Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55201 |
| ensemblid | ENSG00000130479.11 |
| hgncid | 15715 |
| symbol | MAP1S |
| name | microtubule associated protein 1S |
| refseq_nuc | NM_018174.6 |
| refseq_prot | NP_060644.4 |
| ensembl_nuc | ENST00000324096.9 |
| ensembl_prot | ENSP00000325313.3 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 17719480 |
| end | 17734513 |
| strand | + |
| ver | v1.2 |
| region | chr19:17719480-17734513 |
| region5000 | chr19:17714480-17739513 |
| regionname0 | MAP1S_chr19_17719480_17734513 |
| regionname5000 | MAP1S_chr19_17714480_17739513 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1059 | 181 | 49 | 43 | 58 | 8 | 21 | 39 | MAP1S_chr19_17714480_17739513 | MAP1S | MAAVA others(1054): Show |
chr19 | 17714480 | 17739513 |
| a0002 | 0/0 | 1059 | 34 | 7 | 15 | 1 | 3 | 8 | 1 | MAP1S_chr19_17714480_17739513 | MAP1S | MAAVA others(1054): Show |
chr19 | 17714480 | 17739513 |
| a0003 | 0/0 | 1059 | 25 | 0 | 10 | 3 | 3 | 9 | 3 | MAP1S_chr19_17714480_17739513 | MAP1S | MAAVA others(1054): Show |
chr19 | 17714480 | 17739513 |
| a0004 | 0/0 | 1059 | 20 | 18 | 2 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | MAAVA others(1054): Show |
chr19 | 17714480 | 17739513 |
| a0005 | 0/0 | 492 | 11 | 2 | 3 | 2 | 0 | 4 | 2 | MAP1S_chr19_17714480_17739513 | MAP1S | MAAVA others(487): Show |
chr19 | 17714480 | 17739513 |
| a0006 | 0/0 | 1059 | 10 | 10 | 0 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | MAAVA others(1054): Show |
chr19 | 17714480 | 17739513 |
| a0007 | 0/0 | 1059 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | MAAVA others(1054): Show |
chr19 | 17714480 | 17739513 |
| a0008 | 0/0 | 1059 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | MAAVA others(1054): Show |
chr19 | 17714480 | 17739513 |
| a0009 | 0/0 | 1059 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | MAAVA others(1054): Show |
chr19 | 17714480 | 17739513 |
| a0010 | 0/0 | 1059 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | MAAVA others(1054): Show |
chr19 | 17714480 | 17739513 |
| a0011 | 0/0 | 1059 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAP1S_chr19_17714480_17739513 | MAP1S | MAAVA others(1054): Show |
chr19 | 17714480 | 17739513 |
| a0012 | 0/0 | 1059 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAP1S_chr19_17714480_17739513 | MAP1S | MAAVA others(1054): Show |
chr19 | 17714480 | 17739513 |
| a0013 | 0/0 | 1059 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAP1S_chr19_17714480_17739513 | MAP1S | MAAVA others(1054): Show |
chr19 | 17714480 | 17739513 |
| a0014 | 0/0 | 1059 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | MAAVA others(1054): Show |
chr19 | 17714480 | 17739513 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3177 | 164 | 38 | 40 | 56 | 8 | 20 | MAP1S_chr19_17714480_17739513 | MAP1S | ATGGC others(3172): Show |
chr19 | 17714480 | 17739513 | ||
| a0001c0007 | 0/0 | 3177 | 5 | 5 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | ATGGC others(3172): Show |
chr19 | 17714480 | 17739513 | ||
| a0001c0008 | 0/0 | 3177 | 4 | 4 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | ATGGC others(3172): Show |
chr19 | 17714480 | 17739513 | ||
| a0001c0010 | 0/0 | 3177 | 2 | 0 | 2 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | ATGGC others(3172): Show |
chr19 | 17714480 | 17739513 | ||
| a0001c0013 | 0/0 | 3177 | 2 | 2 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | ATGGC others(3172): Show |
chr19 | 17714480 | 17739513 | ||
| a0001c0014 | 0/0 | 3177 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | ATGGC others(3172): Show |
chr19 | 17714480 | 17739513 | ||
| a0001c0019 | 0/0 | 3177 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | ATGGC others(3172): Show |
chr19 | 17714480 | 17739513 | ||
| a0001c0020 | 0/0 | 3177 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1S_chr19_17714480_17739513 | MAP1S | ATGGC others(3172): Show |
chr19 | 17714480 | 17739513 | ||
| a0001c0026 | 0/0 | 3177 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | ATGGC others(3172): Show |
chr19 | 17714480 | 17739513 | ||
| a0002c0002 | 0/0 | 3177 | 32 | 7 | 13 | 1 | 3 | 8 | MAP1S_chr19_17714480_17739513 | MAP1S | ATGGC others(3172): Show |
chr19 | 17714480 | 17739513 | ||
| a0002c0011 | 0/0 | 3177 | 2 | 0 | 2 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | ATGGC others(3172): Show |
chr19 | 17714480 | 17739513 | ||
| a0003c0003 | 0/0 | 3177 | 24 | 0 | 10 | 2 | 3 | 9 | MAP1S_chr19_17714480_17739513 | MAP1S | ATGGC others(3172): Show |
chr19 | 17714480 | 17739513 | ||
| a0003c0024 | 0/0 | 3177 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | ATGGC others(3172): Show |
chr19 | 17714480 | 17739513 | ||
| a0004c0004 | 0/0 | 3177 | 20 | 18 | 2 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | ATGGC others(3172): Show |
chr19 | 17714480 | 17739513 | ||
| a0005c0006 | 0/0 | 3178 | 6 | 1 | 2 | 1 | 0 | 2 | MAP1S_chr19_17714480_17739513 | MAP1S | ATGGC others(3173): Show |
chr19 | 17714480 | 17739513 | ||
| a0005c0009 | 0/0 | 3178 | 3 | 0 | 0 | 1 | 0 | 2 | MAP1S_chr19_17714480_17739513 | MAP1S | ATGGC others(3173): Show |
chr19 | 17714480 | 17739513 | ||
| a0005c0015 | 0/0 | 3178 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | ATGGC others(3173): Show |
chr19 | 17714480 | 17739513 | ||
| a0005c0016 | 0/0 | 3178 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | ATGGC others(3173): Show |
chr19 | 17714480 | 17739513 | ||
| a0006c0005 | 0/0 | 3177 | 10 | 10 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | ATGGC others(3172): Show |
chr19 | 17714480 | 17739513 | ||
| a0007c0012 | 0/0 | 3177 | 2 | 0 | 2 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | ATGGC others(3172): Show |
chr19 | 17714480 | 17739513 | ||
| a0008c0022 | 0/0 | 3177 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | ATGGC others(3172): Show |
chr19 | 17714480 | 17739513 | ||
| a0009c0021 | 0/0 | 3177 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | ATGGC others(3172): Show |
chr19 | 17714480 | 17739513 | ||
| a0010c0027 | 0/0 | 3177 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | ATGGC others(3172): Show |
chr19 | 17714480 | 17739513 | ||
| a0011c0025 | 0/0 | 3177 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | ATGGC others(3172): Show |
chr19 | 17714480 | 17739513 | ||
| a0012c0018 | 0/0 | 3177 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | ATGGC others(3172): Show |
chr19 | 17714480 | 17739513 | ||
| a0013c0023 | 0/0 | 3177 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | ATGGC others(3172): Show |
chr19 | 17714480 | 17739513 | ||
| a0014c0017 | 0/0 | 3177 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | ATGGC others(3172): Show |
chr19 | 17714480 | 17739513 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3288 | 164 | 38 | 40 | 56 | 8 | 20 | MAP1S_chr19_17714480_17739513 | MAP1S | GAGAA others(3283): Show |
chr19 | 17714480 | 17739513 |
| a0001c0007t0001 | 0/0 | 3288 | 5 | 5 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | GAGAA others(3283): Show |
chr19 | 17714480 | 17739513 |
| a0001c0008t0001 | 0/0 | 3288 | 4 | 4 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | GAGAA others(3283): Show |
chr19 | 17714480 | 17739513 |
| a0001c0010t0001 | 0/0 | 3288 | 2 | 0 | 2 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | GAGAA others(3283): Show |
chr19 | 17714480 | 17739513 |
| a0001c0013t0001 | 0/0 | 3288 | 2 | 2 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | GAGAA others(3283): Show |
chr19 | 17714480 | 17739513 |
| a0001c0014t0001 | 0/0 | 3288 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | GAGAA others(3283): Show |
chr19 | 17714480 | 17739513 |
| a0001c0019t0001 | 0/0 | 3288 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | GAGAA others(3283): Show |
chr19 | 17714480 | 17739513 |
| a0001c0020t0001 | 0/0 | 3288 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1S_chr19_17714480_17739513 | MAP1S | GAGAA others(3283): Show |
chr19 | 17714480 | 17739513 |
| a0001c0026t0001 | 0/0 | 3288 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | GAGAA others(3283): Show |
chr19 | 17714480 | 17739513 |
| a0002c0002t0001 | 0/0 | 3288 | 32 | 7 | 13 | 1 | 3 | 8 | MAP1S_chr19_17714480_17739513 | MAP1S | GAGAA others(3283): Show |
chr19 | 17714480 | 17739513 |
| a0002c0011t0001 | 0/0 | 3288 | 2 | 0 | 2 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | GAGAA others(3283): Show |
chr19 | 17714480 | 17739513 |
| a0003c0003t0001 | 0/0 | 3288 | 24 | 0 | 10 | 2 | 3 | 9 | MAP1S_chr19_17714480_17739513 | MAP1S | GAGAA others(3283): Show |
chr19 | 17714480 | 17739513 |
