Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 81558 |
| ensemblid | ENSG00000121104.8 |
| hgncid | 24179 |
| symbol | FAM117A |
| name | family with sequence similarity 117 member A |
| refseq_nuc | NM_030802.4 |
| refseq_prot | NP_110429.1 |
| ensembl_nuc | ENST00000240364.7 |
| ensembl_prot | ENSP00000240364.2 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 49710332 |
| end | 49764131 |
| strand | - |
| ver | v1.2 |
| region | chr17:49710332-49764131 |
| region5000 | chr17:49705332-49769131 |
| regionname0 | FAM117A_chr17_49710332_49764131 |
| regionname5000 | FAM117A_chr17_49705332_49769131 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 453 | 330 | 93 | 71 | 120 | 10 | 34 | 85 | FAM117A_chr17_49705332_49769131 | FAM117A | MAGAA others(448): Show |
chr17 | 49705332 | 49769131 |
| a0002 | 0/0 | 453 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | MAGAA others(448): Show |
chr17 | 49705332 | 49769131 |
| a0003 | 0/0 | 453 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | MAGAA others(448): Show |
chr17 | 49705332 | 49769131 |
| a0004 | 0/0 | 453 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | MAGAA others(448): Show |
chr17 | 49705332 | 49769131 |
| a0005 | 0/0 | 453 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | MAGAA others(448): Show |
chr17 | 49705332 | 49769131 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1359 | 293 | 84 | 61 | 110 | 7 | 29 | FAM117A_chr17_49705332_49769131 | FAM117A | ATGGC others(1354): Show |
chr17 | 49705332 | 49769131 | ||
| a0001c0002 | 0/0 | 1359 | 28 | 5 | 10 | 9 | 2 | 2 | FAM117A_chr17_49705332_49769131 | FAM117A | ATGGC others(1354): Show |
chr17 | 49705332 | 49769131 | ||
| a0001c0003 | 0/0 | 1359 | 5 | 4 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | ATGGC others(1354): Show |
chr17 | 49705332 | 49769131 | ||
| a0001c0005 | 0/0 | 1359 | 2 | 0 | 0 | 0 | 1 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | ATGGC others(1354): Show |
chr17 | 49705332 | 49769131 | ||
| a0001c0006 | 0/0 | 1359 | 2 | 0 | 0 | 1 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | ATGGC others(1354): Show |
chr17 | 49705332 | 49769131 | ||
| a0002c0004 | 0/0 | 1359 | 3 | 3 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | ATGGC others(1354): Show |
chr17 | 49705332 | 49769131 | ||
| a0003c0007 | 0/0 | 1359 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | ATGGC others(1354): Show |
chr17 | 49705332 | 49769131 | ||
| a0004c0009 | 0/0 | 1359 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | ATGGC others(1354): Show |
chr17 | 49705332 | 49769131 | ||
| a0005c0008 | 0/0 | 1359 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | ATGGC others(1354): Show |
chr17 | 49705332 | 49769131 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2329 | 285 | 80 | 59 | 108 | 7 | 29 | FAM117A_chr17_49705332_49769131 | FAM117A | GTGTG others(2324): Show |
chr17 | 49705332 | 49769131 |
| a0001c0001t0004 | 0/0 | 2329 | 3 | 1 | 2 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | GTGTG others(2324): Show |
chr17 | 49705332 | 49769131 |
| a0001c0001t0005 | 0/0 | 2329 | 2 | 2 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | GTGTG others(2324): Show |
chr17 | 49705332 | 49769131 |
| a0001c0001t0006 | 0/0 | 2329 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | GTGTG others(2324): Show |
chr17 | 49705332 | 49769131 |
| a0001c0001t0007 | 0/0 | 2329 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | GTGTG others(2324): Show |
chr17 | 49705332 | 49769131 |
| a0001c0001t0008 | 0/0 | 2329 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | GTGTG others(2324): Show |
chr17 | 49705332 | 49769131 |
| a0001c0002t0002 | 0/0 | 2329 | 28 | 5 | 10 | 9 | 2 | 2 | FAM117A_chr17_49705332_49769131 | FAM117A | GTGTG others(2324): Show |
chr17 | 49705332 | 49769131 |
| a0001c0003t0001 | 0/0 | 2329 | 2 | 1 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | GTGTG others(2324): Show |
chr17 | 49705332 | 49769131 |
| a0001c0003t0003 | 0/0 | 2329 | 3 | 3 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | GTGTG others(2324): Show |
chr17 | 49705332 | 49769131 |
| a0001c0005t0001 | 0/0 | 2329 | 2 | 0 | 0 | 0 | 1 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | GTGTG others(2324): Show |
chr17 | 49705332 | 49769131 |
| a0001c0006t0001 | 0/0 | 2329 | 2 | 0 | 0 | 1 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | GTGTG others(2324): Show |
chr17 | 49705332 | 49769131 |
| a0002c0004t0001 | 0/0 | 2329 | 3 | 3 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | GTGTG others(2324): Show |
chr17 | 49705332 | 49769131 |
| a0003c0007t0001 | 0/0 | 2329 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | GTGTG others(2324): Show |
chr17 | 49705332 | 49769131 |
| a0004c0009t0001 | 0/0 | 2329 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | GTGTG others(2324): Show |
chr17 | 49705332 | 49769131 |
| a0005c0008t0001 | 0/0 | 2329 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | GTGTG others(2324): Show |
chr17 | 49705332 | 49769131 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0011 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0014 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0069 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0004g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0004g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0004g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0005g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0005g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0006g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0007g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0001t0008g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0002t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0002t0002g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0002t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0002t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0002t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0002t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0002t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0002t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0002t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0002t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0002t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0002t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0002t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0002t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0003t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0003t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0003t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0003t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0005t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0005t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0006t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0001c0006t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0002c0004t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0002c0004t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0003c0007t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0004c0009t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| a0005c0008t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0002 | g0264 | EUR | GBR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0213 | EUR | GBR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | GBR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0182 | EUR | GBR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0236 | EUR | FIN | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0030 | EUR | FIN | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0279 | EUR | FIN | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0094 | EUR | FIN | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | CHS | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | CHS | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | CHS | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG00609 | hp1 | a0001 | c0001 | t0008 | g0305 | EAS | CHS | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | CHS | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0053 | EAS | CHS | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0302 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0303 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01256 | hp2 | a0001 | c0002 | t0002 | g0239 | AMR | CLM | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0023 | AMR | CLM | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | CLM | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0255 | AMR | CLM | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01358 | hp2 | a0001 | c0002 | t0002 | g0023 | AMR | CLM | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0295 | AMR | CLM | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01952 | hp1 | a0003 | c0007 | t0001 | g0188 | AMR | PEL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02027 | hp1 | a0004 | c0009 | t0001 | g0204 | EAS | KHV | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02027 | hp2 | a0001 | c0002 | t0002 | g0284 | EAS | KHV | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | KHV | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | KHV | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | KHV | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | CDX | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | CDX | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02258 | hp1 | a0001 | c0002 | t0002 | g0273 | AFR | ACB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0304 | AFR | ACB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02273 | hp1 | a0001 | c0002 | t0002 | g0258 | AMR | PEL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02273 | hp2 | a0001 | c0002 | t0002 | g0254 | AMR | PEL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | ACB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02293 | hp1 | a0001 | c0002 | t0002 | g0253 | AMR | PEL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02293 | hp2 | a0001 | c0002 | t0002 | g0251 | AMR | PEL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PEL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02300 | hp2 | a0001 | c0002 | t0002 | g0257 | AMR | PEL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02630 | hp1 | a0001 | c0002 | t0002 | g0024 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02647 | hp1 | a0002 | c0004 | t0001 | g0129 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02698 | hp1 | a0001 | c0005 | t0001 | g0131 | SAS | PJL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02717 | hp1 | a0001 | c0003 | t0003 | g0133 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0293 | SAS | PJL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0296 | SAS | PJL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0286 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02896 | hp1 | a0001 | c0001 | t0006 | g0259 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02922 | hp2 | a0001 | c0003 | t0003 | g0223 | AFR | ESN | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02965 | hp1 | a0001 | c0002 | t0002 | g0024 | AFR | ESN | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ESN | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0067 | AFR | ESN | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02976 | hp1 | a0002 | c0004 | t0001 | g0007 | AFR | ESN | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | MSL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | MSL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG03225 | hp1 | a0001 | c0003 | t0001 | g0070 | AFR | MSL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | MSL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | MSL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | MSL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG03710 | hp2 | a0001 | c0003 | t0001 | g0138 | SAS | PJL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG03831 | hp1 | a0001 | c0006 | t0001 | g0301 | SAS | BEB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | BEB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | BEB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG03834 | hp2 | a0001 | c0002 | t0002 | g0146 | SAS | BEB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0287 | SAS | BEB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | BEB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | BEB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG03942 | hp2 | a0001 | c0002 | t0002 | g0222 | SAS | BEB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | STU | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | STU | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | STU | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | STU | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18522 | hp1 | a0002 | c0004 | t0001 | g0007 | AFR | YRI | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | CHB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | CHB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18906 | hp1 | a0001 | c0003 | t0003 | g0224 | AFR | YRI | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0256 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18953 | hp2 | a0005 | c0008 | t0001 | g0165 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0100 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18962 | hp2 | a0001 | c0002 | t0002 | g0092 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18994 | hp1 | a0001 | c0006 | t0001 | g0300 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0091 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | LWK | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | LWK | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | LWK | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA19058 | hp2 | a0001 | c0001 | t0007 | g0201 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA19063 | hp2 | a0001 | c0002 | t0002 | g0020 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA19074 | hp1 | a0001 | c0002 | t0002 | g0020 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA19075 | hp2 | a0001 | c0002 | t0002 | g0139 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | YRI | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | YRI | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ASW | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ASW | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA20752 | hp1 | a0001 | c0005 | t0001 | g0132 | EUR | TSI | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA20752 | hp2 | a0001 | c0002 | t0002 | g0250 | EUR | TSI | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | GIH | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | GIH | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | MSL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | USA | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | USA | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA20300 | hp1 | a0001 | c0002 | t0002 | g0272 | AFR | USA | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | USA | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | LWK | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| NA21309 | hp2 | a0001 | c0002 | t0002 | g0152 | AFR | LWK | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0069 | REF | REF | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0011 | REF | REF | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:49710332 | T | G | 1 | a0001 | 2 | HG02809.hp2 HG02970.hp2 |
