Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 81610 |
| ensemblid | ENSG00000101447.15 |
| hgncid | 16122 |
| symbol | FAM83D |
| name | family with sequence similarity 83 member D |
| refseq_nuc | NM_030919.3 |
| refseq_prot | NP_112181.3 |
| ensembl_nuc | ENST00000619850.2 |
| ensembl_prot | ENSP00000481465.1 |
| mane_status | MANE Select |
| chr | chr20 |
| start | 38926417 |
| end | 38953106 |
| strand | + |
| ver | v1.2 |
| region | chr20:38926417-38953106 |
| region5000 | chr20:38921417-38958106 |
| regionname0 | FAM83D_chr20_38926417_38953106 |
| regionname5000 | FAM83D_chr20_38921417_38958106 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 585 | 164 | 32 | 28 | 84 | 3 | 16 | 60 | FAM83D_chr20_38921417_38958106 | FAM83D | MALLS others(580): Show |
chr20 | 38921417 | 38958106 |
| a0002 | 0/1 | 585 | 139 | 31 | 25 | 68 | 3 | 11 | 51 | FAM83D_chr20_38921417_38958106 | FAM83D | MALLS others(580): Show |
chr20 | 38921417 | 38958106 |
| a0003 | 0/0 | 584 | 9 | 8 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | MALLS others(579): Show |
chr20 | 38921417 | 38958106 |
| a0004 | 0/0 | 585 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | MALLS others(580): Show |
chr20 | 38921417 | 38958106 |
| a0005 | 0/0 | 586 | 4 | 0 | 3 | 0 | 0 | 1 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | MALLS others(581): Show |
chr20 | 38921417 | 38958106 |
| a0006 | 0/0 | 586 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | MALLS others(581): Show |
chr20 | 38921417 | 38958106 |
| a0007 | 0/0 | 587 | 3 | 1 | 0 | 2 | 0 | 0 | 2 | FAM83D_chr20_38921417_38958106 | FAM83D | MALLS others(582): Show |
chr20 | 38921417 | 38958106 |
| a0008 | 0/0 | 585 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | FAM83D_chr20_38921417_38958106 | FAM83D | MALLS others(580): Show |
chr20 | 38921417 | 38958106 |
| a0009 | 0/0 | 585 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | MALLS others(580): Show |
chr20 | 38921417 | 38958106 |
| a0010 | 0/0 | 585 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | FAM83D_chr20_38921417_38958106 | FAM83D | MALLS others(580): Show |
chr20 | 38921417 | 38958106 |
| a0011 | 0/0 | 585 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | MALLS others(580): Show |
chr20 | 38921417 | 38958106 |
| a0012 | 0/0 | 585 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | MAMLS others(580): Show |
chr20 | 38921417 | 38958106 |
| a0013 | 0/0 | 585 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | MALLS others(580): Show |
chr20 | 38921417 | 38958106 |
| a0014 | 0/0 | 585 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | MALLS others(580): Show |
chr20 | 38921417 | 38958106 |
| a0015 | 0/0 | 585 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | MALLS others(580): Show |
chr20 | 38921417 | 38958106 |
| a0016 | 0/0 | 585 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM83D_chr20_38921417_38958106 | FAM83D | MALLS others(580): Show |
chr20 | 38921417 | 38958106 |
| a0017 | 0/0 | 559 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM83D_chr20_38921417_38958106 | FAM83D | MALLS others(554): Show |
chr20 | 38921417 | 38958106 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1755 | 156 | 25 | 28 | 83 | 3 | 16 | FAM83D_chr20_38921417_38958106 | FAM83D | ATGGC others(1750): Show |
chr20 | 38921417 | 38958106 | ||
| a0001c0004 | 0/0 | 1755 | 7 | 7 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | ATGGC others(1750): Show |
chr20 | 38921417 | 38958106 | ||
| a0001c0022 | 0/0 | 1755 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | ATGGC others(1750): Show |
chr20 | 38921417 | 38958106 | ||
| a0002c0002 | 0/1 | 1755 | 131 | 27 | 24 | 66 | 3 | 10 | FAM83D_chr20_38921417_38958106 | FAM83D | ATGGC others(1750): Show |
chr20 | 38921417 | 38958106 | ||
| a0002c0006 | 0/0 | 1755 | 5 | 2 | 1 | 1 | 0 | 1 | FAM83D_chr20_38921417_38958106 | FAM83D | ATGGC others(1750): Show |
chr20 | 38921417 | 38958106 | ||
| a0002c0014 | 0/0 | 1755 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | ATGGC others(1750): Show |
chr20 | 38921417 | 38958106 | ||
| a0002c0019 | 0/0 | 1755 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | ATGGC others(1750): Show |
chr20 | 38921417 | 38958106 | ||
| a0003c0005 | 0/0 | 1752 | 6 | 5 | 1 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | ATGGC others(1747): Show |
chr20 | 38921417 | 38958106 | ||
| a0003c0008 | 0/0 | 1752 | 3 | 3 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | ATGGC others(1747): Show |
chr20 | 38921417 | 38958106 | ||
| a0004c0003 | 0/0 | 1755 | 7 | 7 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | ATGGC others(1750): Show |
chr20 | 38921417 | 38958106 | ||
| a0005c0007 | 0/0 | 1758 | 4 | 0 | 3 | 0 | 0 | 1 | FAM83D_chr20_38921417_38958106 | FAM83D | ATGGC others(1753): Show |
chr20 | 38921417 | 38958106 | ||
| a0006c0010 | 0/0 | 1758 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | ATGGC others(1753): Show |
chr20 | 38921417 | 38958106 | ||
| a0006c0021 | 0/0 | 1758 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | ATGGC others(1753): Show |
chr20 | 38921417 | 38958106 | ||
| a0007c0009 | 0/0 | 1761 | 3 | 1 | 0 | 2 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | ATGGC others(1756): Show |
chr20 | 38921417 | 38958106 | ||
| a0008c0012 | 0/0 | 1755 | 2 | 0 | 0 | 2 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | ATGGC others(1750): Show |
chr20 | 38921417 | 38958106 | ||
| a0009c0011 | 0/0 | 1755 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | ATGGC others(1750): Show |
chr20 | 38921417 | 38958106 | ||
| a0010c0013 | 0/0 | 1755 | 2 | 0 | 0 | 2 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | ATGGC others(1750): Show |
chr20 | 38921417 | 38958106 | ||
| a0011c0017 | 0/0 | 1755 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | ATGGC others(1750): Show |
chr20 | 38921417 | 38958106 | ||
| a0012c0015 | 0/0 | 1755 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | ATGGC others(1750): Show |
chr20 | 38921417 | 38958106 | ||
| a0013c0018 | 0/0 | 1755 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | ATGGC others(1750): Show |
chr20 | 38921417 | 38958106 | ||
| a0014c0020 | 0/0 | 1755 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | ATGGC others(1750): Show |
chr20 | 38921417 | 38958106 | ||
| a0015c0024 | 0/0 | 1755 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | ATGGC others(1750): Show |
chr20 | 38921417 | 38958106 | ||
| a0016c0023 | 0/0 | 1755 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | ATGGC others(1750): Show |
chr20 | 38921417 | 38958106 | ||
| a0017c0016 | 0/0 | 1765 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | ATGGC others(1760): Show |
chr20 | 38921417 | 38958106 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2370 | 153 | 23 | 28 | 82 | 3 | 16 | FAM83D_chr20_38921417_38958106 | FAM83D | GAGGG others(2365): Show |
chr20 | 38921417 | 38958106 |
| a0001c0001t0005 | 0/0 | 2370 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | GAGGG others(2365): Show |
chr20 | 38921417 | 38958106 |
| a0001c0001t0010 | 0/0 | 2370 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | GAGGG others(2365): Show |
chr20 | 38921417 | 38958106 |
| a0001c0004t0001 | 0/0 | 2370 | 7 | 7 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | GAGGG others(2365): Show |
chr20 | 38921417 | 38958106 |
| a0001c0022t0001 | 0/0 | 2370 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | GAGGG others(2365): Show |
chr20 | 38921417 | 38958106 |
| a0002c0002t0001 | 0/0 | 2370 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | GAGGG others(2365): Show |
chr20 | 38921417 | 38958106 |
| a0002c0002t0002 | 0/1 | 2370 | 92 | 9 | 23 | 50 | 2 | 7 | FAM83D_chr20_38921417_38958106 | FAM83D | GAGGG others(2365): Show |
chr20 | 38921417 | 38958106 |
| a0002c0002t0003 | 0/0 | 2370 | 31 | 12 | 1 | 14 | 1 | 3 | FAM83D_chr20_38921417_38958106 | FAM83D | GAGGG others(2365): Show |
chr20 | 38921417 | 38958106 |
| a0002c0002t0004 | 0/0 | 2370 | 5 | 5 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | GAGGG others(2365): Show |
chr20 | 38921417 | 38958106 |
| a0002c0002t0008 | 0/0 | 2370 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | CAGGG others(2365): Show |
chr20 | 38921417 | 38958106 |
| a0002c0002t0009 | 0/0 | 2370 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | GAGGG others(2365): Show |
chr20 | 38921417 | 38958106 |
| a0002c0006t0001 | 0/0 | 2370 | 4 | 2 | 1 | 0 | 0 | 1 | FAM83D_chr20_38921417_38958106 | FAM83D | GAGGG others(2365): Show |
chr20 | 38921417 | 38958106 |
| a0002c0006t0007 | 0/0 | 2370 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | CAGGG others(2365): Show |
chr20 | 38921417 | 38958106 |
| a0002c0014t0004 | 0/0 | 2370 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | GAGGG others(2365): Show |
chr20 | 38921417 | 38958106 |
| a0002c0019t0002 | 0/0 | 2370 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | GAGGG others(2365): Show |
chr20 | 38921417 | 38958106 |
| a0003c0005t0004 | 0/0 | 2367 | 6 | 5 | 1 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | GAGGG others(2362): Show |
chr20 | 38921417 | 38958106 |
| a0003c0008t0002 | 0/0 | 2367 | 3 | 3 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | GAGGG others(2362): Show |
chr20 | 38921417 | 38958106 |
| a0004c0003t0004 | 0/0 | 2370 | 5 | 5 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | GAGGG others(2365): Show |
chr20 | 38921417 | 38958106 |
| a0004c0003t0006 | 0/0 | 2370 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | GAGGG others(2365): Show |
chr20 | 38921417 | 38958106 |
| a0005c0007t0001 | 0/0 | 2373 | 4 | 0 | 3 | 0 | 0 | 1 | FAM83D_chr20_38921417_38958106 | FAM83D | GAGGG others(2368): Show |
chr20 | 38921417 | 38958106 |
| a0006c0010t0002 | 0/0 | 2373 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | GAGGG others(2368): Show |
chr20 | 38921417 | 38958106 |
| a0006c0021t0004 | 0/0 | 2373 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | GAGGG others(2368): Show |
chr20 | 38921417 | 38958106 |
| a0007c0009t0001 | 0/0 | 2376 | 3 | 1 | 0 | 2 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | GAGGG others(2371): Show |
chr20 | 38921417 | 38958106 |
| a0008c0012t0001 | 0/0 | 2370 | 2 | 0 | 0 | 2 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | GAGGG others(2365): Show |
chr20 | 38921417 | 38958106 |
| a0009c0011t0001 | 0/0 | 2370 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | GAGGG others(2365): Show |
chr20 | 38921417 | 38958106 |
| a0010c0013t0001 | 0/0 | 2370 | 2 | 0 | 0 | 2 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | GAGGG others(2365): Show |
chr20 | 38921417 | 38958106 |
| a0011c0017t0003 | 0/0 | 2370 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | GAGGG others(2365): Show |
chr20 | 38921417 | 38958106 |
| a0012c0015t0004 | 0/0 | 2370 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | GAGGG others(2365): Show |
chr20 | 38921417 | 38958106 |
| a0013c0018t0004 | 0/0 | 2370 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | GAGGG others(2365): Show |
chr20 | 38921417 | 38958106 |
| a0014c0020t0004 | 0/0 | 2370 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | GAGGG others(2365): Show |
chr20 | 38921417 | 38958106 |
| a0015c0024t0001 | 0/0 | 2370 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | GAGGG others(2365): Show |
chr20 | 38921417 | 38958106 |
| a0016c0023t0001 | 0/0 | 2370 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | GAGGG others(2365): Show |
chr20 | 38921417 | 38958106 |
| a0017c0016t0002 | 0/0 | 2380 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | GAGGG others(2375): Show |
chr20 | 38921417 | 38958106 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 1/0 | 12 | 2 | 3 | 4 | 1 | 1 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0004 | 0/0 | 8 | 2 | 3 | 2 | 0 | 1 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0005 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0006 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0013 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0005g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0005g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0001t0010g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0004t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0004t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0004t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0004t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0004t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0004t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0004t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0001c0022t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0001 | 0/0 | 16 | 0 | 4 | 11 | 1 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0003 | 0/0 | 11 | 0 | 5 | 5 | 0 | 1 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0011 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0020 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0087 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0003g0007 | 0/0 | 6 | 1 | 0 | 4 | 0 | 1 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0003g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0003g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0003g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0003g0026 