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.57+1445_57+1454dup others(10): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840167 | ||||||
| chr2:134840167 | C | CAAAAAAA others(4): Show |
19 | a0001c0001t0001g0003 a0001c0001t0001g0112 a0001c0001t0001g0113 others(16): Show |
21 | HG01361.hp1 HG01361.hp2 HG01516.hp2 others(18): Show |
intron_variant | MODIFIER | c.57+1444_57+1454dup others(11): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840167 | ||||||
| chr2:134840167 | C | CAAAAAAA others(5): Show |
16 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(13): Show |
16 | HG01255.hp1 HG02015.hp1 HG02523.hp2 others(13): Show |
intron_variant | MODIFIER | c.57+1443_57+1454dup others(12): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840167 | ||||||
| chr2:134840167 | C | CAAAAAAA others(6): Show |
15 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(12): Show |
15 | HG00140.hp2 HG01070.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.57+1442_57+1454dup others(13): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840167 | ||||||
| chr2:134840167 | C | CAAAAAAA others(7): Show |
11 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(8): Show |
11 | HG01192.hp2 HG01243.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.57+1441_57+1454dup others(14): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840167 | ||||||
| chr2:134840167 | C | CAAAAAAA others(8): Show |
13 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(10): Show |
13 | HG00639.hp1 HG00735.hp1 HG02602.hp2 others(10): Show |
intron_variant | MODIFIER | c.57+1440_57+1454dup others(15): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840167 | ||||||
| chr2:134840167 | C | CAAAAAAA others(9): Show |
13 | a0001c0001t0001g0006 a0001c0001t0001g0047 a0001c0001t0001g0048 others(10): Show |
14 | HG00642.hp1 HG00673.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.57+1439_57+1454dup others(16): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840167 | ||||||
| chr2:134840167 | C | CAAAAAAA others(10): Show |
7 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(4): Show |
7 | HG03041.hp2 HG03471.hp2 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+1438_57+1454dup others(17): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840167 | ||||||
| chr2:134840167 | C | CAAAAAAA others(11): Show |
3 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 |
3 | HG01081.hp2 NA19079.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.57+1437_57+1454dup others(18): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840167 | ||||||
| chr2:134840167 | C | CAAAAAAA others(12): Show |
3 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 |
3 | HG01257.hp2 NA18612.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.57+1436_57+1454dup others(19): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840167 | ||||||
| chr2:134840167 | C | CAAAAAAA others(13): Show |
1 | a0001c0001t0001g0033 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.57+1435_57+1454dup others(20): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840167 | ||||||
| chr2:134840167 | C | CAAAAAAA others(14): Show |
3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 |
3 | HG01261.hp2 HG01993.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.57+1434_57+1454dup others(21): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840167 | ||||||
| chr2:134840167 | C | CAAAAAAA others(18): Show |
1 | a0001c0001t0001g0029 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.57+1430_57+1454dup others(25): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840167 | ||||||
| chr2:134840167 | C | CAAAAAAA others(19): Show |
1 | a0001c0001t0001g0028 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.57+1429_57+1454dup others(26): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840167 | ||||||
| chr2:134840167 | CA | C | 12 | a0001c0001t0001g0025 a0001c0001t0001g0230 a0001c0001t0001g0322 others(9): Show |
12 | HG00639.hp2 HG01070.hp2 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.57+1454delA | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840167 | ||||||
| chr2:134840167 | CAA | C | 8 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(5): Show |
8 | HG00735.hp2 HG01243.hp1 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.57+1453_57+1454del others(2): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840167 | ||||||
| chr2:134840180 | A | AAAAAAAA others(8): Show |
5 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(2): Show |
5 | HG03654.hp1 NA18943.hp1 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.57+1454_57+1455ins others(15): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840180 | ||||||
| chr2:134840180 | A | AAAAAAAA others(7): Show |
1 | a0001c0001t0001g0015 | 2 | NA18970.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.57+1449_57+1450ins others(14): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840180 | ||||||
| chr2:134840180 | A | AAAAAAAA others(7): Show |
1 | a0001c0001t0001g0228 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.57+1448_57+1449ins others(14): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840180 | ||||||
| chr2:134840181 | A | AAAAAAAA others(3): Show |
2 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
2 | HG00558.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.57+1451_57+1452ins others(10): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840181 | ||||||
| chr2:134840183 | A | AAAAAAAA others(8): Show |
1 | a0001c0001t0001g0140 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.57+1454_57+1455ins others(15): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840183 | ||||||
| chr2:134840183 | AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0001g0229 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.57+1445_57+1455del others(11): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840183 | |||||||
| chr2:134840184 | A | AAAAAAAA others(9): Show |
1 | a0001c0001t0001g0223 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.57+1454_57+1455ins others(16): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840184 | ||||||
| chr2:134840184 | AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0001g0225 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.57+1446_57+1455del others(10): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840184 | |||||||
| chr2:134840185 | AAAAAAAA others(2): Show |
A | 19 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0159 others(16): Show |
22 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.57+1447_57+1455del others(9): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840185 | |||||||
| chr2:134840186 | AAAAAAAA others(1): Show |
A | 8 | a0001c0001t0001g0002 a0001c0001t0001g0161 a0001c0001t0001g0174 others(5): Show |
8 | HG02165.hp2 HG02293.hp1 HG04184.hp2 others(5): Show |
intron_variant | MODIFIER | c.57+1448_57+1455del others(8): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840186 | |||||||
| chr2:134840187 | A | C | 1 | a0001c0001t0001g0333 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.57+1448A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840187 | |||||||
| chr2:134840189 | AAAAAC | A | 7 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0155 others(4): Show |
7 | HG01168.hp1 HG02698.hp2 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.57+1451_57+1455del others(5): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840189 | |||||||
| chr2:134840192 | A | C | 2 | a0001c0004t0001g0171 a0001c0004t0001g0172 |
2 | HG02257.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.57+1453A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840192 | |||||||
| chr2:134840193 | A | AAAAAAAA others(31): Show |
1 | a0001c0001t0001g0011 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.57+1454_57+1455ins others(38): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840193 | |||||||
| chr2:134840193 | A | AAAAAAAA others(30): Show |
1 | a0001c0001t0001g0011 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.57+1454_57+1455ins others(37): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840193 | |||||||
| chr2:134840193 | A | AAAAAAAA others(28): Show |
1 | a0001c0001t0001g0169 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.57+1454_57+1455ins others(35): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840193 | |||||||
| chr2:134840193 | AC | A | 6 | a0001c0001t0001g0151 a0001c0001t0001g0167 a0001c0001t0001g0317 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.57+1456delC | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840193 | ||||||
| chr2:134840194 | C | A | 196 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(193): Show |
206 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.57+1455C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840194 | |||||||
| chr2:134840194 | C | CAAAAAAA others(7): Show |
21 | a0001c0001t0001g0014 a0001c0001t0001g0150 a0001c0001t0001g0194 others(18): Show |
22 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(19): Show |
intron_variant | MODIFIER | c.57+1455_57+1456ins others(14): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840194 | |||||||
| chr2:134840194 | C | CAAAACAA others(8): Show |
1 | a0001c0001t0001g0206 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.57+1455_57+1456ins others(15): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840194 | |||||||
| chr2:134840242 | A | G | 1 | a0001c0001t0001g0321 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.57+1503A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840242 | |||||||
| chr2:134840267 | C | T | 1 | a0001c0001t0001g0339 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.57+1528C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840267 | |||||||
| chr2:134840336 | C | T | 1 | a0001c0001t0001g0014 | 2 | NA18939.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.57+1597C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840336 | |||||||
| chr2:134840497 | G | C | 21 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0230 others(18): Show |
21 | HG00639.hp2 HG00735.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.57+1758G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840497 | |||||||
| chr2:134840559 | G | A | 1 | a0001c0001t0001g0246 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.57+1820G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840559 | |||||||
| chr2:134840597 | G | T | 2 | a0001c0001t0001g0235 a0001c0001t0001g0245 |
2 | HG00597.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.57+1858G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840597 | |||||||
| chr2:134840738 | TTTC | T | 218 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(215): Show |
233 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(230): Show |
intron_variant | MODIFIER | c.57+2008_57+2010del others(3): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840738 | ||||||
| chr2:134840815 | A | G | 1 | a0001c0001t0001g0025 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.57+2076A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840815 | |||||||
| chr2:134840888 | A | G | 1 | a0001c0001t0001g0025 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.57+2149A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840888 | |||||||
| chr2:134840929 | C | T | 54 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0231 others(51): Show |
55 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.57+2190C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840929 | |||||||
| chr2:134841001 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.57+2262G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134841001 | |||||||
| chr2:134841343 | G | A | 77 | a0001c0001t0001g0009 a0001c0001t0001g0030 a0001c0001t0001g0031 others(74): Show |
78 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.57+2604G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134841343 | |||||||
| chr2:134841439 | G | T | 295 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(292): Show |
311 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(308): Show |
intron_variant | MODIFIER | c.57+2700G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134841439 | |||||||
| chr2:134841537 | G | C | 5 | a0001c0001t0001g0011 a0001c0001t0001g0169 a0001c0004t0001g0170 others(2): Show |
6 | HG02109.hp1 HG02257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.57+2798G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134841537 | |||||||
| chr2:134841694 | C | T | 3 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0230 |
3 | HG00741.hp1 NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.57+2955C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134841694 | |||||||
| chr2:134841743 | G | A | 52 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0231 others(49): Show |
53 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.57+3004G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134841743 | |||||||
| chr2:134841794 | A | T | 1 | a0001c0001t0001g0025 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.57+3055A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134841794 | |||||||
| chr2:134841811 | G | A | 295 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(292): Show |
311 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(308): Show |
intron_variant | MODIFIER | c.57+3072G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134841811 | |||||||
| chr2:134841837 | T | C | 270 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(267): Show |
286 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(283): Show |
intron_variant | MODIFIER | c.57+3098T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134841837 | |||||||
| chr2:134841947 | G | C | 2 | a0001c0001t0001g0344 a0001c0001t0001g0345 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.57+3208G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134841947 | |||||||
| chr2:134841956 | T | C | 1 | a0001c0001t0001g0332 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.57+3217T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134841956 | |||||||
| chr2:134841980 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.57+3241G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134841980 | |||||||
| chr2:134842068 | G | A | 1 | a0001c0001t0001g0339 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.58-3165G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134842068 | |||||||
| chr2:134842158 | T | C | 1 | a0002c0002t0001g0026 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.58-3075T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134842158 | |||||||
| chr2:134842164 | C | T | 218 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(215): Show |
233 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(230): Show |
intron_variant | MODIFIER | c.58-3069C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134842164 | |||||||
| chr2:134842169 | C | T | 272 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(269): Show |
288 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(285): Show |
intron_variant | MODIFIER | c.58-3064C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134842169 | |||||||
| chr2:134842172 | C | G | 5 | a0001c0001t0001g0293 a0001c0001t0001g0328 a0001c0001t0001g0329 others(2): Show |
5 | HG02818.hp1 HG02886.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.58-3061C>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134842172 | |||||||
| chr2:134842289 | G | T | 2 | a0001c0001t0001g0225 a0001c0001t0001g0229 |
2 | HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.58-2944G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134842289 | |||||||
| chr2:134842306 | T | C | 18 | a0001c0001t0001g0025 a0001c0001t0001g0293 a0001c0001t0001g0322 others(15): Show |
18 | HG00639.hp2 HG00735.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.58-2927T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134842306 | |||||||
| chr2:134842371 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.58-2862C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134842371 | |||||||
| chr2:134842423 | G | A | 1 | a0001c0001t0001g0333 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.58-2810G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134842423 | |||||||
| chr2:134842455 | G | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0022 |
3 | HG02559.hp1 HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.58-2778G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134842455 | |||||||
| chr2:134842466 | C | T | 38 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(35): Show |
43 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.58-2767C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134842466 | |||||||
| chr2:134842538 | C | T | 4 | a0001c0001t0001g0029 a0001c0001t0001g0101 a0001c0001t0001g0111 others(1): Show |
4 | HG02717.hp1 HG03453.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.58-2695C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134842538 | |||||||
| chr2:134842843 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0148 a0001c0001t0001g0149 |
4 | HG02965.hp1 HG02965.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-2390C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134842843 | |||||||
| chr2:134842847 | T | C | 3 | a0001c0001t0001g0102 a0001c0001t0001g0114 a0001c0001t0001g0173 |
3 | HG02258.hp1 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.58-2386T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134842847 | |||||||
| chr2:134842848 | C | T | 294 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(291): Show |
310 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(307): Show |
intron_variant | MODIFIER | c.58-2385C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134842848 | |||||||
| chr2:134842855 | G | A | 1 | a0005c0010t0001g0115 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.58-2378G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134842855 | |||||||
| chr2:134843031 | T | G | 2 | a0001c0001t0001g0236 a0001c0001t0001g0247 |
2 | NA18940.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.58-2202T>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134843031 | |||||||
| chr2:134843058 | C | A | 2 | a0001c0001t0001g0344 a0001c0001t0001g0345 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.58-2175C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134843058 | |||||||
| chr2:134843109 | T | C | 1 | a0001c0001t0001g0278 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.58-2124T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134843109 | |||||||
| chr2:134843127 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.58-2106T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134843127 | |||||||
| chr2:134843179 | A | G | 46 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0011 others(43): Show |
52 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.58-2054A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134843179 | |||||||
| chr2:134843355 | T | C | 77 | a0001c0001t0001g0009 a0001c0001t0001g0030 a0001c0001t0001g0031 others(74): Show |
78 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.58-1878T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134843355 | |||||||
| chr2:134843735 | T | C | 1 | a0001c0001t0001g0023 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.58-1498T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134843735 | |||||||
| chr2:134843793 | G | A | 2 | a0001c0001t0001g0294 a0001c0001t0001g0295 |
2 | HG03041.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.58-1440G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134843793 | |||||||
| chr2:134843937 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.58-1296C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134843937 | |||||||
| chr2:134843954 | T | A | 77 | a0001c0001t0001g0009 a0001c0001t0001g0030 a0001c0001t0001g0031 others(74): Show |
78 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.58-1279T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134843954 | |||||||
| chr2:134843979 | C | T | 38 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(35): Show |
43 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.58-1254C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134843979 | |||||||
| chr2:134844187 | A | G | 17 | a0001c0001t0001g0293 a0001c0001t0001g0322 a0001c0001t0001g0323 others(14): Show |
17 | HG00639.hp2 HG00735.hp2 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.58-1046A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134844187 | |||||||
| chr2:134844211 | G | A | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0226 others(1): Show |
4 | HG00558.hp1 NA18989.hp2 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-1022G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134844211 | |||||||
| chr2:134844222 | T | C | 2 | a0001c0001t0001g0047 a0001c0001t0001g0151 |
2 | HG01074.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.58-1011T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134844222 | |||||||
| chr2:134844586 | G | A | 221 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(218): Show |
236 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(233): Show |
intron_variant | MODIFIER | c.58-647G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134844586 | |||||||
| chr2:134844624 | C | T | 49 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0234 others(46): Show |
50 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.58-609C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134844624 | |||||||
| chr2:134844839 | T | A | 221 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(218): Show |
236 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(233): Show |
intron_variant | MODIFIER | c.58-394T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134844839 | |||||||
| chr2:134844881 | A | G | 1 | a0001c0001t0001g0292 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.58-352A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134844881 | |||||||
| chr2:134844941 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0148 a0001c0001t0001g0149 |
4 | HG02965.hp1 HG02965.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-292C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134844941 | |||||||
| chr2:134844974 | T | C | 1 | a0001c0001t0001g0204 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.58-259T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134844974 | |||||||
| chr2:134844998 | G | C | 1 | a0001c0001t0001g0030 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.58-235G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134844998 | |||||||
| chr2:134845031 | T | A | 291 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(288): Show |
307 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(304): Show |
intron_variant | MODIFIER | c.58-202T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134845031 | |||||||
| chr2:134845361 | G | A | 17 | a0001c0001t0001g0293 a0001c0001t0001g0322 a0001c0001t0001g0323 others(14): Show |
17 | HG00639.hp2 HG00735.hp2 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.102+84G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134845361 | |||||||
