Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 54757 |
| ensemblid | ENSG00000108950.12 |
| hgncid | 23015 |
| symbol | FAM20A |
| name | FAM20A golgi associated secretory pathway pseudokinase |
| refseq_nuc | NM_017565.4 |
| refseq_prot | NP_060035.2 |
| ensembl_nuc | ENST00000592554.2 |
| ensembl_prot | ENSP00000468308.1 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 68535116 |
| end | 68601367 |
| strand | - |
| ver | v1.2 |
| region | chr17:68535116-68601367 |
| region5000 | chr17:68530116-68606367 |
| regionname0 | FAM20A_chr17_68535116_68601367 |
| regionname5000 | FAM20A_chr17_68530116_68606367 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 541 | 192 | 55 | 23 | 80 | 8 | 26 | 67 | FAM20A_chr17_68530116_68606367 | FAM20A | MPGLR others(536): Show |
chr17 | 68530116 | 68606367 |
| a0002 | 0/0 | 541 | 132 | 18 | 28 | 72 | 5 | 9 | 57 | FAM20A_chr17_68530116_68606367 | FAM20A | MPGLR others(536): Show |
chr17 | 68530116 | 68606367 |
| a0003 | 1/1 | 541 | 44 | 5 | 17 | 9 | 3 | 8 | 5 | FAM20A_chr17_68530116_68606367 | FAM20A | MPGLR others(536): Show |
chr17 | 68530116 | 68606367 |
| a0004 | 0/0 | 541 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | MPGLR others(536): Show |
chr17 | 68530116 | 68606367 |
| a0005 | 0/0 | 541 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | MPVLR others(536): Show |
chr17 | 68530116 | 68606367 |
| a0006 | 0/0 | 541 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | MPGLR others(536): Show |
chr17 | 68530116 | 68606367 |
| a0007 | 0/0 | 541 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | MPGLR others(536): Show |
chr17 | 68530116 | 68606367 |
| a0008 | 0/0 | 541 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | MPGLR others(536): Show |
chr17 | 68530116 | 68606367 |
| a0009 | 0/0 | 541 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | MPGLR others(536): Show |
chr17 | 68530116 | 68606367 |
| a0010 | 0/0 | 541 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | MPVLR others(536): Show |
chr17 | 68530116 | 68606367 |
| a0011 | 0/0 | 541 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | MPGLR others(536): Show |
chr17 | 68530116 | 68606367 |
| a0012 | 0/0 | 541 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | MPGLR others(536): Show |
chr17 | 68530116 | 68606367 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1623 | 127 | 47 | 19 | 35 | 7 | 19 | FAM20A_chr17_68530116_68606367 | FAM20A | ATGCC others(1618): Show |
chr17 | 68530116 | 68606367 | ||
| a0001c0004 | 0/0 | 1623 | 33 | 3 | 1 | 24 | 1 | 4 | FAM20A_chr17_68530116_68606367 | FAM20A | ATGCC others(1618): Show |
chr17 | 68530116 | 68606367 | ||
| a0001c0005 | 0/0 | 1623 | 31 | 4 | 3 | 21 | 0 | 3 | FAM20A_chr17_68530116_68606367 | FAM20A | ATGCC others(1618): Show |
chr17 | 68530116 | 68606367 | ||
| a0001c0017 | 0/0 | 1623 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | ATGCC others(1618): Show |
chr17 | 68530116 | 68606367 | ||
| a0002c0002 | 0/0 | 1623 | 55 | 7 | 12 | 28 | 4 | 4 | FAM20A_chr17_68530116_68606367 | FAM20A | ATGCC others(1618): Show |
chr17 | 68530116 | 68606367 | ||
| a0002c0003 | 0/0 | 1623 | 35 | 11 | 5 | 16 | 1 | 2 | FAM20A_chr17_68530116_68606367 | FAM20A | ATGCC others(1618): Show |
chr17 | 68530116 | 68606367 | ||
| a0002c0007 | 0/0 | 1623 | 28 | 0 | 10 | 17 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | ATGCC others(1618): Show |
chr17 | 68530116 | 68606367 | ||
| a0002c0008 | 0/0 | 1623 | 8 | 0 | 0 | 6 | 0 | 2 | FAM20A_chr17_68530116_68606367 | FAM20A | ATGCC others(1618): Show |
chr17 | 68530116 | 68606367 | ||
| a0002c0010 | 0/0 | 1623 | 4 | 0 | 1 | 3 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | ATGCC others(1618): Show |
chr17 | 68530116 | 68606367 | ||
| a0002c0014 | 0/0 | 1623 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | ATGCC others(1618): Show |
chr17 | 68530116 | 68606367 | ||
| a0003c0006 | 1/0 | 1623 | 31 | 3 | 13 | 4 | 3 | 7 | FAM20A_chr17_68530116_68606367 | FAM20A | ATGCC others(1618): Show |
chr17 | 68530116 | 68606367 | ||
| a0003c0009 | 0/1 | 1623 | 5 | 1 | 3 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | ATGCC others(1618): Show |
chr17 | 68530116 | 68606367 | ||
| a0003c0012 | 0/0 | 1623 | 3 | 0 | 0 | 3 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | ATGCC others(1618): Show |
chr17 | 68530116 | 68606367 | ||
| a0003c0013 | 0/0 | 1623 | 2 | 0 | 1 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | ATGCC others(1618): Show |
chr17 | 68530116 | 68606367 | ||
| a0003c0015 | 0/0 | 1623 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | ATGCC others(1618): Show |
chr17 | 68530116 | 68606367 | ||
| a0003c0018 | 0/0 | 1623 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | ATGCC others(1618): Show |
chr17 | 68530116 | 68606367 | ||
| a0004c0011 | 0/0 | 1623 | 3 | 3 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | ATGCC others(1618): Show |
chr17 | 68530116 | 68606367 | ||
| a0005c0024 | 0/0 | 1623 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | ATGCC others(1618): Show |
chr17 | 68530116 | 68606367 | ||
| a0005c0025 | 0/0 | 1623 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | ATGCC others(1618): Show |
chr17 | 68530116 | 68606367 | ||
| a0006c0023 | 0/0 | 1623 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | ATGCC others(1618): Show |
chr17 | 68530116 | 68606367 | ||
| a0007c0016 | 0/0 | 1623 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | ATGCC others(1618): Show |
chr17 | 68530116 | 68606367 | ||
| a0008c0022 | 0/0 | 1623 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | ATGCC others(1618): Show |
chr17 | 68530116 | 68606367 | ||
| a0009c0021 | 0/0 | 1623 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | ATGCC others(1618): Show |
chr17 | 68530116 | 68606367 | ||
| a0010c0026 | 0/0 | 1623 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | ATGCC others(1618): Show |
chr17 | 68530116 | 68606367 | ||
| a0011c0020 | 0/0 | 1623 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | ATGCC others(1618): Show |
chr17 | 68530116 | 68606367 | ||
| a0012c0019 | 0/0 | 1623 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | ATGCC others(1618): Show |
chr17 | 68530116 | 68606367 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4688 | 52 | 22 | 6 | 14 | 2 | 8 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0001c0001t0002 | 0/0 | 4688 | 41 | 10 | 8 | 12 | 5 | 6 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0001c0001t0003 | 0/0 | 4688 | 10 | 0 | 0 | 5 | 0 | 5 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0001c0001t0004 | 0/0 | 4688 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0001c0001t0005 | 0/0 | 4688 | 10 | 6 | 4 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0001c0001t0006 | 0/0 | 4688 | 6 | 6 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0001c0001t0012 | 0/0 | 4688 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0001c0001t0020 | 0/0 | 4688 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0001c0001t0021 | 0/0 | 4688 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0001c0001t0022 | 0/0 | 4688 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0001c0001t0023 | 0/0 | 4688 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0001c0001t0025 | 0/0 | 4688 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0001c0004t0001 | 0/0 | 4688 | 7 | 0 | 0 | 4 | 1 | 2 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0001c0004t0002 | 0/0 | 4688 | 9 | 0 | 0 | 7 | 0 | 2 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0001c0004t0003 | 0/0 | 4688 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0001c0004t0004 | 0/0 | 4688 | 12 | 0 | 0 | 12 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0001c0004t0008 | 0/0 | 4688 | 3 | 2 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0001c0004t0013 | 0/0 | 4688 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0001c0005t0001 | 0/0 | 4688 | 6 | 0 | 2 | 3 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0001c0005t0002 | 0/0 | 4688 | 16 | 3 | 1 | 10 | 0 | 2 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0001c0005t0003 | 0/0 | 4688 | 7 | 0 | 0 | 7 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0001c0005t0004 | 0/0 | 4688 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0001c0005t0006 | 0/0 | 4688 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0001c0017t0005 | 0/0 | 4688 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0002c0002t0001 | 0/0 | 4688 | 46 | 6 | 11 | 21 | 4 | 4 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0002c0002t0007 | 0/0 | 4688 | 5 | 0 | 0 | 5 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0002c0002t0014 | 0/0 | 4688 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0002c0002t0018 | 0/0 | 4688 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0002c0002t0019 | 0/0 | 4688 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0002c0002t0024 | 0/0 | 4688 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0002c0003t0001 | 0/0 | 4688 | 28 | 8 | 4 | 14 | 1 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0002c0003t0009 | 0/0 | 4688 | 2 | 1 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0002c0003t0010 | 0/0 | 4688 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0002c0003t0011 | 0/0 | 4688 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0002c0003t0016 | 0/0 | 4688 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0002c0003t0017 | 0/0 | 4688 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0002c0007t0001 | 0/0 | 4688 | 28 | 0 | 10 | 17 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0002c0008t0001 | 0/0 | 4688 | 8 | 0 | 0 | 6 | 0 | 2 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0002c0010t0001 | 0/0 | 4688 | 4 | 0 | 1 | 3 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0002c0014t0001 | 0/0 | 4688 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0003c0006t0001 | 1/0 | 4688 | 31 | 3 | 13 | 4 | 3 | 7 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0003c0009t0001 | 0/1 | 4688 | 5 | 1 | 3 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0003c0012t0001 | 0/0 | 4688 | 3 | 0 | 0 | 3 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0003c0013t0001 | 0/0 | 4688 | 2 | 0 | 1 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0003c0015t0001 | 0/0 | 4688 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0003c0018t0001 | 0/0 | 4688 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0004c0011t0002 | 0/0 | 4688 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0004c0011t0005 | 0/0 | 4688 | 2 | 2 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0005c0024t0001 | 0/0 | 4688 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0005c0025t0001 | 0/0 | 4688 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0006c0023t0001 | 0/0 | 4688 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0007c0016t0015 | 0/0 | 4688 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0008c0022t0002 | 0/0 | 4688 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0009c0021t0001 | 0/0 | 4688 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0010c0026t0001 | 0/0 | 4688 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0011c0020t0001 | 0/0 | 4688 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| a0012c0019t0010 | 0/0 | 4688 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | AGTTG others(4683): Show |
chr17 | 68530116 | 68606367 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0003g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0005g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0005g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0005g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0005g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0005g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0005g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0005g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0005g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0005g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0006g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0006g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0006g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0006g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0006g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0006g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0012g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0020g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0021g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0022g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0023g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0025g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0004g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0004g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0004g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0004g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0008g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0008g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0008g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0013g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0006g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0017t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0007g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0007g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0007g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0007g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0007g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0014g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0018g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0019g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0024g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0009g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0009g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0010g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0011g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0011g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0016g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0017g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0007t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0007t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0007t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0007t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0007t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0007t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0007t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0007t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0007t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0007t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0007t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0007t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0007t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0007t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0007t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0007t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0007t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0007t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0007t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0007t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0007t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0007t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0007t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0007t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0007t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0007t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0007t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0008t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0008t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0008t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0008t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0008t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0008t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0008t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0008t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0010t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0010t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0010t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0010t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0014t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0014t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0321 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0009t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0009t0001g0077 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0009t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0009t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0012t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0012t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0012t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0013t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0013t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0015t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0015t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0018t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0004c0011t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0004c0011t0005g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0004c0011t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0005c0024t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0005c0025t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0006c0023t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0007c0016t0015g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0008c0022t0002g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0009c0021t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0010c0026t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0011c0020t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0012c0019t0010g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0289 | EUR | GBR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0231 | EUR | GBR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00140 | hp1 | a0002 | c0003 | t0001 | g0210 | EUR | GBR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0137 | EUR | GBR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0229 | EUR | FIN | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0185 | EUR | FIN | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00323 | hp1 | a0001 | c0004 | t0001 | g0044 | EUR | FIN | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0228 | EUR | FIN | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00408 | hp1 | a0001 | c0004 | t0004 | g0020 | EAS | CHS | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0325 | EAS | CHS | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00544 | hp1 | a0001 | c0005 | t0003 | g0118 | EAS | CHS | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00544 | hp2 | a0001 | c0005 | t0003 | g0078 | EAS | CHS | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0257 | EAS | CHS | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0309 | EAS | CHS | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00597 | hp1 | a0006 | c0023 | t0001 | g0358 | EAS | CHS | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00597 | hp2 | a0003 | c0006 | t0001 | g0203 | EAS | CHS | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00609 | hp1 | a0005 | c0024 | t0001 | g0359 | EAS | CHS | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00609 | hp2 | a0001 | c0004 | t0003 | g0033 | EAS | CHS | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00621 | hp1 | a0001 | c0005 | t0001 | g0090 | EAS | CHS | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00621 | hp2 | a0002 | c0007 | t0001 | g0095 | EAS | CHS | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00673 | hp1 | a0002 | c0008 | t0001 | g0032 | EAS | CHS | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00673 | hp2 | a0003 | c0006 | t0001 | g0170 | EAS | CHS | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0153 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00735 | hp2 | a0002 | c0003 | t0001 | g0290 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0184 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00738 | hp2 | a0003 | c0006 | t0001 | g0320 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00741 | hp1 | a0003 | c0006 | t0001 | g0277 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00741 | hp2 | a0002 | c0007 | t0001 | g0124 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01069 | hp2 | a0001 | c0001 | t0005 | g0286 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01070 | hp1 | a0003 | c0006 | t0001 | g0313 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0244 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01071 | hp1 | a0001 | c0001 | t0005 | g0007 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01071 | hp2 | a0003 | c0006 | t0001 | g0307 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0332 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01074 | hp2 | a0002 | c0003 | t0001 | g0232 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0288 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01099 | hp1 | a0002 | c0007 | t0001 | g0066 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01099 | hp2 | a0001 | c0001 | t0005 | g0354 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0237 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01106 | hp2 | a0001 | c0001 | t0005 | g0007 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0308 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01109 | hp2 | a0001 | c0004 | t0008 | g0012 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0187 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01167 | hp2 | a0002 | c0007 | t0001 | g0001 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01169 | hp1 | a0003 | c0013 | t0001 | g0053 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01169 | hp2 | a0002 | c0007 | t0001 | g0001 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01192 | hp1 | a0002 | c0007 | t0001 | g0067 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01192 | hp2 | a0003 | c0006 | t0001 | g0008 