Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 11061 |
| ensemblid | ENSG00000136110.13 |
| hgncid | 17005 |
| symbol | CNMD |
| name | chondromodulin |
| refseq_nuc | NM_007015.3 |
| refseq_prot | NP_008946.1 |
| ensembl_nuc | ENST00000377962.8 |
| ensembl_prot | ENSP00000367198.3 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 52703264 |
| end | 52739820 |
| strand | - |
| ver | v1.2 |
| region | chr13:52703264-52739820 |
| region5000 | chr13:52698264-52744820 |
| regionname0 | CNMD_chr13_52703264_52739820 |
| regionname5000 | CNMD_chr13_52698264_52744820 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 334 | 305 | 70 | 71 | 119 | 14 | 30 | 83 | CNMD_chr13_52698264_52744820 | CNMD | MTENS others(329): Show |
chr13 | 52698264 | 52744820 |
| a0002 | 0/1 | 334 | 21 | 15 | 1 | 0 | 0 | 4 | 0 | CNMD_chr13_52698264_52744820 | CNMD | MTENS others(329): Show |
chr13 | 52698264 | 52744820 |
| a0003 | 0/0 | 334 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | MTENS others(329): Show |
chr13 | 52698264 | 52744820 |
| a0004 | 0/0 | 334 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | MTENS others(329): Show |
chr13 | 52698264 | 52744820 |
| a0005 | 0/0 | 334 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CNMD_chr13_52698264_52744820 | CNMD | MTENS others(329): Show |
chr13 | 52698264 | 52744820 |
| a0006 | 0/0 | 334 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | MTENS others(329): Show |
chr13 | 52698264 | 52744820 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1002 | 297 | 69 | 69 | 115 | 14 | 29 | CNMD_chr13_52698264_52744820 | CNMD | ATGAC others(997): Show |
chr13 | 52698264 | 52744820 | ||
| a0001c0003 | 0/0 | 1002 | 6 | 0 | 1 | 4 | 0 | 1 | CNMD_chr13_52698264_52744820 | CNMD | ATGAC others(997): Show |
chr13 | 52698264 | 52744820 | ||
| a0001c0008 | 0/0 | 1002 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | ATGAC others(997): Show |
chr13 | 52698264 | 52744820 | ||
| a0001c0009 | 0/0 | 1002 | 1 | 0 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | ATGAC others(997): Show |
chr13 | 52698264 | 52744820 | ||
| a0002c0002 | 0/1 | 1002 | 21 | 15 | 1 | 0 | 0 | 4 | CNMD_chr13_52698264_52744820 | CNMD | ATGAC others(997): Show |
chr13 | 52698264 | 52744820 | ||
| a0003c0006 | 0/0 | 1002 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | ATGAC others(997): Show |
chr13 | 52698264 | 52744820 | ||
| a0004c0007 | 0/0 | 1002 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | ATGAC others(997): Show |
chr13 | 52698264 | 52744820 | ||
| a0005c0004 | 0/0 | 1002 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | ATGAC others(997): Show |
chr13 | 52698264 | 52744820 | ||
| a0006c0005 | 0/0 | 1002 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | ATGAC others(997): Show |
chr13 | 52698264 | 52744820 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1455 | 276 | 63 | 67 | 108 | 14 | 24 | CNMD_chr13_52698264_52744820 | CNMD | AGGCG others(1450): Show |
chr13 | 52698264 | 52744820 |
| a0001c0001t0002 | 0/0 | 1455 | 8 | 0 | 1 | 3 | 0 | 4 | CNMD_chr13_52698264_52744820 | CNMD | AGGCG others(1450): Show |
chr13 | 52698264 | 52744820 |
| a0001c0001t0004 | 1/0 | 1455 | 5 | 3 | 0 | 0 | 0 | 1 | CNMD_chr13_52698264_52744820 | CNMD | AGGCG others(1450): Show |
chr13 | 52698264 | 52744820 |
| a0001c0001t0005 | 0/0 | 1455 | 4 | 3 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | AGGCG others(1450): Show |
chr13 | 52698264 | 52744820 |
| a0001c0001t0006 | 0/0 | 1455 | 3 | 0 | 0 | 3 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | AGGCG others(1450): Show |
chr13 | 52698264 | 52744820 |
| a0001c0001t0007 | 0/0 | 1453 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | AGGCG others(1448): Show |
chr13 | 52698264 | 52744820 |
| a0001c0003t0003 | 0/0 | 1453 | 6 | 0 | 1 | 4 | 0 | 1 | CNMD_chr13_52698264_52744820 | CNMD | AGGCG others(1448): Show |
chr13 | 52698264 | 52744820 |
| a0001c0008t0001 | 0/0 | 1455 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | AGGCG others(1450): Show |
chr13 | 52698264 | 52744820 |
| a0001c0009t0001 | 0/0 | 1455 | 1 | 0 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | AGGCG others(1450): Show |
chr13 | 52698264 | 52744820 |
| a0002c0002t0001 | 0/1 | 1455 | 21 | 15 | 1 | 0 | 0 | 4 | CNMD_chr13_52698264_52744820 | CNMD | AGGCG others(1450): Show |
chr13 | 52698264 | 52744820 |
| a0003c0006t0001 | 0/0 | 1455 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | AGGCG others(1450): Show |
chr13 | 52698264 | 52744820 |
| a0004c0007t0001 | 0/0 | 1455 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | AGGCG others(1450): Show |
chr13 | 52698264 | 52744820 |
| a0005c0004t0001 | 0/0 | 1455 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | AGGCG others(1450): Show |
chr13 | 52698264 | 52744820 |
| a0006c0005t0001 | 0/0 | 1455 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | AGGCG others(1450): Show |
chr13 | 52698264 | 52744820 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 9 | 0 | 4 | 1 | 3 | 1 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0003 | 0/0 | 6 | 0 | 1 | 3 | 0 | 2 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0004 | 0/0 | 6 | 0 | 0 | 3 | 0 | 3 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0006 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0007 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0016 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0043 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0002g0015 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0004g0031 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0005g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0005g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0005g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0006g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0006g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0001t0007g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0003t0003g0013 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0003t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0003t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0003t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0008t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0001c0009t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0002c0002t0001g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0002c0002t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0002c0002t0001g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0002c0002t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0002c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0002c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0002c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0002c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0002c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0002c0002t0001g0185 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0002c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0002c0002t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0002c0002t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0003c0006t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0004c0007t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0005c0004t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| a0006c0005t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0217 | EUR | GBR | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0207 | EUR | GBR | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0201 | EUR | GBR | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | FIN | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0159 | EUR | FIN | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | CHS | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG00544 | hp1 | a0001 | c0003 | t0003 | g0138 | EAS | CHS | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | CHS | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG00609 | hp1 | a0001 | c0001 | t0006 | g0119 | EAS | CHS | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | PUR | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0036 | AMR | PUR | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01099 | hp1 | a0001 | c0003 | t0003 | g0013 | AMR | PUR | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01243 | hp2 | a0001 | c0001 | t0005 | g0161 | AMR | PUR | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0116 | EUR | IBS | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0049 | EUR | IBS | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0049 | EUR | IBS | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01975 | hp2 | a0001 | c0009 | t0001 | g0235 | AMR | PEL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | CDX | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CDX | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0218 | AFR | ACB | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0162 | AFR | ACB | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02523 | hp1 | a0001 | c0001 | t0006 | g0033 | EAS | KHV | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | KHV | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0012 | AFR | GWD | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02615 | hp2 | a0003 | c0006 | t0001 | g0238 | AFR | GWD | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0012 | AFR | GWD | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0012 | AFR | GWD | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0156 | SAS | PJL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0059 | AFR | GWD | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0233 | AFR | GWD | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02896 | hp1 | a0004 | c0007 | t0001 | g0232 | AFR | GWD | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0030 | AFR | GWD | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02897 | hp1 | a0002 | c0002 | t0001 | g0030 | AFR | GWD | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02922 | hp2 | a0001 | c0008 | t0001 | g0237 | AFR | ESN | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | ESN | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0012 | AFR | ESN | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ESN | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0171 | AFR | GWD | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | MSL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ESN | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0114 | AFR | ESN | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0164 | AFR | MSL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0160 | AFR | MSL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0184 | SAS | PJL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0222 | AFR | ESN | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0036 | AFR | GWD | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0183 | SAS | PJL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0038 | SAS | PJL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | STU | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG03688 | hp2 | a0001 | c0003 | t0003 | g0013 | SAS | STU | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0175 | SAS | PJL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0121 | SAS | BEB | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | BEB | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | STU | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | STU | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | STU | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | STU | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | STU | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0038 | SAS | STU | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | YRI | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0057 | AFR | YRI | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | CHB | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | CHB | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0090 | AFR | YRI | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | YRI | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18965 | hp2 | a0001 | c0001 | t0006 | g0033 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18967 | hp1 | a0005 | c0004 | t0001 | g0069 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18967 | hp2 | a0001 | c0001 | t0007 | g0168 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18994 | hp2 | a0001 | c0003 | t0003 | g0050 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA19030 | hp1 | a0006 | c0005 | t0001 | g0125 | AFR | LWK | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | LWK | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | LWK | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | LWK | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA19080 | hp1 | a0001 | c0003 | t0003 | g0013 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA19082 | hp2 | a0001 | c0003 | t0003 | g0051 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | YRI | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0163 | AFR | YRI | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ASW | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0031 | AFR | ASW | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0204 | EUR | TSI | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0226 | SAS | GIH | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0195 | AFR | USA | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | USA | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | USA | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | USA | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | LWK | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | LWK | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0185 | REF | REF | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0031 | REF | REF | CNMD_chr13_52698264_52744820 | CNMD | chr13 | 52698264 | 52744820 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:52703699 | C | T | 1 | a0006 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.901G>A | p.Gly301Arg | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 7/7 | 1020/1455 | 901/1005 | 301/334 | chr13 | 52703699 | |||
