Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 131177 |
| ensemblid | ENSG00000198643.7 |
| hgncid | 18665 |
| symbol | FAM3D |
| name | FAM3 metabolism regulating signaling molecule D |
| refseq_nuc | NM_138805.3 |
| refseq_prot | NP_620160.1 |
| ensembl_nuc | ENST00000358781.7 |
| ensembl_prot | ENSP00000351632.2 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 58633946 |
| end | 58666774 |
| strand | - |
| ver | v1.2 |
| region | chr3:58633946-58666774 |
| region5000 | chr3:58628946-58671774 |
| regionname0 | FAM3D_chr3_58633946_58666774 |
| regionname5000 | FAM3D_chr3_58628946_58671774 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 224 | 364 | 84 | 62 | 161 | 9 | 46 | 125 | FAM3D_chr3_58628946_58671774 | FAM3D | MRVSG others(219): Show |
chr3 | 58628946 | 58671774 |
| a0002 | 0/0 | 224 | 28 | 8 | 11 | 1 | 4 | 4 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | MRVSG others(219): Show |
chr3 | 58628946 | 58671774 |
| a0003 | 0/0 | 224 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | MRVSG others(219): Show |
chr3 | 58628946 | 58671774 |
| a0004 | 0/0 | 224 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | MRVSG others(219): Show |
chr3 | 58628946 | 58671774 |
| a0005 | 0/0 | 224 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | MRVSG others(219): Show |
chr3 | 58628946 | 58671774 |
| a0006 | 0/0 | 224 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | MRVSG others(219): Show |
chr3 | 58628946 | 58671774 |
| a0007 | 0/0 | 224 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | MRVSG others(219): Show |
chr3 | 58628946 | 58671774 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 672 | 350 | 81 | 61 | 158 | 9 | 39 | FAM3D_chr3_58628946_58671774 | FAM3D | ATGAG others(667): Show |
chr3 | 58628946 | 58671774 | ||
| a0001c0003 | 0/0 | 672 | 5 | 1 | 1 | 0 | 0 | 3 | FAM3D_chr3_58628946_58671774 | FAM3D | ATGAG others(667): Show |
chr3 | 58628946 | 58671774 | ||
| a0001c0004 | 0/0 | 672 | 4 | 0 | 0 | 0 | 0 | 4 | FAM3D_chr3_58628946_58671774 | FAM3D | ATGAG others(667): Show |
chr3 | 58628946 | 58671774 | ||
| a0001c0005 | 0/0 | 672 | 3 | 0 | 0 | 3 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | ATGAG others(667): Show |
chr3 | 58628946 | 58671774 | ||
| a0001c0006 | 0/0 | 672 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | ATGAG others(667): Show |
chr3 | 58628946 | 58671774 | ||
| a0002c0002 | 0/0 | 672 | 28 | 8 | 11 | 1 | 4 | 4 | FAM3D_chr3_58628946_58671774 | FAM3D | ATGAG others(667): Show |
chr3 | 58628946 | 58671774 | ||
| a0003c0007 | 0/0 | 672 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | ATGAG others(667): Show |
chr3 | 58628946 | 58671774 | ||
| a0004c0011 | 0/0 | 672 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | ATGAG others(667): Show |
chr3 | 58628946 | 58671774 | ||
| a0005c0010 | 0/0 | 672 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | ATGAG others(667): Show |
chr3 | 58628946 | 58671774 | ||
| a0006c0009 | 0/0 | 672 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | ATGAG others(667): Show |
chr3 | 58628946 | 58671774 | ||
| a0007c0008 | 0/0 | 672 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | ATGAG others(667): Show |
chr3 | 58628946 | 58671774 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1245 | 326 | 66 | 58 | 152 | 9 | 39 | FAM3D_chr3_58628946_58671774 | FAM3D | AACAC others(1240): Show |
chr3 | 58628946 | 58671774 |
| a0001c0001t0002 | 0/0 | 1245 | 12 | 11 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | AACAC others(1240): Show |
chr3 | 58628946 | 58671774 |
| a0001c0001t0003 | 0/0 | 1245 | 6 | 0 | 0 | 6 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | AACAC others(1240): Show |
chr3 | 58628946 | 58671774 |
| a0001c0001t0004 | 0/0 | 1245 | 3 | 2 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | AACAC others(1240): Show |
chr3 | 58628946 | 58671774 |
| a0001c0001t0005 | 0/0 | 1245 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | AACAC others(1240): Show |
chr3 | 58628946 | 58671774 |
| a0001c0001t0007 | 0/0 | 1245 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | AACAC others(1240): Show |
chr3 | 58628946 | 58671774 |
| a0001c0003t0001 | 0/0 | 1245 | 5 | 1 | 1 | 0 | 0 | 3 | FAM3D_chr3_58628946_58671774 | FAM3D | AACAC others(1240): Show |
chr3 | 58628946 | 58671774 |
| a0001c0004t0001 | 0/0 | 1245 | 4 | 0 | 0 | 0 | 0 | 4 | FAM3D_chr3_58628946_58671774 | FAM3D | AACAC others(1240): Show |
chr3 | 58628946 | 58671774 |
| a0001c0005t0001 | 0/0 | 1245 | 3 | 0 | 0 | 3 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | AACAC others(1240): Show |
chr3 | 58628946 | 58671774 |
| a0001c0006t0001 | 0/0 | 1245 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | AACAC others(1240): Show |
chr3 | 58628946 | 58671774 |
| a0001c0006t0006 | 0/0 | 1245 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | AACAC others(1240): Show |
chr3 | 58628946 | 58671774 |
| a0002c0002t0001 | 0/0 | 1245 | 28 | 8 | 11 | 1 | 4 | 4 | FAM3D_chr3_58628946_58671774 | FAM3D | AACAC others(1240): Show |
chr3 | 58628946 | 58671774 |
| a0003c0007t0001 | 0/0 | 1245 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | AACAC others(1240): Show |
chr3 | 58628946 | 58671774 |
| a0004c0011t0001 | 0/0 | 1245 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | AACAC others(1240): Show |
chr3 | 58628946 | 58671774 |
| a0005c0010t0004 | 0/0 | 1245 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | AACAC others(1240): Show |
chr3 | 58628946 | 58671774 |
| a0006c0009t0001 | 0/0 | 1245 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | AACAC others(1240): Show |
chr3 | 58628946 | 58671774 |
| a0007c0008t0001 | 0/0 | 1245 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | AACAC others(1240): Show |
chr3 | 58628946 | 58671774 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 20 | 0 | 1 | 17 | 0 | 2 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0002 | 0/0 | 19 | 0 | 3 | 12 | 3 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0003 | 0/0 | 12 | 1 | 2 | 6 | 1 | 2 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0005 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0009 | 0/0 | 5 | 1 | 4 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 2 | 1 | 1 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0026 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0032 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0044 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0053 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0057 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0166 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0002g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0002g0045 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0003g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0004g0021 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0005g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0001t0007g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0003t0001g0047 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0003t0001g0048 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0003t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0004t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0004t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0004t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0005t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0005t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0005t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0006t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0001c0006t0006g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0002c0002t0001g0007 | 0/0 | 5 | 0 | 2 | 0 | 1 | 2 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0002c0002t0001g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0002c0002t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0002c0002t0001g0041 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0002c0002t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0002c0002t0001g0043 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0002c0002t0001g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0002c0002t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0002c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0003c0007t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0004c0011t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0005c0010t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0006c0009t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| a0007c0008t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | GBR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | FIN | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0094 | EUR | FIN | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0214 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0042 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0191 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0042 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01081 | hp1 | a0001 | c0003 | t0001 | g0047 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01099 | hp1 | a0004 | c0011 | t0001 | g0239 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0182 | AMR | CLM | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0021 | AMR | CLM | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0049 | AMR | CLM | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0184 | AMR | CLM | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0049 | AMR | CLM | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0041 | EUR | IBS | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0202 | EUR | IBS | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0007 | EUR | IBS | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0041 | EUR | IBS | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | ACB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01981 | hp1 | a0001 | c0001 | t0007 | g0151 | AMR | PEL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02027 | hp2 | a0003 | c0007 | t0001 | g0036 | EAS | KHV | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0045 | AFR | ACB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0215 | EAS | KHV | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | CDX | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CDX | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CDX | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0043 | AMR | PEL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0011 | AFR | ACB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0021 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0104 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0193 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02683 | hp1 | a0001 | c0004 | t0001 | g0038 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0185 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02698 | hp2 | a0001 | c0004 | t0001 | g0038 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0206 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0021 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0029 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02897 | hp1 | a0002 | c0002 | t0001 | g0029 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0011 | AFR | ESN | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03098 | hp2 | a0001 | c0006 | t0001 | g0110 | AFR | MSL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03139 | hp2 | a0005 | c0010 | t0004 | g0173 | AFR | ESN | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0192 | AFR | ESN | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0250 | AFR | ESN | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | MSL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0007 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | MSL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03490 | hp1 | a0001 | c0003 | t0001 | g0048 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03492 | hp1 | a0001 | c0003 | t0001 | g0048 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0011 | AFR | ESN | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | MSL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | STU | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03688 | hp2 | a0001 | c0003 | t0001 | g0047 | SAS | STU | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0007 | SAS | BEB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03831 | hp2 | a0001 | c0004 | t0001 | g0112 | SAS | BEB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | BEB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | BEB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | BEB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | STU | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | STU | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | BEB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | STU | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG04199 | hp2 | a0001 | c0004 | t0001 | g0082 | SAS | STU | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | STU | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | STU | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | STU | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | STU | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0176 | AFR | YRI | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | YRI | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | CHB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | CHB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | YRI | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | YRI | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18967 | hp1 | a0001 | c0005 | t0001 | g0133 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18968 | hp2 | a0003 | c0007 | t0001 | g0036 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19012 | hp1 | a0001 | c0005 | t0001 | g0141 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | LWK | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19030 | hp2 | a0001 | c0006 | t0006 | g0179 | AFR | LWK | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | LWK | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0011 | AFR | LWK | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19066 | hp2 | a0001 | c0005 | t0001 | g0216 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0058 | AFR | YRI | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | YRI | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ASW | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ASW | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0043 | EUR | TSI | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0123 | EUR | TSI | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA20805 | hp2 | a0007 | c0008 | t0001 | g0183 | EUR | TSI | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | GIH | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0251 | AFR | ACB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0059 | AFR | ACB | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG03471 | hp2 | a0006 | c0009 | t0001 | g0242 | AFR | MSL | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | USA | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | USA | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | USA | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | USA | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | LWK | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | LWK | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0166 | REF | REF | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0026 | REF | REF | FAM3D_chr3_58628946_58671774 | FAM3D | chr3 | 58628946 | 58671774 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:58637187 | C | T | 1 | a0005 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.412G>A | p.Gly138Arg | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 8/10 | 649/1245 | 412/675 | 138/224 | chr3 | 58637187 | |||