| chr2:134845509 | G | GTC | 40 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0025 others(37): Show |
43 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.102+277_102+278dup others(2): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134845509 | ||||||
| chr2:134845509 | G | GTCTC | 20 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0041 others(17): Show |
22 | HG00609.hp2 HG01361.hp1 HG01517.hp1 others(19): Show |
intron_variant | MODIFIER | c.102+275_102+278dup others(4): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134845509 | ||||||
| chr2:134845509 | G | GTCTCTC | 19 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0034 others(16): Show |
20 | HG01070.hp1 HG01257.hp2 HG01515.hp2 others(17): Show |
intron_variant | MODIFIER | c.102+273_102+278dup others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134845509 | ||||||
| chr2:134845509 | G | GTCTCTCT others(1): Show |
16 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0001g0035 others(13): Show |
16 | HG00140.hp2 HG01192.hp1 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.102+271_102+278dup others(8): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134845509 | ||||||
| chr2:134845509 | G | GTCTCTCT others(3): Show |
14 | a0001c0001t0001g0009 a0001c0001t0001g0030 a0001c0001t0001g0037 others(11): Show |
15 | HG01081.hp2 HG01192.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.102+269_102+278dup others(10): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134845509 | ||||||
| chr2:134845509 | G | GTCTCTCT others(5): Show |
7 | a0001c0001t0001g0044 a0001c0001t0001g0063 a0001c0001t0001g0064 others(4): Show |
7 | HG00639.hp1 HG01243.hp2 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.102+267_102+278dup others(12): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134845509 | ||||||
| chr2:134845509 | G | GTCTCTCT others(7): Show |
8 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(5): Show |
8 | HG00642.hp1 HG00673.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.102+265_102+278dup others(14): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134845509 | ||||||
| chr2:134845509 | G | GTCTCTCT others(9): Show |
2 | a0001c0001t0001g0055 a0001c0001t0001g0069 |
2 | HG00738.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.102+263_102+278dup others(16): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134845509 | ||||||
| chr2:134845509 | G | GTCTCTCT others(11): Show |
1 | a0001c0001t0001g0089 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.102+261_102+278dup others(18): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134845509 | ||||||
| chr2:134845509 | GTC | G | 50 | a0001c0001t0001g0017 a0001c0001t0001g0024 a0001c0001t0001g0027 others(47): Show |
51 | HG00558.hp1 HG00597.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.102+277_102+278del others(2): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134845509 | ||||||
| chr2:134845509 | GTCTC | G | 58 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(55): Show |
68 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.102+275_102+278del others(4): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134845509 | ||||||
| chr2:134845509 | GTCTCTC | G | 47 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0011 others(44): Show |
52 | HG00408.hp2 HG00741.hp2 HG01074.hp2 others(49): Show |
intron_variant | MODIFIER | c.102+273_102+278del others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134845509 | ||||||
| chr2:134845509 | GTCTCTCT others(1): Show |
G | 10 | a0001c0001t0001g0082 a0001c0001t0001g0097 a0001c0001t0001g0098 others(7): Show |
10 | HG02559.hp2 HG02717.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.102+271_102+278del others(8): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134845509 | ||||||
| chr2:134845509 | GTCTCTCT others(3): Show |
G | 1 | a0001c0001t0001g0149 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.102+269_102+278del others(10): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134845509 | ||||||
| chr2:134845509 | GTCTCTCT others(5): Show |
G | 3 | a0001c0001t0001g0040 a0001c0001t0001g0148 a0001c0001t0001g0152 |
3 | HG03041.hp2 HG03831.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.102+267_102+278del others(12): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134845509 | ||||||
| chr2:134845509 | GTCTCTCT others(7): Show |
G | 1 | a0001c0001t0001g0010 | 2 | HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.102+265_102+278del others(14): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134845509 | ||||||
| chr2:134845554 | T | C | 4 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(1): Show |
4 | HG01978.hp2 NA18961.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.102+277T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134845554 | |||||||
| chr2:134845555 | C | CTCTCTCT others(2): Show |
3 | a0001c0001t0001g0001 a0001c0001t0001g0059 a0001c0001t0001g0158 |
3 | HG01123.hp2 HG01175.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.102+278_102+279ins others(9): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134845555 | |||||||
| chr2:134845555 | C | CTCTCTCT others(10): Show |
1 | a0001c0001t0001g0162 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.102+278_102+279ins others(17): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134845555 | |||||||
| chr2:134845640 | A | G | 1 | a0001c0001t0001g0241 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.102+363A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134845640 | |||||||
| chr2:134845728 | A | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0148 a0001c0001t0001g0149 |
4 | HG02965.hp1 HG02965.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+451A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134845728 | |||||||
| chr2:134845854 | T | G | 1 | a0001c0001t0001g0158 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.102+577T>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134845854 | |||||||
| chr2:134846120 | A | G | 295 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(292): Show |
311 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(308): Show |
intron_variant | MODIFIER | c.102+843A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134846120 | |||||||
| chr2:134846227 | T | C | 77 | a0001c0001t0001g0009 a0001c0001t0001g0030 a0001c0001t0001g0031 others(74): Show |
78 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.102+950T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134846227 | |||||||
| chr2:134846389 | C | T | 295 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(292): Show |
311 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(308): Show |
intron_variant | MODIFIER | c.102+1112C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134846389 | |||||||
| chr2:134846613 | T | C | 221 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(218): Show |
236 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(233): Show |
intron_variant | MODIFIER | c.102+1336T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134846613 | |||||||
| chr2:134846820 | G | A | 1 | a0001c0001t0001g0010 | 2 | HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.102+1543G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134846820 | |||||||
| chr2:134846847 | A | C | 1 | a0001c0001t0001g0269 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.102+1570A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134846847 | |||||||
| chr2:134846911 | G | C | 1 | a0001c0001t0001g0025 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.102+1634G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134846911 | |||||||
| chr2:134846919 | C | A | 1 | a0001c0001t0001g0025 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.102+1642C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134846919 | |||||||
| chr2:134846922 | G | A | 17 | a0001c0001t0001g0002 a0001c0001t0001g0028 a0001c0001t0001g0174 others(14): Show |
20 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.102+1645G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134846922 | |||||||
| chr2:134847169 | G | A | 38 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(35): Show |
43 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.102+1892G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134847169 | |||||||
| chr2:134847264 | G | C | 1 | a0001c0001t0001g0174 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.102+1987G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134847264 | |||||||
| chr2:134847290 | C | A | 5 | a0001c0001t0001g0011 a0001c0001t0001g0169 a0001c0004t0001g0170 others(2): Show |
6 | HG02109.hp1 HG02257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+2013C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134847290 | |||||||
| chr2:134847331 | T | C | 3 | a0001c0001t0001g0095 a0001c0001t0001g0109 a0001c0001t0001g0133 |
3 | HG02015.hp1 HG02074.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.102+2054T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134847331 | |||||||
| chr2:134847393 | GATACAGA others(9): Show |
G | 1 | a0001c0001t0001g0248 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.102+2118_102+2133d others(18): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134847393 | ||||||
| chr2:134847395 | T | TATAG | 14 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(11): Show |
14 | HG00735.hp2 HG01256.hp2 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.102+2119_102+2120i others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134847395 | ||||||
| chr2:134847395 | TACAG | T | 63 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(60): Show |
65 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.102+2120_102+2123d others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134847395 | ||||||
| chr2:134847395 | TACAGATA others(1): Show |
T | 90 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0011 others(87): Show |
92 | HG00408.hp2 HG00438.hp2 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.102+2120_102+2127d others(10): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134847395 | ||||||
| chr2:134847395 | TACAGATA others(5): Show |
T | 78 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(75): Show |
81 | HG00639.hp1 HG00642.hp2 HG00738.hp2 others(78): Show |
intron_variant | MODIFIER | c.102+2120_102+2131d others(14): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134847395 | ||||||
| chr2:134847395 | TACAGATA others(9): Show |
T | 15 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0039 others(12): Show |
15 | HG00741.hp1 HG01175.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.102+2120_102+2135d others(18): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134847395 | ||||||
| chr2:134847397 | C | CAGAT | 18 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0017 others(15): Show |
19 | HG01099.hp1 HG01169.hp1 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.102+2170_102+2173d others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134847397 | ||||||
| chr2:134847397 | C | CAGATAGA others(1): Show |
20 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0018 others(17): Show |
21 | HG01123.hp1 HG01175.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.102+2166_102+2173d others(10): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134847397 | ||||||
| chr2:134847397 | C | CAGATAGA others(5): Show |
4 | a0001c0001t0001g0276 a0001c0001t0001g0292 a0001c0001t0001g0309 others(1): Show |
4 | HG00438.hp1 HG02922.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+2162_102+2173d others(14): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134847397 | ||||||
| chr2:134847397 | C | CAGATAGA others(9): Show |
6 | a0001c0001t0001g0004 a0001c0001t0001g0281 a0001c0001t0001g0284 others(3): Show |
6 | HG03098.hp2 HG03453.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+2158_102+2173d others(18): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134847397 | ||||||
| chr2:134847397 | C | T | 48 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(45): Show |
51 | HG00544.hp1 HG00544.hp2 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.102+2120C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134847397 | |||||||
| chr2:134847397 | CAGAT | C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0289 others(1): Show |
4 | HG00140.hp1 HG02155.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+2170_102+2173d others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134847397 | ||||||
| chr2:134847443 | G | GATAGATA others(11): Show |
1 | a0001c0001t0001g0041 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.102+2173_102+2174i others(20): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134847443 | ||||||
| chr2:134847444 | A | G | 77 | a0001c0001t0001g0009 a0001c0001t0001g0030 a0001c0001t0001g0031 others(74): Show |
78 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.102+2167A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134847444 | |||||||
| chr2:134847449 | T | C | 2 | a0001c0001t0001g0030 a0001c0001t0001g0040 |
2 | HG01261.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.102+2172T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134847449 | |||||||
| chr2:134847451 | T | G | 52 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0041 others(49): Show |
53 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.102+2174T>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134847451 | |||||||
| chr2:134847558 | C | T | 2 | a0001c0001t0001g0105 a0001c0001t0001g0108 |
2 | HG02602.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.102+2281C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134847558 | |||||||
| chr2:134847601 | C | T | 3 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0135 |
3 | HG02109.hp2 HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.102+2324C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134847601 | |||||||
| chr2:134847646 | T | C | 1 | a0001c0001t0001g0025 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.102+2369T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134847646 | |||||||
| chr2:134847707 | G | T | 1 | a0001c0001t0001g0022 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.102+2430G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134847707 | |||||||
| chr2:134847850 | T | C | 5 | a0001c0001t0001g0011 a0001c0001t0001g0169 a0001c0004t0001g0170 others(2): Show |
6 | HG02109.hp1 HG02257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+2573T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134847850 | |||||||
| chr2:134847855 | C | CT | 48 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0234 others(45): Show |
49 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.102+2591dupT | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134847855 | ||||||
| chr2:134847855 | CT | C | 238 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(235): Show |
253 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(250): Show |
intron_variant | MODIFIER | c.102+2591delT | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134847855 | ||||||
| chr2:134847856 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0230 |
2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.102+2579T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134847856 | |||||||
| chr2:134847914 | C | T | 1 | a0001c0001t0001g0025 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.102+2637C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134847914 | |||||||
| chr2:134848130 | C | T | 1 | a0001c0001t0001g0175 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.102+2853C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134848130 | |||||||
| chr2:134848249 | T | C | 12 | a0001c0001t0001g0293 a0001c0001t0001g0328 a0001c0001t0001g0329 others(9): Show |
12 | HG00735.hp2 HG01358.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.102+2972T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134848249 | |||||||
| chr2:134848418 | T | C | 7 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0229 others(4): Show |
7 | HG02145.hp2 HG02809.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.102+3141T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134848418 | |||||||
| chr2:134848604 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.102+3327C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134848604 | |||||||
| chr2:134848635 | T | C | 2 | a0001c0001t0001g0225 a0001c0001t0001g0229 |
2 | HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.102+3358T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134848635 | |||||||
| chr2:134849027 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.102+3750G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134849027 | |||||||
| chr2:134849056 | C | T | 10 | a0001c0001t0001g0144 a0001c0001t0001g0150 a0001c0001t0001g0203 others(7): Show |
10 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(7): Show |
intron_variant | MODIFIER | c.102+3779C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134849056 | |||||||
| chr2:134849228 | C | T | 14 | a0001c0001t0001g0248 a0001c0001t0001g0254 a0001c0001t0001g0257 others(11): Show |
15 | NA18951.hp1 NA18952.hp1 NA18962.hp2 others(12): Show |
intron_variant | MODIFIER | c.102+3951C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134849228 | |||||||
| chr2:134849272 | C | CTTAT | 290 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(287): Show |
306 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(303): Show |
intron_variant | MODIFIER | c.102+3998_102+4001d others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134849272 | ||||||
| chr2:134849309 | T | C | 221 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(218): Show |
236 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(233): Show |
intron_variant | MODIFIER | c.102+4032T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134849309 | |||||||
| chr2:134849330 | T | A | 1 | a0001c0001t0001g0291 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.102+4053T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134849330 | |||||||
| chr2:134849525 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.102+4248C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134849525 | |||||||
| chr2:134849689 | G | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0230 |
2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.102+4412G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134849689 | |||||||
| chr2:134849703 | C | T | 2 | a0001c0001t0001g0047 a0001c0001t0001g0151 |
2 | HG01074.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.102+4426C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134849703 | |||||||
| chr2:134849763 | G | A | 291 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(288): Show |
307 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(304): Show |
intron_variant | MODIFIER | c.102+4486G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134849763 | |||||||
| chr2:134849773 | G | A | 1 | a0001c0001t0001g0193 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.102+4496G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134849773 | |||||||
| chr2:134849882 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.102+4605G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134849882 | |||||||
| chr2:134849902 | T | C | 1 | a0001c0001t0001g0301 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.102+4625T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134849902 | |||||||
| chr2:134849963 | A | AAC | 39 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(36): Show |
40 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.102+4721_102+4722d others(4): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134849963 | ||||||
| chr2:134849963 | A | AACAC | 4 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0071 others(1): Show |
4 | HG02602.hp2 NA19005.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.102+4719_102+4722d others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134849963 | ||||||
| chr2:134849963 | AAC | A | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(123): Show |
139 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.102+4721_102+4722d others(4): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134849963 | ||||||
| chr2:134849963 | AACAC | A | 86 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0030 others(83): Show |
88 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.102+4719_102+4722d others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134849963 | ||||||
| chr2:134849963 | AACACAC | A | 46 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(43): Show |
47 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.102+4717_102+4722d others(8): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134849963 | ||||||
| chr2:134849963 | AACACACA others(1): Show |
A | 3 | a0001c0001t0001g0025 a0001c0001t0001g0258 a0001c0001t0001g0316 |
3 | HG02027.hp1 NA18962.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.102+4715_102+4722d others(10): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134849963 | ||||||
| chr2:134849963 | AACACACA others(3): Show |
A | 18 | a0001c0001t0001g0293 a0001c0001t0001g0322 a0001c0001t0001g0323 others(15): Show |
18 | HG00639.hp2 HG00735.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.102+4713_102+4722d others(12): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134849963 | ||||||
| chr2:134850102 | T | G | 1 | a0001c0001t0001g0048 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.102+4825T>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134850102 | |||||||
| chr2:134850205 | C | G | 30 | a0001c0001t0001g0030 a0001c0001t0001g0034 a0001c0001t0001g0037 others(27): Show |
30 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.102+4928C>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134850205 | |||||||
| chr2:134850206 | T | A | 1 | a0001c0001t0001g0044 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.102+4929T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134850206 | |||||||
| chr2:134850269 | C | CT | 9 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0229 others(6): Show |
9 | HG02145.hp2 HG02630.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.102+5006dupT | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134850269 | ||||||
| chr2:134850282 | TTC | T | 8 | a0001c0001t0001g0010 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
9 | HG01168.hp2 HG01169.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.102+5007_102+5008d others(4): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134850282 | ||||||
| chr2:134850283 | TC | T | 201 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(198): Show |
214 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(211): Show |
intron_variant | MODIFIER | c.102+5007delC | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134850283 | |||||||
| chr2:134850284 | C | T | 82 | a0001c0001t0001g0011 a0001c0001t0001g0024 a0001c0001t0001g0025 others(79): Show |
84 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.102+5007C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134850284 | |||||||
| chr2:134850287 | A | G | 1 | a0001c0001t0001g0187 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.102+5010A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134850287 | |||||||