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0003g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0008g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0002t0009g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0006t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0006t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0006t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0006t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0006t0007g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0014t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0014t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0002c0019t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0003c0005t0004g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0003c0005t0004g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0003c0005t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0003c0005t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0003c0005t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0003c0008t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0003c0008t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0003c0008t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0004c0003t0004g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0004c0003t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0004c0003t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0004c0003t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0004c0003t0006g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0005c0007t0001g0004 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0005c0007t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0005c0007t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0006c0010t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0006c0010t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0006c0021t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0007c0009t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0007c0009t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0007c0009t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0008c0012t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0008c0012t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0009c0011t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0009c0011t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0010c0013t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0010c0013t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0011c0017t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0012c0015t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0013c0018t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0014c0020t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0015c0024t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0016c0023t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| a0017c0016t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0186 | EUR | GBR | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG00099 | hp2 | a0002 | c0002 | t0003 | g0123 | EUR | GBR | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG00280 | hp1 | a0002 | c0002 | t0002 | g0084 | EUR | FIN | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG00423 | hp2 | a0002 | c0002 | t0009 | g0135 | EAS | CHS | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG00544 | hp2 | a0002 | c0002 | t0002 | g0054 | EAS | CHS | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | CHS | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | CHS | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0079 | EAS | CHS | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG00673 | hp1 | a0002 | c0002 | t0002 | g0051 | EAS | CHS | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0064 | EAS | CHS | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0062 | AMR | PUR | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG00738 | hp2 | a0005 | c0007 | t0001 | g0153 | AMR | PUR | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG00741 | hp2 | a0002 | c0006 | t0001 | g0109 | AMR | PUR | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01074 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01081 | hp1 | a0002 | c0002 | t0002 | g0078 | AMR | PUR | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01099 | hp1 | a0002 | c0002 | t0002 | g0042 | AMR | PUR | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01099 | hp2 | a0011 | c0017 | t0003 | g0125 | AMR | PUR | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01167 | hp2 | a0002 | c0002 | t0002 | g0019 | AMR | PUR | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01168 | hp1 | a0002 | c0002 | t0002 | g0100 | AMR | PUR | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01168 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01169 | hp1 | a0002 | c0002 | t0002 | g0019 | AMR | PUR | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01169 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | PUR | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01175 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | PUR | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01192 | hp2 | a0005 | c0007 | t0001 | g0221 | AMR | PUR | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01243 | hp1 | a0002 | c0002 | t0003 | g0119 | AMR | PUR | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01255 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | CLM | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01255 | hp2 | a0002 | c0002 | t0002 | g0082 | AMR | CLM | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01346 | hp1 | a0002 | c0002 | t0002 | g0089 | AMR | CLM | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01361 | hp1 | a0003 | c0005 | t0004 | g0103 | AMR | CLM | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01361 | hp2 | a0005 | c0007 | t0001 | g0004 | AMR | CLM | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01433 | hp2 | a0002 | c0002 | t0002 | g0105 | AMR | CLM | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01496 | hp1 | a0002 | c0002 | t0002 | g0086 | AMR | CLM | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0200 | EUR | IBS | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01516 | hp2 | a0002 | c0002 | t0002 | g0001 | EUR | IBS | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01884 | hp1 | a0012 | c0015 | t0004 | g0230 | AFR | ACB | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01884 | hp2 | a0002 | c0002 | t0004 | g0045 | AFR | ACB | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01891 | hp2 | a0002 | c0002 | t0003 | g0026 | AFR | ACB | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01928 | hp1 | a0002 | c0002 | t0002 | g0080 | AMR | PEL | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01928 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01943 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | PEL | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01975 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02055 | hp1 | a0002 | c0002 | t0002 | g0044 | AFR | ACB | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02055 | hp2 | a0001 | c0004 | t0001 | g0199 | AFR | ACB | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02056 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02074 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02080 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | KHV | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | KHV | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02083 | hp2 | a0008 | c0012 | t0001 | g0202 | EAS | KHV | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02129 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02132 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02132 | hp2 | a0002 | c0002 | t0002 | g0055 | EAS | KHV | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02145 | hp1 | a0002 | c0002 | t0004 | g0108 | AFR | ACB | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02145 | hp2 | a0003 | c0008 | t0002 | g0048 | AFR | ACB | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02148 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | PEL | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02148 | hp2 | a0002 | c0002 | t0002 | g0085 | AMR | PEL | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | CDX | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02155 | hp2 | a0002 | c0002 | t0002 | g0077 | EAS | CDX | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CDX | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02165 | hp2 | a0002 | c0002 | t0002 | g0058 | EAS | CDX | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02257 | hp1 | a0002 | c0014 | t0004 | g0056 | AFR | ACB | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02258 | hp1 | a0001 | c0004 | t0001 | g0195 | AFR | ACB | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02258 | hp2 | a0004 | c0003 | t0004 | g0134 | AFR | ACB | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02273 | hp1 | a0002 | c0002 | t0002 | g0018 | AMR | PEL | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02280 | hp1 | a0006 | c0010 | t0002 | g0102 | AFR | ACB | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02280 | hp2 | a0002 | c0002 | t0003 | g0137 | AFR | ACB | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02300 | hp2 | a0002 | c0002 | t0002 | g0050 | AMR | PEL | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02451 | hp1 | a0002 | c0006 | t0001 | g0111 | AFR | ACB | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02451 | hp2 | a0007 | c0009 | t0001 | g0035 | AFR | ACB | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02572 | hp1 | a0004 | c0003 | t0004 | g0025 | AFR | GWD | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02622 | hp2 | a0003 | c0008 | t0002 | g0016 | AFR | GWD | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02630 | hp2 | a0009 | c0011 | t0001 | g0028 | AFR | GWD | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02647 | hp2 | a0002 | c0002 | t0002 | g0063 | AFR | GWD | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02698 | hp2 | a0002 | c0006 | t0001 | g0120 | SAS | PJL | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02717 | hp1 | a0002 | c0002 | t0002 | g0043 | AFR | GWD | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02723 | hp2 | a0004 | c0003 | t0004 | g0025 | AFR | GWD | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02735 | hp1 | a0002 | c0002 | t0002 | g0049 | SAS | PJL | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02809 | hp1 | a0002 | c0014 | t0004 | g0057 | AFR | GWD | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02809 | hp2 | a0009 | c0011 | t0001 | g0009 | AFR | GWD | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02886 | hp1 | a0001 | c0004 | t0001 | g0004 | AFR | GWD | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02886 | hp2 | a0002 | c0002 | t0003 | g0012 | AFR | GWD | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02895 | hp1 | a0004 | c0003 | t0006 | g0024 | AFR | GWD | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02895 | hp2 | a0001 | c0004 | t0001 | g0035 | AFR | GWD | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02896 | hp1 | a0002 | c0002 | t0003 | g0022 | AFR | GWD | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0196 | AFR | GWD | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0211 | AFR | GWD | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02897 | hp2 | a0004 | c0003 | t0006 | g0024 | AFR | GWD | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02922 | hp2 | a0002 | c0002 | t0003 | g0012 | AFR | ESN | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02970 | hp1 | a0002 | c0002 | t0002 | g0011 | AFR | ESN | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02970 | hp2 | a0013 | c0018 | t0004 | g0099 | AFR | ESN | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02976 | hp1 | a0002 | c0002 | t0003 | g0022 | AFR | ESN | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02976 | hp2 | a0001 | c0004 | t0001 | g0174 | AFR | ESN | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG03041 | hp2 | a0003 | c0005 | t0004 | g0021 | AFR | GWD | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG03098 | hp1 | a0002 | c0002 | t0003 | g0117 | AFR | MSL | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG03098 | hp2 | a0014 | c0020 | t0004 | g0132 | AFR | MSL | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG03130 | hp1 | a0002 | c0002 | t0003 | g0012 | AFR | ESN | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG03130 | hp2 | a0003 | c0005 | t0004 | g0104 | AFR | ESN | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG03195 | hp1 | a0002 | c0006 | t0001 | g0110 | AFR | ESN | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ESN | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG03225 | hp1 | a0002 | c0002 | t0004 | g0046 | AFR | MSL | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG03225 | hp2 | a0002 | c0002 | t0002 | g0011 | AFR | MSL | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG03453 | hp1 | a0002 | c0002 | t0001 | g0097 | AFR | MSL | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG03486 | hp1 | a0003 | c0005 | t0004 | g0130 | AFR | MSL | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG03486 | hp2 | a0004 | c0003 | t0004 | g0138 | AFR | MSL | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG03516 | hp1 | a0002 | c0002 | t0002 | g0091 | AFR | ESN | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG03516 | hp2 | a0002 | c0002 | t0003 | g0113 | AFR | ESN | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG03540 | hp2 | a0015 | c0024 | t0001 | g0167 | AFR | GWD | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG03579 | hp1 | a0002 | c0002 | t0002 | g0095 | AFR | MSL | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG03688 | hp1 | a0002 | c0002 | t0002 | g0092 | SAS | STU | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | STU | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG03834 | hp2 | a0002 | c0002 | t0003 | g0007 | SAS | BEB | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG03942 | hp1 | a0005 | c0007 | t0001 | g0004 | SAS | BEB | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG03942 | hp2 | a0002 | c0002 | t0003 | g0115 | SAS | BEB | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG04115 | hp1 | a0002 | c0002 | t0003 | g0136 | SAS | STU | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | STU | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0072 | SAS | STU | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | STU | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0094 | SAS | STU | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG04204 | hp2 | a0002 | c0002 | t0002 | g0003 | SAS | STU | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG04228 | hp1 | a0002 | c0002 | t0002 | g0081 | SAS | STU | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0073 | SAS | STU | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18522 | hp1 | a0002 | c0002 | t0004 | g0098 | AFR | YRI | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | YRI | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHB | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CHB | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18747 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | CHB | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18906 | hp1 | a0001 | c0004 | t0001 | g0002 | AFR | YRI | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18906 | hp2 | a0002 | c0002 | t0004 | g0101 | AFR | YRI | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18939 | hp1 | a0002 | c0002 | t0002 | g0106 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18940 | hp2 | a0002 | c0002 | t0002 | g0052 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18941 | hp2 | a0002 | c0002 | t0003 | g0116 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18943 | hp1 | a0002 | c0002 | t0002 | g0090 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18945 | hp2 | a0002 | c0002 | t0002 | g0068 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18947 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18949 | hp1 | a0002 | c0002 | t0003 | g0114 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18950 | hp2 | a0002 | c0019 | t0002 | g0096 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18953 | hp1 | a0001 | c0001 | t0010 | g0005 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18953 | hp2 | a0016 | c0023 | t0001 | g0194 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18954 | hp2 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18956 | hp1 | a0002 | c0002 | t0002 | g0067 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18957 | hp2 | a0002 | c0002 | t0003 | g0124 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18959 | hp1 | a0017 | c0016 | t0002 | g0074 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18960 | hp2 | a0002 | c0002 | t0002 | g0107 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18962 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18964 | hp1 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18966 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18967 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18969 | hp1 | a0007 | c0009 | t0001 | g0192 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18969 | hp2 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18970 | hp1 | a0002 | c0002 | t0003 | g0023 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18977 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18980 | hp1 | a0002 | c0006 | t0007 | g0093 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18980 | hp2 | a0002 | c0002 | t0002 | g0071 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18983 | hp1 | a0002 | c0002 | t0002 | g0070 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18986 | hp1 | a0002 | c0002 | t0002 | g0041 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18986 | hp2 | a0007 | c0009 | t0001 | g0191 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18988 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18989 | hp1 | a0002 | c0002 | t0002 | g0066 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18990 | hp1 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18994 | hp1 | a0002 | c0002 | t0008 | g0083 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18995 | hp2 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18998 | hp1 | a0002 | c0002 | t0002 | g0075 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA18999 | hp2 | a0001 | c0022 | t0001 | g0141 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19001 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19002 | hp2 | a0002 | c0002 | t0003 | g0112 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19007 | hp2 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19009 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19011 | hp1 | a0002 | c0002 | t0002 | g0061 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19012 | hp1 | a0010 | c0013 | t0001 | g0220 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19030 | hp1 | a0003 | c0008 | t0002 | g0047 | AFR | LWK | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19030 | hp2 | a0002 | c0002 | t0003 | g0118 | AFR | LWK | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19054 | hp1 | a0002 | c0002 | t0002 | g0040 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19054 | hp2 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19056 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19059 | hp2 | a0002 | c0002 | t0002 | g0069 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19062 | hp1 | a0002 | c0002 | t0002 | g0076 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19063 | hp1 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19063 | hp2 | a0008 | c0012 | t0001 | g0229 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19065 | hp2 | a0002 | c0002 | t0003 | g0128 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19067 | hp2 | a0002 | c0002 | t0002 | g0053 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19068 | hp2 | a0002 | c0002 | t0003 | g0026 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19072 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19076 | hp1 | a0010 | c0013 | t0001 | g0219 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19076 | hp2 | a0002 | c0002 | t0002 | g0088 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19079 | hp2 | a0002 | c0002 | t0003 | g0121 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19082 | hp1 | a0002 | c0002 | t0002 | g0060 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19084 | hp1 | a0002 | c0002 | t0003 | g0023 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19084 | hp2 | a0002 | c0002 | t0002 | g0131 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19086 | hp2 | a0002 | c0002 | t0003 | g0122 | EAS | JPT | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | YRI | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | YRI | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ASW | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA20129 | hp2 | a0002 | c0002 | t0003 | g0007 | AFR | ASW | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02109 | hp1 | a0002 | c0002 | t0003 | g0126 | AFR | ACB | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02486 | hp1 | a0004 | c0003 | t0004 | g0133 | AFR | ACB | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02559 | hp1 | a0003 | c0005 | t0004 | g0021 | AFR | ACB | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG02559 | hp2 | a0006 | c0021 | t0004 | g0127 | AFR | ACB | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | MSL | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG06807 | hp1 | a0002 | c0002 | t0002 | g0020 | AFR | USA | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| HG06807 | hp2 | a0006 | c0010 | t0002 | g0016 | AFR | USA | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA20300 | hp1 | a0003 | c0005 | t0004 | g0129 | AFR | USA | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA20300 | hp2 | a0002 | c0002 | t0002 | g0065 | AFR | USA | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| NA21309 | hp2 | a0001 | c0004 | t0001 | g0197 | AFR | LWK | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0002 | g0087 | REF | REF | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0002 | REF | REF | FAM83D_chr20_38921417_38958106 | FAM83D | chr20 | 38921417 | 38958106 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:38926449 | C | A | 1 | a0012 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.7C>A | p.Leu3Met | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/4 | 33/2370 | 7/1758 | 3/585 | chr20 | 38926449 | |||
| chr20:38926473 | G | C | 9 | a0002 a0003 a0004 others(6): Show |
162 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(159): Show |
missense_variant | MODERATE | c.31G>C | p.Val11Leu | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/4 | 57/2370 | 31/1758 | 11/585 | chr20 | 38926473 | |||
| chr20:38926679 | C | CGCG | 2 | a0005 a0006 |
7 | HG00738.hp2 HG01192.hp2 HG01361.hp2 others(4): Show |
disruptive_inframe_insertion | MODERATE | c.255_257dupGGC | p.Ala86dup | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/4 | 284/2370 | 258/1758 | 86/585 | INFO_REALIGN_3_PRIME | chr20 | 38926679 | ||
| chr20:38926679 | C | CGCGGCG | 1 | a0007 | 3 | HG02451.hp2 NA18969.hp1 NA18986.hp2 |
disruptive_inframe_insertion | MODERATE | c.252_257dupGGCGGC | p.Ala85_Ala86dup | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/4 | 284/2370 | 258/1758 | 86/585 | INFO_REALIGN_3_PRIME | chr20 | 38926679 | ||
| chr20:38926679 | CGCG | C | 1 | a0003 | 9 | HG01361.hp1 HG02145.hp2 HG02559.hp1 others(6): Show |
disruptive_inframe_deletion | MODERATE | c.255_257delGGC | p.Ala86del | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/4 | 281/2370 | 255/1758 | 85/585 | INFO_REALIGN_3_PRIME | chr20 | 38926679 | ||
| chr20:38926723 | A | G | 2 | a0004 a0014 |
8 | HG02258.hp2 HG02486.hp1 HG02572.hp1 others(5): Show |
missense_variant | MODERATE | c.281A>G | p.His94Arg | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/4 | 307/2370 | 281/1758 | 94/585 | chr20 | 38926723 | |||
| chr20:38941977 | G | A | 1 | a0009 | 2 | HG02630.hp2 HG02809.hp2 |
missense_variant | MODERATE | c.502G>A | p.Asp168Asn | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/4 | 528/2370 | 502/1758 | 168/585 | chr20 | 38941977 | |||
| chr20:38951550 | C | T | 1 | a0015 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.788C>T | p.Thr263Met | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 4/4 | 814/2370 | 788/1758 | 263/585 | chr20 | 38951550 | |||
| chr20:38951673 | A | G | 2 | a0003 a0006 |
5 | HG02145.hp2 HG02280.hp1 HG02622.hp2 others(2): Show |
missense_variant | MODERATE | c.911A>G | p.His304Arg | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 4/4 | 937/2370 | 911/1758 | 304/585 | chr20 | 38951673 | |||
| chr20:38951742 | G | A | 1 | a0004 | 7 | HG02258.hp2 HG02486.hp1 HG02572.hp1 others(4): Show |
missense_variant | MODERATE | c.980G>A | p.Gly327Asp | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 4/4 | 1006/2370 | 980/1758 | 327/585 | chr20 | 38951742 | |||
| chr20:38951928 | C | A | 1 | a0016 | 1 | NA18953.hp2 | missense_variant | MODERATE | c.1166C>A | p.Ala389Asp | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 4/4 | 1192/2370 | 1166/1758 | 389/585 | chr20 | 38951928 | |||
| chr20:38951972 | G | A | 1 | a0008 | 2 | HG02083.hp2 NA19063.hp2 |
missense_variant | MODERATE | c.1210G>A | p.Val404Met | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 4/4 | 1236/2370 | 1210/1758 | 404/585 | chr20 | 38951972 | |||
| chr20:38952015 | C | G | 1 | a0013 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.1253C>G | p.Ala418Gly | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 4/4 | 1279/2370 | 1253/1758 | 418/585 | chr20 | 38952015 | |||
| chr20:38952027 | C | G | 1 | a0011 | 1 | HG01099.hp2 | missense_variant | MODERATE | c.1265C>G | p.Thr422Ser | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 4/4 | 1291/2370 | 1265/1758 | 422/585 | chr20 | 38952027 | |||
| chr20:38952041 | A | G | 1 | a0016 | 1 | NA18953.hp2 | missense_variant | MODERATE | c.1279A>G | p.Arg427Gly | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 4/4 | 1305/2370 | 1279/1758 | 427/585 | chr20 | 38952041 | |||
| chr20:38952353 | C | T | 1 | a0010 | 2 | NA19012.hp1 NA19076.hp1 |
missense_variant | MODERATE | c.1591C>T | p.Arg531Trp | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 4/4 | 1617/2370 | 1591/1758 | 531/585 | chr20 | 38952353 | |||
| chr20:38952371 | G | GGTATCAG others(3): Show |
1 | a0017 | 1 | NA18959.hp1 | frameshift_variant | HIGH | c.1610_1619dupGTATCA others(4): Show |
p.Arg541fs | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 4/4 | 1646/2370 | 1620/1758 | 540/585 | INFO_REALIGN_3_PRIME | chr20 | 38952371 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:38926457 | C | T | 1 | a0002c0014 | 2 | HG02257.hp1 HG02809.hp1 |
synonymous_variant | LOW | c.15C>T | p.Ser5Ser | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/4 | 41/2370 | 15/1758 | 5/585 | chr20 | 38926457 | |||
| chr20:38926505 | G | A | 1 | a0001c0022 | 1 | NA18999.hp2 | synonymous_variant | LOW | c.63G>A | p.Pro21Pro | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/4 | 89/2370 | 63/1758 | 21/585 | chr20 | 38926505 | |||
| chr20:38926742 | C | T | 1 | a0002c0019 | 1 | NA18950.hp2 | synonymous_variant | LOW | c.300C>T | p.Thr100Thr | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/4 | 326/2370 | 300/1758 | 100/585 | chr20 | 38926742 | |||
| chr20:38942082 | C | T | 15 | a0001c0004 a0002c0002 a0002c0014 others(12): Show |
167 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(164): Show |
synonymous_variant | LOW | c.607C>T | p.Leu203Leu | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/4 | 633/2370 | 607/1758 | 203/585 | chr20 | 38942082 | |||
| chr20:38947980 | C | T | 2 | a0003c0008 a0006c0010 |
5 | HG02145.hp2 HG02280.hp1 HG02622.hp2 others(2): Show |
synonymous_variant | LOW | c.756C>T | p.Arg252Arg | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/4 | 782/2370 | 756/1758 | 252/585 | chr20 | 38947980 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:38926417 | G | C | 2 | a0002c0002t0008 a0002c0006t0007 |
2 | NA18980.hp1 NA18994.hp1 |
5_prime_UTR_variant | MODIFIER | c.-26G>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/4 | 26 | chr20 | 38926417 | ||||||
| chr20:38952735 | T | C | 1 | a0001c0001t0005 | 2 | HG02896.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*215T>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 4/4 | 215 | chr20 | 38952735 | ||||||
| chr20:38952794 | A | G | 6 | a0002c0002t0002 a0002c0002t0008 a0002c0019t0002 others(3): Show |