splice_region_variant | LOW | c.*923A>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 8/8 | chr17 | 49710332 | |||||||
| chr17:49719854 | C | T | 1 | a0004 | 1 | HG02027.hp1 | missense_variant | MODERATE | c.614G>A | p.Arg205Gln | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 5/8 | 658/2329 | 614/1362 | 205/453 | chr17 | 49719854 | |||
| chr17:49720330 | A | G | 1 | a0005 | 1 | NA18953.hp2 | missense_variant | MODERATE | c.569T>C | p.Leu190Pro | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 4/8 | 613/2329 | 569/1362 | 190/453 | chr17 | 49720330 | |||
| chr17:49720396 | C | T | 1 | a0002 | 3 | HG02647.hp1 HG02976.hp1 NA18522.hp1 |
missense_variant | MODERATE | c.503G>A | p.Ser168Asn | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 4/8 | 547/2329 | 503/1362 | 168/453 | chr17 | 49720396 | |||
| chr17:49722560 | C | G | 1 | a0003 | 1 | HG01952.hp1 | missense_variant | MODERATE | c.401G>C | p.Arg134Pro | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 3/8 | 445/2329 | 401/1362 | 134/453 | chr17 | 49722560 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:49711348 | T | C | 1 | a0001c0003 | 5 | HG02717.hp1 HG02922.hp2 HG03225.hp1 others(2): Show |
synonymous_variant | LOW | c.1269A>G | p.Glu423Glu | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 8/8 | 1313/2329 | 1269/1362 | 423/453 | chr17 | 49711348 | |||
| chr17:49711393 | G | A | 1 | a0001c0002 | 28 | HG00099.hp1 HG00673.hp1 HG01256.hp2 others(25): Show |
synonymous_variant | LOW | c.1224C>T | p.Pro408Pro | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 8/8 | 1268/2329 | 1224/1362 | 408/453 | chr17 | 49711393 | |||
| chr17:49717547 | G | A | 1 | a0001c0005 | 2 | HG02698.hp1 NA20752.hp1 |
synonymous_variant | LOW | c.876C>T | p.Ala292Ala | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 6/8 | 920/2329 | 876/1362 | 292/453 | chr17 | 49717547 | |||
| chr17:49763941 | G | A | 1 | a0001c0006 | 2 | HG03831.hp1 NA18994.hp1 |
synonymous_variant | LOW | c.147C>T | p.Pro49Pro | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/8 | 191/2329 | 147/1362 | 49/453 | chr17 | 49763941 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:49710574 | G | A | 1 | a0001c0003t0003 | 3 | HG02717.hp1 HG02922.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*681C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 8/8 | 681 | chr17 | 49710574 | ||||||
| chr17:49710691 | C | T | 1 | a0001c0001t0006 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*564G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 8/8 | 564 | chr17 | 49710691 | ||||||
| chr17:49710743 | C | G | 1 | a0001c0002t0002 | 28 | HG00099.hp1 HG00673.hp1 HG01256.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*512G>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 8/8 | 512 | chr17 | 49710743 | ||||||
| chr17:49711228 | T | C | 1 | a0001c0001t0007 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*27A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 8/8 | 27 | chr17 | 49711228 | ||||||
| chr17:49764097 | G | A | 1 | a0001c0001t0004 | 3 | HG01069.hp1 HG01071.hp2 HG02258.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-10C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/8 | chr17 | 49764097 | |||||||
| chr17:49764099 | C | A | 1 | a0001c0001t0008 | 1 | HG00609.hp1 | 5_prime_UTR_variant | MODIFIER | c.-12G>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/8 | 12 | chr17 | 49764099 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:49711589 | C | T | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1062-34G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49711589 | |||||||
| chr17:49711664 | C | T | 1 | a0001c0003t0001g0138 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1062-109G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49711664 | |||||||
| chr17:49711704 | CT | C | 3 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 |
4 | HG01106.hp2 HG02486.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1062-150delA | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49711704 | |||||||
| chr17:49711720 | T | A | 68 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0022 others(65): Show |
74 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.1062-165A>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49711720 | |||||||
| chr17:49711899 | C | T | 1 | a0001c0001t0001g0027 | 2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1062-344G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49711899 | |||||||
| chr17:49711942 | C | T | 3 | a0001c0001t0004g0302 a0001c0001t0004g0303 a0001c0001t0004g0304 |
3 | HG01069.hp1 HG01071.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1062-387G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49711942 | |||||||
| chr17:49711943 | G | A | 4 | a0001c0001t0001g0095 a0001c0001t0001g0108 a0001c0001t0001g0110 others(1): Show |
4 | HG02630.hp2 HG02717.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1062-388C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49711943 | |||||||
| chr17:49711996 | A | G | 3 | a0001c0001t0001g0179 a0001c0001t0001g0226 a0001c0001t0001g0235 |
3 | HG01123.hp1 HG01361.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1062-441T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49711996 | |||||||
| chr17:49712023 | G | A | 13 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0045 others(10): Show |
16 | HG00558.hp1 HG00621.hp2 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.1062-468C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49712023 | |||||||
| chr17:49712184 | GT | G | 14 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0035 others(11): Show |
15 | HG01106.hp2 HG02145.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.1062-630delA | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49712184 | |||||||
| chr17:49712364 | T | C | 3 | a0001c0001t0001g0004 a0001c0001t0001g0046 a0001c0001t0001g0202 |
4 | HG01070.hp1 HG01943.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1062-809A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49712364 | |||||||
| chr17:49712406 | A | G | 2 | a0001c0005t0001g0131 a0001c0005t0001g0132 |
2 | HG02698.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1062-851T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49712406 | |||||||
| chr17:49712503 | G | C | 251 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(248): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.1062-948C>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49712503 | |||||||
| chr17:49712514 | T | A | 68 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0022 others(65): Show |
74 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.1062-959A>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49712514 | |||||||
| chr17:49713022 | C | T | 1 | a0001c0001t0001g0281 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1062-1467G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49713022 | |||||||
| chr17:49713048 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1062-1493A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49713048 | |||||||
| chr17:49713062 | T | A | 1 | a0001c0001t0001g0210 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1062-1507A>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49713062 | |||||||
| chr17:49713178 | G | A | 6 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0051 others(3): Show |
8 | HG02109.hp2 HG02622.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1062-1623C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49713178 | |||||||
| chr17:49713346 | T | C | 1 | a0001c0001t0001g0114 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1062-1791A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49713346 | |||||||
| chr17:49713505 | T | C | 1 | a0001c0002t0002g0222 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1062-1950A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49713505 | |||||||
| chr17:49713524 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1062-1969A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49713524 | |||||||
| chr17:49713823 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1062-2268G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49713823 | |||||||
| chr17:49713921 | G | A | 7 | a0001c0001t0001g0019 a0001c0001t0001g0026 a0001c0001t0001g0124 others(4): Show |
9 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1061+2244C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49713921 | |||||||
| chr17:49713941 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1061+2224C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49713941 | |||||||
| chr17:49714015 | C | T | 1 | a0001c0003t0001g0138 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1061+2150G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49714015 | |||||||
| chr17:49714334 | C | CT | 6 | a0001c0001t0001g0106 a0001c0001t0001g0116 a0001c0001t0001g0177 others(3): Show |
6 | HG00438.hp1 HG01256.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1061+1830dupA | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49714334 | |||||||
| chr17:49714334 | CT | C | 6 | a0001c0001t0001g0035 a0001c0001t0001g0118 a0001c0001t0001g0180 others(3): Show |
6 | HG00639.hp2 HG01070.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.1061+1830delA | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49714334 | |||||||
| chr17:49714416 | C | A | 31 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0021 others(28): Show |
35 | HG00140.hp1 HG00558.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.1061+1749G>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49714416 | |||||||
| chr17:49714701 | C | T | 4 | a0001c0001t0001g0063 a0001c0001t0001g0099 a0001c0001t0001g0298 others(1): Show |
4 | HG01243.hp1 HG02055.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1061+1464G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49714701 | |||||||
| chr17:49714708 | G | A | 1 | a0001c0003t0001g0138 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1061+1457C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49714708 | |||||||
| chr17:49714749 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1061+1416G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49714749 | |||||||
| chr17:49715338 | C | A | 1 | a0001c0001t0001g0056 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1061+827G>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49715338 | |||||||
| chr17:49715680 | G | A | 58 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0019 others(55): Show |
64 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.1061+485C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49715680 | |||||||
| chr17:49715800 | C | G | 1 | a0001c0001t0001g0005 | 2 | HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1061+365G>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49715800 | |||||||
| chr17:49715806 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1061+359T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49715806 | |||||||
| chr17:49715806 | A | T | 1 | a0001c0001t0001g0005 | 2 | HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1061+359T>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49715806 | |||||||
| chr17:49715813 | G | A | 17 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0077 others(14): Show |
19 | HG00544.hp1 HG01934.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.1061+352C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49715813 | |||||||
| chr17:49716590 | C | T | 1 | a0001c0002t0002g0146 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.911-275G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 6/7 | chr17 | 49716590 | |||||||
| chr17:49716651 | G | A | 7 | a0001c0002t0002g0020 a0001c0002t0002g0139 a0001c0002t0002g0253 others(4): Show |
8 | HG01346.hp2 HG01496.hp1 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.911-336C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 6/7 | chr17 | 49716651 | |||||||