| a0003c0024t0001 | 0/0 | 3288 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | GAGAA others(3283): Show |
chr19 | 17714480 | 17739513 |
| a0004c0004t0001 | 0/0 | 3288 | 20 | 18 | 2 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | GAGAA others(3283): Show |
chr19 | 17714480 | 17739513 |
| a0005c0006t0001 | 0/0 | 3289 | 6 | 1 | 2 | 1 | 0 | 2 | MAP1S_chr19_17714480_17739513 | MAP1S | GAGAA others(3284): Show |
chr19 | 17714480 | 17739513 |
| a0005c0009t0001 | 0/0 | 3289 | 3 | 0 | 0 | 1 | 0 | 2 | MAP1S_chr19_17714480_17739513 | MAP1S | GAGAA others(3284): Show |
chr19 | 17714480 | 17739513 |
| a0005c0015t0001 | 0/0 | 3289 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | GAGAA others(3284): Show |
chr19 | 17714480 | 17739513 |
| a0005c0016t0001 | 0/0 | 3289 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | GAGAA others(3284): Show |
chr19 | 17714480 | 17739513 |
| a0006c0005t0001 | 0/0 | 3288 | 10 | 10 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | GAGAA others(3283): Show |
chr19 | 17714480 | 17739513 |
| a0007c0012t0001 | 0/0 | 3288 | 2 | 0 | 2 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | GAGAA others(3283): Show |
chr19 | 17714480 | 17739513 |
| a0008c0022t0001 | 0/0 | 3288 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | GAGAA others(3283): Show |
chr19 | 17714480 | 17739513 |
| a0009c0021t0001 | 0/0 | 3288 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | GAGAA others(3283): Show |
chr19 | 17714480 | 17739513 |
| a0010c0027t0001 | 0/0 | 3288 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | GAGAA others(3283): Show |
chr19 | 17714480 | 17739513 |
| a0011c0025t0001 | 0/0 | 3288 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | GAGAA others(3283): Show |
chr19 | 17714480 | 17739513 |
| a0012c0018t0001 | 0/0 | 3288 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | GAGAA others(3283): Show |
chr19 | 17714480 | 17739513 |
| a0013c0023t0001 | 0/0 | 3288 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | GAGAA others(3283): Show |
chr19 | 17714480 | 17739513 |
| a0014c0017t0001 | 0/0 | 3288 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | GAGAA others(3283): Show |
chr19 | 17714480 | 17739513 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 83 | 18 | 22 | 27 | 4 | 11 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0001t0001g0005 | 0/0 | 9 | 7 | 2 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0001t0001g0006 | 0/0 | 7 | 0 | 1 | 4 | 0 | 2 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 5 | 0 | 1 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0001t0001g0008 | 0/1 | 5 | 0 | 2 | 0 | 2 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0001t0001g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0001t0001g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0007t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0007t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0007t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0008t0001g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0010t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0013t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0014t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0019t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0020t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0001c0026t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0002c0002t0001g0002 | 0/0 | 23 | 5 | 7 | 1 | 3 | 7 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0002c0002t0001g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0002c0002t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0002c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0002c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0002c0011t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0002c0011t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0003c0003t0001g0003 | 0/0 | 20 | 0 | 9 | 2 | 3 | 6 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0003c0003t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0003c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0003c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0003c0003t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0003c0024t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0004c0004t0001g0011 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0004c0004t0001g0018 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0004c0004t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0004c0004t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0004c0004t0001g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0004c0004t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0004c0004t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0004c0004t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0004c0004t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0005c0006t0001g0001 | 0/0 | 6 | 1 | 2 | 1 | 0 | 2 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0005c0009t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0005c0009t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0005c0009t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0005c0015t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0005c0016t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0006c0005t0001g0004 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0006c0005t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0007c0012t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0008c0022t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0009c0021t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0010c0027t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0011c0025t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0012c0018t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0013c0023t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| a0014c0017t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0002 | EUR | GBR | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | FIN | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0002 | EUR | FIN | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0002 | EUR | FIN | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG00323 | hp2 | a0003 | c0003 | t0001 | g0003 | EUR | FIN | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0025 | AMR | PUR | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG00733 | hp1 | a0003 | c0003 | t0001 | g0003 | AMR | PUR | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG00733 | hp2 | a0008 | c0022 | t0001 | g0002 | AMR | PUR | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG00735 | hp2 | a0005 | c0006 | t0001 | g0001 | AMR | PUR | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0015 | AMR | PUR | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG00741 | hp1 | a0005 | c0006 | t0001 | g0001 | AMR | PUR | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01070 | hp1 | a0003 | c0003 | t0001 | g0003 | AMR | PUR | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0015 | AMR | PUR | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0015 | AMR | PUR | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01081 | hp1 | a0003 | c0003 | t0001 | g0003 | AMR | PUR | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01081 | hp2 | a0003 | c0003 | t0001 | g0031 | AMR | PUR | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01099 | hp1 | a0007 | c0012 | t0001 | g0003 | AMR | PUR | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01109 | hp1 | a0004 | c0004 | t0001 | g0026 | AMR | PUR | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01167 | hp1 | a0003 | c0003 | t0001 | g0003 | AMR | PUR | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01168 | hp2 | a0003 | c0003 | t0001 | g0003 | AMR | PUR | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01169 | hp2 | a0003 | c0003 | t0001 | g0003 | AMR | PUR | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01175 | hp1 | a0007 | c0012 | t0001 | g0003 | AMR | PUR | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01175 | hp2 | a0001 | c0010 | t0001 | g0017 | AMR | PUR | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01192 | hp1 | a0001 | c0014 | t0001 | g0001 | AMR | PUR | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01255 | hp1 | a0002 | c0011 | t0001 | g0066 | AMR | CLM | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01256 | hp2 | a0003 | c0003 | t0001 | g0003 | AMR | CLM | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01258 | hp1 | a0003 | c0003 | t0001 | g0003 | AMR | CLM | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01346 | hp1 | a0002 | c0011 | t0001 | g0002 | AMR | CLM | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01496 | hp2 | a0005 | c0015 | t0001 | g0017 | AMR | CLM | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01516 | hp1 | a0003 | c0003 | t0001 | g0003 | EUR | IBS | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | ACB | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01891 | hp2 | a0004 | c0004 | t0001 | g0026 | AFR | ACB | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0067 | AMR | PEL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01981 | hp1 | a0001 | c0010 | t0001 | g0017 | AMR | PEL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0068 | AMR | PEL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02055 | hp1 | a0004 | c0004 | t0001 | g0011 | AFR | ACB | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02055 | hp2 | a0005 | c0006 | t0001 | g0001 | AFR | ACB | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02056 | hp1 | a0009 | c0021 | t0001 | g0006 | EAS | KHV | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02258 | hp1 | a0004 | c0004 | t0001 | g0073 | AFR | ACB | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02258 | hp2 | a0004 | c0004 | t0001 | g0018 | AFR | ACB | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02280 | hp1 | a0004 | c0004 | t0001 | g0019 | AFR | ACB | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | ACB | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02300 | hp1 | a0003 | c0003 | t0001 | g0003 | AMR | PEL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02572 | hp2 | a0002 | c0002 | t0001 | g0065 | AFR | GWD | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02622 | hp1 | a0004 | c0004 | t0001 | g0027 | AFR | GWD | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02630 | hp1 | a0001 | c0013 | t0001 | g0001 | AFR | GWD | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02630 | hp2 | a0004 | c0004 | t0001 | g0011 | AFR | GWD | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02647 | hp1 | a0006 | c0005 | t0001 | g0004 | AFR | GWD | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02647 | hp2 | a0001 | c0013 | t0001 | g0001 | AFR | GWD | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02698 | hp2 | a0003 | c0003 | t0001 | g0003 | SAS | PJL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02723 | hp1 | a0006 | c0005 | t0001 | g0021 | AFR | GWD | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02723 | hp2 | a0004 | c0004 | t0001 | g0011 | AFR | GWD | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02738 | hp2 | a0005 | c0006 | t0001 | g0001 | SAS | PJL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02818 | hp1 | a0001 | c0008 | t0001 | g0013 | AFR | GWD | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02886 | hp1 | a0006 | c0005 | t0001 | g0004 | AFR | GWD | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02886 | hp2 | a0004 | c0004 | t0001 | g0020 | AFR | GWD | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02895 | hp2 | a0001 | c0007 | t0001 | g0069 | AFR | GWD | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02965 | hp1 | a0004 | c0004 | t0001 | g0011 | AFR | ESN | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02965 | hp2 | a0001 | c0008 | t0001 | g0013 | AFR | ESN | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02970 | hp1 | a0006 | c0005 | t0001 | g0021 | AFR | ESN | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02970 | hp2 | a0004 | c0004 | t0001 | g0071 | AFR | ESN | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0064 | AFR | ESN | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG03041 | hp1 | a0004 | c0004 | t0001 | g0020 | AFR | GWD | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG03041 | hp2 | a0001 | c0007 | t0001 | g0016 | AFR | GWD | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG03098 | hp2 | a0001 | c0008 | t0001 | g0013 | AFR | MSL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG03139 | hp1 | a0001 | c0008 | t0001 | g0013 | AFR | ESN | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | MSL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG03209 | hp2 | a0004 | c0004 | t0001 | g0018 | AFR | MSL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG03453 | hp1 | a0004 | c0004 | t0001 | g0019 | AFR | MSL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG03453 | hp2 | a0001 | c0007 | t0001 | g0016 | AFR | MSL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG03486 | hp1 | a0004 | c0004 | t0001 | g0019 | AFR | MSL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG03486 | hp2 | a0006 | c0005 | t0001 | g0004 | AFR | MSL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG03490 | hp1 | a0003 | c0003 | t0001 | g0032 | SAS | PJL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG03491 | hp2 | a0003 | c0003 | t0001 | g0033 | SAS | PJL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG03540 | hp2 | a0010 | c0027 | t0001 | g0004 | AFR | GWD | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG03579 | hp2 | a0006 | c0005 | t0001 | g0004 | AFR | MSL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG03654 | hp1 | a0003 | c0003 | t0001 | g0003 | SAS | PJL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG03654 | hp2 | a0005 | c0006 | t0001 | g0001 | SAS | PJL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0025 | SAS | PJL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG03669 | hp2 | a0005 | c0009 | t0001 | g0035 | SAS | PJL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG03688 | hp2 | a0003 | c0003 | t0001 | g0003 | SAS | STU | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | BEB | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG03942 | hp2 | a0003 | c0003 | t0001 | g0003 | SAS | BEB | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG04115 | hp1 | a0005 | c0009 | t0001 | g0036 | SAS | STU | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG04115 | hp2 | a0003 | c0003 | t0001 | g0003 | SAS | STU | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | BEB | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG04199 | hp2 | a0001 | c0020 | t0001 | g0001 | SAS | STU | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG04204 | hp2 | a0003 | c0003 | t0001 | g0034 | SAS | STU | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG04228 | hp1 | a0003 | c0003 | t0001 | g0003 | SAS | STU | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | STU | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA18522 | hp1 | a0001 | c0007 | t0001 | g0070 | AFR | YRI | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA18522 | hp2 | a0006 | c0005 | t0001 | g0004 | AFR | YRI | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA18906 | hp1 | a0005 | c0016 | t0001 | g0020 | AFR | YRI | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA18906 | hp2 | a0006 | c0005 | t0001 | g0004 | AFR | YRI | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA18942 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA18942 | hp2 | a0005 | c0006 | t0001 | g0001 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA18946 | hp1 | a0011 | c0025 | t0001 | g0048 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA18952 | hp1 | a0001 | c0019 | t0001 | g0001 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA18991 | hp2 | a0005 | c0009 | t0001 | g0077 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA18994 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA19011 | hp2 | a0012 | c0018 | t0001 | g0001 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA19030 | hp1 | a0006 | c0005 | t0001 | g0004 | AFR | LWK | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | LWK | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA19056 | hp1 | a0013 | c0023 | t0001 | g0002 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA19062 | hp2 | a0003 | c0024 | t0001 | g0030 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA19064 | hp1 | a0001 | c0026 | t0001 | g0001 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | YRI | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ASW | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA20129 | hp2 | a0014 | c0017 | t0001 | g0063 | AFR | ASW | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA20752 | hp1 | a0003 | c0003 | t0001 | g0003 | EUR | TSI | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | TSI | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | GIH | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG01123 | hp2 | a0004 | c0004 | t0001 | g0018 | AMR | CLM | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02109 | hp2 | a0004 | c0004 | t0001 | g0072 | AFR | ACB | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02486 | hp1 | a0006 | c0005 | t0001 | g0004 | AFR | ACB | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | ACB | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | USA | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA20300 | hp1 | a0004 | c0004 | t0001 | g0011 | AFR | USA | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA20300 | hp2 | a0001 | c0007 | t0001 | g0016 | AFR | USA | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA21309 | hp1 | a0004 | c0004 | t0001 | g0027 | AFR | LWK | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0008 | REF | REF | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | MAP1S_chr19_17714480_17739513 | MAP1S | chr19 | 17714480 | 17739513 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:17726160 | A | G | 2 | a0007 a0011 |