99 | HG00280.hp1 HG00544.hp2 HG00597.hp1 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*274A>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 4/4 | 274 | chr20 | 38952794 | ||||||
| chr20:38952814 | T | C | 1 | a0004c0003t0006 | 2 | HG02895.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*294T>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 4/4 | 294 | chr20 | 38952814 | ||||||
| chr20:38952863 | G | A | 18 | a0002c0002t0002 a0002c0002t0003 a0002c0002t0004 others(15): Show |
156 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(153): Show |
3_prime_UTR_variant | MODIFIER | c.*343G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 4/4 | 343 | chr20 | 38952863 | ||||||
| chr20:38952925 | G | A | 1 | a0002c0002t0009 | 1 | HG00423.hp2 | 3_prime_UTR_variant | MODIFIER | c.*405G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 4/4 | 405 | chr20 | 38952925 | ||||||
| chr20:38952929 | A | G | 1 | a0001c0001t0010 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*409A>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 4/4 | 409 | chr20 | 38952929 | ||||||
| chr20:38953064 | C | T | 3 | a0002c0002t0003 a0002c0002t0009 a0011c0017t0003 |
33 | HG00099.hp2 HG00423.hp2 HG01099.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*544C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 4/4 | 544 | chr20 | 38953064 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:38927122 | C | T | 1 | a0001c0001t0001g0231 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.483+197C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38927122 | |||||||
| chr20:38927339 | C | T | 1 | a0012c0015t0004g0230 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.483+414C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38927339 | |||||||
| chr20:38927432 | T | A | 117 | a0001c0001t0001g0059 a0002c0002t0001g0097 a0002c0002t0002g0001 others(114): Show |
163 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.483+507T>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38927432 | |||||||
| chr20:38927498 | C | CT | 26 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0222 others(23): Show |
29 | HG00741.hp2 HG01106.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.483+595dupT | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr20 | 38927498 | ||||||
| chr20:38927498 | C | CTT | 29 | a0002c0002t0002g0131 a0002c0002t0003g0007 a0002c0002t0003g0012 others(26): Show |
40 | HG00099.hp2 HG01099.hp2 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.483+594_483+595dup others(2): Show |
FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr20 | 38927498 | ||||||
| chr20:38927498 | C | CTTT | 5 | a0002c0002t0003g0026 a0002c0002t0003g0136 a0002c0002t0003g0137 others(2): Show |
6 | HG00423.hp2 HG01891.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.483+593_483+595dup others(3): Show |
FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr20 | 38927498 | ||||||
| chr20:38927498 | CT | C | 16 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0139 others(13): Show |
17 | HG01099.hp1 HG02630.hp2 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.483+595delT | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr20 | 38927498 | ||||||
| chr20:38927563 | A | G | 1 | a0005c0007t0001g0221 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.483+638A>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38927563 | |||||||
| chr20:38927727 | G | A | 1 | a0002c0002t0002g0044 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.483+802G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38927727 | |||||||
| chr20:38927978 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.483+1053T>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38927978 | |||||||
| chr20:38928227 | G | A | 3 | a0002c0002t0004g0098 a0012c0015t0004g0230 a0013c0018t0004g0099 |
3 | HG01884.hp1 HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.483+1302G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38928227 | |||||||
| chr20:38928343 | G | A | 1 | a0002c0002t0002g0100 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.483+1418G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38928343 | |||||||
| chr20:38928363 | C | T | 1 | a0010c0013t0001g0220 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.483+1438C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38928363 | |||||||
| chr20:38928424 | G | A | 2 | a0002c0002t0004g0045 a0002c0002t0004g0101 |
2 | HG01884.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.483+1499G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38928424 | |||||||
| chr20:38928542 | G | C | 113 | a0001c0001t0001g0059 a0002c0002t0002g0001 a0002c0002t0002g0003 others(110): Show |
159 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.483+1617G>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38928542 | |||||||
| chr20:38928704 | G | A | 1 | a0002c0002t0004g0046 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.483+1779G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38928704 | |||||||
| chr20:38928820 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.483+1895T>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38928820 | |||||||
| chr20:38928872 | A | G | 1 | a0001c0001t0001g0037 | 2 | HG00408.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.483+1947A>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38928872 | |||||||
| chr20:38928905 | A | G | 112 | a0001c0001t0001g0059 a0002c0002t0002g0001 a0002c0002t0002g0003 others(109): Show |
158 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.483+1980A>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38928905 | |||||||
| chr20:38928905 | A | T | 1 | a0002c0002t0004g0108 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.483+1980A>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38928905 | |||||||
| chr20:38928965 | T | TCAGGAGT others(7): Show |
1 | a0010c0013t0001g0219 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.483+2044_483+2057d others(16): Show |
FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr20 | 38928965 | ||||||
| chr20:38928986 | G | A | 5 | a0003c0008t0002g0016 a0003c0008t0002g0047 a0003c0008t0002g0048 others(2): Show |
5 | HG02145.hp2 HG02280.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.483+2061G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38928986 | |||||||
| chr20:38929005 | C | T | 3 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 |
3 | NA18979.hp2 NA19010.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.483+2080C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38929005 | |||||||
| chr20:38929125 | T | C | 28 | a0002c0002t0003g0007 a0002c0002t0003g0012 a0002c0002t0003g0022 others(25): Show |
38 | HG00099.hp2 HG00423.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.483+2200T>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38929125 | |||||||
| chr20:38929157 | G | C | 1 | a0002c0002t0003g0112 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.483+2232G>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38929157 | |||||||
| chr20:38929179 | G | GA | 20 | a0001c0001t0001g0013 a0001c0001t0001g0029 a0001c0001t0001g0150 others(17): Show |
23 | HG00544.hp1 HG00544.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.483+2273dupA | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr20 | 38929179 | ||||||
| chr20:38929179 | GA | G | 25 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(22): Show |
34 | HG00099.hp2 HG00423.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.483+2273delA | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr20 | 38929179 | ||||||
| chr20:38929196 | A | T | 2 | a0001c0001t0001g0214 a0001c0001t0001g0215 |
2 | HG02040.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.483+2271A>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38929196 | |||||||
| chr20:38929201 | C | G | 10 | a0002c0002t0004g0098 a0002c0002t0004g0108 a0004c0003t0004g0025 others(7): Show |
12 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.483+2276C>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38929201 | |||||||
| chr20:38929207 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.483+2282G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38929207 | |||||||
| chr20:38929251 | A | G | 68 | a0001c0001t0001g0059 a0002c0002t0002g0001 a0002c0002t0002g0003 others(65): Show |
101 | HG00280.hp1 HG00544.hp2 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.483+2326A>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38929251 | |||||||
| chr20:38929456 | G | A | 25 | a0002c0002t0003g0007 a0002c0002t0003g0012 a0002c0002t0003g0022 others(22): Show |
35 | HG00099.hp2 HG00423.hp2 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.483+2531G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38929456 | |||||||
| chr20:38929503 | A | G | 7 | a0002c0014t0004g0056 a0002c0014t0004g0057 a0003c0005t0004g0021 others(4): Show |
8 | HG01361.hp1 HG02257.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.483+2578A>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38929503 | |||||||
| chr20:38929566 | G | A | 6 | a0002c0002t0003g0012 a0002c0002t0003g0022 a0002c0002t0003g0113 others(3): Show |
9 | HG01243.hp1 HG02886.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.483+2641G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38929566 | |||||||
| chr20:38929627 | A | G | 67 | a0001c0001t0001g0059 a0002c0002t0002g0001 a0002c0002t0002g0003 others(64): Show |
100 | HG00280.hp1 HG00544.hp2 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.483+2702A>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38929627 | |||||||
| chr20:38929648 | T | A | 2 | a0003c0005t0004g0103 a0003c0005t0004g0104 |
2 | HG01361.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.483+2723T>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38929648 | |||||||
| chr20:38929650 | T | C | 113 | a0001c0001t0001g0059 a0002c0002t0002g0001 a0002c0002t0002g0003 others(110): Show |
159 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.483+2725T>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38929650 | |||||||
| chr20:38929790 | T | TA | 13 | a0001c0001t0001g0059 a0001c0001t0001g0150 a0001c0001t0001g0159 others(10): Show |
13 | HG00423.hp2 HG00738.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.483+2884dupA | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr20 | 38929790 | ||||||
| chr20:38929790 | TA | T | 9 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0210 others(6): Show |
9 | HG01081.hp2 HG02897.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.483+2884delA | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr20 | 38929790 | ||||||
| chr20:38929837 | T | A | 28 | a0002c0002t0003g0007 a0002c0002t0003g0012 a0002c0002t0003g0022 others(25): Show |
38 | HG00099.hp2 HG00423.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.483+2912T>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38929837 | |||||||
| chr20:38930021 | G | A | 1 | a0002c0002t0002g0063 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.483+3096G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38930021 | |||||||
| chr20:38930227 | G | A | 1 | a0004c0003t0006g0024 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.483+3302G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38930227 | |||||||
| chr20:38930236 | G | A | 1 | a0002c0002t0002g0064 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.483+3311G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38930236 | |||||||
| chr20:38930368 | C | T | 1 | a0002c0002t0002g0094 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.483+3443C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38930368 | |||||||
| chr20:38930391 | G | A | 27 | a0002c0002t0003g0007 a0002c0002t0003g0012 a0002c0002t0003g0022 others(24): Show |
37 | HG00099.hp2 HG00423.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.483+3466G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38930391 | |||||||
| chr20:38930455 | G | A | 1 | a0002c0006t0001g0120 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.483+3530G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38930455 | |||||||
| chr20:38930565 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.483+3640C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38930565 | |||||||
| chr20:38930606 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.483+3681G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38930606 | |||||||
| chr20:38930686 | G | T | 111 | a0002c0002t0002g0001 a0002c0002t0002g0003 a0002c0002t0002g0010 others(108): Show |
157 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.483+3761G>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38930686 | |||||||
| chr20:38930702 | C | T | 1 | a0002c0002t0004g0046 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.483+3777C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38930702 | |||||||
| chr20:38930872 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.483+3947G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38930872 | |||||||
| chr20:38930894 | C | T | 3 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0213 |
3 | HG01069.hp1 HG01071.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.483+3969C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38930894 | |||||||
| chr20:38930931 | C | T | 28 | a0002c0002t0003g0007 a0002c0002t0003g0012 a0002c0002t0003g0022 others(25): Show |
38 | HG00099.hp2 HG00423.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.483+4006C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38930931 | |||||||
| chr20:38931139 | T | C | 1 | a0002c0002t0004g0046 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.483+4214T>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38931139 | |||||||
| chr20:38931144 | T | C | 1 | a0004c0003t0006g0024 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.483+4219T>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38931144 | |||||||
| chr20:38931309 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.483+4384C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38931309 | |||||||