| chr17:49716652 | A | G | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG00438.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.911-337T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 6/7 | chr17 | 49716652 | |||||||
| chr17:49716679 | C | T | 1 | a0001c0001t0001g0078 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.911-364G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 6/7 | chr17 | 49716679 | |||||||
| chr17:49716698 | C | T | 4 | a0001c0002t0002g0251 a0001c0002t0002g0254 a0001c0002t0002g0256 others(1): Show |
4 | HG02273.hp2 HG02293.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.911-383G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 6/7 | chr17 | 49716698 | |||||||
| chr17:49717041 | G | A | 3 | a0001c0001t0004g0302 a0001c0001t0004g0303 a0001c0001t0004g0304 |
3 | HG01069.hp1 HG01071.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.910+472C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 6/7 | chr17 | 49717041 | |||||||
| chr17:49717073 | A | G | 12 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0030 others(9): Show |
13 | HG00280.hp2 HG00323.hp2 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.910+440T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 6/7 | chr17 | 49717073 | |||||||
| chr17:49717220 | C | G | 1 | a0001c0002t0002g0256 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.910+293G>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 6/7 | chr17 | 49717220 | |||||||
| chr17:49717469 | T | C | 32 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0021 others(29): Show |
36 | HG00140.hp1 HG00558.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.910+44A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 6/7 | chr17 | 49717469 | |||||||
| chr17:49717783 | A | G | 1 | a0001c0003t0001g0138 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.709-69T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 5/7 | chr17 | 49717783 | |||||||
| chr17:49717824 | C | A | 1 | a0001c0001t0001g0296 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.709-110G>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 5/7 | chr17 | 49717824 | |||||||
| chr17:49717863 | C | T | 1 | a0001c0001t0001g0057 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.709-149G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 5/7 | chr17 | 49717863 | |||||||
| chr17:49717948 | A | G | 18 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0077 others(15): Show |
20 | HG00544.hp1 HG01934.hp2 HG02080.hp1 others(17): Show |
intron_variant | MODIFIER | c.709-234T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 5/7 | chr17 | 49717948 | |||||||
| chr17:49718673 | A | G | 1 | a0001c0001t0001g0219 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.709-959T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 5/7 | chr17 | 49718673 | |||||||
| chr17:49718742 | G | A | 1 | a0001c0003t0001g0138 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.708+1018C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 5/7 | chr17 | 49718742 | |||||||
| chr17:49718742 | G | T | 1 | a0001c0001t0001g0207 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.708+1018C>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 5/7 | chr17 | 49718742 | |||||||
| chr17:49718868 | T | C | 1 | a0002c0004t0001g0129 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.708+892A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 5/7 | chr17 | 49718868 | |||||||
| chr17:49718954 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.708+806G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 5/7 | chr17 | 49718954 | |||||||
| chr17:49718973 | C | CA | 6 | a0001c0001t0001g0084 a0001c0001t0001g0160 a0001c0001t0001g0233 others(3): Show |
6 | HG02135.hp1 HG02698.hp1 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.708+786dupT | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 5/7 | chr17 | 49718973 | |||||||
| chr17:49718973 | CA | C | 15 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0035 others(12): Show |
16 | HG01106.hp2 HG02145.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.708+786delT | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 5/7 | chr17 | 49718973 | |||||||
| chr17:49718974 | A | C | 4 | a0001c0001t0001g0015 a0001c0001t0001g0121 a0001c0001t0001g0203 others(1): Show |
4 | HG00642.hp1 HG01891.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.708+786T>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 5/7 | chr17 | 49718974 | |||||||
| chr17:49718992 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.708+768C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 5/7 | chr17 | 49718992 | |||||||
| chr17:49719185 | C | T | 1 | a0001c0001t0001g0279 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.708+575G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 5/7 | chr17 | 49719185 | |||||||
| chr17:49719186 | G | A | 1 | a0001c0001t0001g0297 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.708+574C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 5/7 | chr17 | 49719186 | |||||||
| chr17:49719252 | A | T | 1 | a0001c0001t0001g0081 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.708+508T>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 5/7 | chr17 | 49719252 | |||||||
| chr17:49719432 | G | A | 1 | a0001c0006t0001g0300 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.708+328C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 5/7 | chr17 | 49719432 | |||||||
| chr17:49720153 | C | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(84): Show |
94 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.573+173G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 4/7 | chr17 | 49720153 | |||||||
| chr17:49720229 | G | T | 1 | a0001c0001t0001g0181 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.573+97C>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 4/7 | chr17 | 49720229 | |||||||
| chr17:49720284 | T | G | 1 | a0001c0003t0001g0138 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.573+42A>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 4/7 | chr17 | 49720284 | |||||||
| chr17:49720317 | A | G | 11 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0035 others(8): Show |
12 | HG01106.hp2 HG02145.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.573+9T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 4/7 | chr17 | 49720317 | |||||||
| chr17:49720496 | C | G | 10 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0035 others(7): Show |
11 | HG01106.hp2 HG02145.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.463-60G>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 3/7 | chr17 | 49720496 | |||||||
| chr17:49720750 | C | T | 10 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0104 others(7): Show |
10 | HG01123.hp1 HG01346.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.463-314G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 3/7 | chr17 | 49720750 | |||||||
| chr17:49720783 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.463-347C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 3/7 | chr17 | 49720783 | |||||||
| chr17:49721005 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.463-569C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 3/7 | chr17 | 49721005 | |||||||
| chr17:49721160 | T | G | 1 | a0001c0001t0001g0046 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.463-724A>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 3/7 | chr17 | 49721160 | |||||||
| chr17:49721363 | A | G | 251 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(248): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.463-927T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 3/7 | chr17 | 49721363 | |||||||
| chr17:49721373 | A | G | 2 | a0001c0001t0001g0093 a0001c0001t0001g0099 |
2 | HG02647.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.463-937T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 3/7 | chr17 | 49721373 | |||||||
| chr17:49721600 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.462+899C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 3/7 | chr17 | 49721600 | |||||||
| chr17:49721811 | T | G | 1 | a0001c0001t0001g0270 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.462+688A>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 3/7 | chr17 | 49721811 | |||||||
| chr17:49721854 | C | G | 1 | a0001c0001t0001g0219 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.462+645G>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 3/7 | chr17 | 49721854 | |||||||
| chr17:49721876 | G | A | 2 | a0001c0005t0001g0131 a0001c0005t0001g0132 |
2 | HG02698.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.462+623C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 3/7 | chr17 | 49721876 | |||||||
| chr17:49721926 | T | TA | 12 | a0001c0001t0001g0041 a0001c0001t0001g0087 a0001c0001t0001g0088 others(9): Show |
12 | HG01123.hp1 HG01346.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.462+572dupT | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 3/7 | chr17 | 49721926 | |||||||
| chr17:49721926 | TA | T | 6 | a0001c0001t0001g0135 a0001c0001t0001g0180 a0001c0001t0001g0195 others(3): Show |
6 | HG01167.hp1 HG02896.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.462+572delT | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 3/7 | chr17 | 49721926 | |||||||
| chr17:49721942 | T | A | 5 | a0001c0001t0001g0150 a0001c0001t0001g0155 a0001c0001t0001g0161 others(2): Show |
5 | NA18961.hp2 NA18983.hp2 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.462+557A>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 3/7 | chr17 | 49721942 | |||||||
| chr17:49722043 | G | A | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG01243.hp2 HG01884.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.462+456C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 3/7 | chr17 | 49722043 | |||||||
| chr17:49722044 | A | G | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG01243.hp2 HG01884.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.462+455T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 3/7 | chr17 | 49722044 | |||||||
| chr17:49722053 | C | T | 24 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0021 others(21): Show |
28 | HG00140.hp1 HG00558.hp1 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.462+446G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 3/7 | chr17 | 49722053 | |||||||
| chr17:49722305 | G | T | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0217 |
3 | HG01074.hp1 HG02257.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.462+194C>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 3/7 | chr17 | 49722305 | |||||||
| chr17:49722694 | C | T | 1 | a0001c0002t0002g0053 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.367-100G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49722694 | |||||||
| chr17:49722728 | G | A | 2 | a0001c0002t0002g0023 a0001c0002t0002g0239 |
3 | HG01256.hp2 HG01258.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.367-134C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49722728 | |||||||
| chr17:49722871 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.367-277A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49722871 | |||||||
| chr17:49723036 | A | C | 1 | a0001c0001t0001g0037 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.367-442T>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49723036 | |||||||
| chr17:49723182 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.367-588G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49723182 | |||||||
| chr17:49723526 | C | T | 2 | a0001c0001t0001g0269 a0001c0001t0001g0296 |
2 | HG01069.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.367-932G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49723526 | |||||||
| chr17:49724050 | T | C | 10 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0035 others(7): Show |
11 | HG01106.hp2 HG02145.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.367-1456A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49724050 | |||||||
| chr17:49724202 | A | T | 1 | a0001c0001t0001g0094 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.367-1608T>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49724202 | |||||||
| chr17:49724264 | C | T | 1 | a0004c0009t0001g0204 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.367-1670G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49724264 | |||||||
| chr17:49724289 | A | G | 243 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(240): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.367-1695T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49724289 | |||||||
| chr17:49724384 | C | G | 1 | a0001c0001t0001g0299 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.367-1790G>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49724384 | |||||||
| chr17:49724387 | T | A | 1 | a0001c0001t0001g0094 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.367-1793A>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49724387 | |||||||
| chr17:49724822 | GA | G | 6 | a0001c0001t0001g0046 a0001c0001t0001g0248 a0001c0001t0001g0262 others(3): Show |
6 | HG00408.hp1 HG01069.hp1 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.367-2229delT | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49724822 | |||||||
| chr17:49725066 | G | A | 2 | a0001c0001t0001g0051 a0001c0001t0001g0066 |
2 | HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.367-2472C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49725066 | |||||||
| chr17:49725395 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.367-2801C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49725395 | |||||||
| chr17:49725489 | G | C | 13 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0035 others(10): Show |
14 | HG01106.hp2 HG02145.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.367-2895C>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49725489 | |||||||