| chr13:52708596 | A | C | 1 | a0004 | 1 | HG02896.hp1 | missense_variant | MODERATE | c.729T>G | p.Asn243Lys | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/7 | 848/1455 | 729/1005 | 243/334 | chr13 | 52708596 | |||
| chr13:52712815 | C | T | 1 | a0002 | 20 | HG01070.hp1 HG02258.hp2 HG02451.hp1 others(17): Show |
missense_variant | MODERATE | c.523G>A | p.Val175Ile | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 5/7 | 642/1455 | 523/1005 | 175/334 | chr13 | 52712815 | |||
| chr13:52712832 | G | T | 1 | a0003 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.506C>A | p.Ser169Tyr | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 5/7 | 625/1455 | 506/1005 | 169/334 | chr13 | 52712832 | |||
| chr13:52733227 | A | G | 1 | a0005 | 1 | NA18967.hp1 | missense_variant | MODERATE | c.346T>C | p.Phe116Leu | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/7 | 465/1455 | 346/1005 | 116/334 | chr13 | 52733227 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:52703655 | C | T | 1 | a0001c0008 | 1 | HG02922.hp2 | synonymous_variant | LOW | c.945G>A | p.Ser315Ser | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 7/7 | 1064/1455 | 945/1005 | 315/334 | chr13 | 52703655 | |||
| chr13:52708614 | G | A | 1 | a0001c0003 | 6 | HG00544.hp1 HG01099.hp1 HG03688.hp2 others(3): Show |
synonymous_variant | LOW | c.711C>T | p.Gly237Gly | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/7 | 830/1455 | 711/1005 | 237/334 | chr13 | 52708614 | |||
| chr13:52724060 | C | T | 1 | a0006c0005 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.405G>A | p.Ala135Ala | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/7 | 524/1455 | 405/1005 | 135/334 | chr13 | 52724060 | |||
| chr13:52739037 | G | A | 1 | a0001c0009 | 1 | HG01975.hp2 | synonymous_variant | LOW | c.207C>T | p.Asp69Asp | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/7 | 326/1455 | 207/1005 | 69/334 | chr13 | 52739037 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:52703275 | CTG | C | 2 | a0001c0001t0007 a0001c0003t0003 |
7 | HG00544.hp1 HG01099.hp1 HG03688.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*318_*319delCA | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 7/7 | 318 | chr13 | 52703275 | ||||||
| chr13:52703405 | T | G | 1 | a0001c0001t0006 | 3 | HG00609.hp1 HG02523.hp1 NA18965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*190A>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 7/7 | 190 | chr13 | 52703405 | ||||||
| chr13:52703504 | G | A | 11 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(8): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
3_prime_UTR_variant | MODIFIER | c.*91C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 7/7 | 91 | chr13 | 52703504 | ||||||
| chr13:52703511 | T | C | 12 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(9): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
3_prime_UTR_variant | MODIFIER | c.*84A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 7/7 | 84 | chr13 | 52703511 | ||||||
| chr13:52703537 | T | G | 1 | a0001c0001t0002 | 8 | HG00558.hp2 HG00642.hp2 HG02523.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*58A>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 7/7 | 58 | chr13 | 52703537 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:52703854 | A | G | 4 | a0001c0001t0005g0059 a0001c0001t0005g0090 a0001c0001t0005g0160 others(1): Show |
4 | HG01243.hp2 HG02886.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.790-44T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52703854 | |||||||
| chr13:52703863 | G | A | 6 | a0001c0001t0001g0089 a0001c0001t0001g0091 a0001c0001t0001g0189 others(3): Show |
6 | HG01891.hp2 HG02257.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.790-53C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52703863 | |||||||
| chr13:52703932 | T | C | 60 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(57): Show |
102 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.790-122A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52703932 | |||||||
| chr13:52703969 | C | T | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(230): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.790-159G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52703969 | |||||||
| chr13:52704243 | C | A | 1 | a0001c0001t0001g0071 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.790-433G>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52704243 | |||||||
| chr13:52704461 | A | ATATAGT | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.790-652_790-651ins others(6): Show |
CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52704461 | |||||||
| chr13:52704461 | A | ATATAGTT others(30): Show |
1 | a0001c0001t0001g0131 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.790-652_790-651ins others(37): Show |
CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52704461 | |||||||
| chr13:52704545 | T | C | 229 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(226): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.790-735A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52704545 | |||||||
| chr13:52704759 | G | C | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(208): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.790-949C>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52704759 | |||||||
| chr13:52704760 | G | C | 1 | a0001c0001t0001g0131 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.790-950C>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52704760 | |||||||
| chr13:52704785 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.790-975G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52704785 | |||||||
| chr13:52704839 | A | C | 1 | a0001c0001t0001g0149 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.790-1029T>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52704839 | |||||||
| chr13:52704878 | A | C | 2 | a0001c0001t0001g0148 a0001c0001t0001g0151 |
2 | HG00597.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.790-1068T>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52704878 | |||||||
| chr13:52704903 | T | TAAAAATA others(1): Show |
229 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(226): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.790-1094_790-1093i others(10): Show |
CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52704903 | |||||||
| chr13:52705028 | C | T | 7 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(4): Show |
7 | HG02559.hp2 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.790-1218G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52705028 | |||||||
| chr13:52705060 | G | GA | 221 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(218): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.790-1251dupT | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52705060 | |||||||
| chr13:52705060 | G | GAA | 5 | a0001c0001t0001g0016 a0001c0001t0001g0154 a0001c0001t0001g0157 others(2): Show |
7 | HG01243.hp1 HG02965.hp1 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.790-1252_790-1251d others(4): Show |
CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52705060 | |||||||
| chr13:52705283 | A | G | 4 | a0001c0003t0003g0013 a0001c0003t0003g0050 a0001c0003t0003g0051 others(1): Show |
6 | HG00544.hp1 HG01099.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.790-1473T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52705283 | |||||||
| chr13:52705357 | T | A | 1 | a0001c0001t0001g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.790-1547A>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52705357 | |||||||
| chr13:52705407 | T | C | 60 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(57): Show |
102 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.790-1597A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52705407 | |||||||
| chr13:52705435 | A | G | 4 | a0001c0003t0003g0013 a0001c0003t0003g0050 a0001c0003t0003g0051 others(1): Show |
6 | HG00544.hp1 HG01099.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.790-1625T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52705435 | |||||||
| chr13:52705482 | A | T | 1 | a0001c0001t0001g0131 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.790-1672T>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52705482 | |||||||
| chr13:52705598 | A | G | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(215): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.790-1788T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52705598 | |||||||
| chr13:52705623 | G | A | 1 | a0001c0001t0001g0049 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.790-1813C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52705623 | |||||||
| chr13:52705640 | T | G | 1 | a0001c0001t0001g0131 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.790-1830A>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52705640 | |||||||
| chr13:52705655 | T | C | 235 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(232): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.790-1845A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52705655 | |||||||
| chr13:52705672 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.790-1862T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52705672 | |||||||
| chr13:52705673 | C | A | 1 | a0001c0001t0001g0131 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.790-1863G>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52705673 | |||||||
| chr13:52705814 | C | CCTGT | 7 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(4): Show |
7 | HG02559.hp2 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.790-2008_790-2005d others(6): Show |
CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52705814 | |||||||
| chr13:52705878 | G | A | 65 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(62): Show |
109 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.790-2068C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52705878 | |||||||
| chr13:52705973 | G | T | 4 | a0001c0003t0003g0013 a0001c0003t0003g0050 a0001c0003t0003g0051 others(1): Show |
6 | HG00544.hp1 HG01099.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.790-2163C>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52705973 | |||||||
| chr13:52706040 | A | T | 1 | a0001c0001t0001g0131 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.790-2230T>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52706040 | |||||||
| chr13:52706074 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.790-2264A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52706074 | |||||||
| chr13:52706315 | A | G | 1 | a0001c0001t0001g0174 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.789+2221T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52706315 | |||||||
| chr13:52706371 | C | A | 1 | a0001c0001t0001g0131 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.789+2165G>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52706371 | |||||||
| chr13:52706372 | A | T | 1 | a0001c0001t0001g0131 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.789+2164T>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52706372 | |||||||
| chr13:52706376 | G | A | 1 | a0004c0007t0001g0232 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.789+2160C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52706376 | |||||||
| chr13:52706453 | A | G | 42 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(39): Show |