| chr20:38931549 | G | A | 2 | a0002c0002t0003g0023 a0002c0002t0003g0121 |
3 | NA18970.hp1 NA19079.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.483+4624G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38931549 | |||||||
| chr20:38931743 | C | T | 29 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(26): Show |
50 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.483+4818C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38931743 | |||||||
| chr20:38931758 | A | G | 3 | a0001c0001t0001g0154 a0008c0012t0001g0202 a0008c0012t0001g0229 |
3 | HG02083.hp2 NA19060.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.483+4833A>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38931758 | |||||||
| chr20:38932135 | C | T | 3 | a0003c0005t0004g0021 a0003c0005t0004g0129 a0003c0005t0004g0130 |
4 | HG02559.hp1 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.483+5210C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38932135 | |||||||
| chr20:38932275 | A | G | 5 | a0003c0005t0004g0021 a0003c0005t0004g0103 a0003c0005t0004g0104 others(2): Show |
6 | HG01361.hp1 HG02559.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.483+5350A>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38932275 | |||||||
| chr20:38932379 | C | T | 26 | a0002c0002t0003g0007 a0002c0002t0003g0012 a0002c0002t0003g0022 others(23): Show |
36 | HG00099.hp2 HG00423.hp2 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.483+5454C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38932379 | |||||||
| chr20:38932680 | C | T | 6 | a0002c0002t0003g0012 a0002c0002t0003g0022 a0002c0002t0003g0113 others(3): Show |
9 | HG01243.hp1 HG02886.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.483+5755C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38932680 | |||||||
| chr20:38932693 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.483+5768C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38932693 | |||||||
| chr20:38932694 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.483+5769A>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38932694 | |||||||
| chr20:38932920 | G | A | 1 | a0002c0002t0002g0065 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.483+5995G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38932920 | |||||||
| chr20:38933014 | G | A | 1 | a0012c0015t0004g0230 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.483+6089G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38933014 | |||||||
| chr20:38933062 | A | G | 2 | a0002c0002t0002g0054 a0002c0002t0002g0055 |
2 | HG00544.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.483+6137A>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38933062 | |||||||
| chr20:38933134 | G | T | 1 | a0004c0003t0004g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.483+6209G>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38933134 | |||||||
| chr20:38933405 | C | A | 1 | a0002c0002t0002g0060 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.483+6480C>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38933405 | |||||||
| chr20:38933425 | C | A | 1 | a0002c0002t0004g0046 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.483+6500C>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38933425 | |||||||
| chr20:38933441 | C | G | 1 | a0001c0001t0001g0201 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.483+6516C>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38933441 | |||||||
| chr20:38933623 | C | T | 28 | a0002c0002t0003g0007 a0002c0002t0003g0012 a0002c0002t0003g0022 others(25): Show |
38 | HG00099.hp2 HG00423.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.483+6698C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38933623 | |||||||
| chr20:38933864 | CT | C | 8 | a0002c0002t0002g0066 a0002c0014t0004g0056 a0002c0014t0004g0057 others(5): Show |
9 | HG01361.hp1 HG02257.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.483+6952delT | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr20 | 38933864 | ||||||
| chr20:38933886 | C | T | 1 | a0002c0002t0004g0046 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.483+6961C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38933886 | |||||||
| chr20:38933887 | G | A | 14 | a0002c0002t0003g0007 a0002c0002t0003g0023 a0002c0002t0003g0026 others(11): Show |
21 | HG00099.hp2 HG00423.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.483+6962G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38933887 | |||||||
| chr20:38933948 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.483+7023G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38933948 | |||||||
| chr20:38934032 | T | G | 1 | a0001c0001t0001g0162 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.483+7107T>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38934032 | |||||||
| chr20:38934053 | A | C | 1 | a0002c0002t0004g0046 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.483+7128A>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38934053 | |||||||
| chr20:38934133 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.483+7208C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38934133 | |||||||
| chr20:38934190 | CT | C | 28 | a0002c0002t0003g0007 a0002c0002t0003g0012 a0002c0002t0003g0022 others(25): Show |
38 | HG00099.hp2 HG00423.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.483+7266delT | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38934190 | |||||||
| chr20:38934194 | CAGACAGT others(6): Show |
C | 28 | a0002c0002t0003g0007 a0002c0002t0003g0012 a0002c0002t0003g0022 others(25): Show |
38 | HG00099.hp2 HG00423.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.483+7270_483+7282d others(15): Show |
FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38934194 | |||||||
| chr20:38934293 | A | G | 28 | a0002c0002t0003g0007 a0002c0002t0003g0012 a0002c0002t0003g0022 others(25): Show |
38 | HG00099.hp2 HG00423.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.483+7368A>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38934293 | |||||||
| chr20:38934463 | G | A | 1 | a0002c0002t0004g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.484-7496G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38934463 | |||||||
| chr20:38934488 | C | T | 1 | a0006c0021t0004g0127 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.484-7471C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38934488 | |||||||
| chr20:38934493 | C | CA | 99 | a0001c0001t0001g0030 a0001c0001t0001g0059 a0001c0001t0001g0139 others(96): Show |
135 | HG00280.hp1 HG00544.hp2 HG00597.hp1 others(132): Show |
intron_variant | MODIFIER | c.484-7445dupA | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr20 | 38934493 | ||||||
| chr20:38934493 | C | CAA | 6 | a0001c0001t0001g0151 a0001c0001t0001g0163 a0002c0002t0002g0017 others(3): Show |
7 | HG01884.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.484-7446_484-7445d others(4): Show |
FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr20 | 38934493 | ||||||
| chr20:38934493 | CA | C | 11 | a0001c0001t0001g0145 a0001c0001t0001g0198 a0001c0001t0005g0196 others(8): Show |
11 | HG01069.hp2 HG02055.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.484-7445delA | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr20 | 38934493 | ||||||
| chr20:38934698 | A | C | 4 | a0002c0002t0003g0012 a0002c0002t0003g0113 a0002c0002t0003g0118 others(1): Show |
6 | HG01243.hp1 HG02886.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.484-7261A>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38934698 | |||||||
| chr20:38934709 | G | A | 50 | a0001c0001t0001g0059 a0002c0002t0002g0001 a0002c0002t0002g0003 others(47): Show |
80 | HG00280.hp1 HG00544.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.484-7250G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38934709 | |||||||
| chr20:38934783 | C | T | 1 | a0002c0002t0004g0046 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.484-7176C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38934783 | |||||||
| chr20:38934923 | G | A | 2 | a0001c0001t0001g0162 a0001c0001t0001g0169 |
2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.484-7036G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38934923 | |||||||
| chr20:38934975 | T | C | 1 | a0002c0002t0002g0040 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.484-6984T>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38934975 | |||||||
| chr20:38934982 | A | C | 1 | a0002c0002t0003g0124 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.484-6977A>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38934982 | |||||||
| chr20:38935504 | G | T | 1 | a0001c0001t0001g0158 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.484-6455G>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38935504 | |||||||
| chr20:38935557 | C | T | 1 | a0002c0002t0002g0095 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.484-6402C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38935557 | |||||||
| chr20:38935608 | T | A | 2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.484-6351T>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38935608 | |||||||
| chr20:38935740 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.484-6219C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38935740 | |||||||
| chr20:38935741 | G | A | 3 | a0002c0002t0002g0058 a0002c0002t0002g0068 a0002c0002t0002g0106 |
3 | HG02165.hp2 NA18939.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.484-6218G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38935741 | |||||||
| chr20:38935878 | G | A | 24 | a0002c0002t0003g0007 a0002c0002t0003g0012 a0002c0002t0003g0022 others(21): Show |
34 | HG00099.hp2 HG00423.hp2 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.484-6081G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38935878 | |||||||
| chr20:38935883 | T | C | 1 | a0001c0022t0001g0141 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.484-6076T>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38935883 | |||||||
| chr20:38935886 | A | G | 2 | a0003c0005t0004g0103 a0003c0005t0004g0104 |
2 | HG01361.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.484-6073A>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38935886 | |||||||
| chr20:38935897 | A | G | 1 | a0002c0002t0002g0060 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.484-6062A>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38935897 | |||||||
| chr20:38936035 | T | C | 1 | a0002c0002t0004g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.484-5924T>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38936035 | |||||||
| chr20:38936080 | G | A | 28 | a0002c0002t0003g0007 a0002c0002t0003g0012 a0002c0002t0003g0022 others(25): Show |
38 | HG00099.hp2 HG00423.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.484-5879G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38936080 | |||||||
| chr20:38936188 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.484-5771G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38936188 | |||||||
| chr20:38936192 | C | T | 28 | a0002c0002t0003g0007 a0002c0002t0003g0012 a0002c0002t0003g0022 others(25): Show |
38 | HG00099.hp2 HG00423.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.484-5767C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38936192 | |||||||
| chr20:38936402 | C | T | 5 | a0003c0008t0002g0016 a0003c0008t0002g0047 a0003c0008t0002g0048 others(2): Show |
5 | HG02145.hp2 HG02280.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.484-5557C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38936402 | |||||||
| chr20:38936447 | C | G | 1 | a0001c0004t0001g0199 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.484-5512C>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38936447 | |||||||
| chr20:38936536 | G | A | 2 | a0002c0002t0002g0066 a0002c0002t0002g0069 |
2 | NA18989.hp1 NA19059.hp2 |
intron_variant | MODIFIER | c.484-5423G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38936536 | |||||||
| chr20:38936692 | T | C | 111 | a0002c0002t0002g0001 a0002c0002t0002g0003 a0002c0002t0002g0010 others(108): Show |
157 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.484-5267T>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38936692 | |||||||
| chr20:38936751 | A | G | 2 | a0002c0002t0002g0085 a0002c0002t0002g0086 |
2 | HG01496.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.484-5208A>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38936751 | |||||||
| chr20:38936791 | A | T | 1 | a0001c0001t0001g0198 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.484-5168A>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38936791 | |||||||
| chr20:38937107 | C | T | 1 | a0002c0002t0002g0084 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.484-4852C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38937107 | |||||||
| chr20:38937112 | C | T | 25 | a0002c0002t0003g0007 a0002c0002t0003g0012 a0002c0002t0003g0022 others(22): Show |
35 | HG00099.hp2 HG00423.hp2 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.484-4847C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38937112 | |||||||
| chr20:38937123 | C | T | 1 | a0002c0002t0008g0083 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.484-4836C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38937123 | |||||||
| chr20:38937229 | C | G | 1 | a0001c0001t0001g0168 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.484-4730C>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38937229 | |||||||
| chr20:38937351 | GC | G | 61 | a0002c0002t0002g0001 a0002c0002t0002g0003 a0002c0002t0002g0010 others(58): Show |
94 | HG00280.hp1 HG00544.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.484-4606delC | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr20 | 38937351 | ||||||
| chr20:38937425 | C | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0029 a0001c0001t0001g0034 others(3): Show |
12 | HG00558.hp1 HG02056.hp2 NA18950.hp1 others(9): Show |