| chr2:134850299 | G | A | 2 | a0001c0001t0001g0119 a0001c0001t0001g0131 |
2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.102+5022G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134850299 | |||||||
| chr2:134850371 | C | T | 1 | a0001c0001t0001g0348 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.102+5094C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134850371 | |||||||
| chr2:134850618 | A | G | 1 | a0001c0001t0001g0284 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.102+5341A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134850618 | |||||||
| chr2:134850631 | A | T | 1 | a0001c0001t0001g0044 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.102+5354A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134850631 | |||||||
| chr2:134850641 | A | G | 221 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(218): Show |
236 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(233): Show |
intron_variant | MODIFIER | c.102+5364A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134850641 | |||||||
| chr2:134850658 | T | TTTA | 221 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(218): Show |
236 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(233): Show |
intron_variant | MODIFIER | c.102+5395_102+5397d others(5): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134850658 | ||||||
| chr2:134850807 | A | G | 68 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0027 others(65): Show |
69 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.102+5530A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134850807 | |||||||
| chr2:134850916 | A | G | 2 | a0001c0001t0001g0023 a0001c0001t0001g0230 |
2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.102+5639A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134850916 | |||||||
| chr2:134850965 | T | C | 3 | a0001c0001t0001g0038 a0001c0001t0001g0056 a0001c0001t0001g0057 |
3 | NA18985.hp1 NA18991.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.102+5688T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134850965 | |||||||
| chr2:134850973 | A | C | 3 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0135 |
3 | HG02109.hp2 HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.102+5696A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134850973 | |||||||
| chr2:134851209 | C | T | 2 | a0001c0001t0001g0062 a0001c0001t0001g0064 |
2 | HG00639.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.102+5932C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134851209 | |||||||
| chr2:134851231 | A | T | 221 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(218): Show |
236 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(233): Show |
intron_variant | MODIFIER | c.102+5954A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134851231 | |||||||
| chr2:134851283 | G | A | 1 | a0001c0001t0001g0285 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.102+6006G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134851283 | |||||||
| chr2:134851325 | C | G | 2 | a0001c0001t0001g0344 a0001c0001t0001g0345 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.102+6048C>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134851325 | |||||||
| chr2:134851346 | G | T | 4 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 others(1): Show |
4 | HG00639.hp2 HG03710.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+6069G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134851346 | |||||||
| chr2:134851434 | G | A | 1 | a0001c0001t0001g0175 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.102+6157G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134851434 | |||||||
| chr2:134851459 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0230 |
2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.102+6182T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134851459 | |||||||
| chr2:134851460 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.102+6183T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134851460 | |||||||
| chr2:134851539 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.102+6262T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134851539 | |||||||
| chr2:134851597 | C | T | 221 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(218): Show |
236 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(233): Show |
intron_variant | MODIFIER | c.102+6320C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134851597 | |||||||
| chr2:134851633 | G | A | 5 | a0001c0001t0001g0011 a0001c0001t0001g0169 a0001c0004t0001g0170 others(2): Show |
6 | HG02109.hp1 HG02257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+6356G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134851633 | |||||||
| chr2:134851677 | G | A | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(172): Show |
184 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(181): Show |
intron_variant | MODIFIER | c.102+6400G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134851677 | |||||||
| chr2:134851688 | C | A | 1 | a0001c0001t0001g0022 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.102+6411C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134851688 | |||||||
| chr2:134852084 | G | T | 3 | a0002c0002t0001g0197 a0002c0002t0001g0201 a0002c0002t0001g0202 |
3 | HG02145.hp2 HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.102+6807G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134852084 | |||||||
| chr2:134852125 | G | T | 221 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(218): Show |
236 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(233): Show |
intron_variant | MODIFIER | c.102+6848G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134852125 | |||||||
| chr2:134852176 | G | A | 291 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(288): Show |
307 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(304): Show |
intron_variant | MODIFIER | c.102+6899G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134852176 | |||||||
| chr2:134852208 | T | C | 1 | a0001c0001t0001g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.102+6931T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134852208 | |||||||
| chr2:134852226 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.102+6949G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134852226 | |||||||
| chr2:134852342 | G | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0148 a0001c0001t0001g0149 |
4 | HG02965.hp1 HG02965.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-6919G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134852342 | |||||||
| chr2:134852436 | C | T | 1 | a0001c0001t0001g0286 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.103-6825C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134852436 | |||||||
| chr2:134852437 | G | A | 51 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0028 others(48): Show |
56 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.103-6824G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134852437 | |||||||
| chr2:134852458 | G | T | 1 | a0001c0001t0001g0025 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.103-6803G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134852458 | |||||||
| chr2:134852536 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.103-6725C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134852536 | |||||||
| chr2:134852584 | A | G | 295 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(292): Show |
311 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(308): Show |
intron_variant | MODIFIER | c.103-6677A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134852584 | |||||||
| chr2:134852632 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.103-6629G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134852632 | |||||||
| chr2:134852662 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.103-6599G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134852662 | |||||||
| chr2:134852793 | G | A | 2 | a0004c0005t0001g0146 a0004c0005t0001g0222 |
2 | NA18952.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.103-6468G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134852793 | |||||||
| chr2:134852868 | T | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0148 a0001c0001t0001g0149 |
4 | HG02965.hp1 HG02965.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-6393T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134852868 | |||||||
| chr2:134852874 | T | C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0141 |
3 | NA18957.hp2 NA19062.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.103-6387T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134852874 | |||||||
| chr2:134852992 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0230 |
2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.103-6269G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134852992 | |||||||
| chr2:134852995 | T | C | 1 | a0001c0001t0001g0022 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.103-6266T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134852995 | |||||||
| chr2:134853047 | C | T | 2 | a0001c0001t0001g0119 a0001c0001t0001g0131 |
2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.103-6214C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134853047 | |||||||
| chr2:134853112 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.103-6149G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134853112 | |||||||
| chr2:134853167 | T | TA | 173 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(170): Show |
183 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(180): Show |
intron_variant | MODIFIER | c.103-6075dupA | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134853167 | ||||||
| chr2:134853167 | T | TAA | 11 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0086 others(8): Show |
11 | HG02145.hp2 HG02572.hp2 HG02735.hp1 others(8): Show |
intron_variant | MODIFIER | c.103-6076_103-6075d others(4): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134853167 | ||||||
| chr2:134853167 | TA | T | 9 | a0001c0001t0001g0005 a0001c0001t0001g0248 a0001c0001t0001g0254 others(6): Show |
11 | HG01515.hp2 HG02647.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.103-6075delA | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134853167 | ||||||
| chr2:134853167 | TAAAAAAA others(1): Show |
T | 38 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(35): Show |
43 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.103-6082_103-6075d others(10): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134853167 | ||||||
| chr2:134853169 | A | C | 1 | a0001c0001t0001g0276 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.103-6092A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134853169 | |||||||
| chr2:134853311 | T | C | 49 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0234 others(46): Show |
50 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.103-5950T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134853311 | |||||||
| chr2:134853428 | A | G | 1 | a0001c0001t0001g0044 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.103-5833A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134853428 | |||||||
| chr2:134853478 | G | A | 4 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 others(1): Show |
4 | HG00639.hp2 HG03710.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-5783G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134853478 | |||||||
| chr2:134853550 | G | A | 5 | a0001c0001t0001g0011 a0001c0001t0001g0169 a0001c0004t0001g0170 others(2): Show |
6 | HG02109.hp1 HG02257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.103-5711G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134853550 | |||||||
| chr2:134853559 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.103-5702T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134853559 | |||||||
| chr2:134853701 | T | C | 1 | a0001c0001t0001g0322 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.103-5560T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134853701 | |||||||
| chr2:134853736 | T | G | 1 | a0001c0001t0001g0246 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.103-5525T>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134853736 | |||||||
| chr2:134853740 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0230 |
2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.103-5521C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134853740 | |||||||
| chr2:134853751 | G | T | 1 | a0001c0009t0001g0211 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.103-5510G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134853751 | |||||||
| chr2:134853927 | G | A | 1 | a0001c0001t0001g0311 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.103-5334G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134853927 | |||||||
| chr2:134854387 | T | A | 1 | a0001c0001t0001g0213 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.103-4874T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134854387 | |||||||
| chr2:134854740 | C | T | 1 | a0001c0001t0001g0046 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.103-4521C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134854740 | |||||||
| chr2:134854811 | AT | A | 88 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(85): Show |
95 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.103-4446delT | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134854811 | ||||||
| chr2:134854819 | G | GCCTC | 88 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(85): Show |
95 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.103-4442_103-4441i others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134854819 | |||||||
| chr2:134854852 | C | T | 167 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(164): Show |
175 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(172): Show |
intron_variant | MODIFIER | c.103-4409C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134854852 | |||||||
| chr2:134854869 | G | C | 221 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(218): Show |
236 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(233): Show |
intron_variant | MODIFIER | c.103-4392G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134854869 | |||||||
| chr2:134854878 | C | G | 295 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(292): Show |
311 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(308): Show |
intron_variant | MODIFIER | c.103-4383C>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134854878 | |||||||
| chr2:134855014 | T | G | 1 | a0001c0001t0001g0044 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.103-4247T>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134855014 | |||||||
| chr2:134855039 | C | CT | 216 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(213): Show |
231 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(228): Show |
intron_variant | MODIFIER | c.103-4212dupT | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134855039 | ||||||
| chr2:134855149 | G | C | 1 | a0001c0001t0001g0096 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.103-4112G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134855149 | |||||||
| chr2:134855187 | G | A | 49 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0234 others(46): Show |
50 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.103-4074G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134855187 | |||||||
| chr2:134855347 | T | C | 51 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0011 others(48): Show |
57 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.103-3914T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134855347 | |||||||
| chr2:134855812 | T | C | 1 | a0001c0001t0001g0242 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.103-3449T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134855812 | |||||||
| chr2:134855982 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0176 a0001c0001t0001g0195 |
4 | HG00741.hp2 HG01256.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.103-3279G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134855982 | |||||||
| chr2:134856005 | C | T | 6 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0092 others(3): Show |
6 | HG01978.hp2 NA18940.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.103-3256C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134856005 | |||||||
| chr2:134856113 | A | T | 5 | a0001c0001t0001g0224 a0002c0002t0001g0026 a0002c0002t0001g0197 others(2): Show |
5 | HG02145.hp2 HG03130.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.103-3148A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134856113 | |||||||
| chr2:134856364 | C | T | 1 | a0001c0001t0001g0311 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.103-2897C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134856364 | |||||||
| chr2:134856432 | G | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0148 a0001c0001t0001g0149 |
4 | HG02965.hp1 HG02965.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-2829G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134856432 | |||||||
| chr2:134856659 | CCT | C | 4 | a0001c0001t0001g0152 a0001c0001t0001g0155 a0001c0001t0001g0156 others(1): Show |
4 | HG02698.hp2 HG03490.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.103-2601_103-2600d others(4): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134856659 | |||||||
| chr2:134856905 | G | GT | 220 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(217): Show |
235 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(232): Show |
intron_variant | MODIFIER | c.103-2347dupT | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134856905 | ||||||
| chr2:134857097 | C | G | 1 | a0001c0001t0001g0347 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.103-2164C>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134857097 | |||||||
| chr2:134857269 | C | A | 221 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(218): Show |
236 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(233): Show |
intron_variant | MODIFIER | c.103-1992C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134857269 | |||||||
| chr2:134857295 | G | A | 1 | a0001c0001t0001g0286 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.103-1966G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134857295 | |||||||
| chr2:134857306 | C | T | 221 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(218): Show |
236 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(233): Show |
intron_variant | MODIFIER | c.103-1955C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134857306 | |||||||
| chr2:134857387 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0148 a0001c0001t0001g0149 |
4 | HG02965.hp1 HG02965.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-1874G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134857387 | |||||||
| chr2:134857864 | T | C | 1 | a0001c0001t0001g0221 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.103-1397T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134857864 | |||||||
| chr2:134857941 | A | C | 1 | a0001c0001t0001g0204 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.103-1320A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134857941 | |||||||
| chr2:134858072 | T | C | 7 | a0001c0001t0001g0005 a0001c0001t0001g0287 a0001c0001t0001g0288 others(4): Show |
9 | HG02257.hp1 HG02647.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.103-1189T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134858072 | |||||||
| chr2:134858085 | G | A | 2 | a0001c0001t0001g0119 a0001c0001t0001g0131 |
2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.103-1176G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134858085 | |||||||
| chr2:134858126 | A | T | 1 | a0001c0001t0001g0182 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.103-1135A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134858126 | |||||||
| chr2:134858322 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0230 |
2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.103-939T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134858322 | |||||||
| chr2:134858363 | G | A | 7 | a0001c0001t0001g0106 a0001c0001t0001g0117 a0001c0001t0001g0128 others(4): Show |
7 | HG00558.hp1 HG00609.hp1 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.103-898G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134858363 | |||||||
| chr2:134858474 | T | C | 1 | a0002c0002t0001g0026 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.103-787T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134858474 | |||||||
| chr2:134858614 | T | C | 1 | a0001c0001t0001g0347 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.103-647T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134858614 | |||||||
| chr2:134858630 | T | C | 76 | a0001c0001t0001g0009 a0001c0001t0001g0030 a0001c0001t0001g0031 others(73): Show |
77 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.103-631T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134858630 | |||||||
| chr2:134858643 | T | C | 1 | a0001c0001t0001g0286 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.103-618T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134858643 | |||||||
| chr2:134858776 | A | G | 291 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(288): Show |
307 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(304): Show |
intron_variant | MODIFIER | c.103-485A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134858776 | |||||||
| chr2:134858815 | C | T | 295 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(292): Show |
311 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(308): Show |
intron_variant | MODIFIER | c.103-446C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134858815 | |||||||
| chr2:134859046 | T | C | 2 | a0001c0001t0001g0207 a0001c0009t0001g0211 |
2 | HG02735.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.103-215T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134859046 | |||||||
| chr2:134859051 | G | A | 291 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(288): Show |
307 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(304): Show |
intron_variant | MODIFIER | c.103-210G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134859051 | |||||||
| chr2:134859065 | C | G | 91 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(88): Show |
98 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.103-196C>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134859065 | |||||||
| chr2:134859443 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.199+86T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | chr2 | 134859443 | |||||||
| chr2:134859563 | C | T | 19 | a0001c0001t0001g0025 a0001c0001t0001g0293 a0001c0001t0001g0322 others(16): Show |
19 | HG00639.hp2 HG00735.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.199+206C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | chr2 | 134859563 | |||||||
| chr2:134859586 | T | C | 4 | a0001c0001t0001g0102 a0001c0001t0001g0114 a0001c0001t0001g0132 others(1): Show |