| chr17:49725848 | C | T | 1 | a0001c0003t0001g0138 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.367-3254G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49725848 | |||||||
| chr17:49726032 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.367-3438G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49726032 | |||||||
| chr17:49726207 | C | T | 1 | a0001c0001t0001g0279 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.367-3613G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49726207 | |||||||
| chr17:49726400 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.367-3806G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49726400 | |||||||
| chr17:49726432 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.367-3838C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49726432 | |||||||
| chr17:49726561 | C | T | 1 | a0001c0002t0002g0091 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.367-3967G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49726561 | |||||||
| chr17:49726618 | A | G | 1 | a0001c0001t0001g0115 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.367-4024T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49726618 | |||||||
| chr17:49726732 | C | T | 1 | a0001c0002t0002g0053 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.367-4138G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49726732 | |||||||
| chr17:49726813 | A | G | 4 | a0001c0002t0002g0253 a0001c0002t0002g0255 a0001c0002t0002g0258 others(1): Show |
4 | HG01346.hp2 HG01496.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.367-4219T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49726813 | |||||||
| chr17:49726911 | C | T | 1 | a0001c0003t0001g0138 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.367-4317G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49726911 | |||||||
| chr17:49726923 | G | A | 1 | a0001c0003t0001g0138 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.367-4329C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49726923 | |||||||
| chr17:49726945 | C | T | 22 | a0001c0002t0002g0020 a0001c0002t0002g0023 a0001c0002t0002g0053 others(19): Show |
24 | HG00099.hp1 HG00673.hp1 HG01256.hp2 others(21): Show |
intron_variant | MODIFIER | c.367-4351G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49726945 | |||||||
| chr17:49727394 | C | G | 1 | a0001c0002t0002g0139 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.367-4800G>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49727394 | |||||||
| chr17:49727565 | A | T | 1 | a0001c0001t0001g0054 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.367-4971T>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49727565 | |||||||
| chr17:49727583 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.366+4968T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49727583 | |||||||
| chr17:49727703 | T | C | 1 | a0001c0001t0001g0268 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.366+4848A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49727703 | |||||||
| chr17:49727884 | C | T | 1 | a0001c0003t0001g0138 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.366+4667G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49727884 | |||||||
| chr17:49727913 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.366+4638G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49727913 | |||||||
| chr17:49727949 | A | G | 2 | a0001c0005t0001g0131 a0001c0005t0001g0132 |
2 | HG02698.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.366+4602T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49727949 | |||||||
| chr17:49728018 | C | T | 7 | a0001c0002t0002g0020 a0001c0002t0002g0139 a0001c0002t0002g0253 others(4): Show |
8 | HG01346.hp2 HG01496.hp1 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.366+4533G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49728018 | |||||||
| chr17:49728112 | C | A | 1 | a0001c0001t0001g0033 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.366+4439G>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49728112 | |||||||
| chr17:49728305 | T | C | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.366+4246A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49728305 | |||||||
| chr17:49728389 | G | A | 1 | a0001c0001t0001g0059 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.366+4162C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49728389 | |||||||
| chr17:49728409 | C | CT | 6 | a0001c0001t0001g0045 a0001c0001t0001g0054 a0001c0001t0001g0055 others(3): Show |
6 | HG01884.hp2 HG02132.hp2 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.366+4141dupA | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49728409 | |||||||
| chr17:49728688 | A | G | 14 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0035 others(11): Show |
15 | HG01106.hp2 HG02145.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.366+3863T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49728688 | |||||||
| chr17:49729077 | A | ATTCAAGA others(32): Show |
1 | a0001c0002t0002g0139 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.366+3435_366+3473d others(41): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49729077 | |||||||
| chr17:49729083 | G | T | 1 | a0001c0001t0001g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.366+3468C>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49729083 | |||||||
| chr17:49729292 | T | A | 11 | a0001c0001t0001g0021 a0001c0001t0001g0068 a0001c0001t0001g0130 others(8): Show |
12 | HG00140.hp1 HG00741.hp1 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.366+3259A>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49729292 | |||||||
| chr17:49729450 | G | A | 1 | a0001c0001t0001g0090 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.366+3101C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49729450 | |||||||
| chr17:49729503 | CT | C | 90 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(87): Show |
97 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.366+3047delA | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49729503 | |||||||
| chr17:49729503 | CTT | C | 199 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(196): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.366+3046_366+3047d others(4): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49729503 | |||||||
| chr17:49729503 | CTTT | C | 7 | a0001c0001t0001g0051 a0001c0001t0001g0177 a0001c0001t0007g0201 others(4): Show |
7 | HG01256.hp1 HG02717.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.366+3045_366+3047d others(5): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49729503 | |||||||
| chr17:49729538 | C | T | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.366+3013G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49729538 | |||||||
| chr17:49729728 | C | T | 179 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(176): Show |
197 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.366+2823G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49729728 | |||||||
| chr17:49729755 | C | T | 1 | a0001c0001t0001g0078 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.366+2796G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49729755 | |||||||
| chr17:49729853 | T | C | 17 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0077 others(14): Show |
19 | HG00544.hp1 HG01934.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.366+2698A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49729853 | |||||||
| chr17:49730334 | C | T | 1 | a0001c0001t0001g0277 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.366+2217G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49730334 | |||||||
| chr17:49730524 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.366+2027T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49730524 | |||||||
| chr17:49730625 | C | A | 1 | a0001c0001t0001g0299 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.366+1926G>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49730625 | |||||||
| chr17:49730760 | C | G | 1 | a0001c0002t0002g0152 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.366+1791G>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49730760 | |||||||
| chr17:49730845 | C | A | 2 | a0001c0005t0001g0131 a0001c0005t0001g0132 |
2 | HG02698.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.366+1706G>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49730845 | |||||||
| chr17:49730891 | T | C | 2 | a0001c0001t0001g0028 a0001c0001t0001g0117 |
2 | HG03490.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.366+1660A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49730891 | |||||||
| chr17:49731403 | G | A | 4 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(1): Show |
4 | HG00741.hp1 HG00741.hp2 HG01069.hp2 others(1): Show |
intron_variant | MODIFIER | c.366+1148C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49731403 | |||||||
| chr17:49731463 | G | GTGCTCAG others(5): Show |
14 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0035 others(11): Show |
15 | HG01106.hp2 HG02145.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.366+1087_366+1088i others(14): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49731463 | |||||||
| chr17:49731520 | G | A | 1 | a0001c0003t0001g0138 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.366+1031C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49731520 | |||||||
| chr17:49731522 | G | C | 1 | a0001c0001t0001g0163 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.366+1029C>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49731522 | |||||||
| chr17:49731616 | G | C | 1 | a0001c0001t0001g0171 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.366+935C>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49731616 | |||||||
| chr17:49731618 | C | T | 17 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0077 others(14): Show |
19 | HG00544.hp1 HG01934.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.366+933G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49731618 | |||||||
| chr17:49731748 | G | A | 10 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0035 others(7): Show |
11 | HG01106.hp2 HG02145.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.366+803C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49731748 | |||||||
| chr17:49731787 | A | AT | 10 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0035 others(7): Show |
11 | HG01106.hp2 HG02145.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.366+763dupA | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49731787 | |||||||
| chr17:49731888 | C | T | 3 | a0001c0002t0002g0091 a0001c0002t0002g0092 a0001c0002t0002g0100 |
3 | NA18959.hp1 NA18962.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.366+663G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49731888 | |||||||
| chr17:49731975 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.366+576C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49731975 | |||||||
| chr17:49732170 | A | G | 1 | a0001c0001t0001g0299 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.366+381T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49732170 | |||||||
| chr17:49732991 | C | T | 17 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0077 others(14): Show |
19 | HG00544.hp1 HG01934.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.197-271G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49732991 | |||||||
| chr17:49733294 | G | C | 48 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0019 others(45): Show |
54 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.197-574C>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49733294 | |||||||
| chr17:49733631 | C | T | 17 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0077 others(14): Show |
19 | HG00544.hp1 HG01934.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.197-911G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49733631 | |||||||
| chr17:49733908 | C | T | 1 | a0001c0001t0001g0289 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.197-1188G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49733908 | |||||||
| chr17:49733959 | G | A | 3 | a0001c0001t0004g0302 a0001c0001t0004g0303 a0001c0001t0004g0304 |
3 | HG01069.hp1 HG01071.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.197-1239C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49733959 | |||||||
| chr17:49733967 | C | T | 17 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0077 others(14): Show |
19 | HG00544.hp1 HG01934.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.197-1247G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49733967 | |||||||
| chr17:49734100 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.197-1380C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49734100 | |||||||
| chr17:49734142 | C | CA | 6 | a0001c0001t0001g0098 a0001c0001t0001g0105 a0001c0002t0002g0139 others(3): Show |
6 | HG02717.hp1 HG02922.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.197-1423dupT | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49734142 | |||||||
| chr17:49734381 | G | A | 1 | a0001c0003t0001g0138 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.197-1661C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49734381 | |||||||
| chr17:49734431 | C | CA | 7 | a0001c0001t0001g0116 a0001c0001t0001g0135 a0001c0001t0001g0136 others(4): Show |
7 | HG04115.hp1 NA18941.hp2 NA18980.hp1 others(4): Show |
intron_variant | MODIFIER | c.197-1712dupT | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49734431 | |||||||
| chr17:49734435 | A | C | 1 | a0001c0001t0001g0182 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.197-1715T>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49734435 | |||||||