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0211 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01243 | hp2 | a0002 | c0003 | t0009 | g0318 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01255 | hp2 | a0002 | c0003 | t0001 | g0180 | AMR | CLM | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01256 | hp1 | a0003 | c0006 | t0001 | g0005 | AMR | CLM | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01256 | hp2 | a0003 | c0006 | t0001 | g0144 | AMR | CLM | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01257 | hp1 | a0003 | c0009 | t0001 | g0002 | AMR | CLM | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0317 | AMR | CLM | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01258 | hp1 | a0003 | c0009 | t0001 | g0002 | AMR | CLM | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01258 | hp2 | a0003 | c0006 | t0001 | g0005 | AMR | CLM | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01261 | hp1 | a0001 | c0005 | t0002 | g0125 | AMR | CLM | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01261 | hp2 | a0002 | c0010 | t0001 | g0056 | AMR | CLM | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01346 | hp1 | a0002 | c0007 | t0001 | g0068 | AMR | CLM | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01358 | hp1 | a0001 | c0001 | t0012 | g0013 | AMR | CLM | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01358 | hp2 | a0003 | c0006 | t0001 | g0008 | AMR | CLM | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01361 | hp1 | a0001 | c0005 | t0001 | g0088 | AMR | CLM | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0254 | AMR | CLM | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01433 | hp1 | a0003 | c0006 | t0001 | g0345 | AMR | CLM | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01433 | hp2 | a0001 | c0005 | t0001 | g0099 | AMR | CLM | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01496 | hp1 | a0003 | c0006 | t0001 | g0344 | AMR | CLM | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0299 | AMR | CLM | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01515 | hp1 | a0003 | c0006 | t0001 | g0223 | EUR | IBS | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0176 | EUR | IBS | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0175 | EUR | IBS | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01517 | hp2 | a0003 | c0006 | t0001 | g0242 | EUR | IBS | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01884 | hp1 | a0003 | c0006 | t0001 | g0214 | AFR | ACB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01884 | hp2 | a0004 | c0011 | t0002 | g0061 | AFR | ACB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | ACB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0285 | AFR | ACB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0154 | AMR | PEL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | PEL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01934 | hp1 | a0002 | c0007 | t0001 | g0126 | AMR | PEL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0310 | AMR | PEL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0166 | AMR | PEL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0296 | AMR | PEL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0323 | AMR | PEL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01981 | hp2 | a0003 | c0009 | t0001 | g0112 | AMR | PEL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02004 | hp1 | a0003 | c0006 | t0001 | g0316 | AMR | PEL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02004 | hp2 | a0002 | c0007 | t0001 | g0098 | AMR | PEL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0336 | EAS | KHV | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02040 | hp2 | a0003 | c0012 | t0001 | g0164 | EAS | KHV | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0197 | AFR | ACB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0347 | AFR | ACB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0339 | EAS | KHV | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02071 | hp2 | a0002 | c0007 | t0001 | g0101 | EAS | KHV | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02074 | hp1 | a0001 | c0005 | t0002 | g0087 | EAS | KHV | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0337 | EAS | KHV | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02080 | hp1 | a0002 | c0007 | t0001 | g0092 | EAS | KHV | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02080 | hp2 | a0002 | c0003 | t0001 | g0152 | EAS | KHV | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02129 | hp1 | a0002 | c0007 | t0001 | g0064 | EAS | KHV | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0335 | EAS | KHV | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0225 | AFR | ACB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02145 | hp2 | a0001 | c0001 | t0021 | g0202 | AFR | ACB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0305 | AMR | PEL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02148 | hp2 | a0003 | c0006 | t0001 | g0276 | AMR | PEL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02155 | hp1 | a0002 | c0007 | t0001 | g0104 | EAS | CDX | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02155 | hp2 | a0002 | c0003 | t0001 | g0302 | EAS | CDX | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02258 | hp1 | a0001 | c0001 | t0022 | g0362 | AFR | ACB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0273 | AFR | ACB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02280 | hp1 | a0001 | c0005 | t0002 | g0096 | AFR | ACB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0326 | AFR | ACB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02293 | hp1 | a0002 | c0007 | t0001 | g0097 | AMR | PEL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0239 | AMR | PEL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02300 | hp1 | a0002 | c0002 | t0019 | g0294 | AMR | PEL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02300 | hp2 | a0002 | c0007 | t0001 | g0127 | AMR | PEL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0284 | AFR | ACB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0275 | AFR | ACB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02523 | hp1 | a0002 | c0014 | t0001 | g0117 | EAS | KHV | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02523 | hp2 | a0002 | c0002 | t0018 | g0136 | EAS | KHV | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0278 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02602 | hp1 | a0003 | c0013 | t0001 | g0047 | SAS | PJL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0215 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02630 | hp1 | a0001 | c0004 | t0008 | g0011 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0209 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02647 | hp1 | a0007 | c0016 | t0015 | g0015 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0352 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02683 | hp1 | a0003 | c0006 | t0001 | g0160 | SAS | PJL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02717 | hp2 | a0001 | c0005 | t0006 | g0116 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0188 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0312 | SAS | PJL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02735 | hp2 | a0003 | c0006 | t0001 | g0248 | SAS | PJL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02738 | hp1 | a0002 | c0007 | t0001 | g0108 | SAS | PJL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02809 | hp1 | a0002 | c0003 | t0001 | g0349 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0141 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0201 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0279 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02895 | hp2 | a0003 | c0006 | t0001 | g0322 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02922 | hp1 | a0002 | c0003 | t0001 | g0243 | AFR | ESN | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0329 | AFR | ESN | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02965 | hp1 | a0001 | c0004 | t0008 | g0009 | AFR | ESN | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | ESN | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02976 | hp1 | a0002 | c0003 | t0001 | g0200 | AFR | ESN | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0346 | AFR | ESN | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03017 | hp1 | a0003 | c0006 | t0001 | g0241 | SAS | PJL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03041 | hp1 | a0003 | c0006 | t0001 | g0271 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0314 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0348 | AFR | MSL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0280 | AFR | MSL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0218 | AFR | ESN | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0198 | AFR | ESN | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03139 | hp1 | a0001 | c0001 | t0006 | g0208 | AFR | ESN | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03139 | hp2 | a0002 | c0003 | t0001 | g0297 | AFR | ESN | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03195 | hp1 | a0003 | c0009 | t0001 | g0079 | AFR | ESN | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0207 | AFR | ESN | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0283 | AFR | MSL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03225 | hp2 | a0002 | c0002 | t0024 | g0371 | AFR | MSL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03239 | hp1 | a0002 | c0003 | t0016 | g0301 | SAS | PJL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03239 | hp2 | a0001 | c0004 | t0002 | g0041 | SAS | PJL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0353 | AFR | MSL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03453 | hp2 | a0002 | c0003 | t0017 | g0142 | AFR | MSL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0272 | AFR | MSL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03486 | hp2 | a0002 | c0003 | t0001 | g0251 | AFR | MSL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0319 | SAS | PJL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03491 | hp2 | a0003 | c0006 | t0001 | g0006 | SAS | PJL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03492 | hp1 | a0003 | c0006 | t0001 | g0006 | SAS | PJL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03492 | hp2 | a0001 | c0005 | t0001 | g0103 | SAS | PJL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03516 | hp1 | a0001 | c0005 | t0002 | g0082 | AFR | ESN | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0328 | AFR | ESN | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03540 | hp1 | a0001 | c0017 | t0005 | g0014 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03540 | hp2 | a0002 | c0003 | t0010 | g0282 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0330 | AFR | MSL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03579 | hp2 | a0008 | c0022 | t0002 | g0331 | AFR | MSL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03654 | hp1 | a0002 | c0008 | t0001 | g0038 | SAS | PJL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0192 | SAS | PJL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0234 | SAS | PJL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03688 | hp1 | a0001 | c0005 | t0002 | g0111 | SAS | STU | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0226 | SAS | STU | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0324 | SAS | PJL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0245 | SAS | PJL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | BEB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03831 | hp2 | a0002 | c0008 | t0001 | g0031 | SAS | BEB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0179 | SAS | BEB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03834 | hp2 | a0001 | c0005 | t0002 | g0115 | SAS | BEB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0167 | SAS | BEB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | BEB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03942 | hp1 | a0003 | c0006 | t0001 | g0306 | SAS | BEB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0186 | SAS | BEB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG04115 | hp1 | a0001 | c0004 | t0001 | g0046 | SAS | STU | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0206 | SAS | STU | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG04184 | hp1 | a0001 | c0004 | t0001 | g0045 | SAS | BEB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0266 | SAS | BEB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0267 | SAS | STU | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG04199 | hp2 | a0001 | c0004 | t0002 | g0017 | SAS | STU | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | STU | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG04204 | hp2 | a0002 | c0003 | t0001 | g0300 | SAS | STU | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG04228 | hp1 | a0009 | c0021 | t0001 | g0304 | SAS | STU | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG04228 | hp2 | a0003 | c0006 | t0001 | g0205 | SAS | STU | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | YRI | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0350 | AFR | YRI | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18612 | hp1 | a0002 | c0003 | t0001 | g0262 | EAS | CHB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18612 | hp2 | a0002 | c0002 | t0007 | g0367 | EAS | CHB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18747 | hp1 | a0001 | c0004 | t0002 | g0050 | EAS | CHB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18747 | hp2 | a0003 | c0006 | t0001 | g0171 | EAS | CHB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18906 | hp1 | a0001 | c0004 | t0013 | g0010 | AFR | YRI | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18906 | hp2 | a0002 | c0003 | t0001 | g0230 | AFR | YRI | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0334 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18939 | hp2 | a0002 | c0007 | t0001 | g0102 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18942 | hp1 | a0005 | c0025 | t0001 | g0361 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0132 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0162 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0356 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18944 | hp1 | a0001 | c0005 | t0002 | g0074 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18944 | hp2 | a0002 | c0007 | t0001 | g0086 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18945 | hp1 | a0003 | c0006 | t0001 | g0259 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18945 | hp2 | a0001 | c0001 | t0023 | g0365 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18947 | hp1 | a0001 | c0004 | t0004 | g0023 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18948 | hp1 | a0002 | c0003 | t0011 | g0363 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18948 | hp2 | a0002 | c0008 | t0001 | g0039 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18950 | hp1 | a0001 | c0004 | t0004 | g0029 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18952 | hp1 | a0002 | c0003 | t0001 | g0238 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18952 | hp2 | a0002 | c0007 | t0001 | g0093 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0173 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18954 | hp2 | a0001 | c0005 | t0003 | g0069 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18956 | hp1 | a0002 | c0002 | t0014 | g0143 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18956 | hp2 | a0001 | c0005 | t0002 | g0085 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18957 | hp1 | a0001 | c0005 | t0003 | g0065 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18959 | hp1 | a0001 | c0005 | t0002 | g0106 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18959 | hp2 | a0002 | c0008 | t0001 | g0042 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18960 | hp1 | a0001 | c0005 | t0002 | g0083 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18960 | hp2 | a0002 | c0002 | t0007 | g0370 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18961 | hp1 | a0002 | c0007 | t0001 | g0091 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18961 | hp2 | a0001 | c0004 | t0001 | g0021 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18962 | hp1 | a0002 | c0007 | t0001 | g0094 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18962 | hp2 | a0001 | c0005 | t0002 | g0076 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18964 | hp1 | a0001 | c0005 | t0002 | g0084 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18966 | hp1 | a0002 | c0003 | t0001 | g0338 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0178 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18967 | hp1 | a0001 | c0004 | t0004 | g0055 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18967 | hp2 | a0001 | c0005 | t0002 | g0075 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18969 | hp1 | a0003 | c0015 | t0001 | g0113 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18969 | hp2 | a0001 | c0001 | t0025 | g0372 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18970 | hp1 | a0001 | c0004 | t0001 | g0037 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18970 | hp2 | a0002 | c0007 | t0001 | g0080 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18971 | hp1 | a0002 | c0008 | t0001 | g0018 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18974 | hp1 | a0001 | c0005 | t0001 | g0089 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18977 | hp2 | a0003 | c0012 | t0001 | g0227 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18978 | hp1 | a0001 | c0005 | t0002 | g0071 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18978 | hp2 | a0002 | c0002 | t0007 | g0368 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18979 | hp1 | a0003 | c0015 | t0001 | g0114 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0260 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18981 | hp1 | a0001 | c0005 | t0003 | g0119 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18981 | hp2 | a0003 | c0012 | t0001 | g0311 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18983 | hp1 | a0002 | c0003 | t0011 | g0364 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0333 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18984 | hp2 | a0002 | c0003 | t0001 | g0256 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18986 | hp1 | a0002 | c0007 | t0001 | g0109 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0341 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18987 | hp1 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18987 | hp2 | a0002 | c0010 | t0001 | g0052 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18989 | hp1 | a0001 | c0004 | t0002 | g0059 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18992 | hp1 | a0002 | c0002 | t0001 | g0247 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18994 | hp1 | a0001 | c0001 | t0004 | g0138 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18994 | hp2 | a0001 | c0005 | t0001 | g0120 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18997 | hp1 | a0002 | c0003 | t0001 | g0340 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18997 | hp2 | a0001 | c0004 | t0002 | g0057 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18998 | hp1 | a0001 | c0004 | t0001 | g0034 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18998 | hp2 | a0001 | c0001 | t0004 | g0158 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19002 | hp2 | a0001 | c0004 | t0004 | g0027 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19005 | hp2 | a0002 | c0003 | t0001 | g0357 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19006 | hp1 | a0001 | c0004 | t0004 | g0054 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19006 | hp2 | a0002 | c0007 | t0001 | g0072 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19007 | hp1 | a0002 | c0007 | t0001 | g0073 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19007 | hp2 | a0001 | c0005 | t0003 | g0070 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19010 | hp1 | a0001 | c0004 | t0002 | g0049 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19010 | hp2 | a0002 | c0003 | t0001 | g0183 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19011 | hp2 | a0001 | c0004 | t0001 | g0043 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0224 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0351 | AFR | LWK | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | LWK | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19043 | hp1 | a0002 | c0003 | t0001 | g0298 | AFR | LWK | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19043 | hp2 | a0001 | c0001 | t0020 | g0327 | AFR | LWK | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19055 | hp1 | a0002 | c0003 | t0001 | g0249 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19055 | hp2 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19056 | hp1 | a0002 | c0003 | t0001 | g0135 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19056 | hp2 | a0002 | c0008 | t0001 | g0035 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19057 | hp1 | a0001 | c0004 | t0004 | g0022 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19057 | hp2 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19059 | hp1 | a0001 | c0004 | t0004 | g0051 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19059 | hp2 | a0002 | c0010 | t0001 | g0058 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19062 | hp1 | a0001 | c0004 | t0004 | g0025 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19062 | hp2 | a0002 | c0014 | t0001 | g0122 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19063 | hp2 | a0001 | c0004 | t0004 | g0028 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19064 | hp1 | a0001 | c0004 | t0004 | g0048 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0139 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19065 | hp1 | a0001 | c0005 | t0004 | g0081 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19065 | hp2 | a0002 | c0002 | t0007 | g0366 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0263 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19066 | hp2 | a0010 | c0026 | t0001 | g0360 