4 | HG01175.hp2 HG02258.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.199+229T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | chr2 | 134859586 | |||||||
| chr2:134859623 | T | TAAAAATT others(317): Show |
1 | a0001c0001t0001g0345 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.199+279_199+280ins others(324): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 134859623 | ||||||
| chr2:134859623 | T | TAAAAATT others(318): Show |
1 | a0001c0001t0001g0344 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.199+279_199+280ins others(325): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 134859623 | ||||||
| chr2:134860194 | C | T | 3 | a0001c0001t0001g0257 a0003c0003t0001g0021 a0003c0003t0001g0268 |
4 | NA18952.hp1 NA18962.hp2 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.199+837C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | chr2 | 134860194 | |||||||
| chr2:134860212 | G | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0090 a0001c0001t0001g0118 |
5 | HG01099.hp2 HG01361.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.199+855G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | chr2 | 134860212 | |||||||
| chr2:134860234 | G | C | 49 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0234 others(46): Show |
50 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.199+877G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | chr2 | 134860234 | |||||||
| chr2:134860265 | A | G | 46 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0011 others(43): Show |
52 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.199+908A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | chr2 | 134860265 | |||||||
| chr2:134860368 | A | G | 1 | a0001c0001t0001g0029 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.199+1011A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | chr2 | 134860368 | |||||||
| chr2:134860450 | A | G | 3 | a0001c0001t0001g0249 a0001c0001t0001g0253 a0001c0001t0001g0267 |
3 | HG01255.hp2 HG01346.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.199+1093A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | chr2 | 134860450 | |||||||
| chr2:134860637 | G | C | 1 | a0001c0001t0001g0099 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.199+1280G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | chr2 | 134860637 | |||||||
| chr2:134860671 | G | T | 1 | a0001c0001t0001g0154 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.200-1298G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | chr2 | 134860671 | |||||||
| chr2:134860749 | G | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0230 |
2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.200-1220G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | chr2 | 134860749 | |||||||
| chr2:134860856 | C | CA | 16 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0169 others(13): Show |
17 | HG01169.hp1 HG01261.hp1 HG02071.hp1 others(14): Show |
intron_variant | MODIFIER | c.200-1089dupA | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 134860856 | ||||||
| chr2:134860856 | C | CAAA | 32 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0014 others(29): Show |
36 | HG00408.hp1 HG00544.hp1 HG01952.hp2 others(33): Show |
intron_variant | MODIFIER | c.200-1091_200-1089d others(5): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 134860856 | ||||||
| chr2:134860856 | C | CAAAA | 19 | a0001c0001t0001g0008 a0001c0001t0001g0029 a0001c0001t0001g0045 others(16): Show |
20 | HG00609.hp2 HG01175.hp2 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.200-1092_200-1089d others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 134860856 | ||||||
| chr2:134860856 | C | CAAAAA | 43 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(40): Show |
49 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.200-1093_200-1089d others(7): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 134860856 | ||||||
| chr2:134860856 | C | CAAAAAA | 35 | a0001c0001t0001g0025 a0001c0001t0001g0056 a0001c0001t0001g0103 others(32): Show |
36 | HG01243.hp1 HG01255.hp2 HG02027.hp1 others(33): Show |
intron_variant | MODIFIER | c.200-1094_200-1089d others(8): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 134860856 | ||||||
| chr2:134860856 | C | CAAAAAAA | 36 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0027 others(33): Show |
38 | HG00597.hp2 HG00642.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.200-1095_200-1089d others(9): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 134860856 | ||||||
| chr2:134860856 | C | CAAAAAAA others(1): Show |
15 | a0001c0001t0001g0024 a0001c0001t0001g0091 a0001c0001t0001g0092 others(12): Show |
15 | HG00408.hp2 HG00438.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.200-1096_200-1089d others(10): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 134860856 | ||||||
| chr2:134860856 | CA | C | 9 | a0001c0001t0001g0306 a0001c0001t0001g0309 a0001c0001t0001g0313 others(6): Show |
9 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.200-1089delA | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 134860856 | ||||||
| chr2:134860856 | CAAAAAA | C | 78 | a0001c0001t0001g0009 a0001c0001t0001g0030 a0001c0001t0001g0031 others(75): Show |
79 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.200-1094_200-1089d others(8): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 134860856 | ||||||
| chr2:134860965 | G | A | 2 | a0001c0001t0001g0225 a0001c0001t0001g0229 |
2 | HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.200-1004G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | chr2 | 134860965 | |||||||
| chr2:134861412 | T | C | 291 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(288): Show |
307 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(304): Show |
intron_variant | MODIFIER | c.200-557T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | chr2 | 134861412 | |||||||
| chr2:134861445 | A | G | 1 | a0001c0001t0001g0182 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.200-524A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | chr2 | 134861445 | |||||||
| chr2:134861446 | G | A | 1 | a0001c0001t0001g0182 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.200-523G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | chr2 | 134861446 | |||||||
| chr2:134861787 | T | TA | 76 | a0001c0001t0001g0009 a0001c0001t0001g0030 a0001c0001t0001g0031 others(73): Show |
77 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.200-181dupA | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 134861787 | ||||||
| chr2:134861817 | A | AG | 17 | a0001c0001t0001g0293 a0001c0001t0001g0322 a0001c0001t0001g0323 others(14): Show |
17 | HG00639.hp2 HG00735.hp2 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.200-146dupG | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 134861817 | ||||||
| chr2:134861829 | G | A | 1 | a0001c0001t0001g0339 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.200-140G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | chr2 | 134861829 | |||||||
| chr2:134861915 | A | C | 3 | a0002c0002t0001g0197 a0002c0002t0001g0201 a0002c0002t0001g0202 |
3 | HG02145.hp2 HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.200-54A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | chr2 | 134861915 | |||||||
| chr2:134861930 | C | A | 6 | a0001c0001t0001g0012 a0001c0001t0001g0070 a0001c0001t0001g0176 others(3): Show |
7 | HG00741.hp2 HG01256.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.200-39C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | chr2 | 134861930 | |||||||
| chr2:134862075 | A | C | 2 | a0001c0001t0001g0225 a0001c0001t0001g0229 |
2 | HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.249+57A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 4/9 | chr2 | 134862075 | |||||||
| chr2:134862247 | T | C | 19 | a0001c0001t0001g0025 a0001c0001t0001g0293 a0001c0001t0001g0322 others(16): Show |
19 | HG00639.hp2 HG00735.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.249+229T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 4/9 | chr2 | 134862247 | |||||||
| chr2:134862311 | A | T | 1 | a0001c0001t0001g0182 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.249+293A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 4/9 | chr2 | 134862311 | |||||||
| chr2:134862541 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.249+523G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 4/9 | chr2 | 134862541 | |||||||
| chr2:134862585 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0230 |
2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.249+567G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 4/9 | chr2 | 134862585 | |||||||
| chr2:134862615 | G | C | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(141): Show |
152 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(149): Show |
intron_variant | MODIFIER | c.249+597G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 4/9 | chr2 | 134862615 | |||||||
| chr2:134862731 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.250-664C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 4/9 | chr2 | 134862731 | |||||||
| chr2:134862995 | T | C | 1 | a0001c0001t0001g0025 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.250-400T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 4/9 | chr2 | 134862995 | |||||||
| chr2:134863017 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.250-378T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 4/9 | chr2 | 134863017 | |||||||
| chr2:134863057 | A | AG | 90 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(87): Show |
97 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.250-332dupG | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 134863057 | ||||||
| chr2:134863064 | C | A | 1 | a0001c0001t0001g0182 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.250-331C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 4/9 | chr2 | 134863064 | |||||||
| chr2:134863809 | TC | T | 5 | a0001c0001t0001g0010 a0001c0001t0001g0148 a0001c0001t0001g0149 others(2): Show |
6 | HG02486.hp1 HG02965.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.486+180delC | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 134863809 | ||||||
| chr2:134863953 | G | A | 5 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0092 others(2): Show |
5 | HG01978.hp2 NA18940.hp2 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.486+322G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134863953 | |||||||
| chr2:134863986 | T | C | 292 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(289): Show |
308 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(305): Show |
intron_variant | MODIFIER | c.486+355T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134863986 | |||||||
| chr2:134864044 | G | C | 1 | a0001c0001t0001g0182 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.486+413G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134864044 | |||||||
| chr2:134864132 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.486+501G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134864132 | |||||||
| chr2:134864265 | T | A | 1 | a0001c0001t0001g0149 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.486+634T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134864265 | |||||||
| chr2:134864268 | C | CA | 75 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0027 others(72): Show |
76 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.486+652dupA | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 134864268 | ||||||
| chr2:134864333 | T | A | 1 | a0001c0001t0001g0045 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.486+702T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134864333 | |||||||
| chr2:134864348 | G | A | 1 | a0001c0001t0001g0046 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.486+717G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134864348 | |||||||
| chr2:134864372 | G | T | 3 | a0001c0001t0001g0085 a0001c0001t0001g0166 a0001c0001t0001g0167 |
3 | HG02572.hp2 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.486+741G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134864372 | |||||||
| chr2:134864475 | T | G | 2 | a0001c0001t0001g0288 a0001c0001t0001g0308 |
2 | HG02818.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.486+844T>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134864475 | |||||||
| chr2:134864586 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.486+955C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134864586 | |||||||
| chr2:134864624 | A | AT | 290 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(287): Show |
306 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(303): Show |
intron_variant | MODIFIER | c.486+998dupT | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 134864624 | ||||||
| chr2:134864953 | T | C | 40 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(37): Show |
45 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.486+1322T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134864953 | |||||||
| chr2:134865032 | C | A | 2 | a0001c0001t0001g0225 a0001c0001t0001g0229 |
2 | HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.486+1401C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134865032 | |||||||
| chr2:134865158 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.486+1527G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134865158 | |||||||
| chr2:134865238 | C | T | 218 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(215): Show |
233 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(230): Show |
intron_variant | MODIFIER | c.486+1607C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134865238 | |||||||
| chr2:134865290 | T | C | 167 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(164): Show |
175 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(172): Show |
intron_variant | MODIFIER | c.486+1659T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134865290 | |||||||
| chr2:134865330 | A | C | 4 | a0001c0001t0001g0018 a0001c0001t0001g0292 a0001c0001t0001g0301 others(1): Show |
5 | NA18966.hp1 NA18967.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.486+1699A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134865330 | |||||||
| chr2:134865354 | G | A | 2 | a0001c0001t0001g0224 a0002c0002t0001g0026 |
2 | HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.486+1723G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134865354 | |||||||
| chr2:134865541 | T | C | 1 | a0001c0001t0001g0348 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.486+1910T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134865541 | |||||||
| chr2:134865550 | A | G | 47 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0011 others(44): Show |
53 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.486+1919A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134865550 | |||||||
| chr2:134865814 | C | T | 1 | a0001c0001t0001g0073 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.487-1765C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134865814 | |||||||
| chr2:134865947 | C | T | 291 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(288): Show |
307 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(304): Show |
intron_variant | MODIFIER | c.487-1632C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134865947 | |||||||
| chr2:134866039 | T | C | 16 | a0001c0001t0001g0293 a0001c0001t0001g0322 a0001c0001t0001g0323 others(13): Show |
16 | HG00639.hp2 HG00735.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.487-1540T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134866039 | |||||||
| chr2:134866259 | C | A | 40 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(37): Show |
45 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.487-1320C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134866259 | |||||||
| chr2:134866438 | A | C | 291 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(288): Show |
307 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(304): Show |
intron_variant | MODIFIER | c.487-1141A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134866438 | |||||||
| chr2:134866507 | G | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0230 |
2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.487-1072G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134866507 | |||||||
| chr2:134866596 | T | C | 1 | a0001c0001t0001g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.487-983T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134866596 | |||||||
| chr2:134866797 | A | G | 1 | a0001c0001t0001g0192 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.487-782A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134866797 | |||||||
| chr2:134866991 | C | T | 2 | a0001c0001t0001g0076 a0001c0001t0001g0087 |
2 | HG01070.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.487-588C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134866991 | |||||||
| chr2:134867251 | G | C | 1 | a0002c0002t0001g0202 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.487-328G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134867251 | |||||||
| chr2:134867312 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.487-267T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134867312 | |||||||
| chr2:134867479 | C | T | 1 | a0001c0001t0001g0346 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.487-100C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134867479 | |||||||
| chr2:134867552 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0230 |
2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.487-27T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134867552 | |||||||
| chr2:134867709 | C | T | 1 | a0001c0001t0001g0286 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.580+37C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134867709 | |||||||
| chr2:134867803 | T | G | 1 | a0001c0001t0001g0332 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.580+131T>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134867803 | |||||||
| chr2:134867821 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.580+149G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134867821 | |||||||
| chr2:134867829 | C | CTA | 4 | a0001c0001t0001g0045 a0001c0001t0001g0225 a0001c0001t0001g0229 others(1): Show |
4 | HG02071.hp2 HG02809.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.580+172_580+173dup others(2): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 134867829 | ||||||
| chr2:134867838 | T | C | 5 | a0001c0001t0001g0011 a0001c0001t0001g0169 a0001c0004t0001g0170 others(2): Show |
6 | HG02109.hp1 HG02257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.580+166T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134867838 | |||||||
| chr2:134867848 | C | T | 5 | a0001c0001t0001g0011 a0001c0001t0001g0169 a0001c0004t0001g0170 others(2): Show |
6 | HG02109.hp1 HG02257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.580+176C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134867848 | |||||||
| chr2:134868102 | A | G | 53 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0234 others(50): Show |
54 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.580+430A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134868102 | |||||||
| chr2:134868257 | C | T | 2 | a0001c0001t0001g0062 a0001c0001t0001g0064 |
2 | HG00639.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.580+585C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134868257 | |||||||
| chr2:134868279 | G | A | 1 | a0005c0010t0001g0115 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.580+607G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134868279 | |||||||
| chr2:134868331 | T | C | 45 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0011 others(42): Show |
51 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.580+659T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134868331 | |||||||
| chr2:134868347 | T | TA | 6 | a0001c0001t0001g0060 a0001c0001t0001g0073 a0001c0001t0001g0074 others(3): Show |
6 | NA18959.hp1 NA18983.hp1 NA18988.hp1 others(3): Show |
intron_variant | MODIFIER | c.580+676dupA | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 134868347 | ||||||
| chr2:134868386 | A | T | 1 | a0001c0001t0001g0199 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.580+714A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134868386 | |||||||
| chr2:134868451 | C | CT | 215 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(212): Show |
230 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(227): Show |
intron_variant | MODIFIER | c.580+798dupT | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 134868451 | ||||||
| chr2:134868451 | C | CTT | 11 | a0001c0001t0001g0092 a0001c0001t0001g0110 a0001c0001t0001g0145 others(8): Show |
11 | HG01243.hp1 HG01978.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.580+797_580+798dup others(2): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 134868451 | ||||||
| chr2:134868456 | T | C | 1 | a0001c0001t0001g0325 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.580+784T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134868456 | |||||||
| chr2:134868805 | C | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0148 a0001c0001t0001g0149 others(1): Show |
5 | HG02486.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.580+1133C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134868805 | |||||||
| chr2:134868969 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.580+1297G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134868969 | |||||||
| chr2:134869019 | T | C | 1 | a0001c0001t0001g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.580+1347T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134869019 | |||||||
| chr2:134869041 | GC | G | 40 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(37): Show |
45 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.580+1370delC | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134869041 | |||||||
| chr2:134869205 | C | CATTT | 159 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(156): Show |
167 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(164): Show |
intron_variant | MODIFIER | c.580+1555_580+1558d others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 134869205 | ||||||
| chr2:134869205 | C | CATTTATT others(1): Show |
8 | a0001c0001t0001g0039 a0001c0001t0001g0060 a0001c0001t0001g0073 others(5): Show |
8 | HG03831.hp1 NA18959.hp1 NA18983.hp1 others(5): Show |
intron_variant | MODIFIER | c.580+1551_580+1558d others(10): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 134869205 | ||||||
| chr2:134869340 | G | A | 45 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0011 others(42): Show |
51 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.581-1625G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134869340 | |||||||
| chr2:134869358 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.581-1607G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134869358 | |||||||
| chr2:134869369 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.581-1596C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134869369 | |||||||
| chr2:134869443 | CCTCAAGT others(15): Show |