intron_variant | MODIFIER | c.484-4534C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38937425 | |||||||
| chr20:38937729 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.484-4230G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38937729 | |||||||
| chr20:38938068 | C | T | 1 | a0002c0002t0002g0086 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.484-3891C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38938068 | |||||||
| chr20:38938094 | T | C | 62 | a0002c0002t0002g0001 a0002c0002t0002g0003 a0002c0002t0002g0010 others(59): Show |
95 | HG00280.hp1 HG00544.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.484-3865T>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38938094 | |||||||
| chr20:38938157 | A | G | 1 | a0002c0002t0004g0101 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.484-3802A>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38938157 | |||||||
| chr20:38938259 | G | T | 1 | a0002c0002t0002g0058 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.484-3700G>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38938259 | |||||||
| chr20:38938288 | A | C | 2 | a0002c0002t0004g0045 a0002c0002t0004g0046 |
2 | HG01884.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.484-3671A>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38938288 | |||||||
| chr20:38938305 | G | T | 5 | a0004c0003t0004g0025 a0004c0003t0004g0133 a0004c0003t0004g0134 others(2): Show |
7 | HG02258.hp2 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.484-3654G>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38938305 | |||||||
| chr20:38938449 | C | T | 1 | a0002c0002t0004g0046 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.484-3510C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38938449 | |||||||
| chr20:38938522 | G | A | 2 | a0003c0005t0004g0103 a0003c0005t0004g0104 |
2 | HG01361.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.484-3437G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38938522 | |||||||
| chr20:38938585 | A | T | 1 | a0002c0002t0002g0092 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.484-3374A>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38938585 | |||||||
| chr20:38938614 | C | G | 6 | a0003c0005t0004g0021 a0003c0005t0004g0103 a0003c0005t0004g0104 others(3): Show |
7 | HG01361.hp1 HG02559.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.484-3345C>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38938614 | |||||||
| chr20:38938622 | G | A | 1 | a0002c0002t0002g0070 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.484-3337G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38938622 | |||||||
| chr20:38938712 | A | G | 5 | a0004c0003t0004g0025 a0004c0003t0004g0133 a0004c0003t0004g0134 others(2): Show |
7 | HG02258.hp2 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.484-3247A>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38938712 | |||||||
| chr20:38938716 | C | T | 1 | a0002c0002t0002g0082 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.484-3243C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38938716 | |||||||
| chr20:38938780 | G | GCTA | 5 | a0003c0008t0002g0016 a0003c0008t0002g0047 a0003c0008t0002g0048 others(2): Show |
5 | HG02145.hp2 HG02280.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.484-3176_484-3174d others(5): Show |
FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr20 | 38938780 | ||||||
| chr20:38938940 | T | C | 1 | a0001c0001t0001g0150 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.484-3019T>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38938940 | |||||||
| chr20:38938942 | C | A | 1 | a0001c0001t0001g0150 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.484-3017C>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38938942 | |||||||
| chr20:38938977 | C | T | 2 | a0002c0002t0002g0044 a0002c0002t0002g0091 |
2 | HG02055.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.484-2982C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38938977 | |||||||
| chr20:38939066 | C | A | 1 | a0001c0001t0001g0173 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.484-2893C>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38939066 | |||||||
| chr20:38939287 | A | G | 2 | a0002c0002t0003g0022 a0002c0002t0003g0117 |
3 | HG02896.hp1 HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.484-2672A>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38939287 | |||||||
| chr20:38939306 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.484-2653C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38939306 | |||||||
| chr20:38939336 | T | TTTTTG | 5 | a0003c0008t0002g0016 a0003c0008t0002g0047 a0003c0008t0002g0048 others(2): Show |
5 | HG02145.hp2 HG02280.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.484-2598_484-2594d others(7): Show |
FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr20 | 38939336 | ||||||
| chr20:38939336 | TTTTTG | T | 27 | a0001c0001t0001g0162 a0002c0002t0003g0007 a0002c0002t0003g0012 others(24): Show |
37 | HG00099.hp2 HG00423.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.484-2598_484-2594d others(7): Show |
FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr20 | 38939336 | ||||||
| chr20:38939412 | C | T | 24 | a0002c0002t0003g0007 a0002c0002t0003g0012 a0002c0002t0003g0022 others(21): Show |
34 | HG00099.hp2 HG00423.hp2 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.484-2547C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38939412 | |||||||
| chr20:38939488 | G | A | 1 | a0002c0002t0004g0101 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.484-2471G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38939488 | |||||||
| chr20:38939519 | T | C | 1 | a0002c0002t0004g0108 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.484-2440T>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38939519 | |||||||
| chr20:38939823 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.484-2136T>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38939823 | |||||||
| chr20:38939856 | T | C | 1 | a0001c0004t0001g0174 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.484-2103T>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38939856 | |||||||
| chr20:38940039 | C | A | 5 | a0004c0003t0004g0025 a0004c0003t0004g0133 a0004c0003t0004g0134 others(2): Show |
7 | HG02258.hp2 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.484-1920C>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38940039 | |||||||
| chr20:38940069 | A | G | 1 | a0002c0002t0002g0081 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.484-1890A>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38940069 | |||||||
| chr20:38940134 | G | A | 1 | a0011c0017t0003g0125 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.484-1825G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38940134 | |||||||
| chr20:38940465 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.484-1494C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38940465 | |||||||
| chr20:38940473 | G | A | 3 | a0002c0002t0002g0066 a0002c0002t0002g0069 a0002c0002t0002g0071 |
3 | NA18980.hp2 NA18989.hp1 NA19059.hp2 |
intron_variant | MODIFIER | c.484-1486G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38940473 | |||||||
| chr20:38940600 | A | G | 1 | a0012c0015t0004g0230 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.484-1359A>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38940600 | |||||||
| chr20:38940759 | A | G | 33 | a0002c0002t0003g0007 a0002c0002t0003g0012 a0002c0002t0003g0022 others(30): Show |
44 | HG00099.hp2 HG00423.hp2 HG01099.hp2 others(41): Show |
intron_variant | MODIFIER | c.484-1200A>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38940759 | |||||||
| chr20:38940775 | A | C | 2 | a0007c0009t0001g0191 a0007c0009t0001g0192 |
2 | NA18969.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.484-1184A>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38940775 | |||||||
| chr20:38940821 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.484-1138C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38940821 | |||||||
| chr20:38941011 | A | T | 26 | a0002c0002t0003g0007 a0002c0002t0003g0012 a0002c0002t0003g0022 others(23): Show |
36 | HG00099.hp2 HG00423.hp2 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.484-948A>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38941011 | |||||||
| chr20:38941064 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.484-895T>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38941064 | |||||||
| chr20:38941179 | C | T | 2 | a0001c0001t0001g0227 a0002c0002t0002g0090 |
2 | HG02300.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.484-780C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38941179 | |||||||
| chr20:38941180 | G | A | 5 | a0003c0008t0002g0016 a0003c0008t0002g0047 a0003c0008t0002g0048 others(2): Show |
5 | HG02145.hp2 HG02280.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.484-779G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38941180 | |||||||
| chr20:38941346 | A | T | 1 | a0002c0002t0004g0046 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.484-613A>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38941346 | |||||||
| chr20:38941761 | G | T | 61 | a0002c0002t0002g0001 a0002c0002t0002g0003 a0002c0002t0002g0010 others(58): Show |
94 | HG00280.hp1 HG00544.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.484-198G>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38941761 | |||||||
| chr20:38941770 | C | T | 2 | a0002c0002t0002g0042 a0002c0002t0002g0080 |
2 | HG01099.hp1 HG01928.hp1 |
intron_variant | MODIFIER | c.484-189C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38941770 | |||||||
| chr20:38941774 | A | G | 1 | a0002c0002t0004g0108 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.484-185A>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38941774 | |||||||
| chr20:38941777 | G | A | 2 | a0002c0002t0004g0098 a0013c0018t0004g0099 |
2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.484-182G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38941777 | |||||||
| chr20:38941832 | G | A | 110 | a0002c0002t0002g0001 a0002c0002t0002g0003 a0002c0002t0002g0010 others(107): Show |
156 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.484-127G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38941832 | |||||||
| chr20:38941842 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.484-117G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38941842 | |||||||
| chr20:38941858 | G | A | 1 | a0002c0002t0004g0046 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.484-101G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38941858 | |||||||
| chr20:38941900 | C | T | 1 | a0003c0008t0002g0048 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.484-59C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38941900 | |||||||
| chr20:38941925 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.484-34G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 1/3 | chr20 | 38941925 | |||||||
| chr20:38942640 | G | A | 1 | a0002c0002t0004g0108 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.651+514G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38942640 | |||||||
| chr20:38942712 | T | A | 1 | a0001c0001t0001g0150 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.651+586T>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38942712 | |||||||
| chr20:38942726 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.651+600G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38942726 | |||||||
| chr20:38942897 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.651+771C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38942897 | |||||||
| chr20:38943024 | C | CT | 85 | a0001c0001t0001g0151 a0001c0001t0001g0158 a0001c0001t0001g0188 others(82): Show |
128 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.651+913dupT | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr20 | 38943024 | ||||||
| chr20:38943024 | C | CTT | 6 | a0002c0002t0002g0052 a0002c0002t0002g0053 a0002c0002t0002g0060 others(3): Show |
6 | HG01243.hp1 HG02970.hp2 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.651+912_651+913dup others(2): Show |
FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr20 | 38943024 | ||||||
| chr20:38943172 | G | A | 4 | a0001c0001t0001g0036 a0001c0001t0001g0145 a0001c0001t0001g0212 others(1): Show |
5 | HG02976.hp2 NA18982.hp2 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.651+1046G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38943172 | |||||||
| chr20:38943257 | C | T | 23 | a0002c0002t0003g0007 a0002c0002t0003g0012 a0002c0002t0003g0022 others(20): Show |
33 | HG00099.hp2 HG00423.hp2 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.651+1131C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38943257 | |||||||
| chr20:38943319 | C | T | 23 | a0002c0002t0003g0007 a0002c0002t0003g0012 a0002c0002t0003g0022 others(20): Show |
33 | HG00099.hp2 HG00423.hp2 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.651+1193C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38943319 | |||||||
| chr20:38943390 | A | G | 6 | a0003c0005t0004g0021 a0003c0005t0004g0103 a0003c0005t0004g0104 others(3): Show |
7 | HG01361.hp1 HG02559.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.651+1264A>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38943390 | |||||||
| chr20:38943422 | G | C | 2 | a0002c0014t0004g0056 a0002c0014t0004g0057 |
2 | HG02257.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.651+1296G>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38943422 | |||||||
| chr20:38943456 | G | C | 1 | a0002c0002t0004g0108 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.651+1330G>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38943456 | |||||||
| chr20:38943631 | C | G | 6 | a0003c0005t0004g0021 a0003c0005t0004g0103 a0003c0005t0004g0104 others(3): Show |
7 | HG01361.hp1 HG02559.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.651+1505C>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38943631 | |||||||