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19067 | hp2 | a0001 | c0004 | t0002 | g0019 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19068 | hp1 | a0011 | c0020 | t0001 | g0140 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19068 | hp2 | a0002 | c0008 | t0001 | g0040 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19070 | hp2 | a0001 | c0005 | t0003 | g0107 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19074 | hp1 | a0002 | c0007 | t0001 | g0105 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19074 | hp2 | a0002 | c0003 | t0001 | g0163 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19079 | hp1 | a0002 | c0007 | t0001 | g0110 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19079 | hp2 | a0001 | c0004 | t0002 | g0026 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19080 | hp1 | a0002 | c0002 | t0007 | g0369 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19083 | hp1 | a0001 | c0004 | t0004 | g0036 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19084 | hp1 | a0002 | c0003 | t0001 | g0150 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19084 | hp2 | a0001 | c0004 | t0002 | g0030 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0258 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19088 | hp2 | a0002 | c0010 | t0001 | g0024 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19090 | hp1 | a0002 | c0003 | t0001 | g0149 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19090 | hp2 | a0001 | c0005 | t0002 | g0123 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19091 | hp2 | a0002 | c0007 | t0001 | g0100 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19240 | hp1 | a0012 | c0019 | t0010 | g0063 | AFR | YRI | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19240 | hp2 | a0001 | c0005 | t0002 | g0121 | AFR | YRI | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ASW | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA20129 | hp2 | a0002 | c0003 | t0009 | g0343 | AFR | ASW | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA20752 | hp1 | a0003 | c0006 | t0001 | g0342 | EUR | TSI | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0233 | EUR | TSI | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0246 | EUR | TSI | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0172 | EUR | TSI | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0303 | SAS | GIH | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0292 | SAS | GIH | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0291 | AMR | CLM | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01123 | hp2 | a0002 | c0003 | t0001 | g0174 | AMR | CLM | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0217 | AFR | ACB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02486 | hp1 | a0004 | c0011 | t0005 | g0062 | AFR | ACB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0204 | AFR | ACB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02559 | hp1 | a0002 | c0003 | t0001 | g0199 | AFR | ACB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02559 | hp2 | a0004 | c0011 | t0005 | g0060 | AFR | ACB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | USA | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0219 | AFR | USA | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0315 | AFR | USA | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA20300 | hp2 | a0003 | c0018 | t0001 | g0016 | AFR | USA | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| homoSapiens | chm13v2 | a0003 | c0009 | t0001 | g0077 | REF | REF | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| homoSapiens | grch38p0 | a0003 | c0006 | t0001 | g0321 | REF | REF | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:68537488 | A | C | 1 | a0009 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.1615T>G | p.Leu539Val | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 11/11 | 2316/4688 | 1615/1626 | 539/541 | chr17 | 68537488 | |||
| chr17:68537514 | A | G | 9 | a0001 a0002 a0004 others(6): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
missense_variant | MODERATE | c.1589T>C | p.Leu530Ser | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 11/11 | 2290/4688 | 1589/1626 | 530/541 | chr17 | 68537514 | |||
| chr17:68537592 | G | A | 1 | a0008 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.1511C>T | p.Thr504Ile | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 11/11 | 2212/4688 | 1511/1626 | 504/541 | chr17 | 68537592 | |||
| chr17:68542098 | G | T | 5 | a0002 a0005 a0007 others(2): Show |
137 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(134): Show |
missense_variant | MODERATE | c.996C>A | p.Asn332Lys | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 7/11 | 1697/4688 | 996/1626 | 332/541 | chr17 | 68542098 | |||
| chr17:68555621 | C | T | 1 | a0007 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.527G>A | p.Arg176Gln | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 2/11 | 1228/4688 | 527/1626 | 176/541 | chr17 | 68555621 | |||
| chr17:68555639 | C | T | 1 | a0011 | 1 | NA19068.hp1 | missense_variant | MODERATE | c.509G>A | p.Arg170His | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 2/11 | 1210/4688 | 509/1626 | 170/541 | chr17 | 68555639 | |||
| chr17:68600509 | A | T | 2 | a0004 a0012 |
4 | HG01884.hp2 HG02486.hp1 HG02559.hp2 others(1): Show |
missense_variant | MODERATE | c.158T>A | p.Leu53Gln | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/11 | 859/4688 | 158/1626 | 53/541 | chr17 | 68600509 | |||
| chr17:68600534 | G | A | 1 | a0006 | 1 | HG00597.hp1 | missense_variant | MODERATE | c.133C>T | p.Pro45Ser | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/11 | 834/4688 | 133/1626 | 45/541 | chr17 | 68600534 | |||
| chr17:68600659 | C | A | 2 | a0005 a0010 |
3 | HG00609.hp1 NA18942.hp1 NA19066.hp2 |
missense_variant | MODERATE | c.8G>T | p.Gly3Val | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/11 | 709/4688 | 8/1626 | 3/541 | chr17 | 68600659 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:68540862 | G | A | 4 | a0003c0012 a0003c0015 a0010c0026 others(1): Show |
7 | HG02040.hp2 NA18969.hp1 NA18977.hp2 others(4): Show |
synonymous_variant | LOW | c.1206C>T | p.Phe402Phe | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 8/11 | 1907/4688 | 1206/1626 | 402/541 | chr17 | 68540862 | |||
| chr17:68543706 | C | T | 5 | a0002c0002 a0002c0007 a0002c0008 others(2): Show |
93 | HG00280.hp2 HG00408.hp2 HG00558.hp1 others(90): Show |
synonymous_variant | LOW | c.735G>A | p.Glu245Glu | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 5/11 | 1436/4688 | 735/1626 | 245/541 | chr17 | 68543706 | |||
| chr17:68600322 | C | T | 5 | a0001c0005 a0002c0007 a0002c0014 others(2): Show |
67 | HG00544.hp1 HG00544.hp2 HG00621.hp1 others(64): Show |
synonymous_variant | LOW | c.345G>A | p.Ser115Ser | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/11 | 1046/4688 | 345/1626 | 115/541 | chr17 | 68600322 | |||
| chr17:68600628 | C | T | 4 | a0001c0004 a0002c0008 a0002c0010 others(1): Show |
47 | HG00323.hp1 HG00408.hp1 HG00609.hp2 others(44): Show |
synonymous_variant | LOW | c.39G>A | p.Leu13Leu | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/11 | 740/4688 | 39/1626 | 13/541 | chr17 | 68600628 | |||
| chr17:68600649 | C | T | 3 | a0001c0017 a0003c0018 a0007c0016 |
3 | HG02647.hp1 HG03540.hp1 NA20300.hp2 |
synonymous_variant | LOW | c.18G>A | p.Arg6Arg | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/11 | 719/4688 | 18/1626 | 6/541 | chr17 | 68600649 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:68535227 | A | T | 1 | a0002c0002t0019 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2250T>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 11/11 | 2250 | chr17 | 68535227 | ||||||
| chr17:68535356 | T | C | 2 | a0002c0003t0010 a0012c0019t0010 |
2 | HG03540.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2121A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 11/11 | 2121 | chr17 | 68535356 | ||||||
| chr17:68535432 | C | G | 1 | a0001c0001t0012 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2045G>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 11/11 | 2045 | chr17 | 68535432 | ||||||
| chr17:68535472 | A | G | 4 | a0001c0001t0005 a0001c0017t0005 a0002c0002t0018 others(1): Show |
14 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2005T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 11/11 | 2005 | chr17 | 68535472 | ||||||
| chr17:68535502 | C | T | 3 | a0001c0001t0004 a0001c0004t0004 a0001c0005t0004 |
15 | HG00408.hp1 NA18947.hp1 NA18950.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1975G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 11/11 | 1975 | chr17 | 68535502 | ||||||
| chr17:68535667 | A | C | 2 | a0002c0003t0017 a0007c0016t0015 |
2 | HG02647.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1810T>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 11/11 | 1810 | chr17 | 68535667 | ||||||
| chr17:68535683 | G | A | 1 | a0001c0001t0012 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1794C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 11/11 | 1794 | chr17 | 68535683 | ||||||
| chr17:68535757 | C | T | 9 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0023 others(6): Show |
87 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*1720G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 11/11 | 1720 | chr17 | 68535757 | ||||||
| chr17:68535827 | A | T | 1 | a0001c0001t0012 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1650T>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 11/11 | 1650 | chr17 | 68535827 | ||||||
| chr17:68536266 | G | A | 1 | a0001c0001t0012 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1211C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 11/11 | 1211 | chr17 | 68536266 | ||||||
| chr17:68536272 | T | G | 2 | a0001c0001t0020 a0001c0004t0013 |
2 | NA18906.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1205A>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 11/11 | 1205 | chr17 | 68536272 | ||||||
| chr17:68536404 | A | G | 1 | a0002c0003t0009 | 2 | HG01243.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1073T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 11/11 | 1073 | chr17 | 68536404 | ||||||
| chr17:68536604 | A | G | 2 | a0001c0001t0006 a0001c0005t0006 |
7 | HG02451.hp2 HG02572.hp2 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*873T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 11/11 | 873 | chr17 | 68536604 | ||||||
| chr17:68536617 | A | G | 1 | a0002c0003t0016 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*860T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 11/11 | 860 | chr17 | 68536617 | ||||||
| chr17:68536749 | G | A | 12 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(9): Show |
100 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*728C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 11/11 | 728 | chr17 | 68536749 | ||||||
| chr17:68536861 | C | A | 1 | a0001c0001t0021 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*616G>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 11/11 | 616 | chr17 | 68536861 | ||||||
| chr17:68537085 | G | T | 1 | a0007c0016t0015 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*392C>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 11/11 | 392 | chr17 | 68537085 | ||||||
| chr17:68537267 | C | T | 3 | a0001c0001t0003 a0001c0004t0003 a0001c0005t0003 |
18 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*210G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 11/11 | 210 | chr17 | 68537267 | ||||||
| chr17:68537284 | C | T | 1 | a0002c0002t0014 | 1 | NA18956.hp1 | 3_prime_UTR_variant | MODIFIER | c.*193G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 11/11 | 193 | chr17 | 68537284 | ||||||
| chr17:68600712 | G | A | 1 | a0001c0001t0022 | 1 | HG02258.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-46C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/11 | chr17 | 68600712 | |||||||
| chr17:68600923 | G | C | 1 | a0002c0003t0011 | 2 | NA18948.hp1 NA18983.hp1 |
5_prime_UTR_variant | MODIFIER | c.-257C>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/11 | 257 | chr17 | 68600923 | ||||||
| chr17:68600987 | G | A | 2 | a0001c0001t0023 a0002c0002t0007 |
6 | NA18612.hp2 NA18945.hp2 NA18960.hp2 others(3): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-321C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/11 | chr17 | 68600987 | |||||||
| chr17:68601149 | G | A | 1 | a0002c0002t0024 | 1 | HG03225.hp2 | 5_prime_UTR_variant | MODIFIER | c.-483C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/11 | 483 | chr17 | 68601149 | ||||||
| chr17:68601201 | G | A | 1 | a0001c0001t0025 | 1 | NA18969.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-535C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/11 | chr17 | 68601201 | |||||||
| chr17:68601328 | C | G | 3 | a0001c0001t0012 a0001c0004t0008 a0001c0004t0013 |
5 | HG01109.hp2 HG01358.hp1 HG02630.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-662G>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/11 | 662 | chr17 | 68601328 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:68537838 | C | G | 136 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0132 others(133): Show |
137 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.1362-97G>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 10/10 | chr17 | 68537838 | |||||||
| chr17:68537942 | T | C | 1 | a0003c0006t0001g0322 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1362-201A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 10/10 | chr17 | 68537942 | |||||||
| chr17:68538004 | A | G | 83 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(80): Show |
84 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.1362-263T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 10/10 | chr17 | 68538004 | |||||||
| chr17:68538086 | G | A | 1 | a0002c0002t0001g0303 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1362-345C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 10/10 | chr17 | 68538086 | |||||||
| chr17:68538088 | A | C | 1 | a0001c0001t0002g0188 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1362-347T>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 10/10 | chr17 | 68538088 | |||||||
| chr17:68538122 | G | C | 1 | a0002c0010t0001g0052 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1362-381C>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 10/10 | chr17 | 68538122 | |||||||
| chr17:68538369 | G | A | 82 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(79): Show |
83 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1362-628C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 10/10 | chr17 | 68538369 | |||||||
| chr17:68538508 | T | C | 1 | a0001c0001t0001g0352 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1362-767A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 10/10 | chr17 | 68538508 | |||||||
| chr17:68538681 | C | T | 1 | a0002c0002t0001g0219 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1361+656G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 10/10 | chr17 | 68538681 | |||||||
| chr17:68538822 | A | G | 1 | a0001c0001t0012g0013 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1361+515T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 10/10 | chr17 | 68538822 | |||||||
| chr17:68538911 | C | T | 4 | a0001c0001t0001g0212 a0001c0001t0001g0351 a0001c0001t0021g0202 others(1): Show |
4 | HG02145.hp2 HG02258.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1361+426G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 10/10 | chr17 | 68538911 | |||||||
| chr17:68538982 | G | A | 98 | a0001c0001t0002g0004 a0001c0001t0002g0128 a0001c0001t0002g0146 others(95): Show |
100 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.1361+355C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 10/10 | chr17 | 68538982 | |||||||
| chr17:68539134 | G | C | 1 | a0002c0002t0001g0147 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1361+203C>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 10/10 | chr17 | 68539134 | |||||||
| chr17:68539233 | G | A | 1 | a0005c0024t0001g0359 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1361+104C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 10/10 | chr17 | 68539233 | |||||||
| chr17:68539605 | C | T | 136 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0132 others(133): Show |
137 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.1302-209G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 9/10 | chr17 | 68539605 | |||||||
| chr17:68540071 | CAG | C | 93 | a0001c0001t0001g0182 a0001c0001t0001g0189 a0001c0001t0001g0287 others(90): Show |
94 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.1220-107_1220-106d others(4): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 8/10 | chr17 | 68540071 | |||||||
| chr17:68540078 | G | C | 330 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(327): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.1220-112C>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 8/10 | chr17 | 68540078 | |||||||
| chr17:68540083 | C | T | 1 | a0004c0011t0005g0062 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1220-117G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 8/10 | chr17 | 68540083 | |||||||
| chr17:68540153 | G | T | 15 | a0001c0001t0005g0007 a0001c0001t0005g0141 a0001c0001t0005g0201 others(12): Show |
16 | HG00621.hp2 HG00673.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.1220-187C>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 8/10 | chr17 | 68540153 | |||||||
| chr17:68540323 | G | A | 1 | a0002c0007t0001g0108 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1220-357C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 8/10 | chr17 | 68540323 | |||||||
| chr17:68540516 | T | C | 2 | a0001c0001t0005g0007 a0001c0001t0005g0286 |
3 | HG01069.hp2 HG01071.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1219+333A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 8/10 | chr17 | 68540516 | |||||||
| chr17:68540545 | A | G | 2 | a0001c0001t0001g0145 a0001c0001t0001g0157 |
2 | HG02083.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.1219+304T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 8/10 | chr17 | 68540545 | |||||||
| chr17:68540576 | A | G | 1 | a0007c0016t0015g0015 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1219+273T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 8/10 | chr17 | 68540576 | |||||||
| chr17:68540608 | C | T | 78 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(75): Show |
79 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.1219+241G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 8/10 | chr17 | 68540608 | |||||||
| chr17:68540641 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1219+208G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 8/10 | chr17 | 68540641 | |||||||
| chr17:68540779 | C | T | 1 | a0003c0009t0001g0002 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1219+70G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 8/10 | chr17 | 68540779 | |||||||
| chr17:68541010 | C | T | 12 | a0001c0001t0005g0007 a0001c0001t0005g0141 a0001c0001t0005g0201 others(9): Show |
13 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1110-52G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 7/10 | chr17 | 68541010 | |||||||
| chr17:68541042 | C | G | 1 | a0007c0016t0015g0015 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1110-84G>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 7/10 | chr17 | 68541042 | |||||||
| chr17:68541114 | C | T | 1 | a0003c0006t0001g0306 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1110-156G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 7/10 | chr17 | 68541114 | |||||||
| chr17:68541154 | G | A | 21 | a0001c0001t0001g0252 a0001c0001t0005g0007 a0001c0001t0005g0141 others(18): Show |
22 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.1110-196C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 7/10 | chr17 | 68541154 | |||||||
| chr17:68541163 | G | A | 92 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0132 others(89): Show |
93 | HG00280.hp2 HG00408.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.1110-205C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 7/10 | chr17 | 68541163 | |||||||
| chr17:68541185 | G | A | 1 | a0003c0006t0001g0005 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1110-227C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 7/10 | chr17 | 68541185 | |||||||
| chr17:68541233 | G | T | 92 | a0002c0002t0001g0129 a0002c0002t0001g0131 a0002c0002t0001g0132 others(89): Show |
93 | HG00280.hp2 HG00408.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.1110-275C>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 7/10 | chr17 | 68541233 | |||||||
| chr17:68541249 | C | T | 2 | a0002c0002t0001g0333 a0002c0002t0019g0294 |
2 | HG02300.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1110-291G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 7/10 | chr17 | 68541249 | |||||||
| chr17:68541380 | T | C | 1 | a0002c0003t0001g0232 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1110-422A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 7/10 | chr17 | 68541380 | |||||||
| chr17:68541638 | C | G | 3 | a0001c0001t0006g0218 a0001c0001t0006g0314 a0001c0005t0006g0116 |
3 | HG02717.hp2 HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1109+347G>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 7/10 | chr17 | 68541638 | |||||||
| chr17:68541639 | G | A | 1 | a0001c0001t0001g0233 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1109+346C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 7/10 | chr17 | 68541639 | |||||||
| chr17:68541669 | CTG | C | 85 | a0001c0001t0002g0004 a0001c0001t0002g0128 a0001c0001t0002g0146 others(82): Show |
86 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.1109+314_1109+315d others(4): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 7/10 | chr17 | 68541669 | |||||||
| chr17:68542243 | C | T | 1 | a0001c0005t0002g0084 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.929-78G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 6/10 | chr17 | 68542243 | |||||||
| chr17:68542277 | G | A | 75 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(72): Show |