3 | HG01099.hp1 HG01175.hp1 NA18946.hp1 |
missense_variant | MODERATE | c.776A>G | p.Asn259Ser | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/7 | 799/3288 | 776/3180 | 259/1059 | chr19 | 17726160 | |||
| chr19:17726616 | C | G | 3 | a0002 a0008 a0013 |
36 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(33): Show |
missense_variant | MODERATE | c.1232C>G | p.Ser411Cys | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/7 | 1255/3288 | 1232/3180 | 411/1059 | chr19 | 17726616 | |||
| chr19:17726640 | A | AC | 1 | a0005 | 11 | HG00735.hp2 HG00741.hp1 HG01496.hp2 others(8): Show |
frameshift_variant | HIGH | c.1260dupC | p.Ala421fs | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/7 | 1284/3288 | 1261/3180 | 421/1059 | INFO_REALIGN_3_PRIME | chr19 | 17726640 | ||
| chr19:17726703 | G | A | 3 | a0003 a0005 a0007 |
30 | HG00323.hp2 HG00733.hp1 HG01070.hp1 others(27): Show |
missense_variant | MODERATE | c.1319G>A | p.Cys440Tyr | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/7 | 1342/3288 | 1319/3180 | 440/1059 | chr19 | 17726703 | |||
| chr19:17726784 | C | T | 1 | a0009 | 1 | HG02056.hp1 | missense_variant | MODERATE | c.1400C>T | p.Pro467Leu | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/7 | 1423/3288 | 1400/3180 | 467/1059 | chr19 | 17726784 | |||
| chr19:17726997 | C | A | 5 | a0004 a0005 a0006 others(2): Show |
33 | HG01109.hp1 HG01123.hp2 HG01891.hp2 others(30): Show |
missense_variant | MODERATE | c.1613C>A | p.Pro538Gln | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/7 | 1636/3288 | 1613/3180 | 538/1059 | chr19 | 17726997 | |||
| chr19:17727158 | A | C | 1 | a0013 | 1 | NA19056.hp1 | missense_variant | MODERATE | c.1774A>C | p.Ser592Arg | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/7 | 1797/3288 | 1774/3180 | 592/1059 | chr19 | 17727158 | |||
| chr19:17728010 | C | G | 1 | a0010 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.2626C>G | p.Pro876Ala | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/7 | 2649/3288 | 2626/3180 | 876/1059 | chr19 | 17728010 | |||
| chr19:17733193 | G | C | 1 | a0008 | 1 | HG00733.hp2 | missense_variant&splice_region_variant | MODERATE | c.2789G>C | p.Gly930Ala | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 6/7 | 2812/3288 | 2789/3180 | 930/1059 | chr19 | 17733193 | |||
| chr19:17733211 | C | G | 1 | a0012 | 1 | NA19011.hp2 | missense_variant | MODERATE | c.2807C>G | p.Pro936Arg | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 6/7 | 2830/3288 | 2807/3180 | 936/1059 | chr19 | 17733211 | |||
| chr19:17733213 | G | A | 1 | a0014 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.2809G>A | p.Gly937Arg | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 6/7 | 2832/3288 | 2809/3180 | 937/1059 | chr19 | 17733213 | |||
| chr19:17733418 | G | A | 2 | a0006 a0010 |
11 | HG02486.hp1 HG02647.hp1 HG02723.hp1 others(8): Show |
missense_variant | MODERATE | c.3014G>A | p.Arg1005His | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 6/7 | 3037/3288 | 3014/3180 | 1005/1059 | chr19 | 17733418 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:17719547 | A | G | 1 | a0001c0013 | 2 | HG02630.hp1 HG02647.hp2 |
synonymous_variant | LOW | c.45A>G | p.Ser15Ser | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 1/7 | 68/3288 | 45/3180 | 15/1059 | chr19 | 17719547 | |||
| chr19:17719556 | C | T | 2 | a0006c0005 a0010c0027 |
11 | HG02486.hp1 HG02647.hp1 HG02723.hp1 others(8): Show |
synonymous_variant | LOW | c.54C>T | p.Leu18Leu | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 1/7 | 77/3288 | 54/3180 | 18/1059 | chr19 | 17719556 | |||
| chr19:17725153 | G | C | 1 | a0001c0008 | 4 | HG02818.hp1 HG02965.hp2 HG03098.hp2 others(1): Show |
synonymous_variant | LOW | c.408G>C | p.Ser136Ser | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 4/7 | 431/3288 | 408/3180 | 136/1059 | chr19 | 17725153 | |||
| chr19:17726149 | C | T | 1 | a0001c0026 | 1 | NA19064.hp1 | synonymous_variant | LOW | c.765C>T | p.Phe255Phe | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/7 | 788/3288 | 765/3180 | 255/1059 | chr19 | 17726149 | |||
| chr19:17726281 | C | T | 4 | a0003c0003 a0003c0024 a0005c0009 others(1): Show |
30 | HG00323.hp2 HG00733.hp1 HG01070.hp1 others(27): Show |
synonymous_variant | LOW | c.897C>T | p.Pro299Pro | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/7 | 920/3288 | 897/3180 | 299/1059 | chr19 | 17726281 | |||
| chr19:17726449 | G | A | 1 | a0001c0014 | 1 | HG01192.hp1 | synonymous_variant | LOW | c.1065G>A | p.Ala355Ala | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/7 | 1088/3288 | 1065/3180 | 355/1059 | chr19 | 17726449 | |||
| chr19:17726608 | G | A | 2 | a0001c0010 a0005c0015 |
3 | HG01175.hp2 HG01496.hp2 HG01981.hp1 |
synonymous_variant | LOW | c.1224G>A | p.Thr408Thr | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/7 | 1247/3288 | 1224/3180 | 408/1059 | chr19 | 17726608 | |||
| chr19:17727109 | G | A | 1 | a0002c0011 | 2 | HG01255.hp1 HG01346.hp1 |
synonymous_variant | LOW | c.1725G>A | p.Pro575Pro | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/7 | 1748/3288 | 1725/3180 | 575/1059 | chr19 | 17727109 | |||
| chr19:17727166 | C | T | 1 | a0001c0020 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.1782C>T | p.Pro594Pro | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/7 | 1805/3288 | 1782/3180 | 594/1059 | chr19 | 17727166 | |||
| chr19:17727172 | A | G | 12 | a0001c0007 a0001c0010 a0002c0002 others(9): Show |
77 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
synonymous_variant | LOW | c.1788A>G | p.Ala596Ala | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/7 | 1811/3288 | 1788/3180 | 596/1059 | chr19 | 17727172 | |||
| chr19:17727271 | C | T | 1 | a0001c0019 | 1 | NA18952.hp1 | synonymous_variant | LOW | c.1887C>T | p.Ala629Ala | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/7 | 1910/3288 | 1887/3180 | 629/1059 | chr19 | 17727271 | |||
| chr19:17727865 | C | T | 1 | a0005c0016 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.2481C>T | p.Pro827Pro | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/7 | 2504/3288 | 2481/3180 | 827/1059 | chr19 | 17727865 | |||
| chr19:17728138 | C | T | 1 | a0003c0024 | 1 | NA19062.hp2 | synonymous_variant | LOW | c.2754C>T | p.Ser918Ser | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/7 | 2777/3288 | 2754/3180 | 918/1059 | chr19 | 17728138 | |||
| chr19:17733323 | G | A | 2 | a0006c0005 a0010c0027 |
11 | HG02486.hp1 HG02647.hp1 HG02723.hp1 others(8): Show |
synonymous_variant | LOW | c.2919G>A | p.Ala973Ala | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 6/7 | 2942/3288 | 2919/3180 | 973/1059 | chr19 | 17733323 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:17719639 | C | G | 1 | a0005c0009t0001g0077 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.118+19C>G | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 1/6 | chr19 | 17719639 | |||||||
| chr19:17719672 | C | A | 1 | a0001c0001t0001g0029 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.118+52C>A | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 1/6 | chr19 | 17719672 | |||||||
| chr19:17719694 | G | A | 3 | a0006c0005t0001g0004 a0006c0005t0001g0021 a0010c0027t0001g0004 |
11 | HG02486.hp1 HG02647.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.118+74G>A | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 1/6 | chr19 | 17719694 | |||||||
| chr19:17719698 | GGGC | G | 14 | a0001c0007t0001g0016 a0001c0007t0001g0069 a0001c0007t0001g0070 others(11): Show |
41 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.118+99_118+101delC others(2): Show |
MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 17719698 | ||||||
| chr19:17719698 | GGGCGGCG others(2): Show |
G | 22 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0028 others(19): Show |
57 | HG00544.hp1 HG00597.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.118+93_118+101delC others(8): Show |
MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 17719698 | ||||||
| chr19:17719825 | A | G | 23 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0028 others(20): Show |
58 | HG00544.hp1 HG00597.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.118+205A>G | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 1/6 | chr19 | 17719825 | |||||||
| chr19:17719884 | A | G | 1 | a0001c0001t0001g0062 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.118+264A>G | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 1/6 | chr19 | 17719884 | |||||||
| chr19:17719958 | T | C | 49 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(46): Show |
134 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.118+338T>C | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 1/6 | chr19 | 17719958 | |||||||
| chr19:17719968 | T | G | 23 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0028 others(20): Show |
58 | HG00544.hp1 HG00597.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.118+348T>G | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 1/6 | chr19 | 17719968 | |||||||
| chr19:17720084 | G | C | 1 | a0005c0009t0001g0077 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.118+464G>C | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 1/6 | chr19 | 17720084 | |||||||
| chr19:17720166 | C | T | 49 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(46): Show |
138 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.118+546C>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 1/6 | chr19 | 17720166 | |||||||
| chr19:17720328 | G | A | 3 | a0006c0005t0001g0004 a0006c0005t0001g0021 a0010c0027t0001g0004 |
11 | HG02486.hp1 HG02647.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.119-608G>A | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 1/6 | chr19 | 17720328 | |||||||
| chr19:17720565 | G | T | 1 | a0001c0001t0001g0061 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.119-371G>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 1/6 | chr19 | 17720565 | |||||||
| chr19:17720592 | G | A | 2 | a0004c0004t0001g0071 a0004c0004t0001g0072 |
2 | HG02109.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.119-344G>A | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 1/6 | chr19 | 17720592 | |||||||
| chr19:17720676 | A | G | 1 | a0001c0001t0001g0060 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.119-260A>G | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 1/6 | chr19 | 17720676 | |||||||
| chr19:17720764 | C | G | 3 | a0001c0001t0001g0006 a0001c0001t0001g0076 a0009c0021t0001g0006 |
9 | HG00544.hp1 HG00597.hp2 HG00642.hp1 others(6): Show |
intron_variant | MODIFIER | c.119-172C>G | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 1/6 | chr19 | 17720764 | |||||||
| chr19:17720782 | G | A | 11 | a0002c0002t0001g0002 a0002c0002t0001g0015 a0002c0002t0001g0025 others(8): Show |
36 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.119-154G>A | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 1/6 | chr19 | 17720782 | |||||||
| chr19:17720845 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.119-91C>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 1/6 | chr19 | 17720845 | |||||||
| chr19:17721171 | A | AAGCCGTG others(26): Show |
1 | a0001c0001t0001g0058 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.220+138_220+170dup others(33): Show |
MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 17721171 | ||||||
| chr19:17721493 | G | A | 49 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(46): Show |
138 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.220+456G>A | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 2/6 | chr19 | 17721493 | |||||||
| chr19:17721571 | G | A | 2 | a0001c0010t0001g0017 a0005c0015t0001g0017 |
3 | HG01175.hp2 HG01496.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.220+534G>A | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 2/6 | chr19 | 17721571 | |||||||
| chr19:17721661 | T | C | 5 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0037 others(2): Show |
13 | HG00140.hp2 HG00639.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.220+624T>C | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 2/6 | chr19 | 17721661 | |||||||
| chr19:17721683 | CA | C | 1 | a0002c0002t0001g0015 | 3 | HG00738.hp1 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.220+649delA | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 17721683 | ||||||
| chr19:17721689 | A | G | 1 | a0001c0001t0001g0057 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.220+652A>G | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 2/6 | chr19 | 17721689 | |||||||
| chr19:17721865 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.220+828C>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 2/6 | chr19 | 17721865 | |||||||
| chr19:17721939 | G | T | 47 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0028 others(44): Show |
129 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.220+902G>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 2/6 | chr19 | 17721939 | |||||||
| chr19:17722030 | T | C | 1 | a0001c0001t0001g0039 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.220+993T>C | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 2/6 | chr19 | 17722030 | |||||||
| chr19:17722079 | G | C | 3 | a0006c0005t0001g0004 a0006c0005t0001g0021 a0010c0027t0001g0004 |
11 | HG02486.hp1 HG02647.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.220+1042G>C | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 2/6 | chr19 | 17722079 | |||||||
| chr19:17722163 | G | A | 10 | a0003c0003t0001g0003 a0003c0003t0001g0031 a0003c0003t0001g0032 others(7): Show |
30 | HG00323.hp2 HG00733.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.220+1126G>A | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 2/6 | chr19 | 17722163 | |||||||
| chr19:17722272 | T | TGAAACCC others(159): Show |
37 | a0001c0001t0001g0074 a0001c0007t0001g0016 a0001c0007t0001g0069 others(34): Show |
104 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.220+1238_220+1403d others(168): Show |
MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 17722272 | ||||||
| chr19:17722272 | T | TGAAACCC others(325): Show |
2 | a0002c0002t0001g0064 a0002c0002t0001g0065 |
2 | HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.220+1403_220+1404i others(334): Show |
MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 17722272 | ||||||
| chr19:17722366 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.220+1329C>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 2/6 | chr19 | 17722366 | |||||||
| chr19:17722368 | C | CTTTTACC others(160): Show |
1 | a0005c0009t0001g0077 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.220+1403_220+1404i others(169): Show |
MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 17722368 | ||||||
| chr19:17722419 | T | TTCAGCCT others(158): Show |
1 | a0003c0024t0001g0030 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.220+1403_220+1404i others(167): Show |
MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 17722419 | ||||||
| chr19:17722619 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.221-1507A>G | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 2/6 | chr19 | 17722619 | |||||||
| chr19:17722621 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.221-1505C>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 2/6 | chr19 | 17722621 | |||||||
| chr19:17722659 | G | A | 1 | a0003c0003t0001g0031 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.221-1467G>A | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 2/6 | chr19 | 17722659 | |||||||
| chr19:17722766 | A | AGAGG | 10 | a0003c0003t0001g0003 a0003c0003t0001g0031 a0003c0003t0001g0032 others(7): Show |
30 | HG00323.hp2 HG00733.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.221-1342_221-1339d others(6): Show |
MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 17722766 | ||||||
| chr19:17722766 | A | G | 1 | a0001c0008t0001g0013 | 4 | HG02818.hp1 HG02965.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-1360A>G | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 2/6 | chr19 | 17722766 | |||||||
| chr19:17722766 | AGAGG | A | 3 | a0001c0001t0001g0010 a0004c0004t0001g0020 a0005c0016t0001g0020 |
8 | HG01891.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.221-1342_221-1339d others(6): Show |
MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 17722766 | ||||||
| chr19:17722787 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.221-1339G>A | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 2/6 | chr19 | 17722787 | |||||||