| chr20:38943722 | C | T | 1 | a0002c0002t0004g0101 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.651+1596C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38943722 | |||||||
| chr20:38943783 | C | T | 23 | a0002c0002t0003g0007 a0002c0002t0003g0012 a0002c0002t0003g0022 others(20): Show |
33 | HG00099.hp2 HG00423.hp2 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.651+1657C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38943783 | |||||||
| chr20:38943851 | C | T | 1 | a0001c0001t0001g0187 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.651+1725C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38943851 | |||||||
| chr20:38943852 | G | A | 27 | a0002c0002t0003g0007 a0002c0002t0003g0012 a0002c0002t0003g0022 others(24): Show |
37 | HG00099.hp2 HG00423.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.651+1726G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38943852 | |||||||
| chr20:38943953 | A | G | 2 | a0003c0005t0004g0103 a0003c0005t0004g0104 |
2 | HG01361.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.651+1827A>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38943953 | |||||||
| chr20:38944000 | G | A | 66 | a0002c0002t0002g0001 a0002c0002t0002g0003 a0002c0002t0002g0010 others(63): Show |
99 | HG00280.hp1 HG00544.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.651+1874G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38944000 | |||||||
| chr20:38944113 | T | A | 1 | a0001c0001t0001g0150 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.651+1987T>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38944113 | |||||||
| chr20:38944181 | A | G | 8 | a0002c0014t0004g0056 a0002c0014t0004g0057 a0003c0005t0004g0021 others(5): Show |
9 | HG01361.hp1 HG02257.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.651+2055A>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38944181 | |||||||
| chr20:38944271 | G | A | 4 | a0002c0002t0002g0072 a0002c0002t0002g0073 a0002c0002t0002g0084 others(1): Show |
4 | HG00280.hp1 HG04199.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.651+2145G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38944271 | |||||||
| chr20:38944399 | A | G | 1 | a0001c0004t0001g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.651+2273A>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38944399 | |||||||
| chr20:38944551 | A | G | 27 | a0002c0002t0003g0007 a0002c0002t0003g0012 a0002c0002t0003g0022 others(24): Show |
37 | HG00099.hp2 HG00423.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.651+2425A>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38944551 | |||||||
| chr20:38944578 | C | T | 9 | a0002c0002t0004g0098 a0002c0002t0004g0108 a0004c0003t0004g0025 others(6): Show |
11 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.651+2452C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38944578 | |||||||
| chr20:38944596 | T | C | 66 | a0002c0002t0002g0001 a0002c0002t0002g0003 a0002c0002t0002g0010 others(63): Show |
99 | HG00280.hp1 HG00544.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.651+2470T>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38944596 | |||||||
| chr20:38944675 | T | C | 1 | a0002c0002t0004g0046 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.651+2549T>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38944675 | |||||||
| chr20:38944765 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.651+2639G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38944765 | |||||||
| chr20:38944844 | A | C | 33 | a0002c0002t0003g0007 a0002c0002t0003g0012 a0002c0002t0003g0022 others(30): Show |
44 | HG00099.hp2 HG00423.hp2 HG01099.hp2 others(41): Show |
intron_variant | MODIFIER | c.651+2718A>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38944844 | |||||||
| chr20:38944893 | C | T | 3 | a0002c0002t0002g0066 a0002c0002t0002g0069 a0002c0002t0002g0071 |
3 | NA18980.hp2 NA18989.hp1 NA19059.hp2 |
intron_variant | MODIFIER | c.651+2767C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38944893 | |||||||
| chr20:38944938 | C | CA | 12 | a0002c0002t0002g0044 a0002c0002t0002g0067 a0002c0002t0003g0117 others(9): Show |
13 | HG01361.hp1 HG02055.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.651+2827dupA | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr20 | 38944938 | ||||||
| chr20:38945173 | G | A | 66 | a0002c0002t0002g0001 a0002c0002t0002g0003 a0002c0002t0002g0010 others(63): Show |
99 | HG00280.hp1 HG00544.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.652-2703G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38945173 | |||||||
| chr20:38945388 | C | T | 1 | a0002c0002t0002g0079 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.652-2488C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38945388 | |||||||
| chr20:38945586 | G | A | 1 | a0002c0002t0004g0046 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.652-2290G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38945586 | |||||||
| chr20:38945698 | C | T | 26 | a0002c0002t0003g0007 a0002c0002t0003g0012 a0002c0002t0003g0022 others(23): Show |
36 | HG00099.hp2 HG00423.hp2 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.652-2178C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38945698 | |||||||
| chr20:38945736 | A | AC | 98 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(95): Show |
133 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.652-2130dupC | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr20 | 38945736 | ||||||
| chr20:38945743 | C | G | 26 | a0002c0002t0003g0007 a0002c0002t0003g0012 a0002c0002t0003g0022 others(23): Show |
36 | HG00099.hp2 HG00423.hp2 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.652-2133C>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38945743 | |||||||
| chr20:38945744 | C | A | 2 | a0002c0002t0004g0098 a0013c0018t0004g0099 |
2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.652-2132C>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38945744 | |||||||
| chr20:38945746 | C | G | 1 | a0002c0002t0002g0061 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.652-2130C>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38945746 | |||||||
| chr20:38945755 | A | AC | 7 | a0001c0001t0001g0181 a0001c0001t0001g0226 a0003c0005t0004g0021 others(4): Show |
8 | HG02559.hp1 HG03041.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.652-2115dupC | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr20 | 38945755 | ||||||
| chr20:38945762 | G | T | 2 | a0003c0005t0004g0103 a0003c0005t0004g0104 |
2 | HG01361.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.652-2114G>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38945762 | |||||||
| chr20:38945763 | T | G | 1 | a0001c0001t0001g0150 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.652-2113T>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38945763 | |||||||
| chr20:38945772 | T | C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0029 a0001c0001t0001g0034 others(3): Show |
12 | HG00558.hp1 HG02056.hp2 NA18950.hp1 others(9): Show |
intron_variant | MODIFIER | c.652-2104T>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38945772 | |||||||
| chr20:38945804 | C | T | 2 | a0002c0014t0004g0056 a0002c0014t0004g0057 |
2 | HG02257.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.652-2072C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38945804 | |||||||
| chr20:38945816 | T | C | 9 | a0002c0002t0004g0098 a0002c0002t0004g0108 a0004c0003t0004g0025 others(6): Show |
11 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.652-2060T>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38945816 | |||||||
| chr20:38945868 | C | T | 1 | a0002c0002t0002g0073 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.652-2008C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38945868 | |||||||
| chr20:38945869 | G | A | 8 | a0002c0002t0004g0098 a0004c0003t0004g0025 a0004c0003t0004g0133 others(5): Show |
10 | HG01884.hp1 HG02258.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.652-2007G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38945869 | |||||||
| chr20:38945891 | C | T | 1 | a0004c0003t0006g0024 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.652-1985C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38945891 | |||||||
| chr20:38945892 | G | A | 3 | a0002c0002t0002g0131 a0003c0005t0004g0103 a0003c0005t0004g0104 |
3 | HG01361.hp1 HG03130.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.652-1984G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38945892 | |||||||
| chr20:38946010 | C | T | 1 | a0002c0002t0002g0076 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.652-1866C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38946010 | |||||||
| chr20:38946197 | C | CA | 40 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0015 others(37): Show |
49 | HG00423.hp1 HG00639.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.652-1656dupA | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr20 | 38946197 | ||||||
| chr20:38946197 | CA | C | 15 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0225 others(12): Show |
15 | HG00099.hp1 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.652-1656delA | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr20 | 38946197 | ||||||
| chr20:38946197 | CAA | C | 31 | a0002c0002t0002g0010 a0002c0002t0002g0040 a0002c0002t0002g0044 others(28): Show |
43 | HG00099.hp2 HG00423.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.652-1657_652-1656d others(4): Show |
FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr20 | 38946197 | ||||||
| chr20:38946197 | CAAA | C | 60 | a0002c0002t0002g0001 a0002c0002t0002g0003 a0002c0002t0002g0011 others(57): Show |
93 | HG00280.hp1 HG00544.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.652-1658_652-1656d others(5): Show |
FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr20 | 38946197 | ||||||
| chr20:38946197 | CAAAA | C | 7 | a0002c0002t0002g0095 a0003c0005t0004g0021 a0003c0005t0004g0103 others(4): Show |
8 | HG01361.hp1 HG02559.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.652-1659_652-1656d others(6): Show |
FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr20 | 38946197 | ||||||
| chr20:38946214 | A | C | 14 | a0002c0002t0004g0098 a0003c0005t0004g0021 a0003c0005t0004g0103 others(11): Show |
17 | HG01361.hp1 HG01884.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.652-1662A>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38946214 | |||||||
| chr20:38946215 | A | C | 1 | a0001c0001t0001g0180 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.652-1661A>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38946215 | |||||||
| chr20:38946217 | A | C | 1 | a0002c0002t0009g0135 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.652-1659A>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38946217 | |||||||
| chr20:38946218 | A | C | 1 | a0001c0004t0001g0195 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.652-1658A>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38946218 | |||||||
| chr20:38946223 | A | T | 1 | a0016c0023t0001g0194 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.652-1653A>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38946223 | |||||||
| chr20:38946279 | G | A | 2 | a0002c0014t0004g0056 a0002c0014t0004g0057 |
2 | HG02257.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.652-1597G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38946279 | |||||||
| chr20:38946387 | T | A | 1 | a0001c0001t0001g0150 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.652-1489T>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38946387 | |||||||
| chr20:38946400 | C | T | 1 | a0002c0002t0002g0063 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.652-1476C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38946400 | |||||||
| chr20:38946705 | T | A | 1 | a0001c0001t0001g0150 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.652-1171T>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38946705 | |||||||
| chr20:38946830 | T | TC | 26 | a0002c0002t0003g0007 a0002c0002t0003g0012 a0002c0002t0003g0022 others(23): Show |
36 | HG00099.hp2 HG00423.hp2 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.652-1044dupC | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr20 | 38946830 | ||||||
| chr20:38947106 | G | A | 1 | a0002c0002t0002g0042 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.652-770G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38947106 | |||||||
| chr20:38947187 | C | T | 1 | a0002c0002t0002g0095 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.652-689C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38947187 | |||||||
| chr20:38947222 | A | T | 1 | a0002c0002t0002g0078 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.652-654A>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38947222 | |||||||
| chr20:38947223 | T | C | 1 | a0002c0002t0002g0078 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.652-653T>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38947223 | |||||||
| chr20:38947244 | C | T | 1 | a0002c0002t0004g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.652-632C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38947244 | |||||||
| chr20:38947253 | G | A | 1 | a0002c0002t0002g0089 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.652-623G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38947253 | |||||||
| chr20:38947278 | G | A | 2 | a0001c0004t0001g0197 a0002c0002t0001g0097 |
2 | HG03453.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.652-598G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38947278 | |||||||
| chr20:38947517 | T | C | 4 | a0001c0001t0001g0031 a0001c0001t0001g0182 a0001c0001t0001g0209 others(1): Show |
5 | HG00639.hp1 HG01081.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.652-359T>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38947517 | |||||||
| chr20:38947612 | G | A | 59 | a0002c0002t0002g0001 a0002c0002t0002g0003 a0002c0002t0002g0010 others(56): Show |