C | 1 | a0001c0001t0001g0094 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.581-1521_581-1500d others(24): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134869443 | |||||||
| chr2:134869548 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.581-1417G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134869548 | |||||||
| chr2:134869605 | G | T | 218 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(215): Show |
233 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(230): Show |
intron_variant | MODIFIER | c.581-1360G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134869605 | |||||||
| chr2:134869706 | G | GTA | 75 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(72): Show |
84 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.581-1239_581-1238d others(4): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 134869706 | ||||||
| chr2:134869706 | G | GTATA | 6 | a0001c0001t0001g0046 a0001c0001t0001g0143 a0001c0001t0001g0189 others(3): Show |
6 | HG02155.hp2 HG03195.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.581-1241_581-1238d others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 134869706 | ||||||
| chr2:134869706 | G | GTATATAT others(3): Show |
1 | a0001c0001t0001g0230 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.581-1247_581-1238d others(12): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 134869706 | ||||||
| chr2:134869826 | C | T | 1 | a0001c0001t0001g0025 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.581-1139C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134869826 | |||||||
| chr2:134869880 | G | A | 1 | a0001c0001t0001g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.581-1085G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134869880 | |||||||
| chr2:134870179 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.581-786C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134870179 | |||||||
| chr2:134870253 | G | A | 4 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 others(1): Show |
4 | HG00639.hp2 HG03710.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.581-712G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134870253 | |||||||
| chr2:134870351 | G | C | 1 | a0001c0001t0001g0200 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.581-614G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134870351 | |||||||
| chr2:134870393 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0230 |
2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.581-572G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134870393 | |||||||
| chr2:134870460 | C | T | 1 | a0001c0001t0001g0255 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.581-505C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134870460 | |||||||
| chr2:134870504 | G | A | 40 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(37): Show |
45 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.581-461G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134870504 | |||||||
| chr2:134870570 | G | A | 1 | a0001c0001t0001g0117 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.581-395G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134870570 | |||||||
| chr2:134870601 | C | A | 2 | a0001c0001t0001g0225 a0001c0001t0001g0229 |
2 | HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.581-364C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134870601 | |||||||
| chr2:134870643 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.581-322G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134870643 | |||||||
| chr2:134870800 | G | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0148 a0001c0001t0001g0149 others(1): Show |
5 | HG02486.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.581-165G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134870800 | |||||||
| chr2:134870836 | C | T | 28 | a0001c0001t0001g0003 a0001c0001t0001g0038 a0001c0001t0001g0056 others(25): Show |
30 | HG00558.hp1 HG00609.hp1 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.581-129C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134870836 | |||||||
| chr2:134870903 | A | G | 2 | a0001c0001t0001g0072 a0001c0001t0001g0086 |
2 | HG03654.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.581-62A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134870903 | |||||||
| chr2:134871124 | T | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0230 |
2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.676+64T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | chr2 | 134871124 | |||||||
| chr2:134871263 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.676+203T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | chr2 | 134871263 | |||||||
| chr2:134871511 | G | GT | 235 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(232): Show |
244 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(241): Show |
intron_variant | MODIFIER | c.676+463dupT | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 134871511 | ||||||
| chr2:134871511 | G | GTT | 6 | a0001c0001t0001g0083 a0001c0001t0001g0105 a0001c0001t0001g0108 others(3): Show |
6 | HG02602.hp1 HG02630.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.676+462_676+463dup others(2): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 134871511 | ||||||
| chr2:134871582 | C | A | 1 | a0001c0001t0001g0080 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.676+522C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | chr2 | 134871582 | |||||||
| chr2:134871678 | G | GAC | 99 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(96): Show |
105 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.676+620_676+621dup others(2): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 134871678 | ||||||
| chr2:134871678 | G | GACAC | 19 | a0001c0001t0001g0010 a0001c0001t0001g0054 a0001c0001t0001g0071 others(16): Show |
20 | HG00642.hp1 HG00735.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.676+621_676+622ins others(4): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 134871678 | ||||||
| chr2:134871678 | G | GACACAC | 13 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0092 others(10): Show |
13 | HG01978.hp2 HG02717.hp2 HG03098.hp1 others(10): Show |
intron_variant | MODIFIER | c.676+621_676+622ins others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 134871678 | ||||||
| chr2:134871678 | G | GACACACA others(1): Show |
48 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0038 others(45): Show |
50 | HG00558.hp1 HG00609.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.676+621_676+622ins others(8): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 134871678 | ||||||
| chr2:134871678 | G | GACACACA others(3): Show |
25 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0028 others(22): Show |
30 | HG00544.hp2 HG00673.hp1 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.676+621_676+622ins others(10): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 134871678 | ||||||
| chr2:134871678 | G | GACACACA others(5): Show |
3 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0185 |
3 | HG00597.hp1 NA18949.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.676+621_676+622ins others(12): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 134871678 | ||||||
| chr2:134871680 | CAG | C | 9 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0098 others(6): Show |
10 | HG02109.hp1 HG02257.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.676+622_676+623del others(2): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 134871680 | ||||||
| chr2:134871682 | G | C | 213 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(210): Show |
227 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(224): Show |
intron_variant | MODIFIER | c.676+622G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | chr2 | 134871682 | |||||||
| chr2:134871682 | G | GAC | 7 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0230 others(4): Show |
9 | HG02647.hp1 HG02922.hp1 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.676+652_676+653dup others(2): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 134871682 | ||||||
| chr2:134871682 | G | GACAC | 9 | a0001c0001t0001g0224 a0001c0001t0001g0288 a0001c0001t0001g0289 others(6): Show |
9 | HG02257.hp1 HG02818.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.676+650_676+653dup others(4): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 134871682 | ||||||
| chr2:134871682 | G | GACACAC | 3 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0008c0008t0001g0327 |
3 | HG00741.hp1 HG02559.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.676+648_676+653dup others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 134871682 | ||||||
| chr2:134871682 | G | GACACACA others(1): Show |
43 | a0001c0001t0001g0024 a0001c0001t0001g0234 a0001c0001t0001g0235 others(40): Show |
44 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.676+646_676+653dup others(8): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 134871682 | ||||||
| chr2:134871682 | G | GACACACA others(3): Show |
12 | a0001c0001t0001g0272 a0001c0001t0001g0293 a0001c0001t0001g0318 others(9): Show |
12 | HG01243.hp1 HG01358.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.676+644_676+653dup others(10): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 134871682 | ||||||
| chr2:134871682 | G | GACACACA others(5): Show |
6 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(3): Show |
6 | HG00639.hp2 HG03710.hp1 NA19004.hp1 others(3): Show |
intron_variant | MODIFIER | c.676+642_676+653dup others(12): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 134871682 | ||||||
| chr2:134871682 | G | GACACACA others(9): Show |
1 | a0001c0001t0001g0271 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.676+638_676+653dup others(16): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 134871682 | ||||||
| chr2:134871682 | G | GACAGACA others(11): Show |
1 | a0001c0001t0001g0025 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.676+625_676+626ins others(18): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 134871682 | ||||||
| chr2:134871735 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0230 |
2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.676+675G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | chr2 | 134871735 | |||||||
| chr2:134871736 | C | T | 97 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(94): Show |
104 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.676+676C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | chr2 | 134871736 | |||||||
| chr2:134871760 | G | A | 3 | a0001c0001t0001g0082 a0001c0001t0001g0097 a0001c0001t0001g0098 |
3 | HG02559.hp2 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.676+700G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | chr2 | 134871760 | |||||||
| chr2:134871763 | T | C | 1 | a0001c0001t0001g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.676+703T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | chr2 | 134871763 | |||||||
| chr2:134871865 | A | G | 7 | a0001c0001t0001g0106 a0001c0001t0001g0117 a0001c0001t0001g0128 others(4): Show |
7 | HG00558.hp1 HG00609.hp1 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.677-604A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | chr2 | 134871865 | |||||||
| chr2:134871869 | C | T | 218 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(215): Show |
233 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(230): Show |
intron_variant | MODIFIER | c.677-600C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | chr2 | 134871869 | |||||||
| chr2:134871890 | A | G | 2 | a0001c0001t0001g0023 a0001c0001t0001g0230 |
2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.677-579A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | chr2 | 134871890 | |||||||
| chr2:134871960 | C | CT | 256 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(253): Show |
270 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(267): Show |
intron_variant | MODIFIER | c.677-495dupT | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 134871960 | ||||||
| chr2:134871960 | C | CTT | 27 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0094 others(24): Show |
28 | HG00639.hp2 HG00735.hp2 HG01358.hp2 others(25): Show |
intron_variant | MODIFIER | c.677-496_677-495dup others(2): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 134871960 | ||||||
| chr2:134872025 | C | T | 2 | a0001c0001t0001g0025 a0002c0002t0001g0197 |
2 | HG02027.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.677-444C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | chr2 | 134872025 | |||||||
| chr2:134872069 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.677-400G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | chr2 | 134872069 | |||||||
| chr2:134872104 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.677-365G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | chr2 | 134872104 | |||||||
| chr2:134872337 | T | C | 53 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0234 others(50): Show |
54 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.677-132T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | chr2 | 134872337 | |||||||
| chr2:134872357 | C | T | 295 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(292): Show |
311 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(308): Show |
intron_variant | MODIFIER | c.677-112C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | chr2 | 134872357 | |||||||
| chr2:134872928 | A | G | 68 | a0001c0001t0001g0009 a0001c0001t0001g0030 a0001c0001t0001g0031 others(65): Show |
69 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.849+287A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134872928 | |||||||
| chr2:134873078 | A | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0134 |
2 | HG01074.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.849+437A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134873078 | |||||||
| chr2:134873130 | C | T | 1 | a0001c0001t0001g0036 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.849+489C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134873130 | |||||||
| chr2:134873295 | C | T | 1 | a0001c0001t0001g0029 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.849+654C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134873295 | |||||||
| chr2:134873356 | GC | G | 4 | a0001c0001t0001g0010 a0001c0001t0001g0148 a0001c0001t0001g0149 others(1): Show |
5 | HG02486.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+716delC | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134873356 | |||||||
| chr2:134873400 | A | T | 1 | a0001c0001t0001g0242 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.849+759A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134873400 | |||||||
| chr2:134873483 | G | T | 18 | a0001c0001t0001g0025 a0001c0001t0001g0293 a0001c0001t0001g0322 others(15): Show |
18 | HG00639.hp2 HG00735.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.849+842G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134873483 | |||||||
| chr2:134873512 | T | C | 1 | a0001c0001t0001g0008 | 2 | NA18998.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.849+871T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134873512 | |||||||
| chr2:134873761 | A | G | 297 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(294): Show |
313 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(310): Show |
intron_variant | MODIFIER | c.849+1120A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134873761 | |||||||
| chr2:134873830 | C | T | 218 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(215): Show |
233 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(230): Show |
intron_variant | MODIFIER | c.849+1189C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134873830 | |||||||
| chr2:134873863 | G | A | 1 | a0001c0001t0001g0333 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.849+1222G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134873863 | |||||||
| chr2:134873989 | T | C | 3 | a0001c0001t0001g0257 a0003c0003t0001g0021 a0003c0003t0001g0268 |
4 | NA18952.hp1 NA18962.hp2 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.849+1348T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134873989 | |||||||
| chr2:134874149 | G | A | 53 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0234 others(50): Show |
54 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.849+1508G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134874149 | |||||||
| chr2:134874237 | T | C | 3 | a0001c0001t0001g0076 a0001c0001t0001g0087 a0001c0001t0001g0158 |
3 | HG01070.hp1 HG01123.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.849+1596T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134874237 | |||||||
| chr2:134874301 | T | C | 1 | a0001c0001t0001g0278 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.849+1660T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134874301 | |||||||
| chr2:134874447 | C | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0148 a0001c0001t0001g0149 others(1): Show |
5 | HG02486.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+1806C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134874447 | |||||||
| chr2:134874495 | G | C | 1 | a0001c0001t0001g0119 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.849+1854G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134874495 | |||||||
| chr2:134874570 | C | T | 2 | a0001c0004t0001g0171 a0001c0004t0001g0172 |
2 | HG02257.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.849+1929C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134874570 | |||||||
| chr2:134874588 | T | A | 1 | a0001c0001t0001g0025 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.849+1947T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134874588 | |||||||
| chr2:134874621 | T | A | 53 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0234 others(50): Show |
54 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.849+1980T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134874621 | |||||||
| chr2:134874666 | T | C | 1 | a0001c0001t0001g0333 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.849+2025T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134874666 | |||||||
| chr2:134874864 | A | G | 1 | a0001c0001t0001g0325 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.849+2223A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134874864 | |||||||
| chr2:134874983 | A | G | 1 | a0001c0001t0001g0067 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.849+2342A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134874983 | |||||||
| chr2:134875008 | G | C | 2 | a0001c0001t0001g0344 a0001c0001t0001g0345 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.849+2367G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134875008 | |||||||
| chr2:134875053 | C | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0148 a0001c0001t0001g0149 others(1): Show |
5 | HG02486.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+2412C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134875053 | |||||||
| chr2:134875169 | T | C | 1 | a0001c0001t0001g0107 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.849+2528T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134875169 | |||||||
| chr2:134875184 | A | G | 16 | a0001c0001t0001g0293 a0001c0001t0001g0322 a0001c0001t0001g0323 others(13): Show |
16 | HG00639.hp2 HG00735.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.849+2543A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134875184 | |||||||
| chr2:134875292 | C | A | 296 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(293): Show |
312 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(309): Show |
intron_variant | MODIFIER | c.849+2651C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134875292 | |||||||
| chr2:134875411 | C | T | 274 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(271): Show |
290 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(287): Show |
intron_variant | MODIFIER | c.849+2770C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134875411 | |||||||
| chr2:134875581 | G | T | 4 | a0001c0001t0001g0082 a0001c0001t0001g0097 a0001c0001t0001g0098 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+2940G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134875581 | |||||||
| chr2:134875744 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.849+3103G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134875744 | |||||||
| chr2:134875899 | A | C | 1 | a0001c0001t0001g0191 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.849+3258A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134875899 | |||||||
| chr2:134876025 | T | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0148 a0001c0001t0001g0149 others(1): Show |
5 | HG02486.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+3384T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134876025 | |||||||
| chr2:134876115 | G | A | 1 | a0001c0001t0001g0258 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.849+3474G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134876115 | |||||||
| chr2:134876252 | A | T | 1 | a0001c0001t0001g0122 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.849+3611A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134876252 | |||||||
| chr2:134876424 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.849+3783G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134876424 | |||||||
| chr2:134876558 | G | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0148 a0001c0001t0001g0149 others(1): Show |
5 | HG02486.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+3917G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134876558 | |||||||
| chr2:134876574 | C | T | 1 | a0001c0001t0001g0023 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.849+3933C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134876574 | |||||||
| chr2:134876578 | A | G | 1 | a0001c0001t0001g0025 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.849+3937A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134876578 | |||||||
| chr2:134876684 | C | A | 1 | a0001c0001t0001g0140 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.849+4043C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134876684 | |||||||
| chr2:134876707 | C | T | 1 | a0001c0001t0001g0242 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.849+4066C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134876707 | |||||||
| chr2:134876767 | G | A | 5 | a0001c0001t0001g0011 a0001c0001t0001g0169 a0001c0004t0001g0170 others(2): Show |
6 | HG02109.hp1 HG02257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.849+4126G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134876767 | |||||||
| chr2:134876821 | A | C | 4 | a0001c0001t0001g0018 a0001c0001t0001g0292 a0001c0001t0001g0301 others(1): Show |
5 | NA18966.hp1 NA18967.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.849+4180A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134876821 | |||||||
| chr2:134877011 | G | A | 217 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(214): Show |
232 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(229): Show |
intron_variant | MODIFIER | c.849+4370G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134877011 | |||||||