| chr19:17722915 | G | A | 30 | a0001c0007t0001g0016 a0001c0007t0001g0069 a0001c0007t0001g0070 others(27): Show |
77 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.221-1211G>A | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 2/6 | chr19 | 17722915 | |||||||
| chr19:17722975 | T | G | 10 | a0003c0003t0001g0003 a0003c0003t0001g0031 a0003c0003t0001g0032 others(7): Show |
30 | HG00323.hp2 HG00733.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.221-1151T>G | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 2/6 | chr19 | 17722975 | |||||||
| chr19:17723035 | C | G | 3 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0075 |
12 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.221-1091C>G | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 2/6 | chr19 | 17723035 | |||||||
| chr19:17723047 | C | T | 45 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0074 others(42): Show |
124 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.221-1079C>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 2/6 | chr19 | 17723047 | |||||||
| chr19:17723116 | A | G | 1 | a0001c0001t0001g0024 | 2 | HG00673.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.221-1010A>G | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 2/6 | chr19 | 17723116 | |||||||
| chr19:17723228 | C | T | 1 | a0002c0002t0001g0068 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.221-898C>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 2/6 | chr19 | 17723228 | |||||||
| chr19:17723392 | G | C | 30 | a0001c0007t0001g0016 a0001c0007t0001g0069 a0001c0007t0001g0070 others(27): Show |
77 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.221-734G>C | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 2/6 | chr19 | 17723392 | |||||||
| chr19:17723414 | G | A | 10 | a0003c0003t0001g0003 a0003c0003t0001g0031 a0003c0003t0001g0032 others(7): Show |
30 | HG00323.hp2 HG00733.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.221-712G>A | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 2/6 | chr19 | 17723414 | |||||||
| chr19:17723543 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.221-583C>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 2/6 | chr19 | 17723543 | |||||||
| chr19:17723548 | CA | C | 30 | a0001c0007t0001g0016 a0001c0007t0001g0069 a0001c0007t0001g0070 others(27): Show |
77 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.221-569delA | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 17723548 | ||||||
| chr19:17723588 | C | T | 30 | a0001c0007t0001g0016 a0001c0007t0001g0069 a0001c0007t0001g0070 others(27): Show |
77 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.221-538C>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 2/6 | chr19 | 17723588 | |||||||
| chr19:17723616 | C | T | 10 | a0003c0003t0001g0003 a0003c0003t0001g0031 a0003c0003t0001g0032 others(7): Show |
30 | HG00323.hp2 HG00733.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.221-510C>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 2/6 | chr19 | 17723616 | |||||||
| chr19:17723659 | G | A | 14 | a0004c0004t0001g0011 a0004c0004t0001g0018 a0004c0004t0001g0019 others(11): Show |
33 | HG01109.hp1 HG01123.hp2 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.221-467G>A | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 2/6 | chr19 | 17723659 | |||||||
| chr19:17723667 | G | A | 2 | a0001c0010t0001g0017 a0005c0015t0001g0017 |
3 | HG01175.hp2 HG01496.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.221-459G>A | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 2/6 | chr19 | 17723667 | |||||||
| chr19:17723827 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.221-299C>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 2/6 | chr19 | 17723827 | |||||||
| chr19:17723850 | G | A | 3 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0075 |
12 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.221-276G>A | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 2/6 | chr19 | 17723850 | |||||||
| chr19:17723950 | T | C | 10 | a0003c0003t0001g0003 a0003c0003t0001g0031 a0003c0003t0001g0032 others(7): Show |
30 | HG00323.hp2 HG00733.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.221-176T>C | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 2/6 | chr19 | 17723950 | |||||||
| chr19:17723989 | G | T | 11 | a0002c0002t0001g0002 a0002c0002t0001g0015 a0002c0002t0001g0025 others(8): Show |
36 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.221-137G>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 2/6 | chr19 | 17723989 | |||||||
| chr19:17724110 | C | T | 1 | a0001c0001t0001g0029 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.221-16C>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 2/6 | chr19 | 17724110 | |||||||
| chr19:17724282 | C | T | 2 | a0004c0004t0001g0020 a0005c0016t0001g0020 |
3 | HG02886.hp2 HG03041.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.303+74C>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 3/6 | chr19 | 17724282 | |||||||
| chr19:17724461 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.303+253G>A | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 3/6 | chr19 | 17724461 | |||||||
| chr19:17724513 | C | T | 2 | a0001c0010t0001g0017 a0005c0015t0001g0017 |
3 | HG01175.hp2 HG01496.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.303+305C>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 3/6 | chr19 | 17724513 | |||||||
| chr19:17724711 | A | G | 43 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0075 others(40): Show |
119 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.304-338A>G | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 3/6 | chr19 | 17724711 | |||||||
| chr19:17724728 | C | G | 2 | a0001c0010t0001g0017 a0005c0015t0001g0017 |
3 | HG01175.hp2 HG01496.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.304-321C>G | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 3/6 | chr19 | 17724728 | |||||||
| chr19:17724780 | T | A | 1 | a0001c0001t0001g0076 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.304-269T>A | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 3/6 | chr19 | 17724780 | |||||||
| chr19:17724834 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.304-215C>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 3/6 | chr19 | 17724834 | |||||||
| chr19:17724900 | C | T | 14 | a0004c0004t0001g0011 a0004c0004t0001g0018 a0004c0004t0001g0019 others(11): Show |
33 | HG01109.hp1 HG01123.hp2 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.304-149C>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 3/6 | chr19 | 17724900 | |||||||
| chr19:17724934 | G | T | 1 | a0001c0001t0001g0052 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.304-115G>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 3/6 | chr19 | 17724934 | |||||||
| chr19:17725002 | A | ACGT | 2 | a0001c0010t0001g0017 a0005c0015t0001g0017 |
3 | HG01175.hp2 HG01496.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.304-45_304-43dupGT others(1): Show |
MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 17725002 | ||||||
| chr19:17725022 | T | G | 30 | a0001c0007t0001g0016 a0001c0007t0001g0069 a0001c0007t0001g0070 others(27): Show |
77 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.304-27T>G | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 3/6 | chr19 | 17725022 | |||||||
| chr19:17725299 | A | G | 43 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0075 others(40): Show |
119 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.444+110A>G | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 4/6 | chr19 | 17725299 | |||||||
| chr19:17725362 | C | T | 14 | a0001c0007t0001g0016 a0001c0007t0001g0069 a0001c0007t0001g0070 others(11): Show |
41 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.444+173C>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 4/6 | chr19 | 17725362 | |||||||
| chr19:17725454 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.444+265C>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 4/6 | chr19 | 17725454 | |||||||
| chr19:17725503 | A | G | 2 | a0001c0001t0001g0008 a0001c0001t0001g0038 |
5 | HG00140.hp2 HG00741.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.444+314A>G | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 4/6 | chr19 | 17725503 | |||||||
| chr19:17725643 | G | A | 1 | a0001c0001t0001g0040 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.445-186G>A | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 4/6 | chr19 | 17725643 | |||||||
| chr19:17725811 | C | T | 1 | a0005c0009t0001g0036 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.445-18C>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 4/6 | chr19 | 17725811 | |||||||