| chr17:49734475 | C | G | 1 | a0001c0003t0001g0070 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.197-1755G>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49734475 | |||||||
| chr17:49734478 | G | C | 1 | a0001c0003t0001g0138 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.197-1758C>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49734478 | |||||||
| chr17:49734613 | A | T | 1 | a0001c0003t0001g0138 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.197-1893T>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49734613 | |||||||
| chr17:49734667 | A | T | 3 | a0001c0001t0001g0112 a0001c0001t0001g0194 a0001c0001t0001g0291 |
3 | NA18939.hp2 NA18963.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.197-1947T>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49734667 | |||||||
| chr17:49734690 | C | T | 1 | a0001c0001t0001g0283 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.197-1970G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49734690 | |||||||
| chr17:49735385 | G | A | 3 | a0001c0001t0001g0209 a0001c0002t0002g0023 a0001c0002t0002g0239 |
4 | HG01256.hp2 HG01257.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-2665C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49735385 | |||||||
| chr17:49735396 | A | C | 1 | a0001c0001t0001g0175 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.197-2676T>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49735396 | |||||||
| chr17:49735495 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.197-2775C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49735495 | |||||||
| chr17:49735716 | T | C | 1 | a0001c0001t0001g0225 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.197-2996A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49735716 | |||||||
| chr17:49735904 | T | C | 1 | a0001c0001t0001g0010 | 2 | HG00438.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.197-3184A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49735904 | |||||||
| chr17:49735974 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.197-3254C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49735974 | |||||||
| chr17:49736074 | CTGTGTGT others(5): Show |
C | 5 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0037 others(2): Show |
6 | HG01106.hp2 HG02486.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.197-3366_197-3355d others(14): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49736074 | |||||||
| chr17:49736203 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.197-3483T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49736203 | |||||||
| chr17:49736260 | CT | C | 10 | a0001c0001t0001g0021 a0001c0001t0001g0082 a0001c0001t0001g0180 others(7): Show |
11 | HG00140.hp1 HG00741.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.197-3541delA | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49736260 | |||||||
| chr17:49736470 | C | T | 2 | a0001c0001t0001g0298 a0001c0001t0001g0299 |
2 | HG01243.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.197-3750G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49736470 | |||||||
| chr17:49736766 | C | T | 1 | a0001c0001t0001g0298 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.197-4046G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49736766 | |||||||
| chr17:49736857 | C | G | 1 | a0001c0001t0001g0276 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.197-4137G>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49736857 | |||||||
| chr17:49737116 | C | G | 1 | a0001c0001t0001g0143 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.197-4396G>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49737116 | |||||||
| chr17:49737217 | C | T | 4 | a0001c0001t0001g0170 a0001c0001t0001g0208 a0001c0001t0001g0209 others(1): Show |
4 | HG00323.hp1 HG00733.hp1 HG00735.hp2 others(1): Show |
intron_variant | MODIFIER | c.197-4497G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49737217 | |||||||
| chr17:49737375 | C | T | 1 | a0001c0001t0001g0059 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.197-4655G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49737375 | |||||||
| chr17:49737458 | A | T | 1 | a0001c0001t0001g0035 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.197-4738T>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49737458 | |||||||
| chr17:49737476 | A | G | 2 | a0001c0001t0001g0274 a0001c0001t0001g0280 |
2 | HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.197-4756T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49737476 | |||||||
| chr17:49737592 | C | T | 2 | a0001c0001t0001g0005 a0001c0001t0001g0064 |
3 | HG03195.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.197-4872G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49737592 | |||||||
| chr17:49737884 | C | G | 19 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0077 others(16): Show |
21 | HG00544.hp1 HG01934.hp2 HG02027.hp1 others(18): Show |
intron_variant | MODIFIER | c.197-5164G>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49737884 | |||||||
| chr17:49737927 | G | T | 3 | a0001c0001t0004g0302 a0001c0001t0004g0303 a0001c0001t0004g0304 |
3 | HG01069.hp1 HG01071.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.197-5207C>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49737927 | |||||||
| chr17:49737960 | T | C | 1 | a0001c0002t0002g0273 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.197-5240A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49737960 | |||||||
| chr17:49738195 | C | T | 1 | a0001c0003t0001g0138 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.197-5475G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49738195 | |||||||
| chr17:49738200 | A | C | 1 | a0001c0001t0001g0158 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.197-5480T>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49738200 | |||||||
| chr17:49738392 | C | A | 1 | a0001c0003t0001g0138 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.197-5672G>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49738392 | |||||||
| chr17:49738718 | C | G | 9 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0051 others(6): Show |
11 | HG02109.hp2 HG02145.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.197-5998G>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49738718 | |||||||
| chr17:49738742 | C | A | 3 | a0001c0001t0001g0080 a0001c0001t0001g0140 a0001c0001t0001g0249 |
3 | NA18747.hp2 NA18969.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.197-6022G>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49738742 | |||||||
| chr17:49738757 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.197-6037C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49738757 | |||||||
| chr17:49738865 | G | A | 1 | a0001c0002t0002g0092 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.197-6145C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49738865 | |||||||
| chr17:49739229 | G | A | 1 | a0001c0006t0001g0301 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.197-6509C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49739229 | |||||||
| chr17:49739297 | A | G | 1 | a0001c0003t0001g0138 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.197-6577T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49739297 | |||||||
| chr17:49739405 | C | A | 44 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(41): Show |
49 | HG00544.hp1 HG00558.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.197-6685G>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49739405 | |||||||
| chr17:49739442 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.197-6722C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49739442 | |||||||
| chr17:49739467 | A | G | 1 | a0001c0001t0001g0181 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.197-6747T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49739467 | |||||||
| chr17:49739641 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.197-6921G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49739641 | |||||||
| chr17:49739647 | C | T | 2 | a0001c0001t0001g0085 a0001c0001t0001g0287 |
2 | HG02602.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.197-6927G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49739647 | |||||||
| chr17:49740010 | C | G | 1 | a0001c0001t0001g0080 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.197-7290G>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49740010 | |||||||
| chr17:49740011 | A | T | 25 | a0001c0002t0002g0020 a0001c0002t0002g0023 a0001c0002t0002g0024 others(22): Show |
28 | HG00099.hp1 HG00673.hp1 HG01256.hp2 others(25): Show |
intron_variant | MODIFIER | c.197-7291T>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49740011 | |||||||
| chr17:49740173 | C | T | 5 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0233 others(2): Show |
5 | NA18959.hp2 NA18963.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.197-7453G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49740173 | |||||||
| chr17:49740235 | C | T | 2 | a0001c0001t0001g0048 a0001c0001t0007g0201 |
2 | HG00621.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.197-7515G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49740235 | |||||||
| chr17:49740249 | A | AT | 8 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0001g0148 others(5): Show |
8 | HG01123.hp2 HG01361.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.197-7530dupA | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49740249 | |||||||
| chr17:49740325 | T | C | 27 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0018 others(24): Show |
30 | HG00544.hp1 HG01106.hp2 HG01934.hp2 others(27): Show |
intron_variant | MODIFIER | c.197-7605A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49740325 | |||||||
| chr17:49740350 | C | T | 5 | a0001c0001t0001g0052 a0001c0001t0001g0103 a0001c0001t0001g0148 others(2): Show |
5 | HG02451.hp1 HG02559.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.197-7630G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49740350 | |||||||
| chr17:49740351 | G | A | 5 | a0001c0001t0001g0063 a0001c0001t0001g0093 a0001c0001t0001g0099 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.197-7631C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49740351 | |||||||
| chr17:49740440 | G | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0097 |
3 | HG02922.hp1 HG03471.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.197-7720C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49740440 | |||||||
| chr17:49740466 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.197-7746C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49740466 | |||||||
| chr17:49740470 | T | C | 1 | a0001c0001t0001g0241 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.197-7750A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49740470 | |||||||
| chr17:49740623 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.197-7903C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49740623 | |||||||
| chr17:49740628 | T | C | 4 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(1): Show |
4 | HG00741.hp1 HG00741.hp2 HG01069.hp2 others(1): Show |
intron_variant | MODIFIER | c.197-7908A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49740628 | |||||||
| chr17:49740686 | A | C | 14 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0035 others(11): Show |
15 | HG01106.hp2 HG02145.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.197-7966T>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49740686 | |||||||
| chr17:49740876 | C | T | 1 | a0001c0001t0001g0140 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.197-8156G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49740876 | |||||||
| chr17:49741459 | C | T | 10 | a0001c0001t0001g0021 a0001c0001t0001g0179 a0001c0001t0001g0180 others(7): Show |
11 | HG00140.hp1 HG00741.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.197-8739G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49741459 | |||||||
| chr17:49741517 | C | T | 4 | a0001c0001t0001g0170 a0001c0001t0001g0208 a0001c0001t0001g0209 others(1): Show |
4 | HG00323.hp1 HG00733.hp1 HG00735.hp2 others(1): Show |
intron_variant | MODIFIER | c.197-8797G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49741517 | |||||||
| chr17:49741570 | C | G | 10 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0035 others(7): Show |
11 | HG01106.hp2 HG02145.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.197-8850G>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49741570 | |||||||
| chr17:49741590 | C | T | 2 | a0001c0001t0001g0298 a0001c0001t0001g0299 |
2 | HG01243.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.197-8870G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49741590 | |||||||
| chr17:49741689 | G | A | 303 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(300): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.197-8969C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49741689 | |||||||
| chr17:49741812 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.197-9092C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49741812 | |||||||
| chr17:49741849 | A | G | 1 | a0001c0001t0001g0045 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.197-9129T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49741849 | |||||||
| chr17:49742282 | A | G | 1 | a0001c0001t0001g0216 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.197-9562T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49742282 | |||||||
| chr17:49742319 | C | T | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | HG00558.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.197-9599G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49742319 | |||||||
| chr17:49742343 | A | G | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.197-9623T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49742343 | |||||||