71 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.789+2083T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52706453 | |||||||
| chr13:52706658 | G | A | 1 | a0001c0001t0001g0032 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.789+1878C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52706658 | |||||||
| chr13:52706733 | GTGTGTA | G | 2 | a0002c0002t0001g0038 a0002c0002t0001g0184 |
3 | HG03490.hp2 HG03669.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.789+1797_789+1802d others(8): Show |
CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52706733 | |||||||
| chr13:52706735 | GTGTA | G | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(204): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.789+1797_789+1800d others(6): Show |
CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52706735 | |||||||
| chr13:52706737 | GTA | G | 9 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(6): Show |
9 | HG02451.hp1 HG02559.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.789+1797_789+1798d others(4): Show |
CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52706737 | |||||||
| chr13:52706738 | TATGTGTG others(11): Show |
T | 6 | a0001c0001t0001g0089 a0001c0001t0001g0091 a0001c0001t0001g0189 others(3): Show |
6 | HG01891.hp2 HG02257.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.789+1780_789+1797d others(20): Show |
CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52706738 | |||||||
| chr13:52706739 | A | G | 1 | a0006c0005t0001g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.789+1797T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52706739 | |||||||
| chr13:52706740 | T | G | 1 | a0001c0001t0001g0131 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.789+1796A>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52706740 | |||||||
| chr13:52706752 | T | G | 1 | a0006c0005t0001g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.789+1784A>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52706752 | |||||||
| chr13:52706756 | G | T | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(220): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.789+1780C>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52706756 | |||||||
| chr13:52706803 | T | G | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(230): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.789+1733A>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52706803 | |||||||
| chr13:52707042 | C | T | 1 | a0001c0001t0001g0047 | 2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.789+1494G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52707042 | |||||||
| chr13:52707137 | A | G | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(230): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.789+1399T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52707137 | |||||||
| chr13:52707247 | G | A | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(230): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.789+1289C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52707247 | |||||||
| chr13:52707278 | G | A | 4 | a0001c0003t0003g0013 a0001c0003t0003g0050 a0001c0003t0003g0051 others(1): Show |
6 | HG00544.hp1 HG01099.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.789+1258C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52707278 | |||||||
| chr13:52707298 | GCACCTCG others(105): Show |
G | 43 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0034 others(40): Show |
58 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.789+1126_789+1237d others(2): Show |
CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52707298 | |||||||
| chr13:52707326 | C | A | 1 | a0001c0001t0001g0032 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.789+1210G>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52707326 | |||||||
| chr13:52707387 | G | C | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(183): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.789+1149C>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52707387 | |||||||
| chr13:52707395 | C | T | 1 | a0001c0001t0005g0059 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.789+1141G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52707395 | |||||||
| chr13:52707808 | A | C | 1 | a0001c0001t0001g0131 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.789+728T>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52707808 | |||||||
| chr13:52707816 | T | G | 1 | a0001c0001t0001g0131 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.789+720A>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52707816 | |||||||
| chr13:52707847 | G | C | 1 | a0001c0001t0001g0085 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.789+689C>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52707847 | |||||||
| chr13:52707869 | A | C | 1 | a0001c0001t0001g0131 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.789+667T>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52707869 | |||||||
| chr13:52707896 | C | G | 1 | a0001c0001t0001g0131 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.789+640G>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52707896 | |||||||
| chr13:52707997 | C | T | 4 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 others(1): Show |
4 | HG01192.hp1 HG02572.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.789+539G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52707997 | |||||||
| chr13:52708071 | C | A | 1 | a0004c0007t0001g0232 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.789+465G>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52708071 | |||||||
| chr13:52708187 | AT | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.789+348delA | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52708187 | |||||||
| chr13:52708336 | C | T | 4 | a0001c0003t0003g0013 a0001c0003t0003g0050 a0001c0003t0003g0051 others(1): Show |
6 | HG00544.hp1 HG01099.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.789+200G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52708336 | |||||||
| chr13:52708526 | C | T | 4 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 others(1): Show |
4 | HG01192.hp1 HG02572.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.789+10G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 6/6 | chr13 | 52708526 | |||||||
| chr13:52708806 | G | T | 7 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(4): Show |
7 | HG02559.hp2 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.623-104C>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 5/6 | chr13 | 52708806 | |||||||
| chr13:52708879 | TA | T | 4 | a0001c0003t0003g0013 a0001c0003t0003g0050 a0001c0003t0003g0051 others(1): Show |
6 | HG00544.hp1 HG01099.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.623-178delT | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 5/6 | chr13 | 52708879 | |||||||
| chr13:52708881 | G | T | 7 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(4): Show |
7 | HG02559.hp2 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.623-179C>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 5/6 | chr13 | 52708881 | |||||||
| chr13:52708886 | A | C | 1 | a0001c0001t0001g0131 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.623-184T>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 5/6 | chr13 | 52708886 | |||||||
| chr13:52708887 | C | A | 1 | a0001c0001t0001g0131 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.623-185G>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 5/6 | chr13 | 52708887 | |||||||
| chr13:52708888 | A | T | 1 | a0001c0001t0001g0131 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.623-186T>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 5/6 | chr13 | 52708888 | |||||||
| chr13:52708927 | A | G | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(230): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.623-225T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 5/6 | chr13 | 52708927 | |||||||
| chr13:52708984 | G | T | 8 | a0002c0002t0001g0012 a0002c0002t0001g0114 a0002c0002t0001g0162 others(5): Show |
11 | HG02258.hp2 HG02451.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.623-282C>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 5/6 | chr13 | 52708984 | |||||||
| chr13:52709000 | G | A | 6 | a0001c0001t0001g0089 a0001c0001t0001g0091 a0001c0001t0001g0189 others(3): Show |
6 | HG01891.hp2 HG02257.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.623-298C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 5/6 | chr13 | 52709000 | |||||||
| chr13:52709002 | G | A | 3 | a0001c0001t0001g0029 a0001c0001t0001g0111 a0001c0001t0001g0113 |
4 | HG01106.hp1 HG01884.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.623-300C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 5/6 | chr13 | 52709002 | |||||||
| chr13:52709076 | A | G | 1 | a0004c0007t0001g0232 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.623-374T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 5/6 | chr13 | 52709076 | |||||||
| chr13:52709183 | A | G | 66 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(63): Show |
110 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.623-481T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 5/6 | chr13 | 52709183 | |||||||
| chr13:52709250 | A | G | 229 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(226): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.623-548T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 5/6 | chr13 | 52709250 | |||||||
| chr13:52709574 | A | G | 1 | a0001c0001t0001g0077 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.623-872T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 5/6 | chr13 | 52709574 | |||||||
| chr13:52709653 | TGCA | T | 7 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(4): Show |
7 | HG02559.hp2 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.623-954_623-952del others(3): Show |
CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 5/6 | chr13 | 52709653 | |||||||
| chr13:52709765 | G | A | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(222): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.623-1063C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 5/6 | chr13 | 52709765 | |||||||
| chr13:52709900 | G | A | 1 | a0001c0001t0001g0034 | 2 | HG00438.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.623-1198C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 5/6 | chr13 | 52709900 | |||||||
| chr13:52710030 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.623-1328C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 5/6 | chr13 | 52710030 | |||||||
| chr13:52710071 | G | A | 2 | a0001c0001t0001g0220 a0001c0001t0001g0221 |
2 | HG01192.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.623-1369C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 5/6 | chr13 | 52710071 | |||||||
| chr13:52710133 | G | A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0068 |
7 | NA18945.hp2 NA18959.hp1 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.623-1431C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 5/6 | chr13 | 52710133 | |||||||
| chr13:52710223 | A | T | 1 | a0001c0001t0001g0104 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.623-1521T>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 5/6 | chr13 | 52710223 | |||||||
| chr13:52710347 | C | T | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(230): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.623-1645G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 5/6 | chr13 | 52710347 | |||||||
| chr13:52710389 | A | C | 1 | a0006c0005t0001g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.623-1687T>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 5/6 | chr13 | 52710389 | |||||||
| chr13:52710560 | G | A | 8 | a0002c0002t0001g0012 a0002c0002t0001g0114 a0002c0002t0001g0162 others(5): Show |
11 | HG02258.hp2 HG02451.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.623-1858C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 5/6 | chr13 | 52710560 | |||||||
| chr13:52710598 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.623-1896A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 5/6 | chr13 | 52710598 | |||||||
| chr13:52710655 | C | A | 1 | a0001c0001t0001g0155 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.623-1953G>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 5/6 | chr13 | 52710655 | |||||||
| chr13:52710958 | T | C | 229 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(226): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.622+1758A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 5/6 | chr13 | 52710958 | |||||||
| chr13:52710970 | C | T | 1 | a0001c0001t0001g0018 | 3 | HG01261.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.622+1746G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 5/6 | chr13 | 52710970 | |||||||