| chr19:17728196 | G | T | 1 | a0004c0004t0001g0027 | 2 | HG02622.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2788+24G>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17728196 | |||||||
| chr19:17728229 | A | G | 1 | a0002c0002t0001g0067 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2788+57A>G | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17728229 | |||||||
| chr19:17728235 | C | T | 1 | a0002c0002t0001g0025 | 2 | HG00642.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.2788+63C>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17728235 | |||||||
| chr19:17728356 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2788+184C>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17728356 | |||||||
| chr19:17728359 | C | T | 4 | a0004c0004t0001g0011 a0004c0004t0001g0026 a0004c0004t0001g0027 others(1): Show |
10 | HG01109.hp1 HG01891.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.2788+187C>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17728359 | |||||||
| chr19:17728423 | G | A | 45 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0074 others(42): Show |
124 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.2788+251G>A | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17728423 | |||||||
| chr19:17728447 | C | G | 1 | a0001c0001t0001g0049 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2788+275C>G | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17728447 | |||||||
| chr19:17728496 | A | C | 10 | a0003c0003t0001g0003 a0003c0003t0001g0031 a0003c0003t0001g0032 others(7): Show |
30 | HG00323.hp2 HG00733.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.2788+324A>C | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17728496 | |||||||
| chr19:17728542 | C | G | 1 | a0011c0025t0001g0048 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2788+370C>G | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17728542 | |||||||
| chr19:17728558 | CT | C | 8 | a0001c0001t0001g0041 a0001c0007t0001g0069 a0002c0002t0001g0064 others(5): Show |
15 | HG02486.hp1 HG02647.hp1 HG02886.hp1 others(12): Show |
intron_variant | MODIFIER | c.2788+400delT | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 17728558 | ||||||
| chr19:17728680 | C | T | 10 | a0003c0003t0001g0003 a0003c0003t0001g0031 a0003c0003t0001g0032 others(7): Show |
30 | HG00323.hp2 HG00733.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.2788+508C>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17728680 | |||||||
| chr19:17728699 | G | T | 7 | a0004c0004t0001g0011 a0004c0004t0001g0019 a0004c0004t0001g0026 others(4): Show |
15 | HG01109.hp1 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.2788+527G>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17728699 | |||||||
| chr19:17728880 | C | T | 11 | a0002c0002t0001g0002 a0002c0002t0001g0015 a0002c0002t0001g0025 others(8): Show |
36 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.2788+708C>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17728880 | |||||||
| chr19:17728909 | G | T | 1 | a0001c0001t0001g0028 | 2 | HG02572.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2788+737G>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17728909 | |||||||
| chr19:17729021 | A | G | 10 | a0003c0003t0001g0003 a0003c0003t0001g0031 a0003c0003t0001g0032 others(7): Show |
30 | HG00323.hp2 HG00733.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.2788+849A>G | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17729021 | |||||||
| chr19:17729302 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2788+1130A>G | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17729302 | |||||||
| chr19:17729528 | CAG | C | 1 | a0004c0004t0001g0018 | 3 | HG01123.hp2 HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2788+1359_2788+136 others(6): Show |
MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 17729528 | ||||||
| chr19:17729604 | C | T | 3 | a0001c0001t0001g0046 a0001c0007t0001g0016 a0001c0007t0001g0069 |
5 | HG02895.hp2 HG03041.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.2788+1432C>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17729604 | |||||||
| chr19:17729610 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2788+1438A>G | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17729610 | |||||||
| chr19:17729622 | C | T | 3 | a0001c0007t0001g0016 a0001c0007t0001g0069 a0001c0007t0001g0070 |
5 | HG02895.hp2 HG03041.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.2788+1450C>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17729622 | |||||||
| chr19:17729766 | G | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0041 |
6 | HG02015.hp2 NA18946.hp2 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.2788+1594G>A | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17729766 | |||||||
| chr19:17729777 | C | G | 1 | a0004c0004t0001g0019 | 3 | HG02280.hp1 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2788+1605C>G | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17729777 | |||||||
| chr19:17729873 | G | T | 2 | a0001c0007t0001g0016 a0001c0007t0001g0069 |
4 | HG02895.hp2 HG03041.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2788+1701G>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17729873 | |||||||
| chr19:17730033 | C | T | 2 | a0003c0003t0001g0034 a0005c0009t0001g0035 |
2 | HG03669.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.2788+1861C>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17730033 | |||||||
| chr19:17730067 | C | T | 7 | a0004c0004t0001g0011 a0004c0004t0001g0019 a0004c0004t0001g0026 others(4): Show |
15 | HG01109.hp1 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.2788+1895C>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17730067 | |||||||
| chr19:17730265 | T | G | 2 | a0001c0010t0001g0017 a0005c0015t0001g0017 |
3 | HG01175.hp2 HG01496.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.2788+2093T>G | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17730265 | |||||||
| chr19:17730347 | C | T | 14 | a0004c0004t0001g0011 a0004c0004t0001g0018 a0004c0004t0001g0019 others(11): Show |
33 | HG01109.hp1 HG01123.hp2 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.2788+2175C>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17730347 | |||||||
| chr19:17730428 | C | G | 10 | a0003c0003t0001g0003 a0003c0003t0001g0031 a0003c0003t0001g0032 others(7): Show |
30 | HG00323.hp2 HG00733.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.2788+2256C>G | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17730428 | |||||||
| chr19:17730504 | T | C | 45 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0074 others(42): Show |
124 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.2788+2332T>C | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17730504 | |||||||
| chr19:17730699 | G | A | 1 | a0003c0003t0001g0033 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2789-2494G>A | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17730699 | |||||||
| chr19:17730718 | A | G | 1 | a0001c0001t0001g0045 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2789-2475A>G | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17730718 | |||||||
| chr19:17730727 | C | G | 30 | a0001c0007t0001g0016 a0001c0007t0001g0069 a0001c0007t0001g0070 others(27): Show |
77 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.2789-2466C>G | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17730727 | |||||||
| chr19:17730782 | G | A | 30 | a0001c0007t0001g0016 a0001c0007t0001g0069 a0001c0007t0001g0070 others(27): Show |
77 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.2789-2411G>A | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17730782 | |||||||
| chr19:17730821 | C | G | 4 | a0004c0004t0001g0011 a0004c0004t0001g0026 a0004c0004t0001g0027 others(1): Show |
10 | HG01109.hp1 HG01891.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.2789-2372C>G | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17730821 | |||||||
| chr19:17730915 | G | C | 1 | a0001c0001t0001g0074 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2789-2278G>C | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17730915 | |||||||
| chr19:17730953 | C | G | 2 | a0004c0004t0001g0020 a0005c0016t0001g0020 |
3 | HG02886.hp2 HG03041.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2789-2240C>G | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17730953 | |||||||
| chr19:17730987 | T | C | 10 | a0003c0003t0001g0003 a0003c0003t0001g0031 a0003c0003t0001g0032 others(7): Show |
30 | HG00323.hp2 HG00733.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.2789-2206T>C | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17730987 | |||||||