| chr17:49742439 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.197-9719A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49742439 | |||||||
| chr17:49742771 | C | G | 1 | a0001c0001t0001g0130 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.197-10051G>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49742771 | |||||||
| chr17:49742966 | T | C | 1 | a0001c0001t0001g0058 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.197-10246A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49742966 | |||||||
| chr17:49743500 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.197-10780G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49743500 | |||||||
| chr17:49743860 | G | A | 1 | a0001c0001t0001g0145 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.197-11140C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49743860 | |||||||
| chr17:49743952 | C | T | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0217 |
3 | HG01074.hp1 HG02257.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.197-11232G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49743952 | |||||||
| chr17:49744218 | T | C | 1 | a0001c0003t0001g0138 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.197-11498A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49744218 | |||||||
| chr17:49744360 | A | G | 2 | a0001c0001t0001g0005 a0001c0001t0001g0064 |
3 | HG03195.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.197-11640T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49744360 | |||||||
| chr17:49744478 | C | T | 1 | a0001c0003t0001g0138 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.197-11758G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49744478 | |||||||
| chr17:49744548 | G | A | 1 | a0003c0007t0001g0188 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.197-11828C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49744548 | |||||||
| chr17:49744696 | G | A | 3 | a0001c0003t0003g0133 a0001c0003t0003g0223 a0001c0003t0003g0224 |
3 | HG02717.hp1 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.197-11976C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49744696 | |||||||
| chr17:49744761 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.197-12041G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49744761 | |||||||
| chr17:49745013 | C | CA | 22 | a0001c0001t0001g0016 a0001c0001t0001g0048 a0001c0001t0001g0074 others(19): Show |
23 | HG00621.hp2 HG01243.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.197-12294dupT | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49745013 | |||||||
| chr17:49745013 | C | CAA | 31 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0035 others(28): Show |
35 | HG00099.hp1 HG00673.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.197-12295_197-1229 others(6): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49745013 | |||||||
| chr17:49745013 | CA | C | 44 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0025 others(41): Show |
49 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(46): Show |
intron_variant | MODIFIER | c.197-12294delT | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49745013 | |||||||
| chr17:49745029 | A | C | 1 | a0001c0001t0001g0243 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.197-12309T>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49745029 | |||||||
| chr17:49745032 | A | C | 6 | a0001c0001t0001g0065 a0001c0001t0001g0122 a0001c0001t0001g0213 others(3): Show |
6 | HG00099.hp2 HG01192.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.197-12312T>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49745032 | |||||||
| chr17:49745034 | C | A | 3 | a0001c0001t0001g0063 a0001c0001t0001g0298 a0001c0001t0001g0299 |
3 | HG01243.hp1 HG02055.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.197-12314G>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49745034 | |||||||
| chr17:49745306 | T | C | 1 | a0001c0001t0001g0206 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.197-12586A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49745306 | |||||||
| chr17:49745505 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.197-12785A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49745505 | |||||||
| chr17:49745572 | G | C | 1 | a0001c0001t0001g0060 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.197-12852C>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49745572 | |||||||
| chr17:49745697 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.197-12977C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49745697 | |||||||
| chr17:49746337 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.197-13617G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49746337 | |||||||
| chr17:49746692 | C | T | 7 | a0001c0001t0001g0015 a0001c0001t0001g0118 a0001c0001t0001g0120 others(4): Show |
8 | HG00642.hp1 HG00735.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.197-13972G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49746692 | |||||||
| chr17:49746753 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.197-14033C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49746753 | |||||||
| chr17:49746769 | G | A | 1 | a0001c0003t0003g0223 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.197-14049C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49746769 | |||||||
| chr17:49747139 | GA | G | 9 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0051 others(6): Show |
11 | HG02109.hp2 HG02145.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.197-14420delT | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49747139 | |||||||
| chr17:49747243 | A | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(100): Show |
111 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.197-14523T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49747243 | |||||||
| chr17:49747352 | G | A | 3 | a0001c0001t0001g0147 a0001c0001t0001g0162 a0001c0001t0001g0163 |
3 | HG02135.hp2 NA18612.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.197-14632C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49747352 | |||||||
| chr17:49747442 | G | T | 13 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0035 others(10): Show |
14 | HG01106.hp2 HG02145.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.197-14722C>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49747442 | |||||||
| chr17:49747575 | C | T | 89 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(86): Show |
96 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.197-14855G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49747575 | |||||||
| chr17:49747892 | G | T | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG01243.hp2 HG01884.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.197-15172C>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49747892 | |||||||
| chr17:49747918 | G | A | 1 | a0001c0001t0001g0275 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.197-15198C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49747918 | |||||||
| chr17:49747949 | G | A | 6 | a0001c0001t0001g0022 a0001c0001t0001g0237 a0001c0001t0001g0263 others(3): Show |
7 | HG00408.hp2 HG02056.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.197-15229C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49747949 | |||||||
| chr17:49748139 | A | G | 1 | a0001c0003t0001g0138 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.197-15419T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49748139 | |||||||
| chr17:49748248 | A | G | 1 | a0001c0001t0001g0156 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.197-15528T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49748248 | |||||||
| chr17:49748304 | A | C | 2 | a0001c0005t0001g0131 a0001c0005t0001g0132 |
2 | HG02698.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.197-15584T>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49748304 | |||||||
| chr17:49748402 | C | A | 1 | a0001c0001t0001g0221 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.196+15490G>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49748402 | |||||||
| chr17:49748420 | C | T | 1 | a0001c0001t0001g0021 | 2 | HG00140.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.196+15472G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49748420 | |||||||
| chr17:49748456 | A | G | 1 | a0001c0003t0001g0138 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.196+15436T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49748456 | |||||||
| chr17:49748457 | A | C | 1 | a0001c0003t0001g0138 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.196+15435T>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49748457 | |||||||
| chr17:49748650 | T | C | 2 | a0001c0001t0001g0164 a0004c0009t0001g0204 |
2 | HG02027.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.196+15242A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49748650 | |||||||
| chr17:49748915 | G | A | 2 | a0002c0004t0001g0007 a0002c0004t0001g0129 |
3 | HG02647.hp1 HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.196+14977C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49748915 | |||||||
| chr17:49748934 | G | T | 1 | a0001c0001t0006g0259 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.196+14958C>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49748934 | |||||||
| chr17:49749005 | T | C | 38 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0049 others(35): Show |
43 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.196+14887A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49749005 | |||||||
| chr17:49749105 | C | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0099 |
2 | HG02647.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.196+14787G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49749105 | |||||||
| chr17:49749171 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.196+14721G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49749171 | |||||||
| chr17:49749300 | A | G | 1 | a0001c0001t0001g0229 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.196+14592T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49749300 | |||||||
| chr17:49749312 | T | A | 1 | a0001c0001t0001g0114 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.196+14580A>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49749312 | |||||||
| chr17:49749380 | T | G | 1 | a0001c0001t0001g0027 | 2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.196+14512A>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49749380 | |||||||
| chr17:49749387 | C | T | 2 | a0001c0001t0001g0226 a0001c0001t0001g0235 |
2 | HG01123.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.196+14505G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49749387 | |||||||
| chr17:49749403 | C | T | 1 | a0001c0001t0001g0031 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.196+14489G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49749403 | |||||||
| chr17:49749404 | A | G | 1 | a0001c0001t0001g0031 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.196+14488T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49749404 | |||||||
| chr17:49749450 | G | A | 6 | a0001c0002t0002g0020 a0001c0002t0002g0253 a0001c0002t0002g0255 others(3): Show |
7 | HG01346.hp2 HG01496.hp1 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.196+14442C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49749450 | |||||||
| chr17:49749457 | GTCCCAGC others(1056): Show |
G | 10 | a0001c0001t0001g0021 a0001c0001t0001g0179 a0001c0001t0001g0180 others(7): Show |
11 | HG00140.hp1 HG00741.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.196+13372_196+1443 others(4): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49749457 | |||||||
| chr17:49749575 | C | CA | 32 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0030 others(29): Show |
33 | HG00280.hp2 HG01255.hp2 HG01346.hp1 others(30): Show |
intron_variant | MODIFIER | c.196+14316dupT | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49749575 | |||||||
| chr17:49749575 | CA | C | 57 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(54): Show |
63 | HG00438.hp2 HG00544.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.196+14316delT | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49749575 | |||||||
| chr17:49750163 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.196+13729C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49750163 | |||||||
| chr17:49750255 | G | C | 1 | a0001c0001t0001g0066 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.196+13637C>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49750255 | |||||||
| chr17:49750265 | T | C | 1 | a0001c0003t0001g0138 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.196+13627A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49750265 | |||||||
| chr17:49750293 | C | T | 1 | a0001c0003t0001g0138 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.196+13599G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49750293 | |||||||
| chr17:49750445 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.196+13447G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49750445 | |||||||
| chr17:49750599 | A | AC | 8 | a0001c0001t0001g0090 a0001c0002t0002g0091 a0001c0002t0002g0092 others(5): Show |
8 | HG02717.hp1 HG02922.hp2 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.196+13292dupG | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49750599 | |||||||
| chr17:49750600 | C | A | 1 | a0001c0001t0001g0157 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.196+13292G>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49750600 | |||||||
| chr17:49750605 | C | A | 5 | a0001c0001t0001g0063 a0001c0001t0001g0093 a0001c0001t0001g0099 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.196+13287G>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49750605 | |||||||