| chr2:134877150 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.849+4509G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134877150 | |||||||
| chr2:134877157 | A | C | 1 | a0008c0008t0001g0327 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.849+4516A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134877157 | |||||||
| chr2:134877208 | T | C | 1 | a0001c0001t0001g0175 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.849+4567T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134877208 | |||||||
| chr2:134877523 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0230 |
2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.849+4882T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134877523 | |||||||
| chr2:134877577 | G | A | 5 | a0001c0001t0001g0011 a0001c0001t0001g0169 a0001c0004t0001g0170 others(2): Show |
6 | HG02109.hp1 HG02257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.849+4936G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134877577 | |||||||
| chr2:134877697 | AAG | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0148 a0001c0001t0001g0149 others(1): Show |
5 | HG02486.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+5059_849+5060d others(4): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134877697 | ||||||
| chr2:134877700 | A | AG | 52 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0128 others(49): Show |
53 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.849+5067dupG | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134877700 | ||||||
| chr2:134877700 | A | G | 1 | a0001c0001t0001g0269 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.849+5059A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134877700 | |||||||
| chr2:134877709 | A | G | 55 | a0001c0001t0001g0010 a0001c0001t0001g0024 a0001c0001t0001g0027 others(52): Show |
57 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.849+5068A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134877709 | |||||||
| chr2:134877712 | A | G | 5 | a0001c0001t0001g0029 a0001c0001t0001g0099 a0001c0001t0001g0101 others(2): Show |
5 | HG02717.hp1 HG03139.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.849+5071A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134877712 | |||||||
| chr2:134877908 | C | T | 1 | a0001c0001t0001g0305 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.849+5267C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134877908 | |||||||
| chr2:134878384 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.849+5743C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134878384 | |||||||
| chr2:134879556 | A | G | 1 | a0001c0001t0001g0022 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.849+6915A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134879556 | |||||||
| chr2:134879622 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.849+6981T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134879622 | |||||||
| chr2:134879768 | G | A | 284 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(281): Show |
300 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(297): Show |
intron_variant | MODIFIER | c.849+7127G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134879768 | |||||||
| chr2:134879779 | C | T | 53 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0234 others(50): Show |
54 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.849+7138C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134879779 | |||||||
| chr2:134879800 | T | A | 4 | a0001c0001t0001g0274 a0001c0001t0001g0277 a0001c0001t0001g0280 others(1): Show |
4 | NA18970.hp2 NA18978.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.849+7159T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134879800 | |||||||
| chr2:134879813 | A | C | 1 | a0001c0001t0001g0022 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.849+7172A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134879813 | |||||||
| chr2:134880277 | G | A | 284 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(281): Show |
300 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(297): Show |
intron_variant | MODIFIER | c.849+7636G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134880277 | |||||||
| chr2:134880322 | G | C | 1 | a0001c0001t0001g0166 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.849+7681G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134880322 | |||||||
| chr2:134880474 | C | T | 211 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(208): Show |
226 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(223): Show |
intron_variant | MODIFIER | c.849+7833C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134880474 | |||||||
| chr2:134880478 | C | A | 1 | a0001c0001t0001g0025 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.849+7837C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134880478 | |||||||
| chr2:134880532 | A | G | 1 | a0001c0001t0001g0332 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.849+7891A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134880532 | |||||||
| chr2:134880790 | A | G | 11 | a0001c0001t0001g0293 a0001c0001t0001g0328 a0001c0001t0001g0329 others(8): Show |
11 | HG00735.hp2 HG01358.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.849+8149A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134880790 | |||||||
| chr2:134880891 | C | T | 284 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(281): Show |
300 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(297): Show |
intron_variant | MODIFIER | c.849+8250C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134880891 | |||||||
| chr2:134880904 | G | A | 2 | a0001c0001t0001g0179 a0001c0001t0001g0181 |
2 | HG01496.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.849+8263G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134880904 | |||||||
| chr2:134881029 | T | G | 40 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(37): Show |
45 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.849+8388T>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134881029 | |||||||
| chr2:134881260 | C | T | 40 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(37): Show |
45 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.849+8619C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134881260 | |||||||
| chr2:134881301 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0230 |
2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.849+8660C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134881301 | |||||||
| chr2:134881440 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.849+8799T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134881440 | |||||||
| chr2:134881567 | C | A | 1 | a0001c0001t0001g0041 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.849+8926C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134881567 | |||||||
| chr2:134881807 | G | T | 98 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(95): Show |
105 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.849+9166G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134881807 | |||||||
| chr2:134881855 | C | T | 2 | a0001c0001t0001g0248 a0001c0001t0001g0254 |
2 | NA19010.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.849+9214C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134881855 | |||||||
| chr2:134881860 | G | C | 16 | a0001c0001t0001g0293 a0001c0001t0001g0322 a0001c0001t0001g0323 others(13): Show |
16 | HG00639.hp2 HG00735.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.849+9219G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134881860 | |||||||
| chr2:134881948 | T | A | 18 | a0001c0001t0001g0025 a0001c0001t0001g0293 a0001c0001t0001g0322 others(15): Show |
18 | HG00639.hp2 HG00735.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.849+9307T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134881948 | |||||||
| chr2:134882039 | A | G | 2 | a0001c0001t0001g0225 a0001c0001t0001g0229 |
2 | HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.849+9398A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134882039 | |||||||
| chr2:134882324 | T | C | 5 | a0001c0001t0001g0011 a0001c0001t0001g0169 a0001c0004t0001g0170 others(2): Show |
6 | HG02109.hp1 HG02257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.849+9683T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134882324 | |||||||
| chr2:134882405 | C | G | 295 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(292): Show |
311 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(308): Show |
intron_variant | MODIFIER | c.849+9764C>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134882405 | |||||||
| chr2:134882588 | A | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0148 a0001c0001t0001g0149 others(1): Show |
5 | HG02486.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+9947A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134882588 | |||||||
| chr2:134882642 | G | A | 40 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(37): Show |
45 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.849+10001G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134882642 | |||||||
| chr2:134882652 | A | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0148 a0001c0001t0001g0149 others(1): Show |
5 | HG02486.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+10011A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134882652 | |||||||
| chr2:134883065 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.849+10424T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134883065 | |||||||
| chr2:134883162 | A | G | 2 | a0001c0001t0001g0043 a0001c0001t0001g0051 |
2 | NA18963.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.849+10521A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134883162 | |||||||
| chr2:134883243 | G | T | 1 | a0002c0002t0001g0026 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.849+10602G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134883243 | |||||||
| chr2:134883265 | C | CA | 9 | a0001c0001t0001g0003 a0001c0001t0001g0090 a0001c0001t0001g0118 others(6): Show |
11 | HG01099.hp2 HG01361.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.849+10634dupA | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134883265 | ||||||
| chr2:134883332 | A | G | 1 | a0001c0001t0001g0148 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.849+10691A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134883332 | |||||||
| chr2:134883443 | T | C | 1 | a0001c0001t0001g0286 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.849+10802T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134883443 | |||||||
| chr2:134883564 | C | G | 1 | a0001c0001t0001g0271 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.849+10923C>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134883564 | |||||||
| chr2:134883699 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.849+11058C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134883699 | |||||||
| chr2:134883744 | C | A | 1 | a0001c0001t0001g0154 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.849+11103C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134883744 | |||||||
| chr2:134883904 | A | G | 5 | a0001c0001t0001g0011 a0001c0001t0001g0169 a0001c0004t0001g0170 others(2): Show |
6 | HG02109.hp1 HG02257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.849+11263A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134883904 | |||||||
| chr2:134884014 | G | A | 1 | a0001c0001t0001g0291 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.849+11373G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134884014 | |||||||
| chr2:134884238 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.849+11597T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134884238 | |||||||
| chr2:134884410 | A | T | 2 | a0001c0001t0001g0225 a0001c0001t0001g0229 |
2 | HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.849+11769A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134884410 | |||||||
| chr2:134884589 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.849+11948C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134884589 | |||||||
| chr2:134884610 | A | G | 295 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(292): Show |
311 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(308): Show |
intron_variant | MODIFIER | c.849+11969A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134884610 | |||||||
| chr2:134884833 | G | T | 1 | a0001c0001t0001g0333 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.849+12192G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134884833 | |||||||
| chr2:134884849 | G | C | 1 | a0001c0001t0001g0054 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.849+12208G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134884849 | |||||||
| chr2:134884952 | T | TC | 5 | a0001c0001t0001g0011 a0001c0001t0001g0169 a0001c0004t0001g0170 others(2): Show |
6 | HG02109.hp1 HG02257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.849+12311_849+1231 others(5): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134884952 | |||||||
| chr2:134884965 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0230 |
2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.849+12324G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134884965 | |||||||
| chr2:134885012 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.849+12371A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885012 | |||||||
| chr2:134885144 | G | A | 99 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(96): Show |
106 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.849+12503G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885144 | |||||||
| chr2:134885149 | T | A | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(209): Show |
227 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(224): Show |
intron_variant | MODIFIER | c.849+12508T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885149 | |||||||
| chr2:134885208 | C | T | 3 | a0001c0001t0001g0313 a0001c0001t0001g0344 a0001c0001t0001g0345 |
3 | HG02896.hp1 HG02897.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.849+12567C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885208 | |||||||
| chr2:134885236 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.849+12595G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885236 | |||||||
| chr2:134885244 | A | G | 1 | a0001c0001t0001g0025 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.849+12603A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885244 | |||||||
| chr2:134885246 | AT | A | 19 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0217 others(16): Show |
19 | HG00735.hp2 HG01243.hp1 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.849+12608delT | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134885246 | ||||||
| chr2:134885255 | T | A | 1 | a0001c0001t0001g0322 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.849+12614T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885255 | |||||||
| chr2:134885255 | TA | T | 5 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0092 others(2): Show |
5 | HG01978.hp2 NA18940.hp2 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.849+12616delA | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134885255 | ||||||
| chr2:134885256 | A | T | 1 | a0001c0001t0001g0322 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.849+12615A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885256 | |||||||
| chr2:134885256 | AAT | A | 7 | a0001c0001t0001g0011 a0001c0001t0001g0169 a0001c0001t0001g0188 others(4): Show |
8 | HG01358.hp2 HG02109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.849+12625_849+1262 others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134885256 | ||||||
| chr2:134885277 | A | T | 1 | a0001c0001t0001g0259 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.849+12636A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885277 | |||||||
| chr2:134885278 | T | A | 1 | a0001c0001t0001g0259 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.849+12637T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885278 | |||||||
| chr2:134885284 | A | ATAATATA others(3): Show |
1 | a0001c0001t0001g0154 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.849+12644_849+1264 others(14): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134885284 | ||||||
| chr2:134885285 | T | A | 1 | a0001c0001t0001g0259 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.849+12644T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885285 | |||||||
| chr2:134885285 | T | TAATA | 281 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(278): Show |
297 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(294): Show |
intron_variant | MODIFIER | c.849+12644_849+1264 others(8): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885285 | |||||||
| chr2:134885285 | TTATATTT others(39): Show |
T | 1 | a0001c0001t0001g0119 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.849+12645_849+1269 others(50): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885285 | |||||||
| chr2:134885286 | T | A | 1 | a0001c0001t0001g0041 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.849+12645T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885286 | |||||||
| chr2:134885290 | T | TATATTTA others(51): Show |
1 | a0001c0001t0001g0041 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.849+12649_849+1265 others(62): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885290 | |||||||
| chr2:134885291 | T | A | 2 | a0001c0001t0001g0154 a0001c0001t0001g0259 |
2 | HG02083.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.849+12650T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885291 | |||||||
| chr2:134885292 | T | A | 1 | a0001c0001t0001g0041 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.849+12651T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885292 | |||||||
| chr2:134885292 | T | TATATATA | 159 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(156): Show |
168 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(165): Show |
intron_variant | MODIFIER | c.849+12652_849+1265 others(11): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134885292 | ||||||
| chr2:134885292 | T | TATATATA others(1): Show |
4 | a0001c0001t0001g0010 a0001c0001t0001g0148 a0001c0001t0001g0149 others(1): Show |
5 | HG02486.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+12658_849+1265 others(12): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134885292 | ||||||
| chr2:134885293 | A | T | 1 | a0001c0001t0001g0259 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.849+12652A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885293 | |||||||
| chr2:134885298 | T | TA | 42 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(39): Show |
47 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.849+12658dupA | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134885298 | ||||||
| chr2:134885301 | A | G | 52 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0234 others(49): Show |
53 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.849+12660A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885301 | |||||||
| chr2:134885303 | T | A | 44 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(41): Show |
49 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.849+12662T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885303 | |||||||
| chr2:134885303 | T | G | 240 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(237): Show |
251 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(248): Show |
intron_variant | MODIFIER | c.849+12662T>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885303 | |||||||
| chr2:134885305 | A | G | 3 | a0001c0001t0001g0225 a0001c0001t0001g0229 a0001c0001t0001g0259 |
3 | HG02083.hp2 HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.849+12664A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885305 | |||||||
| chr2:134885306 | A | AAT | 32 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0052 others(29): Show |
34 | HG00642.hp2 HG00673.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.849+12677_849+1267 others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134885306 | ||||||
| chr2:134885306 | A | T | 45 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(42): Show |
50 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.849+12665A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885306 | |||||||
| chr2:134885306 | AAT | A | 56 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(53): Show |
57 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.849+12677_849+1267 others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134885306 | ||||||
| chr2:134885308 | T | A | 3 | a0001c0001t0001g0225 a0001c0001t0001g0229 a0001c0001t0001g0259 |
3 | HG02083.hp2 HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.849+12667T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885308 | |||||||
| chr2:134885308 | T | TGTAA | 42 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(39): Show |
47 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.849+12667_849+1266 others(8): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885308 | |||||||
| chr2:134885309 | A | ATATATAT others(42): Show |
3 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 |
3 | HG02630.hp2 HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.849+12671_849+1271 others(53): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134885309 | ||||||
| chr2:134885311 | A | ATAT | 4 | a0001c0001t0001g0010 a0001c0001t0001g0148 a0001c0001t0001g0149 others(1): Show |
5 | HG02486.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+12671_849+1267 others(7): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134885311 | ||||||
| chr2:134885316 | TATA | T | 4 | a0001c0001t0001g0025 a0001c0001t0001g0313 a0001c0001t0001g0344 others(1): Show |
4 | HG02027.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.849+12677_849+1267 others(7): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134885316 | ||||||
| chr2:134885317 | ATAAATAT others(52): Show |
A | 1 | a0001c0001t0001g0241 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.849+12677_849+1273 others(63): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885317 | |||||||
| chr2:134885319 | A | AT | 17 | a0001c0001t0001g0002 a0001c0001t0001g0028 a0001c0001t0001g0096 others(14): Show |
17 | HG00544.hp2 HG00609.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.849+12678_849+1267 others(5): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885319 | |||||||
| chr2:134885319 | A | ATAT | 35 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0038 others(32): Show |
39 | HG00558.hp1 HG00597.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.849+12678_849+1267 others(7): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885319 | |||||||
| chr2:134885319 | A | ATATAT | 5 | a0001c0001t0001g0102 a0001c0001t0001g0107 a0001c0001t0001g0114 others(2): Show |
5 | HG02258.hp1 NA18906.hp2 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+12678_849+1267 others(9): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885319 | |||||||