| chr13:52711302 | G | C | 1 | a0001c0001t0001g0234 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.622+1414C>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 5/6 | chr13 | 52711302 | |||||||
| chr13:52711406 | G | C | 1 | a0001c0001t0001g0112 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.622+1310C>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 5/6 | chr13 | 52711406 | |||||||
| chr13:52711800 | A | G | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG01074.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.622+916T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 5/6 | chr13 | 52711800 | |||||||
| chr13:52711848 | G | GTA | 138 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(135): Show |
182 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.622+866_622+867dup others(2): Show |
CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 5/6 | chr13 | 52711848 | |||||||
| chr13:52711947 | GC | G | 138 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(135): Show |
182 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.622+768delG | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 5/6 | chr13 | 52711947 | |||||||
| chr13:52711991 | G | A | 138 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(135): Show |
182 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.622+725C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 5/6 | chr13 | 52711991 | |||||||
| chr13:52712015 | T | C | 2 | a0001c0001t0001g0032 a0001c0001t0001g0089 |
3 | HG02109.hp1 HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.622+701A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 5/6 | chr13 | 52712015 | |||||||
| chr13:52712090 | C | T | 2 | a0001c0001t0001g0197 a0001c0001t0001g0207 |
2 | HG00099.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.622+626G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 5/6 | chr13 | 52712090 | |||||||
| chr13:52712147 | C | T | 10 | a0001c0001t0001g0091 a0001c0001t0001g0189 a0001c0001t0001g0190 others(7): Show |
10 | HG01243.hp2 HG01891.hp2 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.622+569G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 5/6 | chr13 | 52712147 | |||||||
| chr13:52712164 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.622+552T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 5/6 | chr13 | 52712164 | |||||||
| chr13:52712189 | AG | A | 146 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(143): Show |
191 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.622+526delC | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 5/6 | chr13 | 52712189 | |||||||
| chr13:52712214 | C | G | 1 | a0001c0001t0001g0032 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.622+502G>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 5/6 | chr13 | 52712214 | |||||||
| chr13:52712336 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.622+380G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 5/6 | chr13 | 52712336 | |||||||
| chr13:52712379 | T | TA | 7 | a0001c0001t0001g0032 a0001c0001t0001g0219 a0001c0001t0001g0220 others(4): Show |
8 | HG01192.hp1 HG01243.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.622+336dupT | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 5/6 | chr13 | 52712379 | |||||||
| chr13:52712687 | A | G | 4 | a0001c0001t0001g0014 a0001c0001t0001g0052 a0001c0001t0001g0054 others(1): Show |
6 | HG01255.hp2 HG01256.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.622+29T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 5/6 | chr13 | 52712687 | |||||||
| chr13:52712888 | G | C | 60 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(57): Show |
102 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.469-19C>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52712888 | |||||||
| chr13:52712985 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.469-116G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52712985 | |||||||
| chr13:52713245 | A | C | 2 | a0001c0001t0001g0046 a0001c0001t0001g0216 |
3 | NA18944.hp2 NA18960.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.469-376T>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52713245 | |||||||
| chr13:52713615 | A | G | 11 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0076 others(8): Show |
19 | HG00323.hp1 HG00408.hp2 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.469-746T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52713615 | |||||||
| chr13:52713841 | G | C | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG01074.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.469-972C>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52713841 | |||||||
| chr13:52714125 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.469-1256G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52714125 | |||||||
| chr13:52714367 | A | T | 1 | a0001c0008t0001g0237 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.469-1498T>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52714367 | |||||||
| chr13:52714590 | T | A | 1 | a0004c0007t0001g0232 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.469-1721A>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52714590 | |||||||
| chr13:52714769 | T | TCA | 7 | a0001c0001t0001g0014 a0001c0001t0001g0052 a0001c0001t0001g0054 others(4): Show |
9 | HG01109.hp1 HG01255.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.469-1902_469-1901d others(4): Show |
CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52714769 | |||||||
| chr13:52714819 | T | A | 1 | a0001c0001t0001g0056 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.469-1950A>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52714819 | |||||||
| chr13:52714820 | T | C | 1 | a0001c0001t0005g0090 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.469-1951A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52714820 | |||||||
| chr13:52714853 | A | C | 1 | a0001c0001t0002g0156 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.469-1984T>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52714853 | |||||||
| chr13:52714959 | C | T | 229 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(226): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.469-2090G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52714959 | |||||||
| chr13:52714968 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.469-2099G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52714968 | |||||||
| chr13:52715031 | A | G | 2 | a0001c0003t0003g0050 a0001c0003t0003g0138 |
2 | HG00544.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.469-2162T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52715031 | |||||||
| chr13:52715165 | A | T | 1 | a0001c0001t0001g0189 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.469-2296T>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52715165 | |||||||
| chr13:52715259 | A | T | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(230): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.469-2390T>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52715259 | |||||||
| chr13:52715362 | T | A | 1 | a0001c0001t0001g0167 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.469-2493A>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52715362 | |||||||
| chr13:52715406 | G | A | 1 | a0002c0002t0001g0184 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.469-2537C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52715406 | |||||||
| chr13:52715427 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.469-2558T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52715427 | |||||||
| chr13:52715459 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.469-2590C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52715459 | |||||||
| chr13:52715483 | T | A | 1 | a0004c0007t0001g0232 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.469-2614A>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52715483 | |||||||
| chr13:52715503 | C | A | 1 | a0002c0002t0001g0164 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.469-2634G>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52715503 | |||||||
| chr13:52715527 | G | A | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(216): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.469-2658C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52715527 | |||||||
| chr13:52715804 | A | G | 8 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0231 others(5): Show |
10 | HG00544.hp1 HG01074.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.469-2935T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52715804 | |||||||
| chr13:52716037 | C | T | 6 | a0001c0001t0001g0231 a0001c0003t0003g0013 a0001c0003t0003g0050 others(3): Show |
8 | HG00544.hp1 HG01099.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.469-3168G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52716037 | |||||||
| chr13:52716049 | C | T | 8 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0231 others(5): Show |
10 | HG00544.hp1 HG01074.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.469-3180G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52716049 | |||||||
| chr13:52716079 | G | C | 9 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(6): Show |
9 | HG02559.hp2 HG02886.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.469-3210C>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52716079 | |||||||
| chr13:52716323 | C | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0210 |
5 | NA18949.hp2 NA18959.hp2 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.469-3454G>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52716323 | |||||||
| chr13:52716545 | C | T | 1 | a0001c0001t0001g0225 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.469-3676G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52716545 | |||||||
| chr13:52716711 | C | G | 2 | a0001c0001t0001g0041 a0001c0001t0001g0159 |
3 | HG00323.hp2 HG02602.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.469-3842G>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52716711 | |||||||
| chr13:52716791 | A | G | 8 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0231 others(5): Show |
10 | HG00544.hp1 HG01074.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.469-3922T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52716791 | |||||||
| chr13:52716848 | C | T | 2 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
2 | HG00597.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.469-3979G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52716848 | |||||||
| chr13:52716862 | T | C | 4 | a0002c0002t0001g0114 a0002c0002t0001g0162 a0002c0002t0001g0163 others(1): Show |
4 | HG02451.hp1 HG03195.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.469-3993A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52716862 | |||||||
| chr13:52716886 | A | T | 4 | a0001c0001t0001g0058 a0001c0001t0001g0178 a0001c0001t0001g0179 others(1): Show |
4 | HG02109.hp2 HG02647.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.469-4017T>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52716886 | |||||||
| chr13:52716961 | T | C | 2 | a0001c0001t0001g0231 a0003c0006t0001g0238 |
2 | HG02615.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.469-4092A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52716961 | |||||||
| chr13:52717118 | A | G | 3 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 |
3 | HG02559.hp2 HG03130.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.469-4249T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52717118 | |||||||
| chr13:52717152 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.469-4283A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52717152 | |||||||
| chr13:52717198 | C | T | 1 | a0001c0001t0001g0213 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.469-4329G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52717198 | |||||||
| chr13:52717276 | T | C | 1 | a0001c0001t0001g0135 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.469-4407A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52717276 | |||||||
| chr13:52717555 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.469-4686C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52717555 | |||||||
| chr13:52717916 | G | A | 3 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 |
3 | HG02559.hp2 HG03130.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.469-5047C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52717916 | |||||||
| chr13:52717941 | G | T | 1 | a0001c0001t0001g0054 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.469-5072C>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52717941 | |||||||