76 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.929-112C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 6/10 | chr17 | 68542277 | |||||||
| chr17:68542354 | G | A | 4 | a0001c0001t0001g0268 a0001c0001t0001g0281 a0001c0001t0001g0346 others(1): Show |
4 | HG01346.hp2 HG02615.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.929-189C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 6/10 | chr17 | 68542354 | |||||||
| chr17:68542573 | C | T | 5 | a0001c0001t0001g0130 a0001c0001t0001g0133 a0001c0001t0001g0134 others(2): Show |
5 | NA18950.hp2 NA18969.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.928+121G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 6/10 | chr17 | 68542573 | |||||||
| chr17:68542652 | G | A | 5 | a0002c0002t0001g0131 a0002c0002t0001g0132 a0002c0002t0001g0224 others(2): Show |
5 | HG02293.hp2 NA18942.hp2 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.928+42C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 6/10 | chr17 | 68542652 | |||||||
| chr17:68542678 | C | T | 8 | a0001c0001t0001g0182 a0001c0001t0001g0189 a0001c0001t0001g0287 others(5): Show |
8 | HG02109.hp2 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.928+16G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 6/10 | chr17 | 68542678 | |||||||
| chr17:68542871 | T | C | 12 | a0001c0001t0005g0007 a0001c0001t0005g0141 a0001c0001t0005g0201 others(9): Show |
13 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.813-62A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 5/10 | chr17 | 68542871 | |||||||
| chr17:68542885 | T | G | 4 | a0002c0002t0001g0258 a0002c0002t0001g0325 a0002c0007t0001g0073 others(1): Show |
4 | HG00408.hp2 NA18939.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.813-76A>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 5/10 | chr17 | 68542885 | |||||||
| chr17:68542925 | G | A | 2 | a0001c0001t0002g0280 a0001c0001t0012g0013 |
2 | HG01358.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.813-116C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 5/10 | chr17 | 68542925 | |||||||
| chr17:68542964 | A | G | 1 | a0001c0001t0012g0013 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.813-155T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 5/10 | chr17 | 68542964 | |||||||
| chr17:68543240 | A | G | 1 | a0001c0001t0002g0280 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.812+389T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 5/10 | chr17 | 68543240 | |||||||
| chr17:68543294 | T | C | 45 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(42): Show |
46 | HG00140.hp2 HG00323.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.812+335A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 5/10 | chr17 | 68543294 | |||||||
| chr17:68543420 | G | A | 1 | a0002c0007t0001g0080 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.812+209C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 5/10 | chr17 | 68543420 | |||||||
| chr17:68543580 | G | A | 82 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(79): Show |
83 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.812+49C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 5/10 | chr17 | 68543580 | |||||||
| chr17:68544124 | G | A | 1 | a0001c0001t0002g0172 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.720-403C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68544124 | |||||||
| chr17:68544128 | G | T | 1 | a0003c0006t0001g0205 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.720-407C>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68544128 | |||||||
| chr17:68544248 | T | TC | 135 | a0001c0001t0002g0280 a0001c0001t0012g0013 a0002c0002t0001g0129 others(132): Show |
136 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.720-528dupG | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68544248 | |||||||
| chr17:68544338 | C | A | 1 | a0001c0001t0002g0156 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.720-617G>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68544338 | |||||||
| chr17:68544409 | A | G | 1 | a0001c0001t0002g0228 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.720-688T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68544409 | |||||||
| chr17:68544566 | T | A | 3 | a0001c0001t0002g0292 a0001c0001t0002g0324 a0001c0004t0002g0017 |
3 | HG03704.hp1 HG04199.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.720-845A>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68544566 | |||||||
| chr17:68544669 | A | G | 135 | a0001c0001t0012g0013 a0002c0002t0001g0129 a0002c0002t0001g0131 others(132): Show |
136 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.720-948T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68544669 | |||||||
| chr17:68544711 | GC | G | 4 | a0001c0001t0001g0003 a0001c0001t0001g0137 a0001c0001t0001g0155 others(1): Show |
5 | HG00140.hp2 HG01069.hp1 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.720-991delG | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68544711 | |||||||
| chr17:68544934 | T | C | 176 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(173): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.720-1213A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68544934 | |||||||
| chr17:68545019 | T | G | 7 | a0001c0001t0006g0207 a0001c0001t0006g0208 a0001c0001t0006g0218 others(4): Show |
7 | HG02451.hp2 HG02572.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.720-1298A>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68545019 | |||||||
| chr17:68545272 | C | T | 76 | a0001c0001t0001g0261 a0001c0001t0002g0004 a0001c0001t0002g0128 others(73): Show |
77 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.720-1551G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68545272 | |||||||
| chr17:68545273 | G | A | 1 | a0002c0002t0024g0371 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.720-1552C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68545273 | |||||||
| chr17:68545402 | C | T | 2 | a0001c0001t0001g0240 a0001c0001t0001g0253 |
2 | HG02886.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.720-1681G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68545402 | |||||||
| chr17:68545529 | T | A | 122 | a0001c0001t0001g0233 a0001c0001t0012g0013 a0002c0002t0001g0129 others(119): Show |
123 | HG00280.hp2 HG00408.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.720-1808A>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68545529 | |||||||
| chr17:68545722 | T | C | 4 | a0002c0002t0001g0162 a0002c0007t0001g0064 a0002c0008t0001g0042 others(1): Show |
4 | HG02129.hp1 NA18747.hp2 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.720-2001A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68545722 | |||||||
| chr17:68545907 | T | C | 77 | a0001c0001t0001g0151 a0001c0001t0001g0190 a0001c0001t0001g0191 others(74): Show |
78 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.720-2186A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68545907 | |||||||
| chr17:68545921 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.720-2200C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68545921 | |||||||
| chr17:68545966 | GAGACCAT others(654): Show |
G | 1 | a0001c0001t0002g0217 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.720-2906_720-2246d others(2): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68545966 | |||||||
| chr17:68545985 | C | T | 1 | a0001c0005t0002g0121 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.720-2264G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68545985 | |||||||
| chr17:68546156 | G | A | 1 | a0001c0001t0003g0309 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.720-2435C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68546156 | |||||||
| chr17:68546168 | C | CA | 8 | a0001c0001t0001g0216 a0001c0001t0002g0204 a0001c0001t0002g0221 others(5): Show |
8 | HG01433.hp1 HG01496.hp1 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.720-2448dupT | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68546168 | |||||||
| chr17:68546168 | CAA | C | 30 | a0001c0001t0001g0347 a0001c0001t0002g0004 a0001c0001t0002g0156 others(27): Show |
31 | HG01099.hp2 HG02055.hp2 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.720-2449_720-2448d others(4): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68546168 | |||||||
| chr17:68546168 | CAAA | C | 33 | a0001c0001t0001g0182 a0001c0001t0001g0189 a0001c0001t0001g0268 others(30): Show |
34 | HG01069.hp2 HG01071.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.720-2450_720-2448d others(5): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68546168 | |||||||
| chr17:68546168 | CAAAAAAA | C | 6 | a0001c0001t0001g0195 a0001c0004t0004g0054 a0001c0005t0002g0076 others(3): Show |
6 | HG02155.hp2 HG02895.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.720-2454_720-2448d others(9): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68546168 | |||||||
| chr17:68546168 | CAAAAAAA others(1): Show |
C | 242 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(239): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.720-2455_720-2448d others(10): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68546168 | |||||||
| chr17:68546168 | CAAAAAAA others(2): Show |
C | 7 | a0001c0001t0002g0228 a0001c0004t0004g0051 a0001c0005t0003g0107 others(4): Show |
7 | HG00323.hp2 HG01099.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.720-2456_720-2448d others(11): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68546168 | |||||||
| chr17:68546195 | A | G | 254 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(251): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.720-2474T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68546195 | |||||||
| chr17:68546407 | C | A | 2 | a0002c0002t0001g0197 a0002c0002t0001g0198 |
2 | HG02055.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.720-2686G>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68546407 | |||||||
| chr17:68546414 | A | G | 1 | a0003c0006t0001g0276 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.720-2693T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68546414 | |||||||
| chr17:68546416 | T | A | 1 | a0002c0008t0001g0038 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.720-2695A>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68546416 | |||||||
| chr17:68546627 | A | G | 15 | a0001c0001t0001g0268 a0001c0001t0001g0270 a0001c0001t0001g0281 others(12): Show |
16 | HG01069.hp2 HG01071.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.720-2906T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68546627 | |||||||
| chr17:68546680 | A | G | 6 | a0001c0001t0005g0007 a0001c0001t0005g0141 a0001c0001t0005g0201 others(3): Show |
7 | HG01069.hp2 HG01071.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.720-2959T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68546680 | |||||||
| chr17:68546754 | C | T | 2 | a0002c0002t0001g0197 a0002c0002t0001g0198 |
2 | HG02055.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.720-3033G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68546754 | |||||||
| chr17:68546817 | G | A | 3 | a0001c0001t0002g0188 a0003c0006t0001g0271 a0003c0018t0001g0016 |
3 | HG02723.hp1 HG03041.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.720-3096C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68546817 | |||||||
| chr17:68546829 | C | CA | 54 | a0001c0001t0001g0134 a0001c0001t0001g0190 a0001c0001t0001g0191 others(51): Show |
55 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(52): Show |
intron_variant | MODIFIER | c.720-3109dupT | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68546829 | |||||||
| chr17:68546829 | CA | C | 134 | a0001c0001t0001g0151 a0001c0001t0001g0161 a0001c0001t0001g0233 others(131): Show |
135 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.720-3109delT | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68546829 | |||||||
| chr17:68546940 | C | T | 7 | a0001c0001t0001g0252 a0001c0001t0021g0202 a0001c0001t0022g0362 others(4): Show |
7 | HG01109.hp2 HG02055.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.720-3219G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68546940 | |||||||
| chr17:68546981 | C | T | 1 | a0001c0004t0002g0049 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.720-3260G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68546981 | |||||||
| chr17:68547019 | T | A | 1 | a0001c0001t0001g0355 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.720-3298A>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68547019 | |||||||
| chr17:68547112 | A | T | 71 | a0001c0001t0001g0182 a0001c0001t0001g0189 a0001c0001t0001g0190 others(68): Show |
72 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.720-3391T>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68547112 | |||||||
| chr17:68547277 | A | T | 1 | a0001c0001t0001g0165 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.720-3556T>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68547277 | |||||||
| chr17:68547304 | G | A | 183 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(180): Show |
185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.720-3583C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68547304 | |||||||
| chr17:68547599 | C | T | 2 | a0001c0001t0002g0211 a0001c0001t0002g0273 |
2 | HG01243.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.720-3878G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68547599 | |||||||
| chr17:68547646 | T | C | 1 | a0002c0002t0001g0258 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.720-3925A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68547646 | |||||||
| chr17:68547771 | G | A | 1 | a0001c0001t0012g0013 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.720-4050C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68547771 | |||||||
| chr17:68547832 | T | C | 71 | a0001c0001t0001g0182 a0001c0001t0001g0189 a0001c0001t0001g0190 others(68): Show |
72 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.719+4041A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68547832 | |||||||
| chr17:68547871 | C | T | 70 | a0001c0001t0001g0182 a0001c0001t0001g0189 a0001c0001t0001g0190 others(67): Show |
71 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.719+4002G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68547871 | |||||||
| chr17:68547918 | C | T | 13 | a0001c0001t0001g0346 a0001c0001t0005g0283 a0001c0001t0005g0284 others(10): Show |
13 | HG01099.hp2 HG01891.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.719+3955G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68547918 | |||||||
| chr17:68548024 | ATTG | A | 214 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(211): Show |
218 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.719+3846_719+3848d others(5): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68548024 | |||||||
| chr17:68548120 | T | C | 71 | a0001c0001t0001g0182 a0001c0001t0001g0189 a0001c0001t0001g0190 others(68): Show |
72 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.719+3753A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68548120 | |||||||
| chr17:68548188 | G | C | 3 | a0001c0001t0001g0212 a0001c0001t0001g0216 a0001c0001t0001g0351 |
3 | HG02818.hp1 NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.719+3685C>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68548188 | |||||||
| chr17:68548222 | C | T | 3 | a0001c0001t0006g0218 a0001c0001t0006g0314 a0001c0005t0006g0116 |
3 | HG02717.hp2 HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.719+3651G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68548222 | |||||||
| chr17:68548314 | G | A | 1 | a0001c0001t0001g0352 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.719+3559C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68548314 | |||||||
| chr17:68548328 | G | A | 18 | a0001c0001t0001g0212 a0001c0001t0001g0216 a0001c0001t0001g0252 others(15): Show |
18 | HG01099.hp2 HG01109.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.719+3545C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68548328 | |||||||
| chr17:68548347 | C | T | 1 | a0002c0003t0017g0142 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.719+3526G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68548347 | |||||||
| chr17:68548359 | G | A | 1 | a0001c0001t0002g0184 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.719+3514C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68548359 | |||||||
| chr17:68548378 | A | G | 7 | a0002c0002t0001g0147 a0002c0002t0001g0159 a0002c0002t0001g0333 others(4): Show |
7 | HG00621.hp2 HG00673.hp1 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.719+3495T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68548378 | |||||||
| chr17:68548462 | A | G | 71 | a0001c0001t0001g0182 a0001c0001t0001g0189 a0001c0001t0001g0190 others(68): Show |
72 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.719+3411T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68548462 | |||||||
| chr17:68548522 | T | A | 5 | a0001c0001t0001g0195 a0001c0001t0001g0264 a0001c0001t0001g0265 others(2): Show |
5 | HG03831.hp1 NA18979.hp2 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.719+3351A>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68548522 | |||||||
| chr17:68548616 | C | T | 1 | a0002c0002t0001g0162 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.719+3257G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68548616 | |||||||
| chr17:68548637 | G | A | 1 | a0001c0004t0001g0044 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.719+3236C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68548637 | |||||||
| chr17:68548643 | C | T | 66 | a0001c0001t0001g0182 a0001c0001t0001g0189 a0001c0001t0001g0213 others(63): Show |
67 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.719+3230G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68548643 | |||||||
| chr17:68548723 | A | AT | 16 | a0001c0001t0002g0209 a0001c0001t0002g0272 a0001c0001t0002g0273 others(13): Show |
16 | HG02258.hp2 HG02630.hp2 HG02922.hp1 others(13): Show |
intron_variant | MODIFIER | c.719+3149dupA | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68548723 | |||||||
| chr17:68548723 | A | ATT | 33 | a0001c0001t0001g0191 a0001c0001t0001g0193 a0001c0001t0001g0213 others(30): Show |
34 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.719+3149_719+3150i others(4): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68548723 | |||||||
| chr17:68548723 | A | ATTT | 6 | a0001c0001t0001g0190 a0001c0001t0002g0237 a0001c0001t0002g0310 others(3): Show |
6 | HG01106.hp1 HG01934.hp2 HG04204.hp1 others(3): Show |
intron_variant | MODIFIER | c.719+3149_719+3150i others(5): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68548723 | |||||||
| chr17:68548725 | A | AT | 101 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(98): Show |
103 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.719+3147dupA | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68548725 | |||||||
| chr17:68548725 | A | ATT | 14 | a0001c0001t0001g0195 a0001c0001t0001g0270 a0001c0001t0001g0347 others(11): Show |
14 | HG01123.hp2 HG01884.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.719+3146_719+3147d others(4): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68548725 | |||||||
| chr17:68548725 | A | T | 68 | a0001c0001t0001g0182 a0001c0001t0001g0189 a0001c0001t0001g0190 others(65): Show |
69 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.719+3148T>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68548725 | |||||||
| chr17:68548725 | AT | A | 24 | a0001c0001t0001g0212 a0001c0001t0001g0216 a0001c0001t0001g0351 others(21): Show |
25 | HG00140.hp1 HG00408.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.719+3147delA | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68548725 | |||||||
| chr17:68548725 | ATT | A | 12 | a0001c0001t0001g0346 a0001c0001t0005g0283 a0001c0001t0005g0284 others(9): Show |
12 | HG01099.hp2 HG01891.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.719+3146_719+3147d others(4): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68548725 | |||||||
| chr17:68548728 | T | A | 1 | a0002c0002t0001g0315 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.719+3145A>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68548728 | |||||||
| chr17:68548893 | C | T | 4 | a0001c0001t0002g0179 a0001c0001t0002g0228 a0001c0001t0002g0229 others(1): Show |
4 | HG00280.hp1 HG00323.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.719+2980G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68548893 | |||||||
| chr17:68548894 | G | A | 1 | a0003c0006t0001g0006 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.719+2979C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68548894 | |||||||
| chr17:68548984 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.719+2889T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68548984 | |||||||
| chr17:68549204 | A | G | 76 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0216 others(73): Show |
77 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.719+2669T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68549204 | |||||||
| chr17:68549311 | G | A | 310 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(307): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.719+2562C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68549311 | |||||||
| chr17:68549404 | T | G | 3 | a0001c0001t0021g0202 a0001c0001t0022g0362 a0003c0009t0001g0079 |
3 | HG02145.hp2 HG02258.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.719+2469A>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68549404 | |||||||
| chr17:68549494 | C | CA | 6 | a0001c0001t0002g0280 a0001c0005t0002g0106 a0002c0003t0011g0364 others(3): Show |
6 | HG01070.hp1 HG01071.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.719+2378dupT | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68549494 | |||||||
| chr17:68549494 | C | CAA | 51 | a0001c0001t0001g0213 a0001c0001t0001g0261 a0001c0001t0001g0269 others(48): Show |
52 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.719+2377_719+2378d others(4): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68549494 | |||||||
| chr17:68549510 | G | A | 53 | a0001c0001t0001g0213 a0001c0001t0001g0261 a0001c0001t0001g0269 others(50): Show |