| chr3:58637189 | G | A | 1 | a0004 | 1 | HG01099.hp1 | missense_variant | MODERATE | c.410C>T | p.Pro137Leu | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 8/10 | 647/1245 | 410/675 | 137/224 | chr3 | 58637189 | |||
| chr3:58640148 | C | A | 3 | a0002 a0004 a0007 |
30 | HG00639.hp1 HG00733.hp2 HG01069.hp2 others(27): Show |
missense_variant | MODERATE | c.352G>T | p.Ala118Ser | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/10 | 589/1245 | 352/675 | 118/224 | chr3 | 58640148 | |||
| chr3:58645512 | C | T | 1 | a0006 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.260G>A | p.Arg87His | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/10 | 497/1245 | 260/675 | 87/224 | chr3 | 58645512 | |||
| chr3:58645594 | G | A | 1 | a0003 | 2 | HG02027.hp2 NA18968.hp2 |
missense_variant | MODERATE | c.178C>T | p.Pro60Ser | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/10 | 415/1245 | 178/675 | 60/224 | chr3 | 58645594 | |||
| chr3:58653691 | C | T | 1 | a0007 | 1 | NA20805.hp2 | missense_variant | MODERATE | c.104G>A | p.Arg35His | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/10 | 341/1245 | 104/675 | 35/224 | chr3 | 58653691 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:58636303 | G | A | 1 | a0001c0005 | 3 | NA18967.hp1 NA19012.hp1 NA19066.hp2 |
synonymous_variant | LOW | c.576C>T | p.Pro192Pro | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/10 | 813/1245 | 576/675 | 192/224 | chr3 | 58636303 | |||
| chr3:58637155 | G | A | 1 | a0001c0006 | 2 | HG03098.hp2 NA19030.hp2 |
synonymous_variant | LOW | c.444C>T | p.Asp148Asp | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 8/10 | 681/1245 | 444/675 | 148/224 | chr3 | 58637155 | |||
| chr3:58645541 | G | A | 1 | a0001c0004 | 4 | HG02683.hp1 HG02698.hp2 HG03831.hp2 others(1): Show |
synonymous_variant | LOW | c.231C>T | p.Val77Val | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/10 | 468/1245 | 231/675 | 77/224 | chr3 | 58645541 | |||
| chr3:58653738 | T | G | 1 | a0001c0003 | 5 | HG01081.hp1 HG03490.hp1 HG03492.hp1 others(2): Show |
synonymous_variant | LOW | c.57A>C | p.Thr19Thr | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/10 | 294/1245 | 57/675 | 19/224 | chr3 | 58653738 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:58634104 | G | A | 1 | a0001c0001t0007 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*175C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 10/10 | 175 | chr3 | 58634104 | ||||||
| chr3:58634151 | G | T | 2 | a0001c0001t0004 a0005c0010t0004 |
4 | HG01255.hp2 HG02572.hp1 HG02818.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*128C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 10/10 | 128 | chr3 | 58634151 | ||||||
| chr3:58634169 | C | A | 1 | a0001c0001t0003 | 6 | NA18612.hp1 NA18948.hp1 NA18973.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*110G>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 10/10 | 110 | chr3 | 58634169 | ||||||
| chr3:58634183 | C | G | 1 | a0001c0006t0006 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*96G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 10/10 | 96 | chr3 | 58634183 | ||||||
| chr3:58634184 | C | T | 1 | a0001c0006t0006 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*95G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 10/10 | 95 | chr3 | 58634184 | ||||||
| chr3:58634187 | C | T | 1 | a0001c0006t0006 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*92G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 10/10 | 92 | chr3 | 58634187 | ||||||
| chr3:58634265 | G | C | 1 | a0001c0001t0002 | 12 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*14C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 10/10 | 14 | chr3 | 58634265 | ||||||
| chr3:58666728 | C | T | 1 | a0001c0001t0005 | 2 | HG02559.hp2 NA19240.hp1 |
5_prime_UTR_variant | MODIFIER | c.-191G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/10 | 11165 | chr3 | 58666728 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:58634378 | G | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0199 |
4 | HG02257.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.586-10C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58634378 | |||||||
| chr3:58634378 | G | C | 2 | a0001c0001t0001g0148 a0003c0007t0001g0036 |
3 | HG02027.hp2 HG02135.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.586-10C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58634378 | |||||||
| chr3:58634624 | T | C | 2 | a0001c0001t0001g0046 a0001c0001t0001g0245 |
3 | HG02922.hp2 HG03516.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.586-256A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58634624 | |||||||
| chr3:58634661 | T | A | 2 | a0001c0003t0001g0047 a0001c0003t0001g0048 |
4 | HG01081.hp1 HG03490.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.586-293A>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58634661 | |||||||
| chr3:58634940 | G | T | 4 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(1): Show |
4 | HG00280.hp2 HG00735.hp2 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.586-572C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58634940 | |||||||
| chr3:58634985 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.586-617C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58634985 | |||||||
| chr3:58635049 | C | G | 2 | a0001c0003t0001g0047 a0001c0003t0001g0048 |
4 | HG01081.hp1 HG03490.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.586-681G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58635049 | |||||||
| chr3:58635114 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.586-746C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58635114 | |||||||
| chr3:58635121 | G | T | 1 | a0001c0001t0001g0145 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.586-753C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58635121 | |||||||
| chr3:58635162 | G | A | 2 | a0001c0001t0001g0203 a0006c0009t0001g0242 |
2 | HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.586-794C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58635162 | |||||||
| chr3:58635175 | T | A | 18 | a0001c0001t0001g0044 a0001c0001t0001g0052 a0001c0001t0001g0065 others(15): Show |
20 | HG00642.hp2 HG01099.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.586-807A>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58635175 | |||||||
| chr3:58635209 | A | G | 3 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 |
3 | HG02622.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.586-841T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58635209 | |||||||
| chr3:58635251 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.586-883A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58635251 | |||||||
| chr3:58635390 | C | T | 1 | a0001c0001t0001g0229 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.585+904G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58635390 | |||||||
| chr3:58635509 | G | C | 1 | a0001c0001t0001g0181 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.585+785C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58635509 | |||||||
| chr3:58635521 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.585+773G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58635521 | |||||||
| chr3:58635532 | G | A | 4 | a0001c0001t0002g0012 a0001c0001t0002g0086 a0001c0001t0002g0192 others(1): Show |
7 | HG02109.hp2 HG02280.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.585+762C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58635532 | |||||||
| chr3:58635628 | C | T | 18 | a0001c0001t0001g0044 a0001c0001t0001g0052 a0001c0001t0001g0065 others(15): Show |
20 | HG00642.hp2 HG01099.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.585+666G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58635628 | |||||||
| chr3:58635633 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.585+661G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58635633 | |||||||
| chr3:58635806 | C | T | 3 | a0001c0001t0001g0244 a0001c0001t0004g0021 a0005c0010t0004g0173 |
5 | HG01255.hp2 HG02258.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.585+488G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58635806 | |||||||
| chr3:58635997 | C | T | 8 | a0001c0001t0001g0023 a0001c0001t0002g0045 a0001c0001t0002g0104 others(5): Show |
13 | HG01081.hp1 HG01109.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.585+297G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58635997 | |||||||
| chr3:58636043 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.585+251G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58636043 | |||||||
| chr3:58636171 | G | C | 1 | a0001c0001t0005g0058 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.585+123C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58636171 | |||||||
| chr3:58636208 | C | T | 242 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(239): Show |
384 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.585+86G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 9/9 | chr3 | 58636208 | |||||||
| chr3:58636501 | G | T | 1 | a0001c0001t0001g0119 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.459-81C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 8/9 | chr3 | 58636501 | |||||||
| chr3:58636758 | T | C | 1 | a0001c0001t0001g0051 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.459-338A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 8/9 | chr3 | 58636758 | |||||||
| chr3:58636762 | A | T | 102 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(99): Show |
157 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.459-342T>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 8/9 | chr3 | 58636762 | |||||||
| chr3:58636769 | GT | G | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(235): Show |
378 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(375): Show |
intron_variant | MODIFIER | c.459-350delA | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 8/9 | chr3 | 58636769 | |||||||
| chr3:58636778 | T | C | 5 | a0001c0001t0001g0023 a0001c0003t0001g0047 a0001c0003t0001g0048 others(2): Show |
9 | HG01081.hp1 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.459-358A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 8/9 | chr3 | 58636778 | |||||||
| chr3:58636818 | C | T | 2 | a0001c0001t0001g0108 a0001c0003t0001g0176 |
2 | NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.458+323G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 8/9 | chr3 | 58636818 | |||||||
| chr3:58636893 | G | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(82): Show |
145 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.458+248C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 8/9 | chr3 | 58636893 | |||||||
| chr3:58637004 | G | T | 1 | a0001c0001t0001g0221 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.458+137C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 8/9 | chr3 | 58637004 | |||||||
| chr3:58637058 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.458+83T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 8/9 | chr3 | 58637058 | |||||||
| chr3:58637109 | G | A | 1 | a0001c0001t0001g0157 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.458+32C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 8/9 | chr3 | 58637109 | |||||||
| chr3:58637458 | T | C | 121 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(118): Show |
191 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.374-233A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58637458 | |||||||
| chr3:58637513 | C | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(115): Show |
191 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.374-288G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58637513 | |||||||
| chr3:58637531 | C | T | 96 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(93): Show |
161 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.374-306G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58637531 | |||||||
| chr3:58637616 | C | T | 1 | a0001c0006t0001g0110 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.374-391G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58637616 | |||||||
| chr3:58637617 | G | A | 95 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(92): Show |
160 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.374-392C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58637617 | |||||||
| chr3:58637746 | G | C | 3 | a0001c0001t0001g0035 a0001c0001t0001g0146 a0001c0001t0001g0202 |
4 | HG00639.hp2 HG00741.hp2 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.374-521C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58637746 | |||||||
| chr3:58637789 | C | T | 1 | a0001c0001t0002g0086 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.374-564G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58637789 | |||||||
| chr3:58637878 | G | GATTATT | 6 | a0001c0001t0001g0044 a0001c0001t0001g0180 a0001c0001t0001g0190 others(3): Show |
8 | HG01109.hp2 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.374-659_374-654dup others(6): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58637878 | |||||||
| chr3:58637878 | G | GATTATTA others(2): Show |
28 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0015 others(25): Show |
47 | HG00609.hp1 HG00673.hp1 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.374-662_374-654dup others(9): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58637878 | |||||||
| chr3:58637878 | G | GATTATTA others(5): Show |
182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.374-665_374-654dup others(12): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58637878 | |||||||
| chr3:58637878 | G | GATTATTA others(8): Show |
22 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0053 others(19): Show |
29 | HG00438.hp2 HG00621.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.374-668_374-654dup others(15): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58637878 | |||||||
| chr3:58637878 | G | GATTATTA others(11): Show |
4 | a0001c0001t0001g0111 a0001c0001t0001g0232 a0001c0001t0001g0241 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.374-671_374-654dup others(18): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58637878 | |||||||