| chr13:52718032 | T | C | 1 | a0001c0001t0005g0059 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.469-5163A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52718032 | |||||||
| chr13:52718176 | A | T | 1 | a0001c0001t0001g0116 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.469-5307T>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52718176 | |||||||
| chr13:52718226 | T | C | 22 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(19): Show |
24 | HG00544.hp1 HG01074.hp1 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.469-5357A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52718226 | |||||||
| chr13:52718294 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.469-5425G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52718294 | |||||||
| chr13:52718333 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.469-5464A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52718333 | |||||||
| chr13:52718441 | A | G | 1 | a0001c0001t0001g0018 | 3 | HG01261.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.468+5556T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52718441 | |||||||
| chr13:52718442 | G | A | 1 | a0001c0001t0001g0018 | 3 | HG01261.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.468+5555C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52718442 | |||||||
| chr13:52718448 | G | C | 1 | a0001c0001t0001g0018 | 3 | HG01261.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.468+5549C>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52718448 | |||||||
| chr13:52718471 | G | C | 1 | a0001c0001t0001g0018 | 3 | HG01261.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.468+5526C>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52718471 | |||||||
| chr13:52718474 | AT | A | 1 | a0001c0001t0001g0018 | 3 | HG01261.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.468+5522delA | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52718474 | |||||||
| chr13:52718654 | G | T | 10 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0159 others(7): Show |
16 | HG00323.hp2 HG00544.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.468+5343C>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52718654 | |||||||
| chr13:52718724 | C | G | 1 | a0002c0002t0001g0162 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.468+5273G>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52718724 | |||||||
| chr13:52718794 | T | C | 3 | a0001c0001t0001g0011 a0001c0001t0001g0081 a0001c0001t0001g0215 |
6 | NA18961.hp2 NA18965.hp1 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.468+5203A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52718794 | |||||||
| chr13:52718914 | T | C | 1 | a0001c0001t0002g0175 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.468+5083A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52718914 | |||||||
| chr13:52718921 | C | T | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG01074.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.468+5076G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52718921 | |||||||
| chr13:52719000 | T | C | 5 | a0001c0001t0001g0091 a0001c0001t0001g0189 a0001c0001t0001g0190 others(2): Show |
5 | HG01891.hp2 HG02257.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.468+4997A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52719000 | |||||||
| chr13:52719013 | A | C | 1 | a0001c0001t0001g0101 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.468+4984T>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52719013 | |||||||
| chr13:52719172 | T | G | 6 | a0001c0001t0001g0058 a0001c0001t0001g0178 a0001c0001t0001g0179 others(3): Show |
6 | HG02109.hp2 HG02647.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.468+4825A>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52719172 | |||||||
| chr13:52719341 | T | C | 5 | a0001c0001t0001g0091 a0001c0001t0001g0189 a0001c0001t0001g0190 others(2): Show |
5 | HG01891.hp2 HG02257.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.468+4656A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52719341 | |||||||
| chr13:52719358 | A | T | 5 | a0001c0001t0001g0091 a0001c0001t0001g0189 a0001c0001t0001g0190 others(2): Show |
5 | HG01891.hp2 HG02257.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.468+4639T>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52719358 | |||||||
| chr13:52719393 | C | T | 6 | a0001c0001t0001g0231 a0001c0003t0003g0013 a0001c0003t0003g0050 others(3): Show |
8 | HG00544.hp1 HG01099.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+4604G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52719393 | |||||||
| chr13:52719394 | G | A | 9 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(6): Show |
9 | HG02559.hp2 HG02886.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.468+4603C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52719394 | |||||||
| chr13:52719424 | A | G | 1 | a0004c0007t0001g0232 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.468+4573T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52719424 | |||||||
| chr13:52719466 | G | A | 2 | a0001c0001t0001g0136 a0001c0001t0001g0228 |
2 | HG02027.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.468+4531C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52719466 | |||||||
| chr13:52719768 | T | C | 1 | a0001c0001t0002g0175 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.468+4229A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52719768 | |||||||
| chr13:52719792 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.468+4205G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52719792 | |||||||
| chr13:52720193 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.468+3804C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52720193 | |||||||
| chr13:52720255 | G | T | 9 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(6): Show |
9 | HG02559.hp2 HG02886.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.468+3742C>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52720255 | |||||||
| chr13:52720381 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.468+3616C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52720381 | |||||||
| chr13:52720467 | T | C | 1 | a0002c0002t0001g0233 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.468+3530A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52720467 | |||||||
| chr13:52720599 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.468+3398G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52720599 | |||||||
| chr13:52720682 | T | C | 1 | a0001c0001t0001g0193 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.468+3315A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52720682 | |||||||
| chr13:52720740 | ATCCCTGC others(11): Show |
A | 1 | a0001c0001t0005g0059 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.468+3239_468+3256d others(20): Show |
CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52720740 | |||||||
| chr13:52720885 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.468+3112A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52720885 | |||||||
| chr13:52720907 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.468+3090C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52720907 | |||||||
| chr13:52721082 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.468+2915G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52721082 | |||||||
| chr13:52721330 | C | G | 9 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(6): Show |
9 | HG02559.hp2 HG02886.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.468+2667G>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52721330 | |||||||
| chr13:52721406 | C | T | 5 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(2): Show |
5 | HG02559.hp2 HG02922.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.468+2591G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52721406 | |||||||
| chr13:52721594 | G | T | 1 | a0001c0001t0001g0018 | 3 | HG01261.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.468+2403C>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52721594 | |||||||
| chr13:52721626 | T | G | 4 | a0001c0003t0003g0013 a0001c0003t0003g0050 a0001c0003t0003g0051 others(1): Show |
6 | HG00544.hp1 HG01099.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.468+2371A>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52721626 | |||||||
| chr13:52721694 | T | C | 3 | a0001c0001t0001g0134 a0001c0001t0001g0154 a0001c0001t0001g0155 |
3 | NA18954.hp2 NA18971.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.468+2303A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52721694 | |||||||
| chr13:52721818 | G | A | 1 | a0001c0001t0001g0211 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.468+2179C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52721818 | |||||||
| chr13:52721958 | T | A | 1 | a0001c0001t0001g0225 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.468+2039A>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52721958 | |||||||
| chr13:52722089 | C | T | 8 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0231 others(5): Show |
10 | HG00544.hp1 HG01074.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.468+1908G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52722089 | |||||||
| chr13:52722162 | C | T | 3 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 |
3 | HG02559.hp2 HG03130.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.468+1835G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52722162 | |||||||
| chr13:52722318 | A | G | 2 | a0001c0001t0001g0134 a0001c0001t0001g0154 |
2 | NA18971.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.468+1679T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52722318 | |||||||
| chr13:52722488 | A | G | 1 | a0006c0005t0001g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.468+1509T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52722488 | |||||||
| chr13:52722536 | A | G | 235 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(232): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.468+1461T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52722536 | |||||||
| chr13:52722892 | G | A | 5 | a0001c0001t0001g0091 a0001c0001t0001g0189 a0001c0001t0001g0190 others(2): Show |
5 | HG01891.hp2 HG02257.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.468+1105C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52722892 | |||||||
| chr13:52722984 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.468+1013C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52722984 | |||||||
| chr13:52723095 | G | GT | 6 | a0001c0001t0001g0231 a0001c0003t0003g0013 a0001c0003t0003g0050 others(3): Show |
8 | HG00544.hp1 HG01099.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+901dupA | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52723095 | |||||||
| chr13:52723103 | A | T | 8 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0231 others(5): Show |
10 | HG00544.hp1 HG01074.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.468+894T>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52723103 | |||||||
| chr13:52723345 | G | A | 4 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0093 others(1): Show |
6 | HG02055.hp1 HG02559.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+652C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52723345 | |||||||
| chr13:52723618 | G | A | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(230): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.468+379C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52723618 | |||||||
| chr13:52723621 | C | G | 1 | a0001c0001t0001g0116 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.468+376G>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52723621 | |||||||
| chr13:52723729 | A | C | 1 | a0001c0001t0001g0198 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.468+268T>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52723729 | |||||||
| chr13:52723776 | A | G | 8 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0231 others(5): Show |
10 | HG00544.hp1 HG01074.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.468+221T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52723776 | |||||||
| chr13:52723827 | G | A | 42 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(39): Show |
71 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.468+170C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 4/6 | chr13 | 52723827 | |||||||
| chr13:52724199 | G | A | 9 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(6): Show |
9 | HG02559.hp2 HG02886.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.355-89C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52724199 | |||||||
| chr13:52724417 | C | CA | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.355-308dupT | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52724417 | |||||||