| chr2:134885320 | A | T | 1 | a0001c0001t0001g0068 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.849+12679A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885320 | |||||||
| chr2:134885329 | G | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0148 a0001c0001t0001g0149 others(1): Show |
5 | HG02486.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+12688G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885329 | |||||||
| chr2:134885332 | A | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0148 a0001c0001t0001g0149 others(1): Show |
5 | HG02486.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+12691A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885332 | |||||||
| chr2:134885339 | AT | A | 3 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0340 |
3 | NA18949.hp2 NA18992.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.849+12701delT | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134885339 | ||||||
| chr2:134885346 | TATA | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0099 others(6): Show |
10 | HG02486.hp1 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.849+12709_849+1271 others(7): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134885346 | ||||||
| chr2:134885349 | A | AATATATA others(36): Show |
52 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0234 others(49): Show |
53 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.849+12719_849+1272 others(47): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134885349 | ||||||
| chr2:134885359 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.849+12718T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885359 | |||||||
| chr2:134885359 | T | TAA | 45 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0011 others(42): Show |
51 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.849+12719_849+1272 others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134885359 | ||||||
| chr2:134885361 | C | A | 65 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0027 others(62): Show |
66 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.849+12720C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885361 | |||||||
| chr2:134885361 | C | CAT | 4 | a0001c0001t0001g0099 a0001c0001t0001g0141 a0001c0001t0001g0210 others(1): Show |
4 | HG03139.hp1 NA19005.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.849+12727_849+1272 others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134885361 | ||||||
| chr2:134885361 | C | T | 46 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0011 others(43): Show |
52 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.849+12720C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885361 | |||||||
| chr2:134885368 | A | AT | 3 | a0001c0001t0001g0023 a0001c0001t0001g0230 a0001c0001t0001g0333 |
3 | HG01243.hp1 NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.849+12729dupT | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134885368 | ||||||
| chr2:134885368 | A | ATTTATAT others(23): Show |
1 | a0001c0001t0001g0025 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.849+12729_849+1273 others(34): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134885368 | ||||||
| chr2:134885368 | ATT | A | 13 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(10): Show |
13 | HG02015.hp2 HG02451.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.849+12728_849+1272 others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885368 | |||||||
| chr2:134885369 | T | TTATATAT others(25): Show |
2 | a0001c0001t0001g0344 a0001c0001t0001g0345 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.849+12737_849+1273 others(36): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134885369 | ||||||
| chr2:134885377 | A | T | 1 | a0001c0001t0001g0298 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.849+12736A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885377 | |||||||
| chr2:134885389 | A | T | 1 | a0001c0001t0001g0022 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.849+12748A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885389 | |||||||
| chr2:134885398 | AT | A | 98 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(95): Show |
105 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.849+12760delT | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134885398 | ||||||
| chr2:134885488 | T | TAC | 285 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(282): Show |
301 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(298): Show |
intron_variant | MODIFIER | c.849+12848_849+1284 others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134885488 | ||||||
| chr2:134885728 | C | T | 285 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(282): Show |
301 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(298): Show |
intron_variant | MODIFIER | c.850-12613C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885728 | |||||||
| chr2:134885745 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0230 |
2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.850-12596C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885745 | |||||||
| chr2:134885805 | G | A | 1 | a0001c0001t0001g0014 | 2 | NA18939.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.850-12536G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885805 | |||||||
| chr2:134885851 | G | A | 53 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0234 others(50): Show |
54 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.850-12490G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885851 | |||||||
| chr2:134886097 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.850-12244G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134886097 | |||||||
| chr2:134886233 | C | CATT | 5 | a0001c0001t0001g0011 a0001c0001t0001g0169 a0001c0004t0001g0170 others(2): Show |
6 | HG02109.hp1 HG02257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.850-12095_850-1209 others(7): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134886233 | ||||||
| chr2:134886243 | A | AT | 4 | a0001c0001t0001g0131 a0001c0001t0001g0161 a0001c0001t0001g0287 others(1): Show |
4 | HG02895.hp1 HG03098.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.850-12096dupT | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134886243 | ||||||
| chr2:134886243 | A | ATT | 3 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0247 |
3 | NA18985.hp2 NA18987.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.850-12097_850-1209 others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134886243 | ||||||
| chr2:134886243 | A | ATTT | 38 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0234 others(35): Show |
39 | HG00408.hp2 HG00597.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.850-12096_850-1209 others(7): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134886243 | ||||||
| chr2:134886243 | A | ATTTT | 13 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0240 others(10): Show |
13 | HG00438.hp2 HG01346.hp1 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.850-12096_850-1209 others(8): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134886243 | ||||||
| chr2:134886246 | A | AT | 18 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(15): Show |
18 | HG00544.hp2 HG01175.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.850-12073dupT | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134886246 | ||||||
| chr2:134886246 | A | ATTATTAT others(20): Show |
1 | a0001c0001t0001g0330 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.850-12093_850-1209 others(31): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134886246 | ||||||
| chr2:134886246 | A | ATTATTAT others(21): Show |
2 | a0001c0001t0001g0329 a0001c0001t0001g0338 |
2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.850-12093_850-1209 others(32): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134886246 | ||||||
| chr2:134886246 | A | ATTATTAT others(15): Show |
1 | a0001c0001t0001g0230 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.850-12093_850-1209 others(26): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134886246 | ||||||
| chr2:134886246 | A | ATTATTAT others(19): Show |
2 | a0001c0001t0001g0324 a0001c0001t0001g0326 |
2 | HG03710.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.850-12093_850-1209 others(30): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134886246 | ||||||
| chr2:134886246 | A | ATTATTAT others(20): Show |
1 | a0001c0001t0001g0335 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.850-12093_850-1209 others(31): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134886246 | ||||||
| chr2:134886246 | A | ATTATTAT others(21): Show |
2 | a0001c0001t0001g0334 a0001c0001t0001g0336 |
2 | HG00735.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.850-12093_850-1209 others(32): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134886246 | ||||||
| chr2:134886246 | A | ATTATTAT others(22): Show |
1 | a0001c0001t0001g0339 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.850-12093_850-1209 others(33): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134886246 | ||||||
| chr2:134886246 | A | ATTATTAT others(18): Show |
2 | a0001c0001t0001g0023 a0001c0001t0001g0322 |
2 | HG00639.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.850-12093_850-1209 others(29): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134886246 | ||||||
| chr2:134886246 | A | ATTATTAT others(21): Show |
2 | a0001c0001t0001g0293 a0001c0001t0001g0328 |
2 | HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.850-12093_850-1209 others(32): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134886246 | ||||||
| chr2:134886246 | A | ATTATTAT others(6): Show |
1 | a0001c0001t0001g0025 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.850-12093_850-1209 others(17): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134886246 | ||||||
| chr2:134886246 | A | ATTATTAT others(17): Show |
1 | a0001c0001t0001g0323 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.850-12093_850-1209 others(28): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134886246 | ||||||
| chr2:134886246 | A | ATTATTAT others(20): Show |
1 | a0001c0001t0001g0332 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.850-12093_850-1209 others(31): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134886246 | ||||||
| chr2:134886246 | A | ATTATTAT others(21): Show |
1 | a0001c0001t0001g0337 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.850-12093_850-1209 others(32): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134886246 | ||||||
| chr2:134886246 | A | ATTATTAT others(15): Show |
1 | a0001c0001t0001g0325 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.850-12093_850-1209 others(26): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134886246 | ||||||
| chr2:134886246 | A | T | 73 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0027 others(70): Show |
76 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.850-12095A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134886246 | |||||||
| chr2:134886248 | T | TA | 11 | a0001c0001t0001g0050 a0001c0001t0001g0070 a0001c0001t0001g0072 others(8): Show |
11 | HG01496.hp2 HG03579.hp1 HG03927.hp1 others(8): Show |
intron_variant | MODIFIER | c.850-12093_850-1209 others(5): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134886248 | |||||||
| chr2:134886249 | T | A | 148 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(145): Show |
157 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.850-12092T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134886249 | |||||||
| chr2:134886250 | T | A | 2 | a0001c0001t0001g0022 a0001c0001t0001g0136 |
2 | HG01515.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.850-12091T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134886250 | |||||||
| chr2:134886251 | T | A | 2 | a0001c0001t0001g0070 a0001c0001t0001g0072 |
2 | HG03927.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.850-12090T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134886251 | |||||||
| chr2:134886252 | T | A | 72 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(69): Show |
76 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.850-12089T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134886252 | |||||||
| chr2:134886255 | T | A | 18 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0029 others(15): Show |
20 | HG01257.hp2 HG01261.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.850-12086T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134886255 | |||||||
| chr2:134886258 | T | A | 5 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0148 others(2): Show |
6 | HG02486.hp1 HG02965.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.850-12083T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134886258 | |||||||
| chr2:134886275 | GTC | G | 5 | a0001c0001t0001g0011 a0001c0001t0001g0169 a0001c0004t0001g0170 others(2): Show |
6 | HG02109.hp1 HG02257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.850-12063_850-1206 others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134886275 | ||||||
| chr2:134886279 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0230 |
2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.850-12062C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134886279 | |||||||
| chr2:134886287 | C | T | 1 | a0001c0001t0001g0029 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.850-12054C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134886287 | |||||||
| chr2:134886484 | G | A | 16 | a0001c0001t0001g0293 a0001c0001t0001g0322 a0001c0001t0001g0323 others(13): Show |
16 | HG00639.hp2 HG00735.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.850-11857G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134886484 | |||||||
| chr2:134886699 | T | C | 1 | a0001c0001t0001g0258 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.850-11642T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134886699 | |||||||
| chr2:134886751 | C | A | 5 | a0001c0001t0001g0011 a0001c0001t0001g0169 a0001c0004t0001g0170 others(2): Show |
6 | HG02109.hp1 HG02257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.850-11590C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134886751 | |||||||
| chr2:134886901 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0230 |
2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.850-11440G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134886901 | |||||||
| chr2:134887077 | C | A | 1 | a0001c0001t0001g0230 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.850-11264C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134887077 | |||||||
| chr2:134887194 | C | G | 1 | a0001c0001t0001g0025 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.850-11147C>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134887194 | |||||||
| chr2:134887408 | C | T | 283 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(280): Show |
299 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(296): Show |
intron_variant | MODIFIER | c.850-10933C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134887408 | |||||||
| chr2:134887500 | T | C | 1 | a0002c0002t0001g0026 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.850-10841T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134887500 | |||||||
| chr2:134887737 | C | A | 1 | a0001c0001t0001g0263 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.850-10604C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134887737 | |||||||
| chr2:134887749 | A | C | 53 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0234 others(50): Show |
54 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.850-10592A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134887749 | |||||||
| chr2:134888213 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.850-10128G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134888213 | |||||||
| chr2:134888343 | T | C | 40 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(37): Show |
45 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.850-9998T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134888343 | |||||||
| chr2:134888665 | G | GAAAAAAA others(310): Show |
4 | a0001c0001t0001g0010 a0001c0001t0001g0148 a0001c0001t0001g0149 others(1): Show |
5 | HG02486.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.850-9661_850-9660i others(319): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134888665 | ||||||
| chr2:134889162 | G | A | 1 | a0001c0001t0001g0175 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.850-9179G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134889162 | |||||||
| chr2:134889184 | G | A | 4 | a0001c0001t0001g0017 a0001c0001t0001g0285 a0001c0001t0001g0304 others(1): Show |
5 | HG01123.hp1 HG01192.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.850-9157G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134889184 | |||||||
| chr2:134889209 | G | A | 213 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(210): Show |
228 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(225): Show |
intron_variant | MODIFIER | c.850-9132G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134889209 | |||||||
| chr2:134889252 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.850-9089T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134889252 | |||||||
| chr2:134889428 | A | G | 1 | a0001c0001t0001g0195 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.850-8913A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134889428 | |||||||
| chr2:134889742 | G | C | 1 | a0001c0001t0001g0332 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.850-8599G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134889742 | |||||||
| chr2:134889867 | C | T | 15 | a0001c0001t0001g0293 a0001c0001t0001g0322 a0001c0001t0001g0323 others(12): Show |
15 | HG00639.hp2 HG00735.hp2 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.850-8474C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134889867 | |||||||
| chr2:134889959 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.850-8382C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134889959 | |||||||
| chr2:134890043 | A | C | 41 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(38): Show |
46 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.850-8298A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134890043 | |||||||
| chr2:134890089 | A | C | 285 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(282): Show |
301 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(298): Show |
intron_variant | MODIFIER | c.850-8252A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134890089 | |||||||
| chr2:134890428 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.850-7913G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134890428 | |||||||
| chr2:134890510 | C | A | 1 | a0001c0001t0001g0258 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.850-7831C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134890510 | |||||||
| chr2:134890738 | A | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0033 |
2 | HG01358.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.850-7603A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134890738 | |||||||
| chr2:134890909 | G | C | 1 | a0001c0001t0001g0022 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.850-7432G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134890909 | |||||||
| chr2:134891053 | G | A | 1 | a0001c0001t0001g0339 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.850-7288G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134891053 | |||||||
| chr2:134891300 | T | C | 40 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(37): Show |
45 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.850-7041T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134891300 | |||||||
| chr2:134891324 | T | C | 1 | a0001c0001t0001g0332 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.850-7017T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134891324 | |||||||
| chr2:134891333 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.850-7008G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134891333 | |||||||
| chr2:134891362 | A | G | 2 | a0001c0001t0001g0225 a0001c0001t0001g0229 |
2 | HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.850-6979A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134891362 | |||||||
| chr2:134891493 | T | C | 63 | a0001c0001t0001g0009 a0001c0001t0001g0030 a0001c0001t0001g0031 others(60): Show |
64 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.850-6848T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134891493 | |||||||
| chr2:134891530 | A | C | 1 | a0001c0001t0001g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.850-6811A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134891530 | |||||||
| chr2:134891625 | G | C | 1 | a0001c0001t0001g0333 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.850-6716G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134891625 | |||||||
| chr2:134891689 | A | G | 5 | a0001c0001t0001g0018 a0001c0001t0001g0112 a0001c0001t0001g0292 others(2): Show |
6 | HG04204.hp2 NA18966.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.850-6652A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134891689 | |||||||
| chr2:134891769 | T | C | 6 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0092 others(3): Show |
6 | HG01978.hp2 NA18940.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.850-6572T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134891769 | |||||||
| chr2:134891831 | G | A | 1 | a0002c0002t0001g0201 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.850-6510G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134891831 | |||||||
| chr2:134891955 | T | C | 40 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(37): Show |
45 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.850-6386T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134891955 | |||||||
| chr2:134892083 | G | C | 161 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(158): Show |
169 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(166): Show |
intron_variant | MODIFIER | c.850-6258G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134892083 | |||||||
| chr2:134892143 | G | T | 1 | a0001c0001t0001g0333 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.850-6198G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134892143 | |||||||
| chr2:134892225 | AT | A | 282 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(279): Show |
298 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(295): Show |
intron_variant | MODIFIER | c.850-6106delT | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134892225 | ||||||
| chr2:134892235 | T | A | 284 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(281): Show |
300 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(297): Show |
intron_variant | MODIFIER | c.850-6106T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134892235 | |||||||
| chr2:134892401 | A | C | 2 | a0001c0001t0001g0225 a0001c0001t0001g0229 |
2 | HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.850-5940A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134892401 | |||||||
| chr2:134892462 | A | AAAAT | 40 | a0001c0001t0001g0027 a0001c0001t0001g0224 a0001c0001t0001g0234 others(37): Show |