54 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.719+2363C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68549510 | |||||||
| chr17:68549630 | C | T | 2 | a0002c0002t0001g0333 a0002c0002t0019g0294 |
2 | HG02300.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.719+2243G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68549630 | |||||||
| chr17:68549689 | A | G | 1 | a0002c0002t0001g0219 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.719+2184T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68549689 | |||||||
| chr17:68549773 | TGAGCATT others(8): Show |
T | 1 | a0001c0001t0002g0217 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.719+2085_719+2099d others(17): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68549773 | |||||||
| chr17:68549894 | C | T | 1 | a0002c0003t0009g0318 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.719+1979G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68549894 | |||||||
| chr17:68549901 | G | A | 50 | a0001c0001t0001g0213 a0001c0001t0001g0261 a0001c0001t0001g0269 others(47): Show |
51 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.719+1972C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68549901 | |||||||
| chr17:68549989 | G | A | 50 | a0001c0001t0001g0213 a0001c0001t0001g0261 a0001c0001t0001g0269 others(47): Show |
51 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.719+1884C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68549989 | |||||||
| chr17:68550002 | C | G | 3 | a0001c0001t0001g0145 a0001c0001t0001g0157 a0001c0001t0001g0165 |
3 | HG02083.hp1 HG02083.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.719+1871G>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68550002 | |||||||
| chr17:68550059 | C | T | 63 | a0001c0001t0001g0213 a0001c0001t0001g0261 a0001c0001t0001g0269 others(60): Show |
64 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.719+1814G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68550059 | |||||||
| chr17:68550067 | A | T | 1 | a0002c0003t0017g0142 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.719+1806T>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68550067 | |||||||
| chr17:68550164 | A | C | 1 | a0001c0001t0012g0013 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.719+1709T>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68550164 | |||||||
| chr17:68550280 | A | G | 1 | a0001c0001t0002g0186 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.719+1593T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68550280 | |||||||
| chr17:68550365 | G | A | 12 | a0001c0001t0001g0169 a0001c0001t0003g0168 a0001c0001t0003g0255 others(9): Show |
12 | HG00544.hp2 HG02129.hp1 NA18943.hp2 others(9): Show |
intron_variant | MODIFIER | c.719+1508C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68550365 | |||||||
| chr17:68550369 | C | CT | 11 | a0001c0001t0001g0213 a0001c0001t0002g0279 a0001c0001t0002g0280 others(8): Show |
11 | HG01069.hp2 HG01934.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.719+1503dupA | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68550369 | |||||||
| chr17:68550369 | C | CTT | 48 | a0001c0001t0001g0182 a0001c0001t0001g0189 a0001c0001t0001g0268 others(45): Show |
51 | HG01071.hp1 HG01106.hp2 HG01167.hp2 others(48): Show |
intron_variant | MODIFIER | c.719+1502_719+1503d others(4): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68550369 | |||||||
| chr17:68550369 | C | CTTT | 142 | a0001c0001t0001g0003 a0001c0001t0001g0137 a0001c0001t0001g0145 others(139): Show |
143 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.719+1501_719+1503d others(5): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68550369 | |||||||
| chr17:68550369 | C | CTTTT | 27 | a0001c0001t0001g0130 a0001c0001t0001g0133 a0001c0001t0001g0134 others(24): Show |
27 | HG00544.hp2 HG00741.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.719+1500_719+1503d others(6): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68550369 | |||||||
| chr17:68550393 | TTTTA | T | 12 | a0001c0001t0001g0346 a0001c0001t0005g0283 a0001c0001t0005g0284 others(9): Show |
12 | HG01099.hp2 HG01891.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.719+1476_719+1479d others(6): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68550393 | |||||||
| chr17:68550396 | T | TTTTA | 12 | a0002c0002t0001g0178 a0002c0002t0001g0194 a0002c0002t0007g0367 others(9): Show |
12 | HG02080.hp2 HG02523.hp1 NA18612.hp1 others(9): Show |
intron_variant | MODIFIER | c.719+1476_719+1477i others(6): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68550396 | |||||||
| chr17:68550396 | TA | T | 5 | a0001c0001t0001g0212 a0001c0001t0001g0216 a0001c0001t0001g0261 others(2): Show |
5 | HG01358.hp1 HG02818.hp1 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.719+1476delT | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68550396 | |||||||
| chr17:68550397 | A | T | 54 | a0001c0001t0001g0213 a0001c0001t0001g0269 a0001c0001t0002g0128 others(51): Show |
55 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.719+1476T>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68550397 | |||||||
| chr17:68550443 | C | T | 13 | a0001c0001t0001g0346 a0001c0001t0005g0283 a0001c0001t0005g0284 others(10): Show |
13 | HG01099.hp2 HG01891.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.719+1430G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68550443 | |||||||
| chr17:68550582 | T | C | 1 | a0001c0001t0001g0151 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.719+1291A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68550582 | |||||||
| chr17:68550653 | T | G | 1 | a0002c0002t0007g0366 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.719+1220A>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68550653 | |||||||
| chr17:68550943 | GGCTCTCA others(1): Show |
G | 16 | a0001c0001t0001g0212 a0001c0001t0001g0216 a0001c0001t0001g0346 others(13): Show |
16 | HG01099.hp2 HG01891.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.719+922_719+929del others(8): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68550943 | |||||||
| chr17:68550954 | G | A | 16 | a0001c0001t0001g0212 a0001c0001t0001g0216 a0001c0001t0001g0346 others(13): Show |
16 | HG01099.hp2 HG01891.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.719+919C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68550954 | |||||||
| chr17:68551029 | G | A | 1 | a0002c0007t0001g0102 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.719+844C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68551029 | |||||||
| chr17:68551066 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.719+807G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68551066 | |||||||
| chr17:68551067 | G | A | 1 | a0001c0001t0012g0013 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.719+806C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68551067 | |||||||
| chr17:68551108 | G | A | 49 | a0001c0001t0001g0213 a0001c0001t0001g0261 a0001c0001t0001g0269 others(46): Show |
50 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.719+765C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68551108 | |||||||
| chr17:68551268 | G | C | 34 | a0001c0001t0001g0213 a0001c0001t0001g0261 a0001c0001t0002g0128 others(31): Show |
35 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.719+605C>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68551268 | |||||||
| chr17:68551620 | A | G | 1 | a0003c0006t0001g0242 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.719+253T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68551620 | |||||||
| chr17:68551688 | A | AATT | 123 | a0001c0001t0001g0151 a0001c0001t0001g0161 a0001c0001t0001g0169 others(120): Show |
125 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.719+182_719+184dup others(3): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68551688 | |||||||
| chr17:68551688 | A | AATTATT | 59 | a0001c0001t0001g0133 a0001c0001t0001g0189 a0001c0001t0001g0191 others(56): Show |
61 | HG00621.hp1 HG00735.hp2 HG01109.hp1 others(58): Show |
intron_variant | MODIFIER | c.719+179_719+184dup others(6): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68551688 | |||||||
| chr17:68551688 | A | AATTATTA others(2): Show |
48 | a0001c0001t0001g0130 a0001c0001t0001g0137 a0001c0001t0001g0145 others(45): Show |
48 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.719+176_719+184dup others(9): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68551688 | |||||||
| chr17:68551688 | A | AATTATTA others(5): Show |
3 | a0001c0001t0001g0250 a0002c0002t0001g0131 a0002c0014t0001g0117 |
3 | HG02523.hp1 NA18977.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.719+173_719+184dup others(12): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68551688 | |||||||
| chr17:68551688 | AATT | A | 49 | a0001c0001t0001g0220 a0001c0001t0001g0222 a0001c0001t0001g0236 others(46): Show |
51 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.719+182_719+184del others(3): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68551688 | |||||||
| chr17:68551688 | AATTATTA others(5): Show |
A | 1 | a0001c0001t0002g0217 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.719+173_719+184del others(12): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68551688 | |||||||
| chr17:68551716 | ATTATTAT others(1): Show |
A | 13 | a0001c0001t0001g0346 a0001c0001t0005g0283 a0001c0001t0005g0284 others(10): Show |
13 | HG01099.hp2 HG01891.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.719+149_719+156del others(8): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68551716 | |||||||
| chr17:68551722 | ATT | A | 3 | a0001c0001t0001g0212 a0001c0001t0001g0216 a0001c0001t0001g0351 |
3 | HG02818.hp1 NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.719+149_719+150del others(2): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68551722 | |||||||
| chr17:68551724 | T | TATTATC | 5 | a0001c0001t0002g0211 a0001c0005t0002g0121 a0001c0005t0003g0107 others(2): Show |
6 | HG01243.hp1 HG01256.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.719+148_719+149ins others(6): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68551724 | |||||||
| chr17:68551724 | T | TATTATTA | 3 | a0001c0001t0022g0362 a0002c0002t0001g0197 a0002c0002t0001g0198 |
3 | HG02055.hp1 HG02258.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.719+148_719+149ins others(7): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68551724 | |||||||
| chr17:68551724 | T | TATTATTA others(2): Show |
13 | a0001c0001t0001g0269 a0001c0001t0002g0154 a0001c0001t0002g0237 others(10): Show |
13 | HG01074.hp2 HG01106.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.719+148_719+149ins others(9): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68551724 | |||||||
| chr17:68551724 | T | TATTATTA others(3): Show |
2 | a0001c0001t0021g0202 a0003c0009t0001g0079 |
2 | HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.719+148_719+149ins others(10): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68551724 | |||||||
| chr17:68551724 | T | TATTATTA others(5): Show |
25 | a0001c0001t0001g0003 a0001c0001t0001g0155 a0001c0001t0001g0235 others(22): Show |
26 | HG00280.hp1 HG01069.hp1 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.719+148_719+149ins others(12): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68551724 | |||||||
| chr17:68551724 | T | TATTATTA others(8): Show |
5 | a0001c0001t0001g0261 a0001c0001t0002g0228 a0001c0001t0002g0231 others(2): Show |
5 | HG00099.hp2 HG00323.hp2 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.719+148_719+149ins others(15): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68551724 | |||||||
| chr17:68551724 | T | TATTATTA others(11): Show |
2 | a0001c0001t0002g0335 a0001c0001t0002g0336 |
2 | HG02040.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.719+148_719+149ins others(18): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68551724 | |||||||
| chr17:68552099 | G | A | 3 | a0002c0003t0001g0199 a0002c0003t0001g0200 a0002c0003t0001g0298 |
3 | HG02559.hp1 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.641-148C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68552099 | |||||||
| chr17:68552154 | C | G | 1 | a0001c0001t0002g0280 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.641-203G>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68552154 | |||||||
| chr17:68552172 | G | A | 1 | a0001c0001t0002g0337 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.641-221C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68552172 | |||||||
| chr17:68552242 | G | GA | 14 | a0001c0001t0001g0346 a0001c0001t0005g0283 a0001c0001t0005g0284 others(11): Show |
14 | HG01099.hp2 HG01891.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.641-292dupT | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68552242 | |||||||
| chr17:68552316 | C | T | 235 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(232): Show |
239 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.641-365G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68552316 | |||||||
| chr17:68552345 | C | T | 2 | a0001c0001t0001g0347 a0001c0004t0008g0009 |
2 | HG02055.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.641-394G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68552345 | |||||||
| chr17:68552650 | GTAAACCT others(323): Show |
G | 46 | a0001c0001t0001g0261 a0001c0001t0001g0269 a0001c0001t0002g0128 others(43): Show |
47 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.641-1029_641-700de others(1): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68552650 | |||||||
| chr17:68552654 | ACCTTTAT others(324): Show |
A | 3 | a0001c0001t0001g0213 a0001c0001t0002g0244 a0001c0001t0002g0319 |
3 | HG01070.hp2 HG02738.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.641-1034_641-704de others(1): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68552654 | |||||||
| chr17:68552665 | C | CTTT | 3 | a0001c0001t0006g0275 a0002c0002t0001g0197 a0002c0002t0001g0198 |
3 | HG02055.hp1 HG02451.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.641-715_641-714ins others(3): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68552665 | |||||||
| chr17:68552665 | C | CTTTT | 15 | a0001c0001t0001g0216 a0001c0001t0001g0346 a0001c0001t0001g0351 others(12): Show |
15 | HG01099.hp2 HG01891.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.641-715_641-714ins others(4): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68552665 | |||||||
| chr17:68552665 | C | CTTTTT | 3 | a0001c0001t0001g0212 a0001c0001t0022g0362 a0004c0011t0005g0062 |
3 | HG02258.hp1 HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.641-715_641-714ins others(5): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68552665 | |||||||
| chr17:68552665 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0252 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.641-715_641-714ins others(10): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68552665 | |||||||
| chr17:68552665 | C | CTTTTTTT others(4): Show |
1 | a0001c0004t0008g0012 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.641-715_641-714ins others(11): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68552665 | |||||||
| chr17:68552666 | C | CT | 58 | a0001c0001t0001g0235 a0001c0001t0001g0264 a0001c0001t0001g0293 others(55): Show |
58 | HG00544.hp2 HG00597.hp2 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.641-716dupA | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68552666 | |||||||
| chr17:68552666 | C | CTT | 87 | a0001c0001t0001g0151 a0001c0001t0001g0191 a0001c0001t0001g0193 others(84): Show |
88 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.641-717_641-716dup others(2): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68552666 | |||||||
| chr17:68552666 | C | CTTT | 17 | a0001c0001t0001g0161 a0001c0001t0001g0190 a0001c0001t0002g0146 others(14): Show |
17 | HG00597.hp1 HG01109.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.641-718_641-716dup others(3): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68552666 | |||||||
| chr17:68552666 | C | T | 24 | a0001c0001t0001g0212 a0001c0001t0001g0216 a0001c0001t0001g0252 others(21): Show |
24 | HG01099.hp2 HG01109.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.641-715G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68552666 | |||||||
| chr17:68552666 | CTTTTTTT others(6): Show |
C | 1 | a0002c0003t0001g0180 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.641-728_641-716del others(13): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68552666 | |||||||
| chr17:68552705 | C | T | 2 | a0001c0001t0001g0182 a0008c0022t0002g0331 |
2 | HG02109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.641-754G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68552705 | |||||||
| chr17:68552723 | G | A | 3 | a0002c0003t0001g0199 a0002c0003t0001g0200 a0002c0003t0001g0298 |
3 | HG02559.hp1 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.641-772C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68552723 | |||||||
| chr17:68552743 | G | A | 2 | a0002c0002t0001g0197 a0002c0002t0001g0198 |
2 | HG02055.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.641-792C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68552743 | |||||||
| chr17:68552762 | A | G | 1 | a0001c0001t0003g0309 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.641-811T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68552762 | |||||||
| chr17:68552774 | C | T | 16 | a0001c0001t0001g0252 a0001c0001t0001g0346 a0001c0001t0005g0283 others(13): Show |
16 | HG01099.hp2 HG01109.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.641-823G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68552774 | |||||||
| chr17:68552780 | C | G | 3 | a0001c0001t0001g0212 a0001c0001t0001g0216 a0001c0001t0001g0351 |
3 | HG02818.hp1 NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.641-829G>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68552780 | |||||||
| chr17:68552871 | C | T | 1 | a0001c0005t0002g0125 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.641-920G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68552871 | |||||||
| chr17:68552903 | G | A | 3 | a0002c0003t0001g0199 a0002c0003t0001g0200 a0002c0003t0001g0298 |
3 | HG02559.hp1 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.641-952C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68552903 | |||||||
| chr17:68553090 | G | C | 21 | a0001c0001t0001g0252 a0001c0001t0001g0346 a0001c0001t0002g0280 others(18): Show |
21 | HG01099.hp2 HG01109.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.641-1139C>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68553090 | |||||||
| chr17:68553328 | T | G | 1 | a0001c0001t0001g0165 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.641-1377A>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68553328 | |||||||
| chr17:68553331 | A | T | 3 | a0001c0001t0001g0212 a0001c0001t0001g0216 a0001c0001t0001g0351 |
3 | HG02818.hp1 NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.641-1380T>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68553331 | |||||||
| chr17:68553657 | G | A | 49 | a0001c0001t0001g0213 a0001c0001t0001g0261 a0001c0001t0001g0269 others(46): Show |
50 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.640+1120C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68553657 | |||||||
| chr17:68553685 | G | T | 49 | a0001c0001t0001g0213 a0001c0001t0001g0261 a0001c0001t0001g0269 others(46): Show |
50 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.640+1092C>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68553685 | |||||||
| chr17:68553745 | CACATATA others(3): Show |
C | 2 | a0002c0007t0001g0104 a0003c0006t0001g0170 |
2 | HG00673.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.640+1022_640+1031d others(12): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68553745 | |||||||
| chr17:68553747 | CATATATA others(5): Show |
C | 1 | a0001c0001t0001g0216 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.640+1018_640+1029d others(14): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68553747 | |||||||
| chr17:68553759 | TATATATA others(1): Show |
T | 33 | a0001c0001t0001g0268 a0001c0001t0001g0270 a0001c0001t0001g0274 others(30): Show |
35 | HG01069.hp2 HG01071.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.640+1010_640+1017d others(10): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68553759 | |||||||
| chr17:68553791 | CACAT | C | 51 | a0001c0001t0001g0213 a0001c0001t0001g0252 a0001c0001t0001g0261 others(48): Show |
52 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.640+982_640+985del others(4): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68553791 | |||||||
| chr17:68553889 | T | TACACATA others(21): Show |
20 | a0001c0001t0001g0145 a0001c0001t0001g0157 a0001c0001t0001g0165 others(17): Show |
20 | HG00140.hp1 HG00558.hp2 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.640+860_640+887dup others(28): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68553889 | |||||||
| chr17:68553889 | TACACATA others(21): Show |
T | 49 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0261 others(46): Show |
49 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.640+860_640+887del others(28): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68553889 | |||||||
| chr17:68553910 | A | C | 9 | a0001c0001t0002g0204 a0001c0001t0002g0221 a0001c0001t0002g0280 others(6): Show |
9 | HG01981.hp2 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.640+867T>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68553910 | |||||||
| chr17:68553911 | T | C | 1 | a0002c0003t0001g0135 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.640+866A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68553911 | |||||||
| chr17:68553915 | TACACACA others(23): Show |
T | 21 | a0001c0001t0001g0252 a0001c0001t0001g0346 a0001c0001t0002g0280 others(18): Show |
21 | HG01099.hp2 HG01109.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.640+832_640+861del others(30): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68553915 | |||||||
| chr17:68553937 | CATATATA others(23): Show |
C | 2 | a0001c0001t0002g0154 a0001c0001t0002g0310 |
2 | HG01928.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.640+810_640+839del others(30): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68553937 | |||||||
| chr17:68553938 | A | C | 2 | a0002c0002t0001g0215 a0002c0002t0001g0328 |