| chr13:52724417 | C | CAA | 35 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0042 others(32): Show |
40 | HG00597.hp1 HG00597.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.355-309_355-308dup others(2): Show |
CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52724417 | |||||||
| chr13:52724417 | C | CAAA | 11 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0054 others(8): Show |
13 | HG01069.hp2 HG01071.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.355-310_355-308dup others(3): Show |
CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52724417 | |||||||
| chr13:52724417 | C | CAAAA | 7 | a0001c0001t0001g0086 a0001c0001t0001g0088 a0001c0001t0001g0105 others(4): Show |
7 | HG01884.hp1 HG02896.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.355-311_355-308dup others(4): Show |
CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52724417 | |||||||
| chr13:52724649 | A | T | 1 | a0001c0001t0001g0145 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.355-539T>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52724649 | |||||||
| chr13:52724663 | G | A | 1 | a0001c0001t0005g0059 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.355-553C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52724663 | |||||||
| chr13:52724724 | T | C | 8 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0231 others(5): Show |
10 | HG00544.hp1 HG01074.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.355-614A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52724724 | |||||||
| chr13:52724734 | TA | T | 5 | a0001c0001t0001g0040 a0001c0001t0001g0056 a0001c0001t0001g0158 others(2): Show |
6 | HG01175.hp2 HG01943.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.355-625delT | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52724734 | |||||||
| chr13:52724828 | T | C | 8 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0231 others(5): Show |
10 | HG00544.hp1 HG01074.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.355-718A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52724828 | |||||||
| chr13:52724860 | A | G | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG01074.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.355-750T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52724860 | |||||||
| chr13:52724979 | G | A | 2 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
2 | HG02622.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.355-869C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52724979 | |||||||
| chr13:52725010 | G | A | 2 | a0001c0001t0001g0043 a0001c0001t0001g0212 |
3 | HG00642.hp1 HG02486.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.355-900C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52725010 | |||||||
| chr13:52725097 | C | T | 8 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0231 others(5): Show |
10 | HG00544.hp1 HG01074.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.355-987G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52725097 | |||||||
| chr13:52725113 | C | G | 1 | a0001c0001t0001g0136 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.355-1003G>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52725113 | |||||||
| chr13:52725147 | TTCCTC | T | 6 | a0001c0001t0001g0231 a0001c0003t0003g0013 a0001c0003t0003g0050 others(3): Show |
8 | HG00544.hp1 HG01099.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.355-1042_355-1038d others(7): Show |
CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52725147 | |||||||
| chr13:52725170 | T | C | 1 | a0001c0001t0004g0057 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.355-1060A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52725170 | |||||||
| chr13:52725212 | A | G | 8 | a0001c0001t0001g0037 a0001c0001t0001g0064 a0001c0001t0001g0078 others(5): Show |
10 | HG00609.hp1 HG00673.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.355-1102T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52725212 | |||||||
| chr13:52725430 | G | GCT | 6 | a0001c0001t0001g0231 a0001c0003t0003g0013 a0001c0003t0003g0050 others(3): Show |
8 | HG00544.hp1 HG01099.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.355-1321_355-1320i others(4): Show |
CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52725430 | |||||||
| chr13:52725430 | G | GT | 17 | a0001c0001t0001g0037 a0001c0001t0001g0076 a0001c0001t0001g0086 others(14): Show |
18 | HG00408.hp2 HG00673.hp1 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.355-1321dupA | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52725430 | |||||||
| chr13:52725482 | T | C | 2 | a0001c0001t0001g0193 a0001c0001t0001g0234 |
2 | HG01109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.355-1372A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52725482 | |||||||
| chr13:52725486 | G | A | 8 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0231 others(5): Show |
10 | HG00544.hp1 HG01074.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.355-1376C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52725486 | |||||||
| chr13:52725487 | A | C | 8 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0231 others(5): Show |
10 | HG00544.hp1 HG01074.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.355-1377T>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52725487 | |||||||
| chr13:52725524 | C | A | 1 | a0001c0001t0001g0193 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.355-1414G>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52725524 | |||||||
| chr13:52725599 | T | C | 6 | a0001c0001t0001g0231 a0001c0003t0003g0013 a0001c0003t0003g0050 others(3): Show |
8 | HG00544.hp1 HG01099.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.355-1489A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52725599 | |||||||
| chr13:52725908 | G | A | 5 | a0001c0001t0001g0032 a0001c0001t0001g0219 a0001c0001t0001g0220 others(2): Show |
6 | HG01192.hp1 HG02109.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.355-1798C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52725908 | |||||||
| chr13:52726011 | G | T | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG01074.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.355-1901C>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52726011 | |||||||
| chr13:52726106 | C | G | 1 | a0001c0001t0001g0173 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.355-1996G>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52726106 | |||||||
| chr13:52726147 | T | A | 1 | a0001c0001t0005g0059 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.355-2037A>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52726147 | |||||||
| chr13:52726175 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.355-2065G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52726175 | |||||||
| chr13:52726252 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.355-2142G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52726252 | |||||||
| chr13:52726510 | T | TA | 10 | a0001c0001t0001g0032 a0001c0001t0001g0047 a0001c0001t0001g0065 others(7): Show |
14 | HG00544.hp1 HG01099.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.355-2401dupT | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52726510 | |||||||
| chr13:52726749 | C | A | 1 | a0001c0001t0001g0115 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.355-2639G>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52726749 | |||||||
| chr13:52727001 | C | T | 82 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0016 others(79): Show |
110 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.355-2891G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52727001 | |||||||
| chr13:52727003 | C | T | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG01074.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.355-2893G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52727003 | |||||||
| chr13:52727046 | G | A | 6 | a0001c0001t0001g0231 a0001c0003t0003g0013 a0001c0003t0003g0050 others(3): Show |
8 | HG00544.hp1 HG01099.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.355-2936C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52727046 | |||||||
| chr13:52727143 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.355-3033G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52727143 | |||||||
| chr13:52727259 | A | G | 2 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
2 | HG02622.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.355-3149T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52727259 | |||||||
| chr13:52727440 | C | T | 13 | a0001c0001t0001g0014 a0001c0001t0001g0052 a0001c0001t0001g0053 others(10): Show |
17 | HG00544.hp1 HG01074.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.355-3330G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52727440 | |||||||
| chr13:52727506 | T | A | 1 | a0001c0001t0002g0129 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.355-3396A>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52727506 | |||||||
| chr13:52727546 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.355-3436G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52727546 | |||||||
| chr13:52727745 | A | G | 1 | a0001c0001t0001g0032 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.355-3635T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52727745 | |||||||
| chr13:52727847 | A | C | 8 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0231 others(5): Show |
10 | HG00544.hp1 HG01074.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.355-3737T>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52727847 | |||||||
| chr13:52728040 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.355-3930G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52728040 | |||||||
| chr13:52728153 | C | T | 12 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(9): Show |
12 | HG00642.hp2 HG02257.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.355-4043G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52728153 | |||||||
| chr13:52728376 | CA | C | 9 | a0001c0001t0001g0032 a0001c0001t0001g0094 a0001c0001t0001g0095 others(6): Show |
10 | HG01192.hp1 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.355-4267delT | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52728376 | |||||||
| chr13:52728376 | CAA | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(212): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.355-4268_355-4267d others(4): Show |
CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52728376 | |||||||
| chr13:52728376 | CAAA | C | 7 | a0001c0001t0001g0143 a0001c0001t0001g0231 a0001c0003t0003g0013 others(4): Show |
9 | HG00544.hp1 HG01099.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.355-4269_355-4267d others(5): Show |
CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52728376 | |||||||
| chr13:52728603 | T | C | 4 | a0001c0001t0001g0035 a0001c0001t0001g0123 a0001c0001t0001g0126 others(1): Show |
5 | HG01074.hp2 HG01496.hp2 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.355-4493A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52728603 | |||||||
| chr13:52728720 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.354+4499G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52728720 | |||||||
| chr13:52728923 | A | G | 12 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(9): Show |
12 | HG02257.hp2 HG02486.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.354+4296T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52728923 | |||||||
| chr13:52728939 | G | T | 60 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(57): Show |
102 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.354+4280C>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52728939 | |||||||
| chr13:52728947 | A | T | 8 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0231 others(5): Show |
10 | HG00544.hp1 HG01074.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.354+4272T>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52728947 | |||||||
| chr13:52729044 | G | A | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | NA18954.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.354+4175C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52729044 | |||||||
| chr13:52729075 | T | C | 1 | a0001c0001t0001g0022 | 2 | HG00738.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.354+4144A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52729075 | |||||||
| chr13:52729158 | G | T | 2 | a0001c0001t0001g0064 a0001c0001t0001g0078 |
2 | HG01081.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.354+4061C>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52729158 | |||||||
| chr13:52729534 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0139 a0001c0001t0001g0205 |