| chr3:58637878 | G | GATTATTA others(14): Show |
5 | a0001c0001t0001g0171 a0001c0001t0005g0058 a0001c0004t0001g0038 others(2): Show |
6 | HG02683.hp1 HG02698.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.374-674_374-654dup others(21): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58637878 | |||||||
| chr3:58637878 | G | GATTATTA others(20): Show |
1 | a0005c0010t0004g0173 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.374-654_374-653ins others(27): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58637878 | |||||||
| chr3:58637909 | A | G | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
392 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(389): Show |
intron_variant | MODIFIER | c.374-684T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58637909 | |||||||
| chr3:58637915 | T | G | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
392 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(389): Show |
intron_variant | MODIFIER | c.374-690A>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58637915 | |||||||
| chr3:58638076 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.374-851C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58638076 | |||||||
| chr3:58638176 | C | G | 104 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(101): Show |
176 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.374-951G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58638176 | |||||||
| chr3:58638213 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.374-988A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58638213 | |||||||
| chr3:58638260 | T | C | 3 | a0001c0001t0001g0177 a0001c0001t0001g0199 a0001c0001t0001g0243 |
3 | HG02257.hp1 HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.374-1035A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58638260 | |||||||
| chr3:58638484 | G | A | 14 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0031 others(11): Show |
22 | HG00609.hp1 HG00673.hp1 HG02129.hp2 others(19): Show |
intron_variant | MODIFIER | c.374-1259C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58638484 | |||||||
| chr3:58638521 | T | C | 1 | a0001c0001t0001g0126 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.374-1296A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58638521 | |||||||
| chr3:58638781 | C | T | 2 | a0001c0004t0001g0038 a0001c0004t0001g0112 |
3 | HG02683.hp1 HG02698.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.373+1346G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58638781 | |||||||
| chr3:58638786 | C | G | 1 | a0001c0001t0001g0194 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.373+1341G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58638786 | |||||||
| chr3:58638807 | C | T | 2 | a0001c0004t0001g0038 a0001c0004t0001g0112 |
3 | HG02683.hp1 HG02698.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.373+1320G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58638807 | |||||||
| chr3:58638913 | C | T | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(246): Show |
393 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(390): Show |
intron_variant | MODIFIER | c.373+1214G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58638913 | |||||||
| chr3:58638980 | C | A | 1 | a0001c0001t0001g0055 | 2 | HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.373+1147G>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58638980 | |||||||
| chr3:58639023 | G | A | 1 | a0001c0001t0001g0009 | 5 | HG01256.hp1 HG01258.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.373+1104C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58639023 | |||||||
| chr3:58639043 | A | G | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(108): Show |
164 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.373+1084T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58639043 | |||||||
| chr3:58639344 | C | G | 1 | a0001c0001t0001g0220 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.373+783G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58639344 | |||||||
| chr3:58639347 | T | C | 1 | a0001c0001t0001g0219 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.373+780A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58639347 | |||||||
| chr3:58639447 | G | C | 7 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0083 others(4): Show |
7 | HG00642.hp2 HG01099.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.373+680C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58639447 | |||||||
| chr3:58639479 | C | A | 1 | a0001c0001t0001g0142 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.373+648G>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58639479 | |||||||
| chr3:58639504 | C | T | 21 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0031 others(18): Show |
31 | HG00609.hp1 HG00673.hp1 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.373+623G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58639504 | |||||||
| chr3:58639578 | C | T | 1 | a0001c0001t0001g0210 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.373+549G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58639578 | |||||||
| chr3:58639598 | G | T | 19 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0031 others(16): Show |
27 | HG00609.hp1 HG00673.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.373+529C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58639598 | |||||||
| chr3:58639607 | A | G | 1 | a0006c0009t0001g0242 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.373+520T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58639607 | |||||||
| chr3:58639740 | A | G | 1 | a0001c0006t0001g0110 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.373+387T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58639740 | |||||||
| chr3:58639832 | T | C | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(133): Show |
205 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.373+295A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58639832 | |||||||
| chr3:58639889 | G | T | 1 | a0001c0001t0001g0208 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.373+238C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58639889 | |||||||
| chr3:58639904 | C | T | 15 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0031 others(12): Show |
23 | HG00609.hp1 HG00673.hp1 HG02129.hp2 others(20): Show |
intron_variant | MODIFIER | c.373+223G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58639904 | |||||||
| chr3:58639973 | A | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0175 |
6 | NA18944.hp2 NA18962.hp1 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.373+154T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58639973 | |||||||
| chr3:58640086 | G | A | 2 | a0001c0003t0001g0047 a0001c0003t0001g0048 |
4 | HG01081.hp1 HG03490.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.373+41C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 7/9 | chr3 | 58640086 | |||||||
| chr3:58640248 | C | G | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(109): Show |
168 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.323-71G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58640248 | |||||||
| chr3:58640348 | G | T | 42 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0033 others(39): Show |
65 | HG00408.hp2 HG00733.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.323-171C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58640348 | |||||||
| chr3:58640421 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.323-244C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58640421 | |||||||
| chr3:58640515 | T | C | 103 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(100): Show |
156 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.323-338A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58640515 | |||||||
| chr3:58640615 | C | T | 4 | a0001c0003t0001g0047 a0001c0003t0001g0048 a0001c0003t0001g0176 others(1): Show |
6 | HG01081.hp1 HG03471.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.323-438G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58640615 | |||||||
| chr3:58640896 | G | T | 1 | a0001c0001t0001g0090 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.323-719C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58640896 | |||||||
| chr3:58640986 | G | T | 1 | a0001c0001t0003g0072 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.323-809C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58640986 | |||||||
| chr3:58640992 | C | G | 15 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0031 others(12): Show |
23 | HG00609.hp1 HG00673.hp1 HG02129.hp2 others(20): Show |
intron_variant | MODIFIER | c.323-815G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58640992 | |||||||
| chr3:58640994 | T | C | 1 | a0001c0001t0001g0249 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.323-817A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58640994 | |||||||
| chr3:58641055 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.323-878G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58641055 | |||||||
| chr3:58641091 | C | T | 3 | a0001c0001t0001g0177 a0001c0001t0001g0199 a0001c0001t0001g0243 |
3 | HG02257.hp1 HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.323-914G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58641091 | |||||||
| chr3:58641167 | G | A | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
344 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(341): Show |
intron_variant | MODIFIER | c.323-990C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58641167 | |||||||
| chr3:58641321 | C | T | 6 | a0001c0001t0001g0177 a0001c0001t0001g0199 a0001c0001t0001g0243 others(3): Show |
7 | HG02257.hp1 HG02683.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.323-1144G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58641321 | |||||||
| chr3:58641383 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.323-1206C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58641383 | |||||||
| chr3:58641536 | G | T | 1 | a0001c0001t0001g0200 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.323-1359C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58641536 | |||||||
| chr3:58641544 | G | A | 2 | a0001c0001t0001g0081 a0001c0001t0001g0107 |
2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.323-1367C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58641544 | |||||||
| chr3:58641729 | A | G | 3 | a0001c0004t0001g0038 a0001c0004t0001g0082 a0001c0004t0001g0112 |
4 | HG02683.hp1 HG02698.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.323-1552T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58641729 | |||||||
| chr3:58641753 | A | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0189 |
2 | HG01175.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.323-1576T>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58641753 | |||||||
| chr3:58641879 | T | G | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(109): Show |
168 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.323-1702A>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58641879 | |||||||
| chr3:58641880 | T | G | 1 | a0001c0001t0005g0059 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.323-1703A>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58641880 | |||||||
| chr3:58642185 | A | T | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(108): Show |
165 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.322+1477T>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58642185 | |||||||
| chr3:58642210 | C | A | 27 | a0001c0001t0001g0023 a0001c0001t0001g0044 a0001c0001t0001g0180 others(24): Show |
44 | HG00639.hp1 HG00733.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.322+1452G>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58642210 | |||||||
| chr3:58642276 | C | T | 1 | a0001c0001t0001g0028 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.322+1386G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58642276 | |||||||
| chr3:58642287 | C | T | 1 | a0001c0001t0001g0229 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.322+1375G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58642287 | |||||||
| chr3:58642310 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.322+1352A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58642310 | |||||||
| chr3:58642339 | T | C | 23 | a0001c0001t0001g0023 a0001c0001t0001g0044 a0001c0001t0001g0180 others(20): Show |
38 | HG00639.hp1 HG00733.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.322+1323A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58642339 | |||||||
| chr3:58642375 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.322+1287C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58642375 | |||||||
| chr3:58642484 | C | A | 6 | a0001c0001t0001g0177 a0001c0001t0001g0199 a0001c0001t0001g0243 others(3): Show |
7 | HG02257.hp1 HG02683.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.322+1178G>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58642484 | |||||||
| chr3:58642627 | G | A | 113 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(110): Show |
167 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.322+1035C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58642627 | |||||||
| chr3:58642642 | G | A | 3 | a0001c0001t0001g0057 a0001c0001t0001g0247 a0001c0001t0001g0248 |
4 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.322+1020C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58642642 | |||||||
| chr3:58642648 | C | T | 1 | a0001c0001t0001g0050 | 2 | NA18997.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.322+1014G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58642648 | |||||||
| chr3:58642743 | C | A | 1 | a0001c0001t0005g0059 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.322+919G>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58642743 | |||||||
| chr3:58642743 | C | G | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(109): Show |
166 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.322+919G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58642743 | |||||||
| chr3:58642778 | T | G | 113 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(110): Show |
167 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.322+884A>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58642778 | |||||||
| chr3:58642812 | C | T | 1 | a0001c0001t0005g0058 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.322+850G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58642812 | |||||||
| chr3:58642927 | C | T | 109 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(106): Show |
163 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.322+735G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58642927 | |||||||
| chr3:58642952 | T | C | 1 | a0001c0006t0001g0110 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.322+710A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58642952 | |||||||
| chr3:58642972 | T | C | 110 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(107): Show |