91 | HG00280.hp1 HG00544.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.652-264G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38947612 | |||||||
| chr20:38947705 | T | C | 3 | a0001c0001t0001g0038 a0001c0001t0001g0184 a0001c0001t0001g0227 |
4 | HG01106.hp1 HG01109.hp1 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.652-171T>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 2/3 | chr20 | 38947705 | |||||||
| chr20:38948126 | C | T | 1 | a0002c0002t0002g0051 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.776+126C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38948126 | |||||||
| chr20:38948191 | T | C | 1 | a0001c0001t0001g0205 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.776+191T>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38948191 | |||||||
| chr20:38948279 | A | G | 14 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0139 others(11): Show |
16 | HG01109.hp2 HG01167.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.776+279A>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38948279 | |||||||
| chr20:38948291 | G | T | 2 | a0002c0014t0004g0056 a0002c0014t0004g0057 |
2 | HG02257.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.776+291G>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38948291 | |||||||
| chr20:38948378 | A | C | 1 | a0001c0001t0001g0207 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.776+378A>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38948378 | |||||||
| chr20:38948378 | A | T | 5 | a0004c0003t0004g0025 a0004c0003t0004g0133 a0004c0003t0004g0134 others(2): Show |
7 | HG02258.hp2 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.776+378A>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38948378 | |||||||
| chr20:38948462 | A | T | 1 | a0002c0002t0004g0108 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.776+462A>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38948462 | |||||||
| chr20:38948626 | G | T | 27 | a0002c0002t0003g0007 a0002c0002t0003g0012 a0002c0002t0003g0022 others(24): Show |
37 | HG00099.hp2 HG00423.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.776+626G>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38948626 | |||||||
| chr20:38948633 | T | A | 1 | a0002c0014t0004g0056 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.776+633T>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38948633 | |||||||
| chr20:38948668 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.776+668C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38948668 | |||||||
| chr20:38948720 | A | G | 2 | a0002c0014t0004g0056 a0002c0014t0004g0057 |
2 | HG02257.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.776+720A>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38948720 | |||||||
| chr20:38949005 | A | C | 1 | a0001c0001t0001g0144 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.776+1005A>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38949005 | |||||||
| chr20:38949133 | G | A | 1 | a0001c0001t0001g0185 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.776+1133G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38949133 | |||||||
| chr20:38949164 | C | CT | 103 | a0002c0002t0002g0001 a0002c0002t0002g0003 a0002c0002t0002g0010 others(100): Show |
147 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.776+1178dupT | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr20 | 38949164 | ||||||
| chr20:38949164 | C | CTT | 6 | a0002c0002t0004g0108 a0004c0003t0004g0025 a0004c0003t0004g0133 others(3): Show |
8 | HG02145.hp1 HG02258.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.776+1177_776+1178d others(4): Show |
FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr20 | 38949164 | ||||||
| chr20:38949223 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.776+1223G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38949223 | |||||||
| chr20:38949397 | T | C | 6 | a0002c0002t0003g0012 a0002c0002t0003g0022 a0002c0002t0003g0113 others(3): Show |
9 | HG01243.hp1 HG02886.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.776+1397T>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38949397 | |||||||
| chr20:38949412 | G | T | 61 | a0002c0002t0002g0001 a0002c0002t0002g0003 a0002c0002t0002g0010 others(58): Show |
94 | HG00280.hp1 HG00544.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.776+1412G>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38949412 | |||||||
| chr20:38949452 | G | T | 1 | a0002c0002t0003g0123 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.776+1452G>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38949452 | |||||||
| chr20:38949455 | C | T | 2 | a0002c0002t0002g0068 a0002c0002t0002g0106 |
2 | NA18939.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.776+1455C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38949455 | |||||||
| chr20:38949550 | C | T | 2 | a0002c0014t0004g0056 a0002c0014t0004g0057 |
2 | HG02257.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.776+1550C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38949550 | |||||||
| chr20:38949719 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.776+1719C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38949719 | |||||||
| chr20:38949732 | C | T | 2 | a0010c0013t0001g0219 a0010c0013t0001g0220 |
2 | NA19012.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.776+1732C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38949732 | |||||||
| chr20:38949744 | C | T | 24 | a0002c0002t0003g0007 a0002c0002t0003g0012 a0002c0002t0003g0022 others(21): Show |
34 | HG00099.hp2 HG00423.hp2 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.776+1744C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38949744 | |||||||
| chr20:38949813 | C | T | 2 | a0002c0002t0004g0098 a0013c0018t0004g0099 |
2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.777-1726C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38949813 | |||||||
| chr20:38949825 | TGTTTATT others(67): Show |
T | 1 | a0017c0016t0002g0074 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.777-1710_777-1637d others(76): Show |
FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr20 | 38949825 | ||||||
| chr20:38949904 | C | G | 1 | a0017c0016t0002g0074 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.777-1635C>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38949904 | |||||||
| chr20:38949905 | G | C | 1 | a0017c0016t0002g0074 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.777-1634G>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38949905 | |||||||
| chr20:38949919 | C | T | 2 | a0002c0002t0002g0066 a0002c0002t0002g0069 |
2 | NA18989.hp1 NA19059.hp2 |
intron_variant | MODIFIER | c.777-1620C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38949919 | |||||||
| chr20:38949969 | C | A | 2 | a0003c0005t0004g0103 a0003c0005t0004g0104 |
2 | HG01361.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.777-1570C>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38949969 | |||||||
| chr20:38950053 | C | A | 1 | a0017c0016t0002g0074 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.777-1486C>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38950053 | |||||||
| chr20:38950053 | C | T | 3 | a0002c0002t0002g0058 a0002c0002t0002g0068 a0002c0002t0002g0106 |
3 | HG02165.hp2 NA18939.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.777-1486C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38950053 | |||||||
| chr20:38950095 | A | G | 1 | a0002c0002t0004g0046 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.777-1444A>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38950095 | |||||||
| chr20:38950118 | GC | G | 24 | a0002c0002t0003g0007 a0002c0002t0003g0012 a0002c0002t0003g0022 others(21): Show |
34 | HG00099.hp2 HG00423.hp2 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.777-1419delC | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr20 | 38950118 | ||||||
| chr20:38950184 | A | C | 2 | a0002c0014t0004g0056 a0002c0014t0004g0057 |
2 | HG02257.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.777-1355A>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38950184 | |||||||
| chr20:38950439 | C | T | 33 | a0002c0002t0003g0007 a0002c0002t0003g0012 a0002c0002t0003g0022 others(30): Show |
44 | HG00099.hp2 HG00423.hp2 HG01099.hp2 others(41): Show |
intron_variant | MODIFIER | c.777-1100C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38950439 | |||||||
| chr20:38950452 | G | A | 1 | a0002c0002t0004g0046 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.777-1087G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38950452 | |||||||
| chr20:38950580 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.777-959G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38950580 | |||||||
| chr20:38950711 | G | A | 2 | a0002c0002t0002g0075 a0002c0002t0002g0076 |
2 | NA18998.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.777-828G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38950711 | |||||||
| chr20:38950728 | G | GATGGGGG others(31): Show |
6 | a0003c0005t0004g0021 a0003c0005t0004g0103 a0003c0005t0004g0104 others(3): Show |
7 | HG01361.hp1 HG02559.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.777-804_777-767dup others(38): Show |
FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr20 | 38950728 | ||||||
| chr20:38950828 | A | T | 1 | a0001c0001t0001g0175 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.777-711A>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38950828 | |||||||
| chr20:38950830 | G | A | 1 | a0012c0015t0004g0230 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.777-709G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38950830 | |||||||
| chr20:38950855 | C | T | 2 | a0001c0004t0001g0197 a0002c0002t0001g0097 |
2 | HG03453.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.777-684C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38950855 | |||||||
| chr20:38950862 | T | TCATG | 27 | a0002c0002t0003g0007 a0002c0002t0003g0012 a0002c0002t0003g0022 others(24): Show |
37 | HG00099.hp2 HG00423.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.777-676_777-673dup others(4): Show |
FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr20 | 38950862 | ||||||
| chr20:38950896 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.777-643C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38950896 | |||||||
| chr20:38950912 | G | A | 1 | a0002c0002t0002g0055 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.777-627G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38950912 | |||||||
| chr20:38950931 | C | A | 1 | a0017c0016t0002g0074 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.777-608C>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38950931 | |||||||
| chr20:38950932 | A | C | 1 | a0017c0016t0002g0074 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.777-607A>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38950932 | |||||||
| chr20:38950934 | C | T | 1 | a0017c0016t0002g0074 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.777-605C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38950934 | |||||||
| chr20:38950944 | C | T | 1 | a0002c0002t0002g0131 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.777-595C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38950944 | |||||||
| chr20:38950953 | A | G | 1 | a0002c0006t0001g0111 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.777-586A>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38950953 | |||||||
| chr20:38950976 | C | T | 2 | a0002c0002t0002g0075 a0002c0002t0002g0076 |
2 | NA18998.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.777-563C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38950976 | |||||||
| chr20:38950989 | T | G | 1 | a0017c0016t0002g0074 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.777-550T>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38950989 | |||||||
| chr20:38951012 | A | C | 2 | a0002c0002t0002g0100 a0002c0002t0002g0105 |
2 | HG01168.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.777-527A>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38951012 | |||||||
| chr20:38951112 | C | T | 23 | a0002c0002t0003g0007 a0002c0002t0003g0012 a0002c0002t0003g0022 others(20): Show |
33 | HG00099.hp2 HG00423.hp2 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.777-427C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38951112 | |||||||
| chr20:38951113 | G | A | 1 | a0002c0002t0004g0108 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.777-426G>A | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38951113 | |||||||
| chr20:38951141 | A | G | 1 | a0002c0002t0003g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.777-398A>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38951141 | |||||||
| chr20:38951189 | C | T | 2 | a0002c0002t0002g0040 a0002c0002t0002g0077 |
2 | HG02155.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.777-350C>T | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38951189 | |||||||
| chr20:38951271 | AAAAC | A | 8 | a0001c0001t0001g0032 a0001c0001t0001g0038 a0001c0001t0001g0176 others(5): Show |
10 | HG01106.hp1 HG01109.hp1 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.777-252_777-249del others(4): Show |
FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr20 | 38951271 | ||||||
| chr20:38951300 | T | C | 1 | a0002c0002t0004g0108 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.777-239T>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38951300 | |||||||
| chr20:38951401 | C | G | 5 | a0003c0008t0002g0016 a0003c0008t0002g0047 a0003c0008t0002g0048 others(2): Show |
5 | HG02145.hp2 HG02280.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.777-138C>G | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38951401 | |||||||
| chr20:38951487 | A | C | 110 | a0002c0002t0002g0001 a0002c0002t0002g0003 a0002c0002t0002g0010 others(107): Show |
156 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.777-52A>C | FAM83D | ENSG00000101447.15 | transcript | ENST00000619850.2 | protein_coding | 3/3 | chr20 | 38951487 |