2 | HG02615.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.640+839T>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68553938 | |||||||
| chr17:68553982 | A | G | 1 | a0001c0001t0003g0245 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.640+795T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68553982 | |||||||
| chr17:68553993 | T | C | 1 | a0001c0001t0003g0266 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.640+784A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68553993 | |||||||
| chr17:68553996 | A | C | 2 | a0002c0002t0001g0291 a0002c0002t0001g0317 |
2 | HG01123.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.640+781T>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68553996 | |||||||
| chr17:68554006 | GCATATAT others(1): Show |
G | 2 | a0003c0006t0001g0005 a0003c0006t0001g0160 |
3 | HG01256.hp1 HG01258.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.640+763_640+770del others(8): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68554006 | |||||||
| chr17:68554008 | A | G | 1 | a0002c0002t0001g0257 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.640+769T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68554008 | |||||||
| chr17:68554014 | A | ACATATAT others(11): Show |
3 | a0001c0001t0006g0218 a0001c0001t0006g0314 a0001c0005t0006g0116 |
3 | HG02717.hp2 HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.640+762_640+763ins others(18): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68554014 | |||||||
| chr17:68554014 | A | G | 14 | a0001c0001t0001g0182 a0001c0001t0001g0189 a0001c0001t0001g0287 others(11): Show |
14 | HG02109.hp2 HG02615.hp2 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.640+763T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68554014 | |||||||
| chr17:68554021 | T | TAC | 3 | a0001c0001t0001g0212 a0001c0001t0001g0351 a0002c0002t0001g0332 |
3 | HG01074.hp1 NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.640+754_640+755dup others(2): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68554021 | |||||||
| chr17:68554023 | CATATAT | C | 29 | a0001c0001t0001g0268 a0001c0001t0001g0270 a0001c0001t0001g0281 others(26): Show |
31 | HG01069.hp2 HG01071.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.640+748_640+753del others(6): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68554023 | |||||||
| chr17:68554025 | T | C | 51 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0261 others(48): Show |
51 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.640+752A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68554025 | |||||||
| chr17:68554027 | T | C | 48 | a0001c0001t0001g0213 a0001c0001t0001g0261 a0001c0001t0001g0269 others(45): Show |
48 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.640+750A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68554027 | |||||||
| chr17:68554030 | A | G | 51 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0261 others(48): Show |
51 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.640+747T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68554030 | |||||||
| chr17:68554033 | C | T | 51 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0261 others(48): Show |
51 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.640+744G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68554033 | |||||||
| chr17:68554035 | C | CAT | 24 | a0001c0001t0001g0252 a0001c0001t0001g0346 a0001c0001t0002g0280 others(21): Show |
24 | HG01099.hp2 HG01109.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.640+740_640+741dup others(2): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68554035 | |||||||
| chr17:68554035 | C | CATATGCA others(3): Show |
1 | a0001c0001t0012g0013 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.640+741_640+742ins others(10): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68554035 | |||||||
| chr17:68554035 | C | CATATGCA others(3): Show |
200 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(197): Show |
202 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.640+741_640+742ins others(10): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68554035 | |||||||
| chr17:68554035 | C | T | 83 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0261 others(80): Show |
85 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.640+742G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68554035 | |||||||
| chr17:68554038 | G | A | 252 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(249): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.640+739C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68554038 | |||||||
| chr17:68554038 | G | GCATATAT others(1): Show |
4 | a0001c0001t0002g0184 a0001c0001t0002g0187 a0001c0001t0002g0188 others(1): Show |
4 | HG00738.hp1 HG01167.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.640+731_640+738dup others(8): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68554038 | |||||||
| chr17:68554049 | C | T | 54 | a0001c0001t0001g0252 a0001c0001t0001g0268 a0001c0001t0001g0270 others(51): Show |
57 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.640+728G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68554049 | |||||||
| chr17:68554057 | C | T | 256 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(253): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.640+720G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68554057 | |||||||
| chr17:68554061 | T | TACATATA others(5): Show |
1 | a0003c0006t0001g0005 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.640+715_640+716ins others(12): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68554061 | |||||||
| chr17:68554061 | TAC | T | 32 | a0001c0001t0001g0268 a0001c0001t0001g0270 a0001c0001t0001g0281 others(29): Show |
34 | HG01069.hp2 HG01071.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.640+714_640+715del others(2): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68554061 | |||||||
| chr17:68554063 | C | CATATAT | 21 | a0001c0001t0001g0252 a0001c0001t0001g0346 a0001c0001t0002g0280 others(18): Show |
21 | HG01099.hp2 HG01109.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.640+713_640+714ins others(6): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68554063 | |||||||
| chr17:68554067 | C | CACAT | 48 | a0001c0001t0001g0213 a0001c0001t0001g0261 a0001c0001t0001g0269 others(45): Show |
48 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.640+709_640+710ins others(4): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68554067 | |||||||
| chr17:68554067 | C | T | 33 | a0001c0001t0001g0268 a0001c0001t0001g0270 a0001c0001t0001g0281 others(30): Show |
36 | HG01069.hp2 HG01071.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.640+710G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68554067 | |||||||
| chr17:68554091 | TAC | T | 15 | a0001c0001t0001g0252 a0001c0001t0001g0346 a0001c0001t0005g0283 others(12): Show |
15 | HG01099.hp2 HG01109.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.640+684_640+685del others(2): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68554091 | |||||||
| chr17:68554127 | C | CAT | 28 | a0001c0001t0001g0130 a0001c0001t0001g0133 a0001c0001t0001g0134 others(25): Show |
28 | HG00544.hp2 HG02071.hp1 HG02071.hp2 others(25): Show |
intron_variant | MODIFIER | c.640+648_640+649dup others(2): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68554127 | |||||||
| chr17:68554127 | CAT | C | 109 | a0001c0001t0001g0195 a0001c0001t0001g0212 a0001c0001t0001g0213 others(106): Show |
112 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.640+648_640+649del others(2): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68554127 | |||||||
| chr17:68554237 | T | C | 1 | a0001c0001t0012g0013 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.640+540A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68554237 | |||||||
| chr17:68554292 | G | C | 1 | a0002c0002t0001g0258 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.640+485C>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68554292 | |||||||
| chr17:68554352 | C | T | 49 | a0001c0001t0001g0213 a0001c0001t0001g0261 a0001c0001t0001g0269 others(46): Show |
50 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.640+425G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68554352 | |||||||
| chr17:68554397 | G | A | 1 | a0001c0001t0002g0244 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.640+380C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68554397 | |||||||
| chr17:68554676 | C | T | 1 | a0002c0008t0001g0042 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.640+101G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68554676 | |||||||
| chr17:68554746 | G | A | 49 | a0001c0001t0001g0213 a0001c0001t0001g0261 a0001c0001t0001g0269 others(46): Show |
50 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.640+31C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68554746 | |||||||
| chr17:68554766 | A | G | 14 | a0001c0001t0001g0182 a0001c0001t0001g0189 a0001c0001t0001g0287 others(11): Show |
14 | HG02109.hp2 HG02615.hp2 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.640+11T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 3/10 | chr17 | 68554766 | |||||||
| chr17:68554869 | T | C | 15 | a0001c0001t0001g0252 a0001c0001t0001g0346 a0001c0001t0005g0283 others(12): Show |
15 | HG01099.hp2 HG01109.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.590-42A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 2/10 | chr17 | 68554869 | |||||||
| chr17:68555783 | T | A | 1 | a0002c0003t0001g0230 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.405-40A>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68555783 | |||||||
| chr17:68555820 | T | G | 1 | a0002c0002t0001g0299 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.405-77A>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68555820 | |||||||
| chr17:68555887 | T | G | 13 | a0001c0001t0001g0346 a0001c0001t0005g0283 a0001c0001t0005g0284 others(10): Show |
13 | HG01099.hp2 HG01891.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.405-144A>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68555887 | |||||||
| chr17:68556002 | T | C | 53 | a0001c0001t0001g0213 a0001c0001t0001g0261 a0001c0001t0001g0269 others(50): Show |
54 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.405-259A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68556002 | |||||||
| chr17:68556097 | G | A | 8 | a0001c0001t0001g0130 a0001c0001t0001g0133 a0001c0001t0001g0134 others(5): Show |
8 | NA18942.hp2 NA18950.hp2 NA18969.hp2 others(5): Show |
intron_variant | MODIFIER | c.405-354C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68556097 | |||||||
| chr17:68556154 | A | G | 53 | a0001c0001t0001g0213 a0001c0001t0001g0261 a0001c0001t0001g0269 others(50): Show |
54 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.405-411T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68556154 | |||||||
| chr17:68556248 | G | T | 13 | a0001c0001t0001g0346 a0001c0001t0005g0283 a0001c0001t0005g0284 others(10): Show |
13 | HG01099.hp2 HG01891.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.405-505C>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68556248 | |||||||
| chr17:68556270 | G | T | 4 | a0001c0004t0002g0030 a0001c0004t0002g0057 a0001c0004t0002g0059 others(1): Show |
4 | HG02074.hp1 NA18989.hp1 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.405-527C>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68556270 | |||||||
| chr17:68556442 | C | T | 1 | a0003c0006t0001g0214 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.405-699G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68556442 | |||||||
| chr17:68556469 | A | C | 53 | a0001c0001t0001g0213 a0001c0001t0001g0261 a0001c0001t0001g0269 others(50): Show |
54 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.405-726T>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68556469 | |||||||
| chr17:68556469 | A | T | 1 | a0001c0001t0012g0013 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.405-726T>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68556469 | |||||||
| chr17:68556544 | A | C | 1 | a0001c0005t0002g0085 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.405-801T>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68556544 | |||||||
| chr17:68556574 | A | G | 53 | a0001c0001t0001g0213 a0001c0001t0001g0261 a0001c0001t0001g0269 others(50): Show |
54 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.405-831T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68556574 | |||||||
| chr17:68556580 | G | C | 1 | a0001c0001t0001g0252 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.405-837C>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68556580 | |||||||
| chr17:68556580 | G | T | 4 | a0001c0001t0002g0280 a0001c0001t0021g0202 a0001c0001t0022g0362 others(1): Show |
4 | HG02145.hp2 HG02258.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.405-837C>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68556580 | |||||||
| chr17:68556581 | G | C | 53 | a0001c0001t0001g0213 a0001c0001t0001g0261 a0001c0001t0001g0269 others(50): Show |
54 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.405-838C>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68556581 | |||||||
| chr17:68556585 | G | T | 1 | a0002c0003t0017g0142 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.405-842C>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68556585 | |||||||
| chr17:68556600 | G | A | 1 | a0002c0002t0001g0162 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.405-857C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68556600 | |||||||
| chr17:68556641 | A | G | 13 | a0001c0001t0001g0346 a0001c0001t0005g0283 a0001c0001t0005g0284 others(10): Show |
13 | HG01099.hp2 HG01891.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.405-898T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68556641 | |||||||
| chr17:68556816 | G | C | 21 | a0001c0001t0001g0182 a0001c0001t0001g0189 a0001c0001t0001g0212 others(18): Show |
21 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.405-1073C>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68556816 | |||||||
| chr17:68556823 | C | T | 2 | a0001c0001t0002g0237 a0004c0011t0002g0061 |
2 | HG01106.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.405-1080G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68556823 | |||||||
| chr17:68556867 | T | C | 56 | a0001c0001t0001g0213 a0001c0001t0001g0252 a0001c0001t0001g0261 others(53): Show |
57 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.405-1124A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68556867 | |||||||
| chr17:68556914 | C | T | 1 | a0001c0001t0002g0187 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.405-1171G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68556914 | |||||||
| chr17:68556939 | G | C | 2 | a0001c0001t0001g0347 a0001c0004t0008g0009 |
2 | HG02055.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.405-1196C>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68556939 | |||||||
| chr17:68557178 | C | T | 2 | a0001c0001t0021g0202 a0001c0001t0022g0362 |
2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.405-1435G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68557178 | |||||||
| chr17:68557179 | G | A | 4 | a0001c0001t0005g0283 a0001c0001t0005g0284 a0001c0001t0005g0285 others(1): Show |
4 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.405-1436C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68557179 | |||||||
| chr17:68557180 | A | T | 1 | a0001c0001t0012g0013 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.405-1437T>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68557180 | |||||||
| chr17:68557200 | T | TA | 56 | a0001c0001t0001g0213 a0001c0001t0001g0261 a0001c0001t0001g0269 others(53): Show |
57 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.405-1458dupT | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68557200 | |||||||
| chr17:68557338 | T | C | 2 | a0001c0001t0002g0228 a0001c0001t0002g0229 |
2 | HG00280.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.405-1595A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68557338 | |||||||
| chr17:68557502 | G | A | 1 | a0001c0001t0002g0217 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.405-1759C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68557502 | |||||||
| chr17:68557574 | T | C | 13 | a0001c0001t0001g0182 a0001c0001t0001g0189 a0001c0001t0001g0287 others(10): Show |
13 | HG02109.hp2 HG02615.hp2 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.405-1831A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68557574 | |||||||
| chr17:68557639 | C | T | 1 | a0001c0005t0002g0083 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.405-1896G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68557639 | |||||||
| chr17:68557756 | A | G | 1 | a0001c0001t0002g0217 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.405-2013T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68557756 | |||||||
| chr17:68557773 | C | A | 2 | a0003c0006t0001g0342 a0003c0013t0001g0053 |
2 | HG01169.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.405-2030G>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68557773 | |||||||
| chr17:68557884 | T | C | 1 | a0012c0019t0010g0063 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.405-2141A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68557884 | |||||||
| chr17:68557886 | G | C | 1 | a0003c0006t0001g0170 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.405-2143C>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68557886 | |||||||
| chr17:68557958 | G | A | 53 | a0001c0001t0001g0213 a0001c0001t0001g0261 a0001c0001t0001g0269 others(50): Show |
54 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.405-2215C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68557958 | |||||||
| chr17:68558152 | C | T | 1 | a0001c0001t0012g0013 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.405-2409G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68558152 | |||||||
| chr17:68558199 | G | A | 2 | a0002c0002t0001g0185 a0002c0002t0001g0246 |
2 | HG00280.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.405-2456C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68558199 | |||||||
| chr17:68558215 | T | C | 1 | a0002c0003t0001g0230 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.405-2472A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68558215 | |||||||
| chr17:68558334 | A | G | 2 | a0001c0001t0002g0217 a0001c0001t0012g0013 |
2 | HG01358.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.405-2591T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68558334 | |||||||
| chr17:68558360 | C | G | 1 | a0001c0001t0012g0013 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.405-2617G>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68558360 | |||||||
| chr17:68558386 | C | G | 2 | a0001c0001t0002g0217 a0001c0001t0012g0013 |
2 | HG01358.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.405-2643G>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68558386 | |||||||
| chr17:68558391 | G | A | 3 | a0001c0001t0005g0201 a0001c0017t0005g0014 a0004c0011t0005g0060 |
3 | HG02559.hp2 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.405-2648C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68558391 | |||||||
| chr17:68558409 | T | G | 2 | a0001c0001t0002g0217 a0001c0001t0012g0013 |
2 | HG01358.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.405-2666A>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68558409 | |||||||
| chr17:68558536 | C | T | 3 | a0001c0001t0002g0186 a0002c0003t0001g0251 a0002c0003t0001g0349 |
3 | HG02809.hp1 HG03486.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.405-2793G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68558536 | |||||||
| chr17:68558600 | A | G | 1 | a0001c0001t0012g0013 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.405-2857T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68558600 | |||||||
| chr17:68558651 | C | G | 2 | a0001c0001t0001g0212 a0001c0001t0001g0351 |
2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.405-2908G>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68558651 | |||||||
| chr17:68559037 | C | T | 4 | a0001c0001t0002g0179 a0001c0001t0002g0226 a0001c0001t0002g0228 others(1): Show |
4 | HG00280.hp1 HG00323.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.405-3294G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68559037 | |||||||
| chr17:68559084 | C | T | 1 | a0004c0011t0005g0062 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.405-3341G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68559084 | |||||||
| chr17:68559129 | G | C | 2 | a0001c0001t0001g0347 a0001c0004t0008g0009 |
2 | HG02055.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.405-3386C>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68559129 | |||||||
| chr17:68559183 | G | A | 1 | a0001c0004t0002g0049 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.405-3440C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68559183 | |||||||
| chr17:68559345 | C | T | 2 | a0001c0001t0001g0133 a0001c0001t0025g0372 |
2 | NA18969.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.405-3602G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68559345 | |||||||
| chr17:68559353 | T | C | 1 | a0001c0004t0004g0027 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.405-3610A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68559353 | |||||||
| chr17:68559406 | C | A | 4 | a0001c0001t0001g0347 a0001c0004t0008g0009 a0001c0005t0002g0121 others(1): Show |
4 | HG02055.hp2 HG02965.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.405-3663G>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68559406 | |||||||
| chr17:68559582 | T | A | 1 | a0002c0007t0001g0102 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.405-3839A>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68559582 | |||||||
| chr17:68559670 | A | G | 1 | a0002c0003t0017g0142 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.405-3927T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68559670 | |||||||
| chr17:68559724 | G | A | 1 | a0001c0004t0001g0044 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.405-3981C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68559724 | |||||||