164 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.322+690A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58642972 | |||||||
| chr3:58643012 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.322+650G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58643012 | |||||||
| chr3:58643017 | A | T | 1 | a0001c0001t0001g0028 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.322+645T>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58643017 | |||||||
| chr3:58643027 | G | T | 108 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(105): Show |
161 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.322+635C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58643027 | |||||||
| chr3:58643050 | T | G | 159 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(156): Show |
238 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.322+612A>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58643050 | |||||||
| chr3:58643178 | C | T | 5 | a0001c0001t0001g0177 a0001c0001t0001g0199 a0001c0001t0001g0243 others(2): Show |
6 | HG02257.hp1 HG02683.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.322+484G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58643178 | |||||||
| chr3:58643182 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.322+480G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58643182 | |||||||
| chr3:58643188 | C | T | 2 | a0001c0001t0001g0171 a0005c0010t0004g0173 |
2 | HG03139.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.322+474G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58643188 | |||||||
| chr3:58643192 | C | T | 19 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0031 others(16): Show |
28 | HG00609.hp1 HG00673.hp1 HG02129.hp2 others(25): Show |
intron_variant | MODIFIER | c.322+470G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58643192 | |||||||
| chr3:58643203 | A | T | 1 | a0001c0003t0001g0176 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.322+459T>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58643203 | |||||||
| chr3:58643212 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.322+450G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58643212 | |||||||
| chr3:58643244 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.322+418A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58643244 | |||||||
| chr3:58643254 | C | T | 2 | a0001c0001t0001g0135 a0001c0001t0001g0147 |
2 | HG03669.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.322+408G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58643254 | |||||||
| chr3:58643392 | G | T | 2 | a0001c0001t0002g0109 a0001c0006t0001g0110 |
2 | HG01891.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.322+270C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58643392 | |||||||
| chr3:58643531 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.322+131G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58643531 | |||||||
| chr3:58643608 | C | T | 2 | a0001c0001t0001g0171 a0005c0010t0004g0173 |
2 | HG03139.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.322+54G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 6/9 | chr3 | 58643608 | |||||||
| chr3:58643960 | G | C | 14 | a0002c0002t0001g0007 a0002c0002t0001g0041 a0002c0002t0001g0042 others(11): Show |
22 | HG00639.hp1 HG00733.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.264-240C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/9 | chr3 | 58643960 | |||||||
| chr3:58644007 | C | T | 1 | a0001c0001t0001g0019 | 3 | HG00423.hp1 HG00609.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.264-287G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/9 | chr3 | 58644007 | |||||||
| chr3:58644113 | A | T | 1 | a0001c0005t0001g0133 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.264-393T>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/9 | chr3 | 58644113 | |||||||
| chr3:58644179 | G | C | 2 | a0001c0001t0001g0005 a0001c0001t0001g0128 |
4 | HG01074.hp2 HG01358.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.264-459C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/9 | chr3 | 58644179 | |||||||
| chr3:58644332 | C | T | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(82): Show |
137 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.264-612G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/9 | chr3 | 58644332 | |||||||
| chr3:58644339 | G | A | 1 | a0001c0003t0001g0176 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.264-619C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/9 | chr3 | 58644339 | |||||||
| chr3:58644340 | C | G | 1 | a0001c0003t0001g0176 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.264-620G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/9 | chr3 | 58644340 | |||||||
| chr3:58644498 | T | C | 8 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0083 others(5): Show |
8 | HG00642.hp2 HG01099.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.264-778A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/9 | chr3 | 58644498 | |||||||
| chr3:58644524 | A | C | 1 | a0001c0001t0001g0081 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.264-804T>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/9 | chr3 | 58644524 | |||||||
| chr3:58644576 | C | A | 3 | a0001c0001t0001g0177 a0001c0001t0001g0199 a0001c0001t0001g0243 |
3 | HG02257.hp1 HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.264-856G>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/9 | chr3 | 58644576 | |||||||
| chr3:58644594 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.264-874G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/9 | chr3 | 58644594 | |||||||
| chr3:58644632 | A | G | 1 | a0001c0001t0001g0205 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.263+877T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/9 | chr3 | 58644632 | |||||||
| chr3:58644774 | A | G | 110 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(107): Show |
165 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.263+735T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/9 | chr3 | 58644774 | |||||||
| chr3:58644924 | C | T | 1 | a0001c0001t0001g0229 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.263+585G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/9 | chr3 | 58644924 | |||||||
| chr3:58645264 | A | G | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(126): Show |
195 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.263+245T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/9 | chr3 | 58645264 | |||||||
| chr3:58645278 | T | G | 3 | a0001c0001t0001g0177 a0001c0001t0001g0199 a0001c0001t0001g0243 |
3 | HG02257.hp1 HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.263+231A>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/9 | chr3 | 58645278 | |||||||
| chr3:58645283 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.263+226C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/9 | chr3 | 58645283 | |||||||
| chr3:58645289 | C | T | 3 | a0001c0004t0001g0038 a0001c0004t0001g0082 a0001c0004t0001g0112 |
4 | HG02683.hp1 HG02698.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.263+220G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/9 | chr3 | 58645289 | |||||||
| chr3:58645457 | G | GAAATA | 116 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(113): Show |
175 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.263+47_263+51dupTA others(3): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/9 | chr3 | 58645457 | |||||||
| chr3:58645457 | G | GAAATAAA others(3): Show |
3 | a0001c0001t0001g0091 a0001c0001t0001g0094 a0001c0001t0001g0188 |
3 | HG00280.hp2 HG00735.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.263+42_263+51dupTA others(8): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 5/9 | chr3 | 58645457 | |||||||
| chr3:58645692 | GAGGGCCA others(5): Show |
G | 2 | a0001c0003t0001g0047 a0001c0003t0001g0048 |
4 | HG01081.hp1 HG03490.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.146-78_146-67delAG others(10): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58645692 | |||||||
| chr3:58645933 | C | T | 2 | a0001c0001t0001g0181 a0001c0006t0006g0179 |
2 | HG01243.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.146-307G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58645933 | |||||||
| chr3:58646179 | A | T | 104 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(101): Show |
155 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.146-553T>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58646179 | |||||||
| chr3:58646414 | C | T | 1 | a0001c0001t0001g0034 | 2 | HG02738.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.146-788G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58646414 | |||||||
| chr3:58646460 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.146-834G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58646460 | |||||||
| chr3:58646539 | T | C | 1 | a0001c0001t0001g0244 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.146-913A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58646539 | |||||||
| chr3:58646557 | C | T | 3 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 |
3 | HG02622.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.146-931G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58646557 | |||||||
| chr3:58646635 | C | T | 3 | a0001c0004t0001g0038 a0001c0004t0001g0082 a0001c0004t0001g0112 |
4 | HG02683.hp1 HG02698.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.146-1009G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58646635 | |||||||
| chr3:58646740 | G | C | 1 | a0003c0007t0001g0036 | 2 | HG02027.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.146-1114C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58646740 | |||||||
| chr3:58646748 | C | G | 1 | a0001c0001t0001g0178 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.146-1122G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58646748 | |||||||
| chr3:58646772 | C | T | 1 | a0001c0001t0005g0059 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.146-1146G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58646772 | |||||||
| chr3:58646788 | G | A | 6 | a0001c0001t0001g0177 a0001c0001t0001g0199 a0001c0001t0001g0243 others(3): Show |
7 | HG02257.hp1 HG02683.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.146-1162C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58646788 | |||||||
| chr3:58646828 | T | C | 6 | a0001c0001t0001g0177 a0001c0001t0001g0199 a0001c0001t0001g0243 others(3): Show |
7 | HG02257.hp1 HG02683.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.146-1202A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58646828 | |||||||
| chr3:58646846 | G | C | 6 | a0001c0001t0001g0177 a0001c0001t0001g0199 a0001c0001t0001g0243 others(3): Show |
7 | HG02257.hp1 HG02683.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.146-1220C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58646846 | |||||||
| chr3:58646924 | C | T | 23 | a0001c0001t0001g0023 a0001c0001t0001g0044 a0001c0001t0001g0180 others(20): Show |
38 | HG00639.hp1 HG00733.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.146-1298G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58646924 | |||||||
| chr3:58646950 | C | A | 1 | a0001c0001t0001g0063 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.146-1324G>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58646950 | |||||||
| chr3:58647009 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.146-1383G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58647009 | |||||||
| chr3:58647014 | T | C | 123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(120): Show |
186 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.146-1388A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58647014 | |||||||
| chr3:58647152 | C | G | 3 | a0001c0004t0001g0038 a0001c0004t0001g0082 a0001c0004t0001g0112 |
4 | HG02683.hp1 HG02698.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.146-1526G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58647152 | |||||||
| chr3:58647244 | C | T | 6 | a0001c0001t0001g0177 a0001c0001t0001g0199 a0001c0001t0001g0243 others(3): Show |
7 | HG02257.hp1 HG02683.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.146-1618G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58647244 | |||||||
| chr3:58647534 | T | A | 157 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(154): Show |
234 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.145+1781A>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58647534 | |||||||
| chr3:58647547 | C | G | 6 | a0001c0001t0001g0108 a0001c0001t0005g0058 a0001c0003t0001g0047 others(3): Show |
8 | HG01081.hp1 HG03471.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.145+1768G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58647547 | |||||||
| chr3:58647777 | G | A | 1 | a0001c0001t0005g0058 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.145+1538C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58647777 | |||||||
| chr3:58647820 | A | G | 1 | a0001c0001t0001g0213 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.145+1495T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58647820 | |||||||
| chr3:58647850 | G | C | 1 | a0002c0002t0001g0042 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.145+1465C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58647850 | |||||||
| chr3:58647949 | G | A | 3 | a0001c0004t0001g0038 a0001c0004t0001g0082 a0001c0004t0001g0112 |
4 | HG02683.hp1 HG02698.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.145+1366C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58647949 | |||||||
| chr3:58647965 | T | G | 1 | a0001c0001t0001g0248 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.145+1350A>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58647965 | |||||||
| chr3:58648222 | G | A | 23 | a0001c0001t0001g0023 a0001c0001t0001g0044 a0001c0001t0001g0180 others(20): Show |
38 | HG00639.hp1 HG00733.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.145+1093C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58648222 | |||||||
| chr3:58648236 | A | G | 154 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(151): Show |
228 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.145+1079T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58648236 | |||||||
| chr3:58648516 | C | T | 12 | a0001c0001t0001g0016 a0001c0001t0001g0031 a0001c0001t0001g0068 others(9): Show |
17 | HG00438.hp1 HG00609.hp1 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.145+799G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58648516 | |||||||
| chr3:58648745 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.145+570C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58648745 | |||||||
| chr3:58648777 | G | T | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(133): Show |
204 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.145+538C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58648777 | |||||||
| chr3:58648818 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.145+497T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58648818 | |||||||