6 | HG00323.hp1 HG00733.hp2 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.354+3685C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52729534 | |||||||
| chr13:52729571 | C | T | 2 | a0001c0001t0001g0193 a0001c0001t0001g0234 |
2 | HG01109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.354+3648G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52729571 | |||||||
| chr13:52729617 | G | A | 4 | a0001c0001t0001g0026 a0001c0001t0001g0104 a0001c0001t0001g0105 others(1): Show |
5 | HG01069.hp2 HG01071.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.354+3602C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52729617 | |||||||
| chr13:52729827 | T | A | 2 | a0001c0001t0001g0108 a0001c0001t0002g0156 |
2 | HG02735.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.354+3392A>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52729827 | |||||||
| chr13:52729828 | A | T | 2 | a0001c0001t0005g0059 a0002c0002t0001g0183 |
2 | HG02886.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.354+3391T>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52729828 | |||||||
| chr13:52729851 | T | C | 1 | a0001c0001t0001g0206 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.354+3368A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52729851 | |||||||
| chr13:52729853 | A | C | 3 | a0001c0001t0005g0059 a0001c0001t0005g0090 a0001c0001t0005g0160 |
3 | HG02886.hp1 HG03486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.354+3366T>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52729853 | |||||||
| chr13:52729885 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.354+3334A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52729885 | |||||||
| chr13:52729940 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.354+3279A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52729940 | |||||||
| chr13:52729997 | G | A | 2 | a0001c0001t0001g0043 a0001c0001t0001g0212 |
3 | HG00642.hp1 HG02486.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.354+3222C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52729997 | |||||||
| chr13:52730006 | C | T | 8 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0231 others(5): Show |
10 | HG00544.hp1 HG01074.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.354+3213G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52730006 | |||||||
| chr13:52730167 | G | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0060 |
3 | NA18999.hp1 NA19011.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.354+3052C>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52730167 | |||||||
| chr13:52730259 | C | T | 137 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(134): Show |
181 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.354+2960G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52730259 | |||||||
| chr13:52730274 | C | A | 8 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0231 others(5): Show |
10 | HG00544.hp1 HG01074.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.354+2945G>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52730274 | |||||||
| chr13:52730285 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.354+2934C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52730285 | |||||||
| chr13:52730301 | A | G | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG01074.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.354+2918T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52730301 | |||||||
| chr13:52730394 | C | T | 6 | a0001c0001t0001g0014 a0001c0001t0001g0052 a0001c0001t0001g0053 others(3): Show |
8 | HG01106.hp2 HG01255.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.354+2825G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52730394 | |||||||
| chr13:52730443 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.354+2776A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52730443 | |||||||
| chr13:52730470 | C | A | 4 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 others(1): Show |
4 | HG01192.hp1 HG02572.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.354+2749G>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52730470 | |||||||
| chr13:52730488 | T | G | 1 | a0001c0001t0001g0080 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.354+2731A>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52730488 | |||||||
| chr13:52730507 | C | T | 8 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0231 others(5): Show |
10 | HG00544.hp1 HG01074.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.354+2712G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52730507 | |||||||
| chr13:52730508 | T | C | 8 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0231 others(5): Show |
10 | HG00544.hp1 HG01074.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.354+2711A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52730508 | |||||||
| chr13:52730689 | T | G | 8 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0231 others(5): Show |
10 | HG00544.hp1 HG01074.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.354+2530A>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52730689 | |||||||
| chr13:52730693 | T | C | 1 | a0001c0001t0005g0059 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.354+2526A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52730693 | |||||||
| chr13:52730863 | G | T | 1 | a0001c0001t0001g0089 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.354+2356C>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52730863 | |||||||
| chr13:52730917 | G | T | 1 | a0001c0001t0001g0139 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.354+2302C>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52730917 | |||||||
| chr13:52731075 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0067 |
2 | HG02027.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.354+2144C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52731075 | |||||||
| chr13:52731208 | C | A | 4 | a0001c0003t0003g0013 a0001c0003t0003g0050 a0001c0003t0003g0051 others(1): Show |
6 | HG00544.hp1 HG01099.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.354+2011G>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52731208 | |||||||
| chr13:52731310 | G | A | 1 | a0001c0001t0001g0044 | 2 | HG00738.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.354+1909C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52731310 | |||||||
| chr13:52731366 | T | C | 5 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(2): Show |
5 | HG02257.hp2 HG02486.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.354+1853A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52731366 | |||||||
| chr13:52731461 | A | G | 8 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0231 others(5): Show |
10 | HG00544.hp1 HG01074.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.354+1758T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52731461 | |||||||
| chr13:52731666 | T | C | 12 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(9): Show |
12 | HG02257.hp2 HG02486.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.354+1553A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52731666 | |||||||
| chr13:52731721 | A | G | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG01074.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.354+1498T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52731721 | |||||||
| chr13:52731725 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0157 |
4 | HG01243.hp1 HG02965.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.354+1494C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52731725 | |||||||
| chr13:52731921 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.354+1298C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52731921 | |||||||
| chr13:52731932 | T | C | 1 | a0001c0001t0001g0032 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.354+1287A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52731932 | |||||||
| chr13:52732021 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.354+1198G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52732021 | |||||||
| chr13:52732143 | A | G | 1 | a0001c0001t0001g0068 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.354+1076T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52732143 | |||||||
| chr13:52732169 | A | G | 115 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(112): Show |
155 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.354+1050T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52732169 | |||||||
| chr13:52732202 | G | T | 1 | a0001c0001t0001g0178 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.354+1017C>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52732202 | |||||||
| chr13:52732463 | A | C | 1 | a0001c0001t0001g0206 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.354+756T>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52732463 | |||||||
| chr13:52732465 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.354+754T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52732465 | |||||||
| chr13:52732745 | G | A | 6 | a0001c0001t0001g0035 a0001c0001t0001g0122 a0001c0001t0001g0123 others(3): Show |
7 | HG01074.hp2 HG01496.hp2 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.354+474C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52732745 | |||||||
| chr13:52733205 | T | G | 4 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0093 others(1): Show |
6 | HG02055.hp1 HG02559.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.354+14A>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 3/6 | chr13 | 52733205 | |||||||
| chr13:52733471 | T | C | 1 | a0003c0006t0001g0238 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.214-112A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52733471 | |||||||
| chr13:52733613 | T | C | 9 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0231 others(6): Show |
11 | HG00544.hp1 HG00642.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.214-254A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52733613 | |||||||
| chr13:52733818 | C | T | 4 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(1): Show |
4 | HG02559.hp2 HG02922.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-459G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52733818 | |||||||
| chr13:52733993 | A | G | 17 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(14): Show |
31 | HG00323.hp1 HG00408.hp2 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.214-634T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52733993 | |||||||
| chr13:52734136 | C | T | 1 | a0001c0001t0001g0032 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.214-777G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52734136 | |||||||
| chr13:52734241 | T | C | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.214-882A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52734241 | |||||||
| chr13:52734291 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.214-932C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52734291 | |||||||
| chr13:52734490 | A | G | 1 | a0001c0001t0001g0134 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.214-1131T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52734490 | |||||||
| chr13:52734688 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.214-1329C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52734688 | |||||||
| chr13:52734747 | C | G | 1 | a0001c0001t0005g0059 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.214-1388G>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52734747 | |||||||
| chr13:52734788 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.214-1429T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52734788 | |||||||
| chr13:52735009 | A | C | 5 | a0001c0001t0001g0014 a0001c0001t0001g0052 a0001c0001t0001g0053 others(2): Show |
7 | HG01106.hp2 HG01255.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.214-1650T>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52735009 | |||||||
| chr13:52735062 | T | TGTC | 22 | a0001c0001t0001g0058 a0001c0001t0001g0089 a0001c0001t0001g0096 others(19): Show |
25 | HG01070.hp1 HG01243.hp2 HG01943.hp1 others(22): Show |
intron_variant | MODIFIER | c.214-1706_214-1704d others(5): Show |
CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52735062 | |||||||
| chr13:52735259 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.214-1900C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52735259 | |||||||
| chr13:52735298 | T | C | 10 | a0001c0001t0001g0014 a0001c0001t0001g0052 a0001c0001t0001g0053 others(7): Show |
14 | HG00544.hp1 HG00642.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.214-1939A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52735298 | |||||||
| chr13:52735369 | GT | G | 178 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(175): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.214-2011delA | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52735369 | |||||||