| chr19:17731065 | T | G | 2 | a0001c0001t0001g0055 a0003c0003t0001g0034 |
2 | HG00621.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.2789-2128T>G | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17731065 | |||||||
| chr19:17731202 | A | G | 1 | a0001c0001t0001g0023 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2789-1991A>G | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17731202 | |||||||
| chr19:17731275 | G | C | 1 | a0004c0004t0001g0026 | 2 | HG01109.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.2789-1918G>C | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17731275 | |||||||
| chr19:17731396 | G | A | 10 | a0003c0003t0001g0003 a0003c0003t0001g0031 a0003c0003t0001g0032 others(7): Show |
30 | HG00323.hp2 HG00733.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.2789-1797G>A | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17731396 | |||||||
| chr19:17731412 | G | C | 45 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0074 others(42): Show |
124 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.2789-1781G>C | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17731412 | |||||||
| chr19:17731530 | T | C | 30 | a0001c0007t0001g0016 a0001c0007t0001g0069 a0001c0007t0001g0070 others(27): Show |
77 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.2789-1663T>C | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17731530 | |||||||
| chr19:17731811 | A | G | 40 | a0001c0007t0001g0016 a0001c0007t0001g0069 a0001c0007t0001g0070 others(37): Show |
107 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.2789-1382A>G | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17731811 | |||||||
| chr19:17732050 | A | G | 3 | a0006c0005t0001g0004 a0006c0005t0001g0021 a0010c0027t0001g0004 |
11 | HG02486.hp1 HG02647.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.2789-1143A>G | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17732050 | |||||||
| chr19:17732143 | C | T | 2 | a0001c0001t0001g0022 a0001c0001t0001g0046 |
3 | HG02257.hp2 NA19240.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2789-1050C>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17732143 | |||||||
| chr19:17732294 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2789-899C>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17732294 | |||||||
| chr19:17732302 | G | T | 2 | a0001c0010t0001g0017 a0005c0015t0001g0017 |
3 | HG01175.hp2 HG01496.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.2789-891G>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17732302 | |||||||
| chr19:17732330 | G | A | 3 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0075 |
12 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.2789-863G>A | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17732330 | |||||||
| chr19:17732422 | T | G | 1 | a0001c0007t0001g0070 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2789-771T>G | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17732422 | |||||||
| chr19:17732523 | G | A | 1 | a0004c0004t0001g0071 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2789-670G>A | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17732523 | |||||||
| chr19:17732528 | C | T | 2 | a0004c0004t0001g0020 a0005c0016t0001g0020 |
3 | HG02886.hp2 HG03041.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2789-665C>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17732528 | |||||||
| chr19:17732537 | G | A | 1 | a0002c0011t0001g0066 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2789-656G>A | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17732537 | |||||||
| chr19:17732554 | G | A | 1 | a0001c0001t0001g0010 | 5 | HG01891.hp1 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2789-639G>A | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17732554 | |||||||
| chr19:17732723 | G | T | 1 | a0001c0001t0001g0014 | 3 | HG00280.hp1 HG01109.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.2789-470G>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17732723 | |||||||
| chr19:17732779 | G | A | 14 | a0004c0004t0001g0011 a0004c0004t0001g0018 a0004c0004t0001g0019 others(11): Show |
33 | HG01109.hp1 HG01123.hp2 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.2789-414G>A | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17732779 | |||||||
| chr19:17732794 | G | A | 10 | a0003c0003t0001g0003 a0003c0003t0001g0031 a0003c0003t0001g0032 others(7): Show |
30 | HG00323.hp2 HG00733.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.2789-399G>A | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17732794 | |||||||
| chr19:17732911 | G | T | 2 | a0001c0007t0001g0016 a0001c0007t0001g0069 |
4 | HG02895.hp2 HG03041.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2789-282G>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17732911 | |||||||
| chr19:17732938 | T | G | 30 | a0001c0007t0001g0016 a0001c0007t0001g0069 a0001c0007t0001g0070 others(27): Show |
77 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.2789-255T>G | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17732938 | |||||||
| chr19:17732986 | T | C | 44 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0074 others(41): Show |
120 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.2789-207T>C | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17732986 | |||||||
| chr19:17733008 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2789-185G>A | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17733008 | |||||||
| chr19:17733052 | A | G | 14 | a0001c0007t0001g0016 a0001c0007t0001g0069 a0001c0007t0001g0070 others(11): Show |
41 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.2789-141A>G | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17733052 | |||||||
| chr19:17733180 | C | A | 4 | a0004c0004t0001g0011 a0004c0004t0001g0026 a0004c0004t0001g0027 others(1): Show |
10 | HG01109.hp1 HG01891.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.2789-13C>A | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 5/6 | chr19 | 17733180 | |||||||
| chr19:17733516 | T | C | 44 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0074 others(41): Show |
120 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.3024+88T>C | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 6/6 | chr19 | 17733516 | |||||||
| chr19:17733641 | G | A | 2 | a0001c0001t0001g0043 a0001c0001t0001g0054 |
2 | HG01256.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.3024+213G>A | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 6/6 | chr19 | 17733641 | |||||||
| chr19:17733712 | G | A | 1 | a0001c0008t0001g0013 | 4 | HG02818.hp1 HG02965.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.3024+284G>A | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 6/6 | chr19 | 17733712 | |||||||
| chr19:17733761 | C | T | 1 | a0001c0001t0001g0023 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.3024+333C>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 6/6 | chr19 | 17733761 | |||||||
| chr19:17733828 | T | C | 44 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0074 others(41): Show |
120 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.3024+400T>C | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 6/6 | chr19 | 17733828 | |||||||
| chr19:17733863 | G | A | 1 | a0001c0007t0001g0070 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3025-410G>A | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 6/6 | chr19 | 17733863 | |||||||
| chr19:17733993 | T | A | 1 | a0003c0003t0001g0032 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3025-280T>A | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 6/6 | chr19 | 17733993 | |||||||
| chr19:17734039 | C | T | 1 | a0004c0004t0001g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3025-234C>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 6/6 | chr19 | 17734039 | |||||||
| chr19:17734085 | A | G | 40 | a0001c0007t0001g0016 a0001c0007t0001g0069 a0001c0007t0001g0070 others(37): Show |
107 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.3025-188A>G | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 6/6 | chr19 | 17734085 | |||||||
| chr19:17734133 | G | T | 30 | a0001c0007t0001g0016 a0001c0007t0001g0069 a0001c0007t0001g0070 others(27): Show |
77 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.3025-140G>T | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 6/6 | chr19 | 17734133 | |||||||
| chr19:17734258 | C | G | 1 | a0001c0001t0001g0044 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3025-15C>G | MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 6/6 | chr19 | 17734258 |