| chr3:58648824 | G | T | 121 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(118): Show |
184 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.145+491C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58648824 | |||||||
| chr3:58648884 | T | G | 1 | a0001c0001t0001g0147 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.145+431A>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58648884 | |||||||
| chr3:58648923 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.145+392T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58648923 | |||||||
| chr3:58649104 | AG | A | 18 | a0001c0001t0001g0016 a0001c0001t0001g0031 a0001c0001t0001g0068 others(15): Show |
24 | HG00438.hp1 HG00609.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.145+210delC | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58649104 | |||||||
| chr3:58649228 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.145+87C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58649228 | |||||||
| chr3:58649258 | G | C | 3 | a0001c0004t0001g0038 a0001c0004t0001g0082 a0001c0004t0001g0112 |
4 | HG02683.hp1 HG02698.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.145+57C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58649258 | |||||||
| chr3:58649284 | G | A | 1 | a0001c0001t0001g0090 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.145+31C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 4/9 | chr3 | 58649284 | |||||||
| chr3:58649350 | A | G | 2 | a0001c0001t0001g0181 a0001c0006t0006g0179 |
2 | HG01243.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.122-12T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58649350 | |||||||
| chr3:58649374 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.122-36T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58649374 | |||||||
| chr3:58649470 | G | A | 149 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(146): Show |
223 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.122-132C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58649470 | |||||||
| chr3:58649548 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.122-210G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58649548 | |||||||
| chr3:58649558 | T | C | 1 | a0001c0001t0001g0225 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.122-220A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58649558 | |||||||
| chr3:58649560 | T | C | 1 | a0001c0001t0001g0225 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.122-222A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58649560 | |||||||
| chr3:58649567 | GCA | G | 6 | a0001c0001t0001g0033 a0001c0001t0001g0075 a0001c0001t0001g0117 others(3): Show |
7 | HG00621.hp1 HG00733.hp1 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.122-231_122-230del others(2): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58649567 | |||||||
| chr3:58649605 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.122-267A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58649605 | |||||||
| chr3:58649647 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.122-309G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58649647 | |||||||
| chr3:58649665 | C | CAT | 3 | a0001c0004t0001g0038 a0001c0004t0001g0082 a0001c0004t0001g0112 |
4 | HG02683.hp1 HG02698.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-328_122-327ins others(2): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58649665 | |||||||
| chr3:58649666 | G | A | 15 | a0001c0001t0001g0016 a0001c0001t0001g0031 a0001c0001t0001g0068 others(12): Show |
20 | HG00438.hp1 HG00609.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.122-328C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58649666 | |||||||
| chr3:58649670 | A | G | 15 | a0001c0001t0001g0016 a0001c0001t0001g0031 a0001c0001t0001g0068 others(12): Show |
20 | HG00438.hp1 HG00609.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.122-332T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58649670 | |||||||
| chr3:58649671 | C | T | 15 | a0001c0001t0001g0016 a0001c0001t0001g0031 a0001c0001t0001g0068 others(12): Show |
20 | HG00438.hp1 HG00609.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.122-333G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58649671 | |||||||
| chr3:58649677 | C | T | 3 | a0001c0001t0001g0020 a0001c0001t0001g0196 a0001c0001t0001g0198 |
5 | HG02615.hp2 HG02965.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.122-339G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58649677 | |||||||
| chr3:58649773 | A | AC | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(133): Show |
204 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.122-436dupG | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58649773 | |||||||
| chr3:58649867 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.122-529G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58649867 | |||||||
| chr3:58650082 | T | G | 1 | a0001c0001t0001g0149 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.122-744A>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58650082 | |||||||
| chr3:58650224 | A | G | 3 | a0001c0004t0001g0038 a0001c0004t0001g0082 a0001c0004t0001g0112 |
4 | HG02683.hp1 HG02698.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-886T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58650224 | |||||||
| chr3:58650400 | A | G | 1 | a0006c0009t0001g0242 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.122-1062T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58650400 | |||||||
| chr3:58650417 | C | G | 17 | a0001c0001t0001g0016 a0001c0001t0001g0031 a0001c0001t0001g0068 others(14): Show |
23 | HG00438.hp1 HG00609.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.122-1079G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58650417 | |||||||
| chr3:58650452 | G | T | 17 | a0001c0001t0001g0016 a0001c0001t0001g0031 a0001c0001t0001g0068 others(14): Show |
23 | HG00438.hp1 HG00609.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.122-1114C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58650452 | |||||||
| chr3:58650467 | C | T | 2 | a0001c0001t0001g0199 a0001c0001t0001g0243 |
2 | HG02257.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.122-1129G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58650467 | |||||||
| chr3:58650473 | A | T | 1 | a0001c0001t0001g0130 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.122-1135T>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58650473 | |||||||
| chr3:58650474 | G | T | 3 | a0001c0004t0001g0038 a0001c0004t0001g0082 a0001c0004t0001g0112 |
4 | HG02683.hp1 HG02698.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-1136C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58650474 | |||||||
| chr3:58650502 | A | G | 1 | a0001c0001t0001g0218 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.122-1164T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58650502 | |||||||
| chr3:58650749 | G | A | 1 | a0002c0002t0001g0042 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.122-1411C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58650749 | |||||||
| chr3:58650836 | A | G | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(136): Show |
208 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.122-1498T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58650836 | |||||||
| chr3:58650843 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.122-1505T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58650843 | |||||||
| chr3:58651039 | T | G | 1 | a0001c0001t0001g0249 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.122-1701A>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58651039 | |||||||
| chr3:58651051 | T | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0150 a0001c0001t0007g0151 |
6 | HG01192.hp1 HG01928.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.122-1713A>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58651051 | |||||||
| chr3:58651126 | T | C | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(147): Show |
225 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.122-1788A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58651126 | |||||||
| chr3:58651174 | T | C | 1 | a0002c0002t0001g0215 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.122-1836A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58651174 | |||||||
| chr3:58651177 | T | G | 3 | a0002c0002t0001g0049 a0002c0002t0001g0214 a0002c0002t0001g0215 |
4 | HG00733.hp2 HG01258.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-1839A>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58651177 | |||||||
| chr3:58651273 | T | C | 2 | a0001c0001t0001g0180 a0001c0001t0001g0190 |
2 | HG02647.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.122-1935A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58651273 | |||||||
| chr3:58651300 | G | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0201 a0001c0001t0004g0021 |
9 | HG01255.hp2 HG01884.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.122-1962C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58651300 | |||||||
| chr3:58651333 | A | C | 1 | a0001c0001t0001g0129 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.122-1995T>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58651333 | |||||||
| chr3:58651436 | T | A | 1 | a0001c0001t0001g0152 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.122-2098A>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58651436 | |||||||
| chr3:58651530 | G | C | 3 | a0001c0004t0001g0038 a0001c0004t0001g0082 a0001c0004t0001g0112 |
4 | HG02683.hp1 HG02698.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.121+2144C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58651530 | |||||||
| chr3:58651633 | C | G | 1 | a0001c0001t0001g0199 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.121+2041G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58651633 | |||||||
| chr3:58651641 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.121+2033T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58651641 | |||||||
| chr3:58651704 | C | T | 5 | a0001c0001t0001g0077 a0001c0001t0001g0127 a0001c0001t0001g0159 others(2): Show |
5 | NA18961.hp2 NA18964.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.121+1970G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58651704 | |||||||
| chr3:58651790 | A | C | 35 | a0001c0001t0001g0016 a0001c0001t0001g0031 a0001c0001t0001g0068 others(32): Show |
53 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.121+1884T>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58651790 | |||||||
| chr3:58651818 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.121+1856C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58651818 | |||||||
| chr3:58651842 | C | T | 1 | a0001c0001t0005g0058 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.121+1832G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58651842 | |||||||
| chr3:58651870 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.121+1804T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58651870 | |||||||
| chr3:58651884 | C | G | 1 | a0001c0001t0001g0055 | 2 | HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.121+1790G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58651884 | |||||||
| chr3:58652374 | C | CCATT | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
341 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(338): Show |
intron_variant | MODIFIER | c.121+1296_121+1299d others(6): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652374 | |||||||
| chr3:58652374 | C | CCATTCAT others(5): Show |
1 | a0005c0010t0004g0173 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.121+1288_121+1299d others(14): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652374 | |||||||
| chr3:58652400 | A | G | 1 | a0001c0001t0001g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.121+1274T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652400 | |||||||
| chr3:58652416 | ACCATCTA others(72): Show |
A | 2 | a0001c0001t0001g0171 a0005c0010t0004g0173 |
2 | HG03139.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.121+1179_121+1257d others(81): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652416 | |||||||
| chr3:58652499 | T | A | 2 | a0001c0001t0001g0171 a0005c0010t0004g0173 |
2 | HG03139.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.121+1175A>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652499 | |||||||
| chr3:58652515 | C | G | 4 | a0001c0001t0001g0171 a0002c0002t0001g0250 a0002c0002t0001g0251 others(1): Show |
4 | HG02109.hp1 HG03139.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.121+1159G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652515 | |||||||
| chr3:58652559 | T | TCATCCAT others(346): Show |
1 | a0001c0003t0001g0176 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.121+1114_121+1115i others(355): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652559 | |||||||
| chr3:58652730 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.121+944G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652730 | |||||||
| chr3:58652731 | G | A | 34 | a0001c0001t0001g0016 a0001c0001t0001g0031 a0001c0001t0001g0068 others(31): Show |
52 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.121+943C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652731 | |||||||
| chr3:58652801 | T | G | 2 | a0001c0004t0001g0038 a0001c0004t0001g0112 |
3 | HG02683.hp1 HG02698.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.121+873A>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652801 | |||||||
| chr3:58652825 | C | G | 1 | a0001c0001t0001g0217 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.121+849G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652825 | |||||||
| chr3:58652861 | T | C | 2 | a0001c0004t0001g0038 a0001c0004t0001g0112 |
3 | HG02683.hp1 HG02698.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.121+813A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652861 | |||||||
| chr3:58652862 | G | A | 2 | a0001c0004t0001g0038 a0001c0004t0001g0112 |
3 | HG02683.hp1 HG02698.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.121+812C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652862 | |||||||
| chr3:58652862 | G | GTCCA | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(73): Show |
125 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.121+808_121+811dup others(4): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652862 | |||||||
| chr3:58652862 | G | GTCCATCC others(1): Show |
46 | a0001c0001t0001g0030 a0001c0001t0001g0037 a0001c0001t0001g0065 others(43): Show |
60 | HG00280.hp2 HG00408.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.121+804_121+811dup others(8): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652862 | |||||||
| chr3:58652862 | G | GTCCATCC others(5): Show |
4 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0002c0002t0001g0043 others(1): Show |
6 | HG01258.hp1 HG01496.hp2 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.121+800_121+811dup others(12): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652862 | |||||||
| chr3:58652862 | G | GTCCATCC others(9): Show |