41 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.850-5842_850-5839d others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134892462 | ||||||
| chr2:134892462 | A | AAAATAAA others(1): Show |
21 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0235 others(18): Show |
21 | HG00597.hp2 HG01255.hp2 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.850-5846_850-5839d others(10): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134892462 | ||||||
| chr2:134892462 | A | AAAATAAA others(5): Show |
2 | a0001c0001t0001g0249 a0001c0001t0001g0315 |
2 | HG02148.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.850-5850_850-5839d others(14): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134892462 | ||||||
| chr2:134892462 | AAAAT | A | 19 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0022 others(16): Show |
22 | HG00639.hp2 HG01099.hp2 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.850-5842_850-5839d others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134892462 | ||||||
| chr2:134892462 | AAAATAAA others(1): Show |
A | 198 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(195): Show |
209 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(206): Show |
intron_variant | MODIFIER | c.850-5846_850-5839d others(10): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134892462 | ||||||
| chr2:134892462 | AAAATAAA others(5): Show |
A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0148 a0001c0001t0001g0149 others(1): Show |
5 | HG02486.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.850-5850_850-5839d others(14): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134892462 | ||||||
| chr2:134892462 | AAAATAAA others(9): Show |
A | 1 | a0001c0001t0001g0343 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.850-5854_850-5839d others(18): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134892462 | ||||||
| chr2:134892655 | T | C | 1 | a0001c0001t0001g0175 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.850-5686T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134892655 | |||||||
| chr2:134892663 | T | A | 16 | a0001c0001t0001g0293 a0001c0001t0001g0322 a0001c0001t0001g0323 others(13): Show |
16 | HG00639.hp2 HG00735.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.850-5678T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134892663 | |||||||
| chr2:134892983 | G | T | 1 | a0001c0001t0001g0191 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.850-5358G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134892983 | |||||||
| chr2:134893196 | T | C | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(162): Show |
174 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(171): Show |
intron_variant | MODIFIER | c.850-5145T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134893196 | |||||||
| chr2:134893198 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.850-5143T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134893198 | |||||||
| chr2:134893209 | A | AT | 10 | a0001c0001t0001g0224 a0001c0001t0001g0234 a0001c0001t0001g0238 others(7): Show |
11 | HG02809.hp2 HG03130.hp2 HG03471.hp1 others(8): Show |
intron_variant | MODIFIER | c.850-5114dupT | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134893209 | ||||||
| chr2:134893209 | A | ATT | 43 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0235 others(40): Show |
43 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.850-5115_850-5114d others(4): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134893209 | ||||||
| chr2:134893209 | AT | A | 153 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(150): Show |
165 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(162): Show |
intron_variant | MODIFIER | c.850-5114delT | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134893209 | ||||||
| chr2:134893209 | ATT | A | 68 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(65): Show |
71 | HG00140.hp2 HG00609.hp1 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.850-5115_850-5114d others(4): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134893209 | ||||||
| chr2:134893299 | T | G | 1 | a0001c0001t0001g0008 | 2 | NA18998.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.850-5042T>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134893299 | |||||||
| chr2:134893339 | C | A | 1 | a0001c0001t0001g0025 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.850-5002C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134893339 | |||||||
| chr2:134893552 | T | C | 1 | a0001c0001t0001g0022 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.850-4789T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134893552 | |||||||
| chr2:134893602 | C | G | 1 | a0001c0001t0001g0184 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.850-4739C>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134893602 | |||||||
| chr2:134893743 | C | T | 40 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(37): Show |
45 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.850-4598C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134893743 | |||||||
| chr2:134893986 | A | C | 2 | a0001c0001t0001g0225 a0001c0001t0001g0229 |
2 | HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.850-4355A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134893986 | |||||||
| chr2:134894142 | T | A | 1 | a0001c0001t0001g0033 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.850-4199T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134894142 | |||||||
| chr2:134894144 | T | C | 1 | a0001c0001t0001g0230 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.850-4197T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134894144 | |||||||
| chr2:134894304 | G | A | 2 | a0001c0001t0001g0047 a0001c0001t0001g0151 |
2 | HG01074.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.850-4037G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134894304 | |||||||
| chr2:134894437 | A | G | 2 | a0001c0001t0001g0023 a0001c0001t0001g0230 |
2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.850-3904A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134894437 | |||||||
| chr2:134894782 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.850-3559G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134894782 | |||||||
| chr2:134894829 | C | A | 285 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(282): Show |
301 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(298): Show |
intron_variant | MODIFIER | c.850-3512C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134894829 | |||||||
| chr2:134894985 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0230 |
2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.850-3356C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134894985 | |||||||
| chr2:134895088 | A | C | 2 | a0001c0001t0001g0225 a0001c0001t0001g0229 |
2 | HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.850-3253A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134895088 | |||||||
| chr2:134895158 | T | C | 1 | a0001c0004t0001g0171 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.850-3183T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134895158 | |||||||
| chr2:134895165 | G | C | 16 | a0001c0001t0001g0293 a0001c0001t0001g0322 a0001c0001t0001g0323 others(13): Show |
16 | HG00639.hp2 HG00735.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.850-3176G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134895165 | |||||||
| chr2:134895226 | C | T | 1 | a0002c0002t0001g0201 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.850-3115C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134895226 | |||||||
| chr2:134895316 | A | ATATATAT others(20): Show |
1 | a0001c0001t0001g0055 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.850-3025_850-3024i others(29): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134895316 | |||||||
| chr2:134895316 | A | T | 57 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(54): Show |
58 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.850-3025A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134895316 | |||||||
| chr2:134895328 | T | TTACATAT others(23): Show |
1 | a0001c0001t0001g0053 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.850-3011_850-3010i others(32): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134895328 | ||||||
| chr2:134895328 | T | TTACATAT others(25): Show |
11 | a0001c0001t0001g0011 a0001c0001t0001g0052 a0001c0001t0001g0066 others(8): Show |
12 | HG00673.hp2 HG01496.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.850-3011_850-3010i others(34): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134895328 | ||||||
| chr2:134895328 | T | TTACATAT others(21): Show |
5 | a0001c0001t0001g0010 a0001c0001t0001g0148 a0001c0001t0001g0149 others(2): Show |
6 | HG02486.hp1 HG02965.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.850-3011_850-3010i others(30): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134895328 | ||||||
| chr2:134895328 | T | TTACATAT others(23): Show |
189 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(186): Show |
202 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(199): Show |
intron_variant | MODIFIER | c.850-3011_850-3010i others(32): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134895328 | ||||||
| chr2:134895328 | T | TTACATAT others(25): Show |
1 | a0004c0005t0001g0222 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.850-3011_850-3010i others(34): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134895328 | ||||||
| chr2:134895328 | T | TTACATAT others(24): Show |
2 | a0001c0001t0001g0095 a0001c0001t0001g0109 |
2 | HG02015.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.850-3011_850-3010i others(33): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134895328 | ||||||
| chr2:134895331 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.850-3010T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134895331 | |||||||
| chr2:134895335 | T | C | 1 | a0001c0001t0001g0022 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.850-3006T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134895335 | |||||||
| chr2:134895356 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.850-2985A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134895356 | |||||||
| chr2:134895358 | A | AAT | 4 | a0001c0001t0001g0010 a0001c0001t0001g0148 a0001c0001t0001g0149 others(1): Show |
5 | HG02486.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.850-2972_850-2971d others(4): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134895358 | ||||||
| chr2:134895358 | A | T | 1 | a0001c0001t0001g0190 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.850-2983A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134895358 | |||||||
| chr2:134895368 | TATGTTAC others(183): Show |
T | 1 | a0001c0001t0001g0190 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.850-2972_850-2783d others(2): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134895368 | |||||||
| chr2:134895375 | C | T | 5 | a0001c0001t0001g0011 a0001c0001t0001g0169 a0001c0004t0001g0170 others(2): Show |
6 | HG02109.hp1 HG02257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.850-2966C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134895375 | |||||||
| chr2:134895524 | T | G | 40 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(37): Show |
45 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.850-2817T>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134895524 | |||||||
| chr2:134895638 | A | G | 4 | a0001c0001t0001g0060 a0001c0001t0001g0074 a0001c0001t0001g0083 others(1): Show |
4 | NA18988.hp1 NA19058.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.850-2703A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134895638 | |||||||
| chr2:134895785 | C | T | 161 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(158): Show |
169 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(166): Show |
intron_variant | MODIFIER | c.850-2556C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134895785 | |||||||
| chr2:134896013 | A | T | 1 | a0001c0001t0001g0179 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.850-2328A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134896013 | |||||||
| chr2:134896278 | C | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0230 |
2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.850-2063C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134896278 | |||||||
| chr2:134896374 | C | T | 2 | a0001c0001t0001g0224 a0002c0002t0001g0026 |
2 | HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.850-1967C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134896374 | |||||||
| chr2:134896598 | G | A | 289 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(286): Show |
305 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(302): Show |
intron_variant | MODIFIER | c.850-1743G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134896598 | |||||||
| chr2:134896689 | T | C | 2 | a0001c0001t0001g0076 a0001c0001t0001g0087 |
2 | HG01070.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.850-1652T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134896689 | |||||||
| chr2:134896768 | T | C | 285 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(282): Show |
301 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(298): Show |
intron_variant | MODIFIER | c.850-1573T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134896768 | |||||||
| chr2:134896924 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.850-1417C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134896924 | |||||||
| chr2:134896931 | T | C | 1 | a0001c0001t0001g0031 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.850-1410T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134896931 | |||||||
| chr2:134896962 | G | T | 2 | a0001c0001t0001g0344 a0001c0001t0001g0345 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.850-1379G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134896962 | |||||||
| chr2:134897010 | TGTGGTTA others(5): Show |
T | 53 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0234 others(50): Show |
54 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.850-1329_850-1318d others(14): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134897010 | ||||||
| chr2:134897065 | G | GATTACAC others(29): Show |
1 | a0001c0001t0001g0183 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.850-1271_850-1236d others(38): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134897065 | ||||||
| chr2:134897119 | G | C | 53 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0234 others(50): Show |
54 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.850-1222G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134897119 | |||||||
| chr2:134897437 | A | AT | 53 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0234 others(50): Show |
54 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.850-901dupT | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134897437 | ||||||
| chr2:134897603 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.850-738C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134897603 | |||||||
| chr2:134897814 | T | C | 2 | a0001c0001t0001g0039 a0001c0001t0001g0134 |
2 | HG01074.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.850-527T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134897814 | |||||||
| chr2:134897885 | G | GT | 93 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(90): Show |
99 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.850-443dupT | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134897885 | ||||||
| chr2:134897891 | T | G | 8 | a0001c0001t0001g0011 a0001c0001t0001g0169 a0001c0001t0001g0225 others(5): Show |
9 | HG02109.hp1 HG02257.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.850-450T>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134897891 | |||||||
| chr2:134898149 | G | A | 1 | a0001c0001t0001g0183 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.850-192G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134898149 | |||||||
| chr2:134898149 | G | GA | 53 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0234 others(50): Show |
54 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.850-183dupA | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134898149 | ||||||
| chr2:134898189 | T | C | 1 | a0001c0001t0001g0025 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.850-152T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134898189 | |||||||
| chr2:134898236 | G | A | 1 | a0001c0001t0001g0298 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.850-105G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134898236 | |||||||
| chr2:134898537 | G | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0148 a0001c0001t0001g0149 others(1): Show |
5 | HG02486.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.948+98G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134898537 | |||||||
| chr2:134898544 | T | C | 1 | a0001c0001t0001g0230 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.948+105T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134898544 | |||||||
| chr2:134898572 | C | G | 1 | a0002c0002t0001g0197 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.948+133C>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134898572 | |||||||
| chr2:134898684 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.948+245T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134898684 | |||||||
| chr2:134898712 | T | C | 4 | a0001c0001t0001g0334 a0001c0001t0001g0335 a0001c0001t0001g0336 others(1): Show |
4 | HG00735.hp2 HG02145.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.948+273T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134898712 | |||||||
| chr2:134898779 | G | C | 3 | a0001c0001t0001g0313 a0001c0001t0001g0344 a0001c0001t0001g0345 |
3 | HG02896.hp1 HG02897.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.948+340G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134898779 | |||||||
| chr2:134898876 | T | C | 1 | a0001c0001t0001g0243 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.948+437T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134898876 | |||||||
| chr2:134898920 | G | A | 5 | a0001c0001t0001g0029 a0001c0001t0001g0099 a0001c0001t0001g0101 others(2): Show |
5 | HG02717.hp1 HG03139.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.948+481G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134898920 | |||||||
| chr2:134898933 | C | G | 9 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0064 others(6): Show |
9 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(6): Show |
intron_variant | MODIFIER | c.948+494C>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134898933 | |||||||
| chr2:134898935 | T | A | 1 | a0001c0001t0001g0022 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.948+496T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134898935 | |||||||
| chr2:134899025 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.948+586C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134899025 | |||||||
| chr2:134899053 | T | G | 1 | a0001c0001t0001g0339 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.948+614T>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134899053 | |||||||
| chr2:134899080 | C | A | 3 | a0001c0001t0001g0249 a0001c0001t0001g0253 a0001c0001t0001g0267 |
3 | HG01255.hp2 HG01346.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.948+641C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134899080 | |||||||
| chr2:134899303 | T | C | 5 | a0001c0001t0001g0238 a0001c0001t0001g0246 a0001c0001t0001g0250 others(2): Show |
5 | NA18939.hp2 NA18941.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.948+864T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134899303 | |||||||
| chr2:134899874 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0230 |
2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.948+1435G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134899874 | |||||||
| chr2:134899901 | C | A | 285 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(282): Show |
301 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(298): Show |
intron_variant | MODIFIER | c.948+1462C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134899901 | |||||||
| chr2:134899917 | A | C | 1 | a0001c0001t0001g0333 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.948+1478A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134899917 | |||||||
| chr2:134900378 | T | C | 1 | a0001c0001t0001g0022 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.949-1420T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134900378 | |||||||
| chr2:134900505 | G | A | 1 | a0002c0002t0001g0026 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.949-1293G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134900505 | |||||||
| chr2:134900621 | C | G | 3 | a0001c0001t0001g0048 a0001c0001t0001g0155 a0001c0001t0001g0157 |
3 | HG02698.hp2 HG03490.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.949-1177C>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134900621 | |||||||
| chr2:134900677 | T | C | 2 | a0001c0001t0001g0225 a0001c0001t0001g0229 |
2 | HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.949-1121T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134900677 | |||||||
| chr2:134900763 | A | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0230 |
2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.949-1035A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134900763 | |||||||
| chr2:134900926 | G | C | 2 | a0001c0001t0001g0278 a0001c0001t0001g0300 |
2 | HG03927.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.949-872G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134900926 | |||||||
| chr2:134901281 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.949-517G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134901281 | |||||||
| chr2:134901303 | A | T | 1 | a0001c0001t0001g0325 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.949-495A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134901303 | |||||||
| chr2:134901491 | T | G | 3 | a0001c0001t0001g0329 a0001c0001t0001g0330 a0001c0001t0001g0338 |
3 | HG02886.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.949-307T>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134901491 | |||||||
| chr2:134901610 | A | T | 1 | a0001c0001t0001g0333 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.949-188A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134901610 | |||||||
| chr2:134901692 | T | C | 2 | a0002c0002t0001g0197 a0002c0002t0001g0202 |
2 | HG02145.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.949-106T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134901692 | |||||||
| chr2:134901702 | T | C | 8 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(5): Show |
11 | HG02080.hp1 HG03704.hp2 NA18947.hp2 others(8): Show |
intron_variant | MODIFIER | c.949-96T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134901702 | |||||||
| chr2:134901740 | C | A | 1 | a0001c0001t0001g0112 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.949-58C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134901740 |