| chr17:68559757 | G | T | 1 | a0001c0004t0004g0036 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.405-4014C>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68559757 | |||||||
| chr17:68559817 | G | A | 1 | a0001c0001t0002g0280 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.405-4074C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68559817 | |||||||
| chr17:68560048 | A | T | 2 | a0001c0001t0021g0202 a0001c0001t0022g0362 |
2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.405-4305T>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68560048 | |||||||
| chr17:68560124 | T | C | 275 | a0001c0001t0001g0130 a0001c0001t0001g0133 a0001c0001t0001g0134 others(272): Show |
278 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(275): Show |
intron_variant | MODIFIER | c.405-4381A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68560124 | |||||||
| chr17:68560169 | T | C | 1 | a0002c0003t0017g0142 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.405-4426A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68560169 | |||||||
| chr17:68560193 | A | G | 15 | a0001c0001t0001g0189 a0001c0001t0001g0287 a0001c0001t0001g0293 others(12): Show |
15 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.405-4450T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68560193 | |||||||
| chr17:68560294 | G | A | 18 | a0001c0001t0001g0189 a0001c0001t0001g0216 a0001c0001t0001g0287 others(15): Show |
18 | HG01358.hp1 HG02055.hp1 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.405-4551C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68560294 | |||||||
| chr17:68560322 | C | T | 1 | a0001c0001t0001g0351 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.405-4579G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68560322 | |||||||
| chr17:68560339 | A | G | 1 | a0001c0001t0002g0217 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.405-4596T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68560339 | |||||||
| chr17:68560343 | C | CA | 7 | a0001c0001t0001g0220 a0001c0001t0001g0236 a0001c0001t0001g0348 others(4): Show |
7 | HG01070.hp1 HG01071.hp2 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.405-4601dupT | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68560343 | |||||||
| chr17:68560343 | CA | C | 202 | a0001c0001t0001g0003 a0001c0001t0001g0151 a0001c0001t0001g0155 others(199): Show |
206 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(203): Show |
intron_variant | MODIFIER | c.405-4601delT | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68560343 | |||||||
| chr17:68560382 | A | G | 3 | a0002c0003t0001g0199 a0002c0003t0001g0200 a0002c0003t0001g0298 |
3 | HG02559.hp1 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.405-4639T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68560382 | |||||||
| chr17:68560436 | C | T | 1 | a0001c0005t0002g0082 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.405-4693G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68560436 | |||||||
| chr17:68560442 | A | G | 2 | a0002c0002t0001g0197 a0002c0002t0001g0198 |
2 | HG02055.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.405-4699T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68560442 | |||||||
| chr17:68560469 | A | C | 1 | a0001c0004t0004g0048 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.405-4726T>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68560469 | |||||||
| chr17:68560563 | T | C | 154 | a0001c0001t0001g0003 a0001c0001t0001g0151 a0001c0001t0001g0155 others(151): Show |
156 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.405-4820A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68560563 | |||||||
| chr17:68560656 | C | T | 2 | a0003c0015t0001g0113 a0003c0015t0001g0114 |
2 | NA18969.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.405-4913G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68560656 | |||||||
| chr17:68560698 | T | C | 1 | a0002c0007t0001g0095 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.405-4955A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68560698 | |||||||
| chr17:68560851 | T | A | 1 | a0002c0010t0001g0058 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.405-5108A>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68560851 | |||||||
| chr17:68560917 | A | G | 5 | a0001c0001t0001g0274 a0001c0001t0005g0141 a0001c0001t0005g0201 others(2): Show |
5 | HG02559.hp2 HG02809.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.405-5174T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68560917 | |||||||
| chr17:68560943 | C | T | 1 | a0001c0005t0006g0116 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.405-5200G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68560943 | |||||||
| chr17:68561318 | A | G | 133 | a0001c0001t0001g0003 a0001c0001t0001g0151 a0001c0001t0001g0155 others(130): Show |
135 | HG00280.hp2 HG00544.hp1 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.405-5575T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68561318 | |||||||
| chr17:68561338 | C | G | 2 | a0001c0001t0001g0216 a0002c0003t0017g0142 |
2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.405-5595G>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68561338 | |||||||
| chr17:68561591 | C | CT | 18 | a0001c0001t0001g0189 a0001c0001t0001g0216 a0001c0001t0001g0287 others(15): Show |
18 | HG00597.hp2 HG01070.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.405-5849dupA | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68561591 | |||||||
| chr17:68561591 | CT | C | 167 | a0001c0001t0001g0003 a0001c0001t0001g0151 a0001c0001t0001g0155 others(164): Show |
169 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(166): Show |
intron_variant | MODIFIER | c.405-5849delA | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68561591 | |||||||
| chr17:68561591 | CTT | C | 9 | a0001c0001t0001g0347 a0001c0001t0003g0206 a0001c0001t0003g0245 others(6): Show |
9 | HG02004.hp2 HG02055.hp2 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.405-5850_405-5849d others(4): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68561591 | |||||||
| chr17:68561610 | T | A | 1 | a0002c0002t0001g0194 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.405-5867A>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68561610 | |||||||
| chr17:68561675 | G | A | 1 | a0003c0009t0001g0079 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.405-5932C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68561675 | |||||||
| chr17:68561705 | A | C | 2 | a0001c0001t0001g0216 a0002c0003t0017g0142 |
2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.405-5962T>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68561705 | |||||||
| chr17:68561764 | G | A | 1 | a0003c0006t0001g0223 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.405-6021C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68561764 | |||||||
| chr17:68561855 | C | T | 133 | a0001c0001t0001g0003 a0001c0001t0001g0151 a0001c0001t0001g0155 others(130): Show |
135 | HG00280.hp2 HG00544.hp1 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.405-6112G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68561855 | |||||||
| chr17:68561892 | G | C | 13 | a0001c0001t0001g0189 a0001c0001t0001g0287 a0001c0001t0001g0293 others(10): Show |
13 | HG02055.hp1 HG02615.hp2 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.405-6149C>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68561892 | |||||||
| chr17:68561907 | C | T | 129 | a0001c0001t0001g0003 a0001c0001t0001g0151 a0001c0001t0001g0155 others(126): Show |
131 | HG00280.hp2 HG00544.hp1 HG00558.hp1 others(128): Show |
intron_variant | MODIFIER | c.405-6164G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68561907 | |||||||
| chr17:68561981 | A | G | 8 | a0001c0001t0001g0189 a0001c0001t0001g0287 a0001c0001t0001g0329 others(5): Show |
8 | HG02647.hp2 HG02723.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.405-6238T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68561981 | |||||||
| chr17:68562052 | C | G | 154 | a0001c0001t0001g0003 a0001c0001t0001g0151 a0001c0001t0001g0155 others(151): Show |
156 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.405-6309G>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68562052 | |||||||
| chr17:68562576 | C | T | 1 | a0001c0004t0002g0049 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.405-6833G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68562576 | |||||||
| chr17:68562611 | T | TA | 9 | a0001c0005t0001g0089 a0002c0002t0001g0194 a0002c0003t0001g0152 others(6): Show |
9 | HG02080.hp2 HG02523.hp1 NA18612.hp1 others(6): Show |
intron_variant | MODIFIER | c.405-6869_405-6868i others(3): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68562611 | |||||||
| chr17:68562611 | T | TC | 76 | a0001c0001t0001g0189 a0001c0001t0001g0268 a0001c0001t0001g0269 others(73): Show |
79 | HG00597.hp1 HG00741.hp2 HG01069.hp2 others(76): Show |
intron_variant | MODIFIER | c.405-6869dupG | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68562611 | |||||||
| chr17:68562732 | A | G | 1 | a0005c0025t0001g0361 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.405-6989T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68562732 | |||||||
| chr17:68562809 | T | C | 1 | a0006c0023t0001g0358 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.405-7066A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68562809 | |||||||
| chr17:68562982 | G | T | 5 | a0001c0001t0002g0217 a0001c0001t0002g0280 a0002c0002t0001g0197 others(2): Show |
5 | HG02055.hp1 HG02109.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.405-7239C>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68562982 | |||||||
| chr17:68562987 | C | T | 3 | a0002c0002t0001g0175 a0002c0002t0001g0176 a0002c0002t0001g0288 |
3 | HG01081.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.405-7244G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68562987 | |||||||
| chr17:68563037 | G | T | 12 | a0001c0001t0001g0252 a0001c0001t0006g0208 a0001c0001t0006g0275 others(9): Show |
12 | HG01109.hp2 HG02451.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.405-7294C>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68563037 | |||||||
| chr17:68563056 | C | T | 3 | a0003c0006t0001g0144 a0003c0006t0001g0248 a0003c0006t0001g0276 |
3 | HG01256.hp2 HG02148.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.405-7313G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68563056 | |||||||
| chr17:68563062 | G | A | 3 | a0002c0007t0001g0066 a0002c0007t0001g0067 a0002c0007t0001g0068 |
3 | HG01099.hp1 HG01192.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.405-7319C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68563062 | |||||||
| chr17:68563112 | G | A | 1 | a0002c0002t0001g0325 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.405-7369C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68563112 | |||||||
| chr17:68563310 | C | T | 1 | a0001c0001t0002g0187 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.405-7567G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68563310 | |||||||
| chr17:68563356 | A | G | 5 | a0001c0001t0002g0188 a0001c0005t0002g0121 a0003c0006t0001g0271 others(2): Show |
5 | HG02647.hp1 HG02723.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.405-7613T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68563356 | |||||||
| chr17:68563386 | CA | C | 250 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(247): Show |
255 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(252): Show |
intron_variant | MODIFIER | c.405-7644delT | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68563386 | |||||||
| chr17:68563386 | CAA | C | 6 | a0001c0001t0001g0213 a0001c0001t0002g0187 a0001c0005t0002g0082 others(3): Show |
6 | HG01167.hp1 HG01943.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.405-7645_405-7644d others(4): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68563386 | |||||||
| chr17:68563386 | CAAA | C | 99 | a0001c0001t0001g0137 a0001c0001t0001g0220 a0001c0001t0001g0222 others(96): Show |
102 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(99): Show |
intron_variant | MODIFIER | c.405-7646_405-7644d others(5): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68563386 | |||||||
| chr17:68563481 | A | G | 1 | a0002c0002t0024g0371 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.405-7738T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68563481 | |||||||
| chr17:68563641 | A | G | 7 | a0001c0001t0001g0216 a0001c0001t0002g0188 a0001c0001t0002g0211 others(4): Show |
7 | HG01243.hp1 HG01358.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.405-7898T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68563641 | |||||||
| chr17:68563705 | G | C | 38 | a0001c0001t0001g0212 a0001c0001t0001g0252 a0001c0001t0001g0268 others(35): Show |
38 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.405-7962C>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68563705 | |||||||
| chr17:68563742 | T | C | 1 | a0001c0001t0002g0279 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.405-7999A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68563742 | |||||||
| chr17:68563809 | T | C | 36 | a0001c0001t0001g0182 a0001c0001t0001g0212 a0001c0001t0001g0268 others(33): Show |
36 | HG01099.hp2 HG01243.hp1 HG01346.hp2 others(33): Show |
intron_variant | MODIFIER | c.405-8066A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68563809 | |||||||
| chr17:68563956 | G | A | 63 | a0001c0001t0001g0213 a0001c0001t0001g0220 a0001c0001t0001g0268 others(60): Show |
65 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.405-8213C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68563956 | |||||||
| chr17:68564148 | G | GC | 115 | a0001c0001t0001g0189 a0001c0001t0001g0212 a0001c0001t0001g0213 others(112): Show |
117 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.405-8406dupG | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68564148 | |||||||
| chr17:68564232 | C | G | 3 | a0001c0001t0002g0279 a0001c0001t0005g0141 a0001c0005t0006g0116 |
3 | HG02717.hp2 HG02809.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.405-8489G>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68564232 | |||||||
| chr17:68564251 | G | C | 301 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(298): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.405-8508C>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68564251 | |||||||
| chr17:68564377 | A | G | 2 | a0001c0001t0001g0351 a0001c0001t0001g0353 |
2 | HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.405-8634T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68564377 | |||||||
| chr17:68564586 | T | C | 3 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0002c0003t0001g0251 |
3 | HG02717.hp1 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.405-8843A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68564586 | |||||||
| chr17:68564629 | A | G | 2 | a0004c0011t0005g0062 a0012c0019t0010g0063 |
2 | HG02486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.405-8886T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68564629 | |||||||
| chr17:68564767 | C | G | 1 | a0002c0002t0001g0219 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.405-9024G>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68564767 | |||||||
| chr17:68564863 | C | T | 72 | a0001c0001t0001g0003 a0001c0001t0001g0151 a0001c0001t0001g0155 others(69): Show |
75 | HG00280.hp2 HG00673.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.405-9120G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68564863 | |||||||
| chr17:68565062 | T | C | 73 | a0001c0001t0001g0003 a0001c0001t0001g0151 a0001c0001t0001g0155 others(70): Show |
76 | HG00280.hp2 HG00673.hp2 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.405-9319A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68565062 | |||||||
| chr17:68565068 | G | A | 38 | a0001c0001t0001g0250 a0001c0001t0001g0261 a0001c0001t0001g0264 others(35): Show |
40 | HG00558.hp1 HG00597.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.405-9325C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68565068 | |||||||
| chr17:68565107 | A | G | 2 | a0001c0001t0001g0274 a0001c0001t0002g0273 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.405-9364T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68565107 | |||||||
| chr17:68565130 | A | G | 1 | a0001c0001t0002g0335 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.405-9387T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68565130 | |||||||
| chr17:68565133 | TCAGG | T | 17 | a0001c0001t0001g0269 a0001c0001t0001g0348 a0001c0001t0002g0188 others(14): Show |
17 | HG01109.hp2 HG01243.hp1 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.405-9394_405-9391d others(6): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68565133 | |||||||
| chr17:68565256 | G | C | 35 | a0001c0001t0001g0130 a0001c0001t0001g0133 a0001c0001t0001g0134 others(32): Show |
35 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.405-9513C>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68565256 | |||||||
| chr17:68565383 | C | CT | 27 | a0001c0001t0001g0220 a0001c0001t0001g0293 a0001c0001t0001g0323 others(24): Show |
27 | HG00597.hp2 HG00741.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.405-9641dupA | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68565383 | |||||||
| chr17:68565383 | C | CTTTTTTT others(3): Show |
6 | a0001c0001t0002g0211 a0001c0001t0006g0218 a0001c0004t0008g0011 others(3): Show |
6 | HG01109.hp2 HG01243.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.405-9650_405-9641d others(12): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68565383 | |||||||
| chr17:68565383 | C | CTTTTTTT others(4): Show |
1 | a0001c0004t0013g0010 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.405-9651_405-9641d others(13): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68565383 | |||||||
| chr17:68565383 | C | CTTTTTTT others(5): Show |
2 | a0001c0001t0002g0188 a0007c0016t0015g0015 |
2 | HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.405-9652_405-9641d others(14): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68565383 | |||||||
| chr17:68565383 | C | CTTTTTTT others(6): Show |
2 | a0001c0017t0005g0014 a0003c0018t0001g0016 |
2 | HG03540.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.405-9653_405-9641d others(15): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68565383 | |||||||
| chr17:68565383 | CT | C | 28 | a0001c0001t0001g0134 a0001c0001t0001g0252 a0001c0001t0001g0253 others(25): Show |
28 | HG00609.hp2 HG00673.hp1 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.405-9641delA | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68565383 | |||||||
| chr17:68565383 | CTTTTT | C | 64 | a0001c0001t0001g0003 a0001c0001t0001g0151 a0001c0001t0001g0155 others(61): Show |
67 | HG00280.hp2 HG00673.hp2 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.405-9645_405-9641d others(7): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68565383 | |||||||
| chr17:68565383 | CTTTTTTT others(4): Show |
C | 5 | a0001c0001t0001g0270 a0001c0001t0002g0272 a0001c0001t0003g0266 others(2): Show |
5 | HG02572.hp1 HG03041.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.405-9651_405-9641d others(13): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68565383 | |||||||
| chr17:68565383 | CTTTTTTT others(5): Show |
C | 41 | a0001c0001t0001g0212 a0001c0001t0001g0216 a0001c0001t0001g0250 others(38): Show |
43 | HG00558.hp1 HG00597.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.405-9652_405-9641d others(14): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68565383 | |||||||
| chr17:68565383 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0005g0285 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.405-9653_405-9641d others(15): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68565383 | |||||||
| chr17:68565609 | G | A | 1 | a0001c0004t0002g0041 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.405-9866C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68565609 | |||||||
| chr17:68565678 | G | A | 2 | a0001c0001t0001g0274 a0001c0001t0002g0273 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.405-9935C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68565678 | |||||||
| chr17:68565789 | C | A | 2 | a0004c0011t0002g0061 a0004c0011t0005g0060 |
2 | HG01884.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.405-10046G>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68565789 | |||||||
| chr17:68565878 | A | G | 1 | a0002c0002t0001g0339 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.405-10135T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68565878 | |||||||
| chr17:68565897 | C | G | 1 | a0001c0004t0001g0044 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.405-10154G>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68565897 | |||||||
| chr17:68566072 | C | T | 79 | a0001c0001t0001g0003 a0001c0001t0001g0151 a0001c0001t0001g0155 others(76): Show |
82 | HG00280.hp2 HG00673.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.405-10329G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68566072 | |||||||
| chr17:68566190 | A | G | 10 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0346 others(7): Show |
10 | HG02055.hp2 HG02109.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.405-10447T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68566190 | |||||||
| chr17:68566353 | C | T | 74 | a0001c0001t0001g0003 a0001c0001t0001g0151 a0001c0001t0001g0155 others(71): Show |
77 | HG00280.hp2 HG00673.hp2 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.405-10610G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68566353 | |||||||
| chr17:68566355 | G | A | 17 | a0001c0001t0001g0269 a0001c0001t0001g0348 a0001c0001t0002g0188 others(14): Show |
17 | HG01109.hp2 HG01243.hp1 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.405-10612C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68566355 | |||||||
| chr17:68566502 | A | G | 2 | a0002c0002t0001g0197 a0002c0002t0001g0198 |
2 | HG02055.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.405-10759T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68566502 | |||||||
| chr17:68566508 | C | T | 87 | a0001c0001t0001g0130 a0001c0001t0001g0133 a0001c0001t0001g0134 others(84): Show |