1 | a0001c0001t0001g0097 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.121+796_121+811dup others(16): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652862 | |||||||
| chr3:58652862 | GTCCA | G | 22 | a0001c0001t0001g0016 a0001c0001t0001g0023 a0001c0001t0001g0031 others(19): Show |
30 | HG00438.hp1 HG00609.hp1 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.121+808_121+811del others(4): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652862 | |||||||
| chr3:58652866 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.121+808T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652866 | |||||||
| chr3:58652870 | A | ATCCATCT others(5): Show |
1 | a0001c0001t0001g0199 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.121+803_121+804ins others(12): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652870 | |||||||
| chr3:58652955 | C | A | 1 | a0001c0001t0001g0158 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.121+719G>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652955 | |||||||
| chr3:58652967 | T | A | 1 | a0001c0001t0001g0124 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.121+707A>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652967 | |||||||
| chr3:58652977 | C | CATCT | 17 | a0001c0001t0001g0016 a0001c0001t0001g0031 a0001c0001t0001g0065 others(14): Show |
22 | HG00438.hp1 HG00609.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.121+696_121+697ins others(4): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652977 | |||||||
| chr3:58652977 | C | CATCTG | 37 | a0001c0001t0001g0030 a0001c0001t0001g0091 a0001c0001t0001g0093 others(34): Show |
50 | HG00280.hp2 HG00639.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.121+696_121+697ins others(5): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652977 | |||||||
| chr3:58652977 | C | CATCTGT | 79 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(76): Show |
129 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.121+696_121+697ins others(6): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652977 | |||||||
| chr3:58652977 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.121+697G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652977 | |||||||
| chr3:58652978 | G | A | 3 | a0001c0003t0001g0047 a0001c0003t0001g0048 a0001c0003t0001g0176 |
5 | HG01081.hp1 HG03490.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.121+696C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652978 | |||||||
| chr3:58652978 | G | T | 118 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(115): Show |
181 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.121+696C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652978 | |||||||
| chr3:58652978 | GT | G | 6 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(3): Show |
7 | HG01358.hp1 HG02273.hp2 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.121+695delA | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652978 | |||||||
| chr3:58652979 | T | TCTG | 3 | a0001c0003t0001g0047 a0001c0003t0001g0048 a0001c0003t0001g0176 |
5 | HG01081.hp1 HG03490.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.121+694_121+695ins others(3): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58652979 | |||||||
| chr3:58653326 | C | T | 14 | a0002c0002t0001g0007 a0002c0002t0001g0041 a0002c0002t0001g0042 others(11): Show |
22 | HG00639.hp1 HG00733.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.121+348G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58653326 | |||||||
| chr3:58653462 | G | A | 3 | a0001c0001t0001g0171 a0001c0001t0001g0244 a0005c0010t0004g0173 |
3 | HG02258.hp1 HG03139.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.121+212C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 3/9 | chr3 | 58653462 | |||||||
| chr3:58654135 | T | A | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(132): Show |
203 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.14-354A>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58654135 | |||||||
| chr3:58654201 | G | A | 2 | a0001c0004t0001g0038 a0001c0004t0001g0112 |
3 | HG02683.hp1 HG02698.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.14-420C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58654201 | |||||||
| chr3:58654334 | A | T | 122 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(119): Show |
185 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.14-553T>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58654334 | |||||||
| chr3:58654378 | C | G | 4 | a0001c0001t0001g0033 a0001c0001t0001g0117 a0001c0001t0001g0123 others(1): Show |
5 | HG00733.hp1 HG00741.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.14-597G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58654378 | |||||||
| chr3:58654538 | G | A | 4 | a0001c0001t0001g0052 a0001c0001t0001g0207 a0001c0001t0001g0227 others(1): Show |
5 | HG01934.hp2 HG02630.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.14-757C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58654538 | |||||||
| chr3:58654572 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.14-791C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58654572 | |||||||
| chr3:58654617 | C | T | 60 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(57): Show |
112 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.14-836G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58654617 | |||||||
| chr3:58654628 | T | G | 1 | a0001c0001t0001g0201 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.14-847A>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58654628 | |||||||
| chr3:58654767 | C | T | 1 | a0001c0001t0005g0058 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.13+784G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58654767 | |||||||
| chr3:58654770 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0197 a0001c0001t0001g0235 |
5 | HG00099.hp2 HG00738.hp1 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.13+781C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58654770 | |||||||
| chr3:58654782 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.13+769C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58654782 | |||||||
| chr3:58654809 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.13+742G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58654809 | |||||||
| chr3:58654821 | T | C | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(135): Show |
207 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.13+730A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58654821 | |||||||
| chr3:58654915 | C | A | 2 | a0001c0001t0001g0171 a0005c0010t0004g0173 |
2 | HG03139.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.13+636G>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58654915 | |||||||
| chr3:58654916 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.13+635A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58654916 | |||||||
| chr3:58655020 | C | T | 14 | a0002c0002t0001g0007 a0002c0002t0001g0041 a0002c0002t0001g0042 others(11): Show |
22 | HG00639.hp1 HG00733.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.13+531G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58655020 | |||||||
| chr3:58655060 | AC | A | 6 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(3): Show |
7 | HG01109.hp2 HG02055.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.13+490delG | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58655060 | |||||||
| chr3:58655109 | A | G | 4 | a0001c0001t0001g0023 a0001c0001t0001g0044 a0001c0001t0001g0180 others(1): Show |
7 | HG01243.hp1 HG02486.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.13+442T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58655109 | |||||||
| chr3:58655184 | A | G | 240 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(237): Show |
382 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(379): Show |
intron_variant | MODIFIER | c.13+367T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58655184 | |||||||
| chr3:58655189 | G | A | 3 | a0001c0001t0001g0171 a0001c0001t0002g0012 a0005c0010t0004g0173 |
6 | HG02109.hp2 HG02280.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.13+362C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58655189 | |||||||
| chr3:58655220 | T | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0245 |
3 | HG02922.hp2 HG03516.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.13+331A>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58655220 | |||||||
| chr3:58655397 | C | T | 2 | a0001c0001t0001g0171 a0001c0001t0002g0012 |
5 | HG02109.hp2 HG02280.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.13+154G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58655397 | |||||||
| chr3:58655447 | C | T | 1 | a0001c0001t0002g0109 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.13+104G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58655447 | |||||||
| chr3:58655457 | C | T | 5 | a0001c0001t0001g0023 a0001c0001t0001g0044 a0001c0001t0001g0180 others(2): Show |
9 | HG01109.hp2 HG01243.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.13+94G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 2/9 | chr3 | 58655457 | |||||||
| chr3:58655620 | C | A | 1 | a0001c0001t0005g0058 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-38-19G>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58655620 | |||||||
| chr3:58655625 | C | T | 58 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0020 others(55): Show |
86 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.-38-24G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58655625 | |||||||
| chr3:58655710 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-38-109A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58655710 | |||||||
| chr3:58655786 | C | T | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG03017.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-38-185G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58655786 | |||||||
| chr3:58656001 | T | C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(238): Show |
382 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(379): Show |
intron_variant | MODIFIER | c.-38-400A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58656001 | |||||||
| chr3:58656002 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-38-401C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58656002 | |||||||
| chr3:58656039 | C | T | 2 | a0002c0002t0001g0250 a0002c0002t0001g0251 |
2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-38-438G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58656039 | |||||||
| chr3:58656073 | CT | C | 26 | a0001c0001t0001g0044 a0001c0001t0001g0177 a0001c0001t0001g0180 others(23): Show |
35 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-38-473delA | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58656073 | |||||||
| chr3:58656121 | G | A | 10 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0197 others(7): Show |
20 | HG00099.hp2 HG00738.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.-38-520C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58656121 | |||||||
| chr3:58656165 | G | A | 26 | a0001c0001t0001g0044 a0001c0001t0001g0177 a0001c0001t0001g0180 others(23): Show |
35 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-38-564C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58656165 | |||||||
| chr3:58656181 | A | G | 26 | a0001c0001t0001g0044 a0001c0001t0001g0177 a0001c0001t0001g0180 others(23): Show |
35 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-38-580T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58656181 | |||||||
| chr3:58656201 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-38-600G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58656201 | |||||||
| chr3:58656208 | C | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(55): Show |
114 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.-38-607G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58656208 | |||||||
| chr3:58656454 | A | G | 5 | a0001c0001t0001g0004 a0001c0001t0001g0174 a0001c0001t0001g0210 others(2): Show |
11 | NA18946.hp2 NA18950.hp1 NA18952.hp1 others(8): Show |
intron_variant | MODIFIER | c.-38-853T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58656454 | |||||||
| chr3:58656521 | AC | A | 61 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0027 others(58): Show |
72 | HG00280.hp2 HG00438.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.-38-921delG | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58656521 | |||||||
| chr3:58656648 | C | T | 1 | a0002c0002t0001g0182 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-38-1047G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58656648 | |||||||
| chr3:58656686 | T | C | 1 | a0001c0003t0001g0048 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-38-1085A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58656686 | |||||||
| chr3:58656725 | A | G | 61 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0027 others(58): Show |
72 | HG00280.hp2 HG00438.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.-38-1124T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58656725 | |||||||
| chr3:58656931 | G | A | 88 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(85): Show |
151 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.-38-1330C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58656931 | |||||||
| chr3:58656948 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-38-1347G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58656948 | |||||||
| chr3:58656999 | T | C | 2 | a0002c0002t0001g0250 a0002c0002t0001g0251 |
2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-38-1398A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58656999 | |||||||
| chr3:58657012 | A | G | 240 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(237): Show |
381 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(378): Show |
intron_variant | MODIFIER | c.-38-1411T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58657012 | |||||||
| chr3:58657046 | C | T | 2 | a0001c0001t0001g0181 a0001c0006t0006g0179 |
2 | HG01243.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-38-1445G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58657046 | |||||||
| chr3:58657094 | C | T | 240 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(237): Show |
381 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(378): Show |
intron_variant | MODIFIER | c.-38-1493G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58657094 | |||||||
| chr3:58657143 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-38-1542G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58657143 | |||||||
| chr3:58657148 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-38-1547A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58657148 | |||||||
| chr3:58657193 | C | T | 240 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(237): Show |
381 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(378): Show |
intron_variant | MODIFIER | c.-38-1592G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58657193 | |||||||