| chr17:49750727 | G | T | 1 | a0001c0001t0001g0169 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.196+13165C>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49750727 | |||||||
| chr17:49750931 | T | G | 1 | a0001c0001t0001g0044 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.196+12961A>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49750931 | |||||||
| chr17:49751213 | G | T | 1 | a0001c0001t0001g0213 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.196+12679C>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49751213 | |||||||
| chr17:49751237 | G | A | 1 | a0001c0001t0005g0286 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.196+12655C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49751237 | |||||||
| chr17:49751275 | T | C | 1 | a0001c0001t0001g0294 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.196+12617A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49751275 | |||||||
| chr17:49751279 | C | CA | 20 | a0001c0001t0001g0008 a0001c0001t0001g0077 a0001c0001t0001g0080 others(17): Show |
21 | HG00408.hp1 HG00438.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.196+12612dupT | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49751279 | |||||||
| chr17:49751279 | C | CAAAAAAA others(3): Show |
1 | a0001c0003t0001g0138 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.196+12603_196+1261 others(14): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49751279 | |||||||
| chr17:49751299 | A | AG | 4 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0298 others(1): Show |
4 | HG00558.hp1 HG01243.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.196+12592dupC | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49751299 | |||||||
| chr17:49751299 | A | G | 22 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0045 others(19): Show |
25 | HG00621.hp2 HG01069.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.196+12593T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49751299 | |||||||
| chr17:49751473 | G | A | 26 | a0001c0001t0001g0090 a0001c0002t0002g0020 a0001c0002t0002g0023 others(23): Show |
29 | HG00099.hp1 HG00673.hp1 HG01256.hp2 others(26): Show |
intron_variant | MODIFIER | c.196+12419C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49751473 | |||||||
| chr17:49751528 | C | T | 1 | a0001c0001t0005g0067 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.196+12364G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49751528 | |||||||
| chr17:49751943 | C | CA | 50 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(47): Show |
53 | HG00099.hp1 HG00673.hp1 HG01106.hp2 others(50): Show |
intron_variant | MODIFIER | c.196+11948dupT | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49751943 | |||||||
| chr17:49751943 | CA | C | 41 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0019 others(38): Show |
47 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.196+11948delT | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49751943 | |||||||
| chr17:49752185 | A | C | 1 | a0001c0003t0001g0138 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.196+11707T>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49752185 | |||||||
| chr17:49752189 | G | A | 9 | a0001c0001t0001g0021 a0001c0001t0001g0179 a0001c0001t0001g0180 others(6): Show |
10 | HG00140.hp1 HG00741.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.196+11703C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49752189 | |||||||
| chr17:49752302 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.196+11590G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49752302 | |||||||
| chr17:49752488 | A | T | 1 | a0001c0001t0001g0210 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.196+11404T>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49752488 | |||||||
| chr17:49752808 | T | C | 1 | a0001c0001t0001g0261 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.196+11084A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49752808 | |||||||
| chr17:49753003 | A | G | 1 | a0001c0003t0001g0138 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.196+10889T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49753003 | |||||||
| chr17:49753407 | C | T | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG01243.hp2 HG01884.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.196+10485G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49753407 | |||||||
| chr17:49753419 | T | C | 1 | a0001c0001t0001g0247 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.196+10473A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49753419 | |||||||
| chr17:49753543 | C | T | 4 | a0001c0001t0001g0090 a0001c0002t0002g0091 a0001c0002t0002g0092 others(1): Show |
4 | NA18959.hp1 NA18962.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.196+10349G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49753543 | |||||||
| chr17:49753558 | G | C | 1 | a0001c0001t0001g0105 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.196+10334C>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49753558 | |||||||
| chr17:49753595 | C | T | 10 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0035 others(7): Show |
11 | HG01106.hp2 HG02145.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.196+10297G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49753595 | |||||||
| chr17:49753618 | C | G | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.196+10274G>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49753618 | |||||||
| chr17:49753852 | G | A | 9 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0051 others(6): Show |
11 | HG02109.hp2 HG02145.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.196+10040C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49753852 | |||||||
| chr17:49753942 | C | G | 1 | a0001c0002t0002g0152 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.196+9950G>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49753942 | |||||||
| chr17:49754461 | C | T | 2 | a0001c0001t0001g0062 a0001c0001t0001g0200 |
2 | HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.196+9431G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49754461 | |||||||
| chr17:49754487 | G | C | 65 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0019 others(62): Show |
72 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(69): Show |
intron_variant | MODIFIER | c.196+9405C>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49754487 | |||||||
| chr17:49754550 | C | T | 2 | a0001c0001t0001g0203 a0001c0001t0001g0207 |
2 | HG00642.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.196+9342G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49754550 | |||||||
| chr17:49754600 | G | A | 3 | a0001c0003t0003g0133 a0001c0003t0003g0223 a0001c0003t0003g0224 |
3 | HG02717.hp1 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.196+9292C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49754600 | |||||||
| chr17:49754750 | C | T | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | NA19058.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.196+9142G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49754750 | |||||||
| chr17:49754981 | T | C | 3 | a0001c0001t0004g0302 a0001c0001t0004g0303 a0001c0001t0004g0304 |
3 | HG01069.hp1 HG01071.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.196+8911A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49754981 | |||||||
| chr17:49754986 | C | T | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.196+8906G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49754986 | |||||||
| chr17:49755038 | C | CA | 31 | a0001c0001t0001g0042 a0001c0001t0001g0050 a0001c0001t0001g0062 others(28): Show |
31 | HG00140.hp2 HG00558.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.196+8853dupT | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49755038 | |||||||
| chr17:49755038 | CA | C | 33 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(30): Show |
37 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.196+8853delT | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49755038 | |||||||
| chr17:49755276 | T | C | 1 | a0001c0003t0001g0138 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.196+8616A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49755276 | |||||||
| chr17:49755715 | C | T | 1 | a0001c0003t0001g0138 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.196+8177G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49755715 | |||||||
| chr17:49755724 | C | T | 1 | a0004c0009t0001g0204 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.196+8168G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49755724 | |||||||
| chr17:49755740 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.196+8152C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49755740 | |||||||
| chr17:49755789 | C | G | 1 | a0001c0001t0001g0203 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.196+8103G>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49755789 | |||||||
| chr17:49756299 | G | A | 1 | a0001c0002t0002g0100 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.196+7593C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49756299 | |||||||
| chr17:49756624 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.196+7268T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49756624 | |||||||
| chr17:49756916 | CA | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
180 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.196+6975delT | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49756916 | |||||||
| chr17:49756916 | CAA | C | 6 | a0001c0001t0001g0034 a0001c0001t0001g0107 a0001c0001t0001g0108 others(3): Show |
6 | HG00673.hp1 HG01943.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.196+6974_196+6975d others(4): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49756916 | |||||||
| chr17:49756945 | A | G | 1 | a0001c0003t0001g0138 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.196+6947T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49756945 | |||||||
| chr17:49756967 | C | T | 1 | a0001c0002t0002g0254 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.196+6925G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49756967 | |||||||
| chr17:49757025 | G | A | 1 | a0001c0001t0001g0227 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.196+6867C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49757025 | |||||||
| chr17:49757056 | C | A | 1 | a0001c0001t0001g0274 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.196+6836G>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49757056 | |||||||
| chr17:49757086 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0219 |
3 | HG02886.hp1 HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.196+6806C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49757086 | |||||||
| chr17:49757211 | C | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0199 |
3 | HG02109.hp2 HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.196+6681G>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49757211 | |||||||
| chr17:49757414 | A | G | 14 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0035 others(11): Show |
15 | HG01106.hp2 HG02145.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.196+6478T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49757414 | |||||||
| chr17:49757697 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.196+6195G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49757697 | |||||||
| chr17:49757813 | G | A | 1 | a0001c0001t0001g0009 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.196+6079C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49757813 | |||||||
| chr17:49757817 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0220 a0001c0001t0001g0236 |
4 | HG00280.hp1 HG00733.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.196+6075C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49757817 | |||||||
| chr17:49757971 | A | G | 1 | a0001c0003t0001g0138 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.196+5921T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49757971 | |||||||
| chr17:49758008 | C | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0227 |
2 | NA19060.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.196+5884G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758008 | |||||||
| chr17:49758159 | G | A | 3 | a0001c0001t0001g0088 a0001c0001t0001g0106 a0001c0001t0001g0183 |
3 | HG01346.hp1 HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.196+5733C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758159 | |||||||
| chr17:49758186 | G | T | 2 | a0001c0001t0001g0085 a0001c0001t0001g0287 |
2 | HG02602.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.196+5706C>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758186 | |||||||
| chr17:49758231 | C | G | 1 | a0001c0003t0001g0138 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.196+5661G>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758231 | |||||||
| chr17:49758511 | C | T | 3 | a0001c0003t0003g0133 a0001c0003t0003g0223 a0001c0003t0003g0224 |
3 | HG02717.hp1 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.196+5381G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758511 | |||||||
| chr17:49758621 | C | CA | 55 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0028 others(52): Show |
60 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.196+5270dupT | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758621 | |||||||
| chr17:49758632 | A | AT | 4 | a0001c0001t0001g0085 a0001c0001t0001g0153 a0001c0001t0001g0155 others(1): Show |
4 | HG02602.hp2 HG03927.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.196+5259_196+5260i others(3): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758632 | |||||||