| chr13:52735579 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.214-2220G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52735579 | |||||||
| chr13:52735605 | A | G | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(230): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.214-2246T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52735605 | |||||||
| chr13:52735618 | T | C | 178 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(175): Show |
235 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.214-2259A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52735618 | |||||||
| chr13:52735682 | T | A | 4 | a0001c0001t0001g0037 a0001c0001t0001g0166 a0001c0001t0001g0167 others(1): Show |
5 | HG00673.hp1 HG02040.hp2 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.214-2323A>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52735682 | |||||||
| chr13:52735682 | T | TA | 6 | a0001c0001t0001g0049 a0001c0001t0001g0060 a0001c0001t0001g0065 others(3): Show |
7 | HG01516.hp2 HG01517.hp2 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.214-2324dupT | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52735682 | |||||||
| chr13:52735682 | TA | T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(45): Show |
76 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(73): Show |
intron_variant | MODIFIER | c.214-2324delT | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52735682 | |||||||
| chr13:52735754 | C | T | 40 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(37): Show |
68 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(65): Show |
intron_variant | MODIFIER | c.214-2395G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52735754 | |||||||
| chr13:52735794 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.214-2435C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52735794 | |||||||
| chr13:52735818 | G | A | 1 | a0001c0001t0005g0059 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.214-2459C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52735818 | |||||||
| chr13:52735819 | C | A | 3 | a0001c0001t0002g0200 a0001c0003t0003g0013 a0001c0003t0003g0051 |
5 | HG00642.hp2 HG01099.hp1 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.214-2460G>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52735819 | |||||||
| chr13:52735827 | C | CT | 24 | a0001c0001t0001g0052 a0001c0001t0001g0062 a0001c0001t0001g0063 others(21): Show |
24 | HG00609.hp1 HG01109.hp2 HG01496.hp2 others(21): Show |
intron_variant | MODIFIER | c.214-2469dupA | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52735827 | |||||||
| chr13:52735827 | CT | C | 60 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(57): Show |
95 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(92): Show |
intron_variant | MODIFIER | c.214-2469delA | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52735827 | |||||||
| chr13:52735910 | A | T | 1 | a0001c0001t0001g0117 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.214-2551T>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52735910 | |||||||
| chr13:52735914 | C | T | 5 | a0001c0001t0001g0014 a0001c0001t0001g0052 a0001c0001t0001g0053 others(2): Show |
7 | HG01106.hp2 HG01255.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.214-2555G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52735914 | |||||||
| chr13:52735996 | AT | A | 16 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0019 others(13): Show |
27 | HG00673.hp2 HG02155.hp2 HG02300.hp2 others(24): Show |
intron_variant | MODIFIER | c.214-2638delA | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52735996 | |||||||
| chr13:52736055 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.214-2696T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52736055 | |||||||
| chr13:52736121 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.214-2762C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52736121 | |||||||
| chr13:52736195 | T | C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(114): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.213+2836A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52736195 | |||||||
| chr13:52736216 | C | G | 42 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0021 others(39): Show |
55 | HG00408.hp2 HG00438.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.213+2815G>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52736216 | |||||||
| chr13:52736230 | G | A | 5 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 others(2): Show |
5 | HG02647.hp1 HG03139.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.213+2801C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52736230 | |||||||
| chr13:52736254 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.213+2777C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52736254 | |||||||
| chr13:52736373 | C | G | 1 | a0001c0001t0001g0061 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.213+2658G>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52736373 | |||||||
| chr13:52736408 | C | T | 40 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0021 others(37): Show |
53 | HG00408.hp2 HG00438.hp2 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.213+2623G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52736408 | |||||||
| chr13:52736414 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.213+2617G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52736414 | |||||||
| chr13:52736421 | G | A | 6 | a0001c0001t0001g0058 a0001c0001t0001g0086 a0001c0001t0001g0087 others(3): Show |
6 | HG02109.hp2 HG02559.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.213+2610C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52736421 | |||||||
| chr13:52736613 | G | A | 1 | a0001c0008t0001g0237 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.213+2418C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52736613 | |||||||
| chr13:52736613 | G | T | 17 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0029 others(14): Show |
25 | HG01106.hp1 HG01106.hp2 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.213+2418C>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52736613 | |||||||
| chr13:52736868 | G | A | 3 | a0002c0002t0001g0038 a0002c0002t0001g0183 a0002c0002t0001g0184 |
4 | HG03490.hp2 HG03654.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+2163C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52736868 | |||||||
| chr13:52737063 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.213+1968A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52737063 | |||||||
| chr13:52737095 | C | G | 46 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0021 others(43): Show |
59 | HG00408.hp2 HG00438.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.213+1936G>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52737095 | |||||||
| chr13:52737095 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.213+1936G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52737095 | |||||||
| chr13:52737189 | C | T | 1 | a0001c0008t0001g0237 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.213+1842G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52737189 | |||||||
| chr13:52737232 | T | G | 1 | a0001c0001t0001g0217 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.213+1799A>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52737232 | |||||||
| chr13:52737235 | G | A | 9 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 others(6): Show |
12 | HG01109.hp1 HG01192.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.213+1796C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52737235 | |||||||
| chr13:52737239 | T | C | 2 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
2 | HG00597.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.213+1792A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52737239 | |||||||
| chr13:52737347 | C | T | 5 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(2): Show |
5 | HG02257.hp2 HG02486.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.213+1684G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52737347 | |||||||
| chr13:52737422 | C | A | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(134): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.213+1609G>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52737422 | |||||||
| chr13:52737453 | C | T | 24 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(21): Show |
28 | HG01069.hp2 HG01071.hp1 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.213+1578G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52737453 | |||||||
| chr13:52737601 | T | G | 2 | a0001c0001t0001g0224 a0001c0001t0001g0225 |
2 | NA18961.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.213+1430A>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52737601 | |||||||
| chr13:52737720 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.213+1311T>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52737720 | |||||||
| chr13:52737856 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.213+1175A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52737856 | |||||||
| chr13:52737877 | G | C | 1 | a0001c0001t0004g0226 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.213+1154C>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52737877 | |||||||
| chr13:52737950 | C | T | 2 | a0001c0001t0001g0231 a0003c0006t0001g0238 |
2 | HG02615.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.213+1081G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52737950 | |||||||
| chr13:52738011 | C | T | 40 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0021 others(37): Show |
52 | HG00408.hp2 HG00438.hp2 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.213+1020G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52738011 | |||||||
| chr13:52738342 | G | A | 3 | a0001c0001t0001g0058 a0001c0001t0004g0057 a0001c0001t0005g0059 |
3 | HG02109.hp2 HG02886.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.213+689C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52738342 | |||||||
| chr13:52738363 | T | C | 1 | a0001c0001t0001g0047 | 2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.213+668A>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52738363 | |||||||
| chr13:52738562 | C | G | 2 | a0001c0001t0001g0021 a0001c0001t0001g0060 |
3 | NA18999.hp1 NA19011.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.213+469G>C | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52738562 | |||||||
| chr13:52738625 | G | A | 5 | a0001c0001t0001g0048 a0001c0001t0001g0227 a0001c0001t0001g0228 others(2): Show |
6 | HG00408.hp1 HG01943.hp2 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.213+406C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52738625 | |||||||
| chr13:52738924 | G | C | 2 | a0001c0001t0001g0231 a0004c0007t0001g0232 |
2 | HG02630.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.213+107C>G | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52738924 | |||||||
| chr13:52738956 | C | A | 3 | a0001c0001t0001g0234 a0002c0002t0001g0012 a0002c0002t0001g0233 |
6 | HG01109.hp1 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.213+75G>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52738956 | |||||||
| chr13:52738965 | C | T | 4 | a0001c0001t0001g0058 a0001c0001t0004g0057 a0001c0001t0005g0059 others(1): Show |
4 | HG02109.hp2 HG02615.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+66G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52738965 | |||||||
| chr13:52738977 | C | T | 6 | a0001c0001t0001g0014 a0001c0001t0001g0052 a0001c0001t0001g0053 others(3): Show |
8 | HG01106.hp2 HG01175.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.213+54G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 2/6 | chr13 | 52738977 | |||||||
| chr13:52739242 | G | A | 2 | a0001c0001t0001g0049 a0001c0001t0001g0236 |
3 | HG01516.hp2 HG01517.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.73-71C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 1/6 | chr13 | 52739242 | |||||||
| chr13:52739266 | G | A | 1 | a0001c0008t0001g0237 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.73-95C>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 1/6 | chr13 | 52739266 | |||||||
| chr13:52739522 | C | T | 3 | a0001c0003t0003g0013 a0001c0003t0003g0050 a0001c0003t0003g0051 |
5 | HG01099.hp1 HG03688.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.72+108G>A | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 1/6 | chr13 | 52739522 | |||||||
| chr13:52739564 | C | A | 1 | a0003c0006t0001g0238 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.72+66G>T | CNMD | ENSG00000136110.13 | transcript | ENST00000377962.8 | protein_coding | 1/6 | chr13 | 52739564 |