| chr3:58657228 | G | A | 1 | a0001c0004t0001g0112 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-38-1627C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58657228 | |||||||
| chr3:58657276 | T | A | 2 | a0001c0001t0001g0177 a0001c0003t0001g0176 |
2 | NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-38-1675A>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58657276 | |||||||
| chr3:58657383 | A | AAG | 54 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0027 others(51): Show |
65 | HG00280.hp2 HG00438.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.-38-1784_-38-1783d others(4): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58657383 | |||||||
| chr3:58657383 | A | AAGAG | 8 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0091 others(5): Show |
8 | HG00735.hp2 HG01358.hp1 HG02273.hp2 others(5): Show |
intron_variant | MODIFIER | c.-38-1786_-38-1783d others(6): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58657383 | |||||||
| chr3:58657443 | G | A | 62 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0027 others(59): Show |
73 | HG00280.hp2 HG00438.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.-38-1842C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58657443 | |||||||
| chr3:58657457 | A | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.-38-1856T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58657457 | |||||||
| chr3:58657468 | C | G | 2 | a0001c0001t0005g0058 a0001c0001t0005g0059 |
2 | HG02559.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-38-1867G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58657468 | |||||||
| chr3:58657638 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-38-2037C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58657638 | |||||||
| chr3:58657726 | C | G | 86 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(83): Show |
148 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.-38-2125G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58657726 | |||||||
| chr3:58657850 | A | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.-38-2249T>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58657850 | |||||||
| chr3:58657915 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-38-2314G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58657915 | |||||||
| chr3:58657917 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-38-2316G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58657917 | |||||||
| chr3:58657947 | G | T | 1 | a0001c0001t0001g0067 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-38-2346C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58657947 | |||||||
| chr3:58658002 | T | G | 1 | a0001c0001t0001g0040 | 2 | NA18940.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.-38-2401A>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58658002 | |||||||
| chr3:58658307 | A | G | 2 | a0002c0002t0001g0250 a0002c0002t0001g0251 |
2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-38-2706T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58658307 | |||||||
| chr3:58658368 | G | A | 1 | a0001c0001t0001g0237 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-38-2767C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58658368 | |||||||
| chr3:58658394 | A | G | 1 | a0001c0001t0001g0027 | 2 | NA18939.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.-38-2793T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58658394 | |||||||
| chr3:58658475 | G | A | 240 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(237): Show |
381 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(378): Show |
intron_variant | MODIFIER | c.-38-2874C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58658475 | |||||||
| chr3:58658486 | C | G | 88 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(85): Show |
151 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.-38-2885G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58658486 | |||||||
| chr3:58658491 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-38-2890C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58658491 | |||||||
| chr3:58658497 | C | A | 10 | a0001c0001t0001g0030 a0001c0001t0001g0091 a0001c0001t0001g0092 others(7): Show |
11 | HG00280.hp2 HG00735.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-38-2896G>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58658497 | |||||||
| chr3:58658559 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-38-2958T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58658559 | |||||||
| chr3:58658635 | C | G | 61 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0027 others(58): Show |
72 | HG00280.hp2 HG00438.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.-38-3034G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58658635 | |||||||
| chr3:58658638 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-38-3037C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58658638 | |||||||
| chr3:58658799 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-38-3198C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58658799 | |||||||
| chr3:58658810 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-38-3209G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58658810 | |||||||
| chr3:58658896 | C | T | 22 | a0001c0001t0001g0044 a0001c0001t0001g0180 a0001c0001t0001g0181 others(19): Show |
31 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.-38-3295G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58658896 | |||||||
| chr3:58658999 | G | A | 92 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0027 others(89): Show |
113 | HG00280.hp2 HG00438.hp1 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.-38-3398C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58658999 | |||||||
| chr3:58659063 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-38-3462C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58659063 | |||||||
| chr3:58659181 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-38-3580G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58659181 | |||||||
| chr3:58659229 | G | C | 29 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0177 others(26): Show |
39 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.-38-3628C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58659229 | |||||||
| chr3:58659654 | G | A | 242 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(239): Show |
383 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.-38-4053C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58659654 | |||||||
| chr3:58659868 | A | G | 90 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(87): Show |
153 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.-38-4267T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58659868 | |||||||
| chr3:58659990 | C | T | 236 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(233): Show |
376 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(373): Show |
intron_variant | MODIFIER | c.-38-4389G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58659990 | |||||||
| chr3:58660076 | A | G | 1 | a0001c0004t0001g0112 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-38-4475T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58660076 | |||||||
| chr3:58660262 | C | G | 1 | a0001c0001t0001g0207 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-38-4661G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58660262 | |||||||
| chr3:58660482 | G | A | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
348 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.-38-4881C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58660482 | |||||||
| chr3:58660493 | C | G | 70 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(67): Show |
128 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.-38-4892G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58660493 | |||||||
| chr3:58660493 | C | T | 28 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0027 others(25): Show |
37 | HG00438.hp1 HG00609.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.-38-4892G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58660493 | |||||||
| chr3:58660638 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-38-5037A>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58660638 | |||||||
| chr3:58660721 | G | A | 7 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(4): Show |
7 | HG01496.hp1 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-38-5120C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58660721 | |||||||
| chr3:58660757 | A | G | 242 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(239): Show |
383 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.-38-5156T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58660757 | |||||||
| chr3:58660825 | T | A | 1 | a0001c0001t0001g0194 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-38-5224A>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58660825 | |||||||
| chr3:58660825 | T | C | 236 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(233): Show |
377 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(374): Show |
intron_variant | MODIFIER | c.-38-5224A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58660825 | |||||||
| chr3:58660975 | G | C | 1 | a0001c0001t0001g0194 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-38-5374C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58660975 | |||||||
| chr3:58661154 | C | A | 4 | a0001c0001t0001g0044 a0001c0001t0001g0180 a0001c0001t0001g0190 others(1): Show |
6 | HG01109.hp2 HG01243.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.-39+5422G>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58661154 | |||||||
| chr3:58661170 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-39+5406G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58661170 | |||||||
| chr3:58661191 | G | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.-39+5385C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58661191 | |||||||
| chr3:58661209 | C | A | 1 | a0004c0011t0001g0239 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-39+5367G>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58661209 | |||||||
| chr3:58661235 | T | C | 1 | a0001c0004t0001g0112 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-39+5341A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58661235 | |||||||
| chr3:58661237 | G | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(173): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.-39+5339C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58661237 | |||||||
| chr3:58661308 | C | T | 1 | a0001c0004t0001g0112 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-39+5268G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58661308 | |||||||
| chr3:58661310 | T | C | 1 | a0001c0001t0001g0252 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-39+5266A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58661310 | |||||||
| chr3:58661431 | T | C | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(173): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.-39+5145A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58661431 | |||||||
| chr3:58661442 | G | C | 2 | a0001c0001t0001g0054 a0001c0001t0003g0240 |
3 | HG02040.hp1 NA19004.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.-39+5134C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58661442 | |||||||
| chr3:58661464 | C | T | 1 | a0001c0001t0001g0055 | 2 | HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-39+5112G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58661464 | |||||||
| chr3:58661584 | G | A | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.-39+4992C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58661584 | |||||||
| chr3:58661654 | C | A | 1 | a0001c0004t0001g0112 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-39+4922G>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58661654 | |||||||
| chr3:58661658 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-39+4918A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58661658 | |||||||
| chr3:58661669 | T | C | 2 | a0001c0001t0002g0109 a0001c0006t0001g0110 |
2 | HG01891.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-39+4907A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58661669 | |||||||
| chr3:58661716 | C | T | 1 | a0001c0006t0006g0179 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-39+4860G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58661716 | |||||||
| chr3:58661725 | A | G | 1 | a0001c0001t0001g0055 | 2 | HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-39+4851T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58661725 | |||||||
| chr3:58661809 | C | G | 1 | a0001c0001t0001g0114 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-39+4767G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58661809 | |||||||
| chr3:58661848 | C | T | 2 | a0001c0001t0001g0065 a0001c0001t0001g0066 |
2 | HG01099.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.-39+4728G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58661848 | |||||||
| chr3:58661985 | C | T | 1 | a0001c0004t0001g0112 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-39+4591G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58661985 | |||||||
| chr3:58662147 | G | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.-39+4429C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58662147 | |||||||
| chr3:58662148 | G | C | 2 | a0002c0002t0001g0250 a0002c0002t0001g0251 |
2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-39+4428C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58662148 | |||||||
| chr3:58662149 | T | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.-39+4427A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58662149 | |||||||
| chr3:58662153 | G | A | 61 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0027 others(58): Show |
72 | HG00280.hp2 HG00438.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.-39+4423C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58662153 | |||||||
| chr3:58662154 | TA | T | 87 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(84): Show |
150 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.-39+4421delT | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58662154 | |||||||
| chr3:58662161 | G | C | 2 | a0001c0001t0001g0195 a0002c0002t0001g0011 |
5 | HG02280.hp2 HG02451.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-39+4415C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58662161 | |||||||
| chr3:58662165 | A | T | 1 | a0001c0001t0001g0114 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-39+4411T>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58662165 | |||||||
| chr3:58662278 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-39+4298G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58662278 | |||||||
| chr3:58662304 | T | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.-39+4272A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58662304 | |||||||
| chr3:58662318 | G | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.-39+4258C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58662318 | |||||||