| chr17:49758632 | A | T | 129 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(126): Show |
141 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.196+5260T>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758632 | |||||||
| chr17:49758633 | A | T | 6 | a0001c0001t0001g0013 a0001c0001t0001g0052 a0001c0001t0004g0302 others(3): Show |
6 | HG01069.hp1 HG01071.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.196+5259T>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758633 | |||||||
| chr17:49758634 | A | AT | 4 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0094 others(1): Show |
5 | HG00323.hp2 HG01255.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.196+5257_196+5258i others(3): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758634 | |||||||
| chr17:49758634 | A | T | 1 | a0001c0001t0001g0030 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.196+5258T>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758634 | |||||||
| chr17:49758634 | AAAT | A | 10 | a0001c0001t0001g0044 a0001c0001t0001g0071 a0001c0001t0001g0072 others(7): Show |
10 | HG01884.hp1 HG02559.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.196+5255_196+5257d others(5): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758634 | |||||||
| chr17:49758634 | AAATAAAA others(9): Show |
A | 1 | a0001c0003t0001g0138 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.196+5242_196+5257d others(18): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758634 | |||||||
| chr17:49758637 | T | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0052 others(21): Show |
28 | HG00558.hp2 HG00639.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.196+5255A>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758637 | |||||||
| chr17:49758638 | A | AAAAT | 23 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(20): Show |
24 | HG00673.hp1 HG01167.hp2 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.196+5250_196+5253d others(6): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758638 | |||||||
| chr17:49758638 | A | AT | 4 | a0001c0001t0001g0017 a0001c0001t0001g0084 a0001c0001t0001g0134 others(1): Show |
5 | HG02129.hp2 NA18945.hp2 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.196+5253_196+5254i others(3): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758638 | |||||||
| chr17:49758638 | A | T | 5 | a0001c0001t0001g0052 a0001c0001t0001g0143 a0001c0001t0001g0144 others(2): Show |
5 | HG02293.hp1 HG02451.hp1 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.196+5254T>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758638 | |||||||
| chr17:49758638 | AAAAT | A | 87 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(84): Show |
100 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.196+5250_196+5253d others(6): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758638 | |||||||
| chr17:49758638 | AAAATAAA others(5): Show |
A | 8 | a0001c0001t0001g0008 a0001c0001t0001g0077 a0001c0001t0001g0079 others(5): Show |
9 | HG01934.hp2 HG02055.hp2 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.196+5242_196+5253d others(14): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758638 | |||||||
| chr17:49758638 | AAAATAAA others(9): Show |
A | 1 | a0001c0001t0001g0066 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.196+5238_196+5253d others(18): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758638 | |||||||
| chr17:49758640 | A | T | 1 | a0001c0001t0001g0097 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.196+5252T>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758640 | |||||||
| chr17:49758641 | A | T | 7 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(4): Show |
7 | HG01884.hp1 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.196+5251T>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758641 | |||||||
| chr17:49758642 | T | A | 22 | a0001c0001t0001g0001 a0001c0001t0001g0044 a0001c0001t0001g0057 others(19): Show |
24 | HG00639.hp2 HG01106.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.196+5250A>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758642 | |||||||
| chr17:49758646 | T | A | 5 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0137 others(2): Show |
5 | HG00639.hp2 HG01928.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.196+5246A>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758646 | |||||||
| chr17:49758669 | A | T | 3 | a0001c0003t0003g0133 a0001c0003t0003g0223 a0001c0003t0003g0224 |
3 | HG02717.hp1 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.196+5223T>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758669 | |||||||
| chr17:49758678 | T | A | 3 | a0001c0001t0001g0006 a0002c0004t0001g0007 a0002c0004t0001g0129 |
5 | HG01358.hp1 HG02109.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.196+5214A>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758678 | |||||||
| chr17:49758993 | A | G | 7 | a0001c0001t0001g0008 a0001c0001t0001g0077 a0001c0001t0001g0079 others(4): Show |
8 | HG01934.hp2 HG02080.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.196+4899T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758993 | |||||||
| chr17:49759088 | C | T | 2 | a0001c0005t0001g0131 a0001c0005t0001g0132 |
2 | HG02698.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.196+4804G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49759088 | |||||||
| chr17:49759526 | C | A | 1 | a0001c0001t0001g0075 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.196+4366G>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49759526 | |||||||
| chr17:49759544 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.196+4348A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49759544 | |||||||
| chr17:49759783 | C | T | 1 | a0001c0001t0001g0078 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.196+4109G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49759783 | |||||||
| chr17:49759865 | A | G | 1 | a0001c0002t0002g0251 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.196+4027T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49759865 | |||||||
| chr17:49759995 | G | T | 1 | a0001c0002t0002g0250 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.196+3897C>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49759995 | |||||||
| chr17:49760049 | A | G | 1 | a0001c0001t0001g0142 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.196+3843T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49760049 | |||||||
| chr17:49760058 | A | T | 1 | a0001c0001t0001g0077 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.196+3834T>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49760058 | |||||||
| chr17:49760092 | A | G | 1 | a0001c0001t0001g0226 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.196+3800T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49760092 | |||||||
| chr17:49760189 | G | A | 4 | a0001c0001t0001g0068 a0001c0001t0001g0130 a0001c0001t0005g0067 others(1): Show |
4 | HG02615.hp1 HG02809.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.196+3703C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49760189 | |||||||
| chr17:49760321 | A | C | 3 | a0001c0001t0004g0302 a0001c0001t0004g0303 a0001c0001t0004g0304 |
3 | HG01069.hp1 HG01071.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.196+3571T>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49760321 | |||||||
| chr17:49760417 | A | T | 1 | a0001c0001t0001g0051 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.196+3475T>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49760417 | |||||||
| chr17:49760484 | A | G | 3 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0249 |
3 | NA18747.hp2 NA18969.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.196+3408T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49760484 | |||||||
| chr17:49760666 | T | C | 1 | a0001c0002t0002g0284 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.196+3226A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49760666 | |||||||
| chr17:49760680 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.196+3212G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49760680 | |||||||
| chr17:49760717 | T | C | 1 | a0001c0002t0002g0222 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.196+3175A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49760717 | |||||||
| chr17:49760723 | A | T | 1 | a0001c0003t0001g0138 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.196+3169T>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49760723 | |||||||
| chr17:49761008 | C | A | 2 | a0001c0005t0001g0131 a0001c0005t0001g0132 |
2 | HG02698.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.196+2884G>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49761008 | |||||||
| chr17:49761014 | A | G | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG01243.hp2 HG01884.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.196+2878T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49761014 | |||||||
| chr17:49761037 | C | A | 10 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0035 others(7): Show |
11 | HG01106.hp2 HG02145.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.196+2855G>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49761037 | |||||||
| chr17:49761094 | A | C | 1 | a0001c0002t0002g0139 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.196+2798T>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49761094 | |||||||
| chr17:49761154 | G | C | 3 | a0001c0003t0003g0133 a0001c0003t0003g0223 a0001c0003t0003g0224 |
3 | HG02717.hp1 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.196+2738C>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49761154 | |||||||
| chr17:49761775 | T | C | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.196+2117A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49761775 | |||||||
| chr17:49762039 | G | A | 10 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0035 others(7): Show |
11 | HG01106.hp2 HG02145.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.196+1853C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49762039 | |||||||
| chr17:49762164 | T | C | 4 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0248 others(1): Show |
4 | NA18941.hp2 NA18980.hp1 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.196+1728A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49762164 | |||||||
| chr17:49762168 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.196+1724G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49762168 | |||||||
| chr17:49762263 | C | T | 1 | a0001c0003t0001g0138 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.196+1629G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49762263 | |||||||
| chr17:49762668 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.196+1224T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49762668 | |||||||
| chr17:49763123 | T | TAC | 30 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(27): Show |
33 | HG00280.hp1 HG00738.hp1 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.196+767_196+768dup others(2): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49763123 | |||||||
| chr17:49763123 | T | TACAC | 48 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0025 others(45): Show |
56 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.196+765_196+768dup others(4): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49763123 | |||||||
| chr17:49763123 | TAC | T | 77 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0028 others(74): Show |
79 | HG00323.hp2 HG00544.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.196+767_196+768del others(2): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49763123 | |||||||
| chr17:49763123 | TACAC | T | 23 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0051 others(20): Show |
26 | HG00673.hp1 HG01243.hp1 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.196+765_196+768del others(4): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49763123 | |||||||
| chr17:49763123 | TACACAC | T | 9 | a0001c0001t0001g0004 a0001c0001t0001g0043 a0001c0001t0001g0044 others(6): Show |
10 | HG00558.hp1 HG00621.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.196+763_196+768del others(6): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49763123 | |||||||
| chr17:49763123 | TACACACA others(1): Show |
T | 10 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0035 others(7): Show |
11 | HG01106.hp2 HG02145.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.196+761_196+768del others(8): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49763123 | |||||||
| chr17:49763123 | TACACACA others(3): Show |
T | 1 | a0001c0001t0001g0033 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.196+759_196+768del others(10): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49763123 | |||||||
| chr17:49763123 | TACACACA others(5): Show |
T | 4 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(1): Show |
4 | HG00280.hp2 HG00673.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.196+757_196+768del others(12): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49763123 | |||||||
| chr17:49763698 | C | G | 1 | a0001c0001t0001g0028 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.196+194G>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49763698 | |||||||
| chr17:49763838 | G | GC | 12 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0001g0289 others(9): Show |
12 | HG00408.hp1 HG01109.hp1 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.196+53dupG | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49763838 | |||||||
| chr17:49763864 | C | A | 2 | a0001c0001t0001g0298 a0001c0001t0001g0299 |
2 | HG01243.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.196+28G>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49763864 |