| chr3:58662362 | A | G | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.-39+4214T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58662362 | |||||||
| chr3:58662433 | T | C | 1 | a0002c0002t0001g0191 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-39+4143A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58662433 | |||||||
| chr3:58662452 | A | T | 36 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0027 others(33): Show |
46 | HG00438.hp1 HG00609.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.-39+4124T>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58662452 | |||||||
| chr3:58662453 | G | T | 36 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0027 others(33): Show |
46 | HG00438.hp1 HG00609.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.-39+4123C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58662453 | |||||||
| chr3:58662797 | C | A | 1 | a0001c0001t0001g0106 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-39+3779G>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58662797 | |||||||
| chr3:58662828 | C | A | 59 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(56): Show |
116 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.-39+3748G>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58662828 | |||||||
| chr3:58662849 | G | A | 3 | a0001c0001t0001g0046 a0001c0001t0002g0192 a0001c0001t0002g0193 |
4 | HG02615.hp1 HG02922.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-39+3727C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58662849 | |||||||
| chr3:58662991 | C | T | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
304 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.-39+3585G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58662991 | |||||||
| chr3:58663001 | C | T | 4 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(1): Show |
4 | HG01358.hp1 HG02273.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.-39+3575G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58663001 | |||||||
| chr3:58663019 | C | G | 2 | a0001c0001t0005g0058 a0001c0001t0005g0059 |
2 | HG02559.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-39+3557G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58663019 | |||||||
| chr3:58663048 | G | A | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.-39+3528C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58663048 | |||||||
| chr3:58663233 | G | A | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.-39+3343C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58663233 | |||||||
| chr3:58663310 | C | T | 61 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0027 others(58): Show |
72 | HG00280.hp2 HG00438.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.-39+3266G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58663310 | |||||||
| chr3:58663316 | C | T | 1 | a0001c0004t0001g0112 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-39+3260G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58663316 | |||||||
| chr3:58663369 | A | C | 2 | a0001c0001t0005g0058 a0001c0001t0005g0059 |
2 | HG02559.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-39+3207T>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58663369 | |||||||
| chr3:58663378 | C | T | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
309 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.-39+3198G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58663378 | |||||||
| chr3:58663390 | G | T | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.-39+3186C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58663390 | |||||||
| chr3:58663441 | T | C | 2 | a0001c0001t0001g0177 a0001c0003t0001g0176 |
2 | NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-39+3135A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58663441 | |||||||
| chr3:58663485 | G | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.-39+3091C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58663485 | |||||||
| chr3:58663552 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-39+3024G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58663552 | |||||||
| chr3:58663582 | C | G | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.-39+2994G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58663582 | |||||||
| chr3:58663608 | G | C | 59 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0027 others(56): Show |
70 | HG00280.hp2 HG00438.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.-39+2968C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58663608 | |||||||
| chr3:58663623 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-39+2953G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58663623 | |||||||
| chr3:58663630 | C | T | 2 | a0001c0001t0005g0058 a0001c0001t0005g0059 |
2 | HG02559.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-39+2946G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58663630 | |||||||
| chr3:58663648 | G | A | 240 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(237): Show |
381 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(378): Show |
intron_variant | MODIFIER | c.-39+2928C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58663648 | |||||||
| chr3:58663784 | G | A | 1 | a0001c0004t0001g0112 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-39+2792C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58663784 | |||||||
| chr3:58663787 | C | T | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG03017.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-39+2789G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58663787 | |||||||
| chr3:58663837 | G | A | 86 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(83): Show |
149 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.-39+2739C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58663837 | |||||||
| chr3:58663847 | A | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(148): Show |
271 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.-39+2729T>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58663847 | |||||||
| chr3:58664002 | T | G | 60 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(57): Show |
117 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.-39+2574A>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58664002 | |||||||
| chr3:58664023 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-39+2553C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58664023 | |||||||
| chr3:58664076 | G | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(173): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.-39+2500C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58664076 | |||||||
| chr3:58664087 | T | C | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(173): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.-39+2489A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58664087 | |||||||
| chr3:58664089 | C | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(173): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.-39+2487G>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58664089 | |||||||
| chr3:58664091 | C | CAGATAAA others(1): Show |
176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(173): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.-39+2484_-39+2485i others(10): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58664091 | |||||||
| chr3:58664092 | T | C | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(173): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.-39+2484A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58664092 | |||||||
| chr3:58664106 | C | A | 1 | a0001c0001t0001g0108 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-39+2470G>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58664106 | |||||||
| chr3:58664195 | T | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(174): Show |
307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.-39+2381A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58664195 | |||||||
| chr3:58664229 | T | C | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(173): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.-39+2347A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58664229 | |||||||
| chr3:58664230 | G | A | 24 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0180 others(21): Show |
34 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.-39+2346C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58664230 | |||||||
| chr3:58664251 | T | G | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(173): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.-39+2325A>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58664251 | |||||||
| chr3:58664255 | C | T | 2 | a0001c0001t0001g0195 a0002c0002t0001g0011 |
5 | HG02280.hp2 HG02451.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-39+2321G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58664255 | |||||||
| chr3:58664267 | G | A | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(144): Show |
267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.-39+2309C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58664267 | |||||||
| chr3:58664368 | G | A | 1 | a0001c0001t0001g0031 | 2 | NA18969.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.-39+2208C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58664368 | |||||||
| chr3:58664383 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-39+2193C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58664383 | |||||||
| chr3:58664411 | T | A | 1 | a0001c0001t0001g0194 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-39+2165A>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58664411 | |||||||
| chr3:58664423 | T | TA | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.-39+2152_-39+2153i others(3): Show |
FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58664423 | |||||||
| chr3:58664482 | G | T | 1 | a0001c0001t0001g0178 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-39+2094C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58664482 | |||||||
| chr3:58664509 | C | T | 59 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0027 others(56): Show |
70 | HG00280.hp2 HG00438.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.-39+2067G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58664509 | |||||||
| chr3:58664522 | A | G | 1 | a0001c0001t0001g0055 | 2 | HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-39+2054T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58664522 | |||||||
| chr3:58664658 | C | T | 2 | a0001c0001t0001g0177 a0001c0003t0001g0176 |
2 | NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-39+1918G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58664658 | |||||||
| chr3:58665012 | G | C | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(235): Show |
379 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(376): Show |
intron_variant | MODIFIER | c.-39+1564C>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58665012 | |||||||
| chr3:58665036 | T | G | 1 | a0001c0001t0001g0111 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-39+1540A>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58665036 | |||||||
| chr3:58665310 | T | G | 1 | a0001c0004t0001g0112 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-39+1266A>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58665310 | |||||||
| chr3:58665351 | A | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0175 |
6 | NA18944.hp2 NA18962.hp1 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.-39+1225T>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58665351 | |||||||
| chr3:58665372 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-39+1204A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58665372 | |||||||
| chr3:58665373 | C | G | 1 | a0001c0001t0001g0252 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-39+1203G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58665373 | |||||||
| chr3:58665431 | C | T | 1 | a0001c0001t0001g0174 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-39+1145G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58665431 | |||||||
| chr3:58665437 | C | T | 1 | a0001c0001t0001g0060 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-39+1139G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58665437 | |||||||
| chr3:58665459 | T | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.-39+1117A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58665459 | |||||||
| chr3:58665554 | T | G | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(235): Show |
379 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(376): Show |
intron_variant | MODIFIER | c.-39+1022A>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58665554 | |||||||
| chr3:58665655 | T | C | 1 | a0001c0004t0001g0112 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-39+921A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58665655 | |||||||
| chr3:58665747 | C | G | 3 | a0001c0001t0001g0171 a0001c0001t0002g0172 a0005c0010t0004g0173 |
3 | HG02723.hp1 HG03139.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-39+829G>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58665747 | |||||||
| chr3:58665748 | G | A | 2 | a0001c0001t0005g0058 a0001c0001t0005g0059 |
2 | HG02559.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-39+828C>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58665748 | |||||||
| chr3:58665878 | T | C | 1 | a0001c0004t0001g0112 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-39+698A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58665878 | |||||||
| chr3:58666121 | G | T | 1 | a0001c0004t0001g0112 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-39+455C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58666121 | |||||||
| chr3:58666126 | C | T | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.-39+450G>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58666126 | |||||||
| chr3:58666304 | T | C | 1 | a0001c0001t0001g0170 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-39+272A>G | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58666304 | |||||||
| chr3:58666489 | A | G | 71 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(68): Show |
119 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.-39+87T>C | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58666489 | |||||||
| chr3:58666531 | T | A | 1 | a0001c0001t0001g0252 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-39+45A>T | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58666531 | |||||||
| chr3:58666534 | G | T | 1 | a0001c0004t0001g0112 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-39+42C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58666534 | |||||||
| chr3:58666565 | G | T | 60 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0027 others(57): Show |
71 | HG00280.hp2 HG00438.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.-39+11C>A | FAM3D | ENSG00000198643.7 | transcript | ENST00000358781.7 | protein_coding | 1/9 | chr3 | 58666565 |