89 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.405-10765G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68566508 | |||||||
| chr17:68566569 | C | G | 97 | a0001c0001t0001g0189 a0001c0001t0001g0212 a0001c0001t0001g0216 others(94): Show |
98 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.405-10826G>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68566569 | |||||||
| chr17:68566603 | C | T | 35 | a0001c0004t0001g0034 a0001c0004t0001g0037 a0001c0004t0001g0043 others(32): Show |
35 | HG00408.hp1 HG00609.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.405-10860G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68566603 | |||||||
| chr17:68566683 | A | G | 72 | a0001c0001t0001g0003 a0001c0001t0001g0151 a0001c0001t0001g0155 others(69): Show |
75 | HG00280.hp2 HG00673.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.405-10940T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68566683 | |||||||
| chr17:68566967 | G | C | 5 | a0001c0001t0002g0225 a0003c0006t0001g0144 a0003c0006t0001g0241 others(2): Show |
5 | HG01256.hp2 HG01517.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.405-11224C>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68566967 | |||||||
| chr17:68567006 | TTTTTTCT others(2072): Show |
T | 2 | a0002c0002t0001g0197 a0002c0002t0001g0198 |
2 | HG02055.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.405-13342_405-1126 others(4): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68567006 | |||||||
| chr17:68567053 | C | T | 3 | a0001c0001t0001g0348 a0001c0001t0002g0350 a0002c0003t0001g0349 |
3 | HG02809.hp1 HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.405-11310G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68567053 | |||||||
| chr17:68567233 | G | A | 15 | a0001c0001t0001g0281 a0001c0001t0001g0287 a0001c0001t0002g0209 others(12): Show |
16 | HG01069.hp2 HG01071.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.405-11490C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68567233 | |||||||
| chr17:68567278 | T | C | 2 | a0003c0015t0001g0113 a0003c0015t0001g0114 |
2 | NA18969.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.405-11535A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68567278 | |||||||
| chr17:68567318 | G | T | 70 | a0001c0001t0001g0003 a0001c0001t0001g0151 a0001c0001t0001g0155 others(67): Show |
73 | HG00280.hp2 HG00673.hp2 HG00735.hp1 others(70): Show |
intron_variant | MODIFIER | c.405-11575C>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68567318 | |||||||
| chr17:68567666 | T | C | 73 | a0001c0001t0001g0003 a0001c0001t0001g0151 a0001c0001t0001g0155 others(70): Show |
76 | HG00280.hp2 HG00673.hp2 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.405-11923A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68567666 | |||||||
| chr17:68567719 | C | T | 1 | a0001c0001t0002g0004 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.405-11976G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68567719 | |||||||
| chr17:68567752 | C | T | 5 | a0001c0005t0003g0118 a0002c0002t0001g0339 a0002c0007t0001g0091 others(2): Show |
5 | HG00544.hp1 HG00621.hp2 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.405-12009G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68567752 | |||||||
| chr17:68567846 | T | C | 3 | a0001c0001t0006g0275 a0001c0001t0020g0327 a0002c0002t0001g0328 |
3 | HG02451.hp2 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.405-12103A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68567846 | |||||||
| chr17:68568149 | C | CT | 4 | a0001c0001t0001g0274 a0001c0001t0002g0273 a0004c0011t0002g0061 others(1): Show |
4 | HG01884.hp2 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.405-12407_405-1240 others(5): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68568149 | |||||||
| chr17:68568150 | A | C | 4 | a0001c0001t0001g0274 a0001c0001t0002g0273 a0004c0011t0002g0061 others(1): Show |
4 | HG01884.hp2 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.405-12407T>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68568150 | |||||||
| chr17:68568222 | T | C | 76 | a0001c0001t0001g0003 a0001c0001t0001g0151 a0001c0001t0001g0155 others(73): Show |
79 | HG00280.hp2 HG00673.hp2 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.405-12479A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68568222 | |||||||
| chr17:68568327 | G | A | 1 | a0002c0002t0024g0371 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.405-12584C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68568327 | |||||||
| chr17:68568328 | C | T | 1 | a0001c0001t0003g0168 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.405-12585G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68568328 | |||||||
| chr17:68568353 | AGCTACTC others(11): Show |
A | 1 | a0002c0002t0001g0173 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.405-12628_405-1261 others(22): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68568353 | |||||||
| chr17:68568469 | A | AAAAT | 11 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0346 others(8): Show |
11 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.405-12730_405-1272 others(8): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68568469 | |||||||
| chr17:68568513 | A | G | 2 | a0004c0011t0002g0061 a0004c0011t0005g0060 |
2 | HG01884.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.405-12770T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68568513 | |||||||
| chr17:68568674 | T | C | 1 | a0002c0010t0001g0052 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.405-12931A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68568674 | |||||||
| chr17:68568771 | T | C | 3 | a0001c0001t0006g0275 a0001c0001t0020g0327 a0002c0002t0001g0328 |
3 | HG02451.hp2 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.405-13028A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68568771 | |||||||
| chr17:68568793 | G | C | 4 | a0001c0001t0001g0274 a0001c0001t0002g0273 a0004c0011t0002g0061 others(1): Show |
4 | HG01884.hp2 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.405-13050C>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68568793 | |||||||
| chr17:68568799 | CT | C | 78 | a0001c0001t0001g0003 a0001c0001t0001g0151 a0001c0001t0001g0155 others(75): Show |
81 | HG00280.hp2 HG00673.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.405-13057delA | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68568799 | |||||||
| chr17:68568916 | A | C | 78 | a0001c0001t0001g0003 a0001c0001t0001g0151 a0001c0001t0001g0155 others(75): Show |
81 | HG00280.hp2 HG00673.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.405-13173T>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68568916 | |||||||
| chr17:68569124 | G | A | 1 | a0002c0003t0009g0318 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.405-13381C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68569124 | |||||||
| chr17:68569253 | C | T | 2 | a0004c0011t0005g0062 a0012c0019t0010g0063 |
2 | HG02486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.405-13510G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68569253 | |||||||
| chr17:68569312 | T | C | 1 | a0001c0001t0022g0362 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.405-13569A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68569312 | |||||||
| chr17:68569354 | A | T | 2 | a0001c0001t0001g0274 a0001c0001t0002g0273 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.405-13611T>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68569354 | |||||||
| chr17:68569465 | C | G | 1 | a0001c0001t0001g0212 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.405-13722G>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68569465 | |||||||
| chr17:68569634 | C | T | 6 | a0001c0001t0001g0157 a0001c0001t0003g0181 a0002c0003t0001g0149 others(3): Show |
6 | NA18948.hp1 NA18983.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.405-13891G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68569634 | |||||||
| chr17:68569647 | G | A | 15 | a0001c0001t0001g0212 a0001c0001t0001g0216 a0001c0001t0001g0270 others(12): Show |
15 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.405-13904C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68569647 | |||||||
| chr17:68569830 | G | A | 4 | a0001c0001t0002g0188 a0001c0017t0005g0014 a0003c0018t0001g0016 others(1): Show |
4 | HG02647.hp1 HG02723.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.405-14087C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68569830 | |||||||
| chr17:68569922 | G | A | 78 | a0001c0001t0001g0003 a0001c0001t0001g0151 a0001c0001t0001g0155 others(75): Show |
81 | HG00280.hp2 HG00673.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.405-14179C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68569922 | |||||||
| chr17:68570092 | C | T | 237 | a0001c0001t0001g0003 a0001c0001t0001g0151 a0001c0001t0001g0155 others(234): Show |
241 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.405-14349G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68570092 | |||||||
| chr17:68570351 | G | A | 1 | a0001c0005t0002g0084 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.405-14608C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68570351 | |||||||
| chr17:68570432 | G | C | 3 | a0001c0001t0001g0330 a0001c0001t0006g0278 a0008c0022t0002g0331 |
3 | HG02572.hp2 HG03579.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.405-14689C>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68570432 | |||||||
| chr17:68570454 | C | T | 1 | a0002c0002t0001g0224 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.405-14711G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68570454 | |||||||
| chr17:68570905 | A | G | 1 | a0001c0001t0006g0275 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.405-15162T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68570905 | |||||||
| chr17:68571192 | G | C | 35 | a0001c0004t0001g0034 a0001c0004t0001g0037 a0001c0004t0001g0043 others(32): Show |
35 | HG00408.hp1 HG00609.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.405-15449C>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68571192 | |||||||
| chr17:68571209 | T | C | 1 | a0001c0005t0002g0121 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.405-15466A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68571209 | |||||||
| chr17:68571400 | C | T | 3 | a0001c0001t0006g0275 a0001c0001t0020g0327 a0002c0002t0001g0328 |
3 | HG02451.hp2 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.405-15657G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68571400 | |||||||
| chr17:68571528 | C | A | 1 | a0002c0003t0001g0183 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.405-15785G>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68571528 | |||||||
| chr17:68571691 | T | A | 1 | a0001c0001t0002g0226 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.405-15948A>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68571691 | |||||||
| chr17:68571833 | G | A | 3 | a0002c0002t0001g0167 a0002c0002t0001g0175 a0002c0002t0001g0176 |
3 | HG01515.hp2 HG01517.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.405-16090C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68571833 | |||||||
| chr17:68571939 | AATATATA others(43): Show |
A | 2 | a0001c0004t0001g0046 a0001c0004t0004g0055 |
2 | HG04115.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.405-16246_405-1619 others(54): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68571939 | |||||||
| chr17:68571939 | AATATATA others(47): Show |
A | 4 | a0001c0004t0001g0034 a0001c0004t0001g0045 a0001c0004t0002g0017 others(1): Show |
4 | HG04184.hp1 HG04199.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.405-16250_405-1619 others(58): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68571939 | |||||||
| chr17:68571939 | AATATATA others(49): Show |
A | 1 | a0003c0013t0001g0047 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.405-16252_405-1619 others(60): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68571939 | |||||||
| chr17:68571939 | AATATATA others(51): Show |
A | 6 | a0001c0004t0001g0037 a0001c0004t0001g0043 a0001c0004t0004g0023 others(3): Show |
6 | HG03654.hp1 NA18947.hp1 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.405-16254_405-1619 others(62): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68571939 | |||||||
| chr17:68571939 | AATATATA others(53): Show |
A | 10 | a0001c0004t0002g0026 a0001c0004t0002g0041 a0001c0004t0002g0057 others(7): Show |
10 | HG00408.hp1 HG00673.hp1 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.405-16256_405-1619 others(64): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68571939 | |||||||
| chr17:68571939 | AATATATA others(55): Show |
A | 3 | a0001c0004t0004g0048 a0001c0004t0004g0051 a0002c0008t0001g0042 |
3 | NA18959.hp2 NA19059.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.405-16258_405-1619 others(66): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68571939 | |||||||
| chr17:68571939 | AATATATA others(57): Show |
A | 8 | a0001c0004t0002g0019 a0001c0004t0002g0030 a0001c0004t0003g0033 others(5): Show |
8 | HG00609.hp2 HG02074.hp1 NA18987.hp2 others(5): Show |
intron_variant | MODIFIER | c.405-16260_405-1619 others(68): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68571939 | |||||||
| chr17:68571987 | C | CAT | 25 | a0001c0001t0001g0130 a0001c0001t0001g0134 a0001c0001t0001g0137 others(22): Show |
26 | HG00099.hp1 HG00140.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.405-16246_405-1624 others(6): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68571987 | |||||||
| chr17:68571987 | C | CATAT | 10 | a0001c0001t0002g0221 a0001c0004t0002g0049 a0002c0002t0001g0131 others(7): Show |
10 | HG01943.hp1 HG02040.hp2 HG02683.hp1 others(7): Show |
intron_variant | MODIFIER | c.405-16248_405-1624 others(8): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68571987 | |||||||
| chr17:68571987 | C | CATATAT | 9 | a0001c0001t0001g0264 a0001c0001t0001g0355 a0001c0001t0002g0146 others(6): Show |
10 | HG01069.hp2 HG01071.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.405-16250_405-1624 others(10): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68571987 | |||||||
| chr17:68571987 | C | CATATATA others(3): Show |
3 | a0001c0001t0002g0004 a0002c0002t0001g0178 a0002c0003t0001g0302 |
3 | HG02155.hp2 NA18964.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.405-16254_405-1624 others(14): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68571987 | |||||||
| chr17:68571987 | C | CATATATA others(7): Show |
1 | a0003c0006t0001g0322 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.405-16258_405-1624 others(18): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68571987 | |||||||
| chr17:68571987 | C | T | 1 | a0003c0006t0001g0005 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.405-16244G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68571987 | |||||||
| chr17:68571987 | CAT | C | 29 | a0001c0001t0001g0191 a0001c0001t0001g0265 a0001c0001t0001g0274 others(26): Show |
29 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.405-16246_405-1624 others(6): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68571987 | |||||||
| chr17:68571987 | CATAT | C | 27 | a0001c0001t0001g0145 a0001c0001t0001g0151 a0001c0001t0001g0193 others(24): Show |
27 | HG00323.hp1 HG00673.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.405-16248_405-1624 others(8): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68571987 | |||||||
| chr17:68571987 | CATATAT | C | 19 | a0001c0001t0001g0133 a0001c0001t0001g0182 a0001c0001t0001g0252 others(16): Show |
19 | HG00735.hp1 HG01346.hp1 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.405-16250_405-1624 others(10): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68571987 | |||||||
| chr17:68571987 | CATATATA others(1): Show |
C | 17 | a0001c0001t0001g0212 a0001c0001t0001g0270 a0001c0001t0002g0156 others(14): Show |
17 | HG02145.hp2 HG02572.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.405-16252_405-1624 others(12): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68571987 | |||||||
| chr17:68571987 | CATATATA others(3): Show |
C | 23 | a0001c0001t0001g0268 a0001c0001t0001g0293 a0001c0001t0001g0347 others(20): Show |
23 | HG00280.hp2 HG00558.hp1 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.405-16254_405-1624 others(14): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68571987 | |||||||
| chr17:68571987 | CATATATA others(5): Show |
C | 16 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0250 others(13): Show |
16 | HG00738.hp1 HG01243.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.405-16256_405-1624 others(16): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68571987 | |||||||
| chr17:68571987 | CATATATA others(7): Show |
C | 16 | a0001c0001t0006g0208 a0001c0005t0001g0090 a0001c0005t0002g0074 others(13): Show |
16 | HG00621.hp1 HG01243.hp2 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.405-16258_405-1624 others(18): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68571987 | |||||||
| chr17:68571987 | CATATATA others(9): Show |
C | 6 | a0001c0001t0002g0188 a0001c0001t0002g0209 a0001c0001t0002g0324 others(3): Show |
6 | HG01981.hp2 HG02300.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.405-16260_405-1624 others(20): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68571987 | |||||||
| chr17:68571987 | CATATATA others(11): Show |
C | 7 | a0001c0001t0025g0372 a0001c0005t0002g0125 a0002c0002t0001g0139 others(4): Show |
8 | HG00621.hp2 HG00741.hp2 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.405-16262_405-1624 others(22): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68571987 | |||||||
| chr17:68571987 | CATATATA others(13): Show |
C | 8 | a0001c0005t0002g0106 a0001c0005t0002g0121 a0001c0005t0003g0107 others(5): Show |
8 | HG02148.hp1 NA18959.hp1 NA18986.hp1 others(5): Show |
intron_variant | MODIFIER | c.405-16264_405-1624 others(24): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68571987 | |||||||
| chr17:68571987 | CATATATA others(15): Show |
C | 14 | a0001c0001t0001g0003 a0001c0001t0001g0155 a0001c0001t0003g0255 others(11): Show |
15 | HG00544.hp1 HG01069.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.405-16266_405-1624 others(26): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68571987 | |||||||
| chr17:68571987 | CATATATA others(17): Show |
C | 9 | a0001c0001t0002g0279 a0001c0001t0002g0280 a0001c0001t0005g0283 others(6): Show |
9 | HG01891.hp2 HG02451.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.405-16268_405-1624 others(28): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68571987 | |||||||
| chr17:68571987 | CATATATA others(19): Show |
C | 4 | a0001c0001t0001g0281 a0001c0001t0001g0330 a0001c0001t0006g0278 others(1): Show |
4 | HG01109.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.405-16270_405-1624 others(30): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68571987 | |||||||
| chr17:68571987 | CATATATA others(21): Show |
C | 1 | a0003c0006t0001g0316 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.405-16272_405-1624 others(32): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68571987 | |||||||
| chr17:68571987 | CATATATA others(25): Show |
C | 3 | a0001c0001t0002g0179 a0002c0003t0001g0180 a0003c0006t0001g0006 |
4 | HG01255.hp2 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.405-16276_405-1624 others(36): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68571987 | |||||||
| chr17:68571987 | CATATATA others(27): Show |
C | 3 | a0001c0001t0005g0141 a0004c0011t0005g0062 a0012c0019t0010g0063 |
3 | HG02486.hp1 HG02809.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.405-16278_405-1624 others(38): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68571987 | |||||||
| chr17:68571991 | T | C | 55 | a0001c0001t0001g0213 a0001c0001t0001g0220 a0001c0001t0001g0222 others(52): Show |
55 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.405-16248A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68571991 | |||||||
| chr17:68571993 | T | C | 1 | a0002c0002t0024g0371 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.405-16250A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68571993 | |||||||
| chr17:68571995 | T | C | 1 | a0001c0001t0001g0253 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.405-16252A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68571995 | |||||||
| chr17:68571997 | T | C | 1 | a0001c0001t0001g0252 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.405-16254A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68571997 | |||||||
| chr17:68571999 | T | C | 3 | a0001c0001t0001g0270 a0001c0001t0002g0272 a0001c0001t0021g0202 |
3 | HG02145.hp2 HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.405-16256A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68571999 | |||||||
| chr17:68571999 | T | TATATATA others(25): Show |
1 | a0002c0002t0001g0198 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.405-16257_405-1625 others(36): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68571999 | |||||||
| chr17:68572001 | T | C | 1 | a0001c0001t0001g0268 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.405-16258A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68572001 | |||||||
| chr17:68572001 | T | TATATAAT others(21): Show |
1 | a0002c0002t0001g0197 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.405-16259_405-1625 others(32): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68572001 | |||||||
| chr17:68572001 | TATATA | T | 7 | a0001c0001t0003g0206 a0001c0004t0013g0010 a0002c0002t0001g0239 others(4): Show |
7 | HG00597.hp2 HG00609.hp1 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.405-16263_405-1625 others(9): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68572001 | |||||||
| chr17:68572001 | TATATATA | T | 11 | a0001c0001t0001g0220 a0001c0001t0001g0222 a0001c0001t0001g0233 others(8): Show |
11 | HG00099.hp2 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.405-16265_405-1625 others(11): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68572001 | |||||||
| chr17:68572001 | TATATATA others(2): Show |
T | 24 | a0001c0001t0001g0213 a0001c0001t0001g0235 a0001c0001t0001g0240 others(21): Show |
24 | HG00140.hp1 HG00323.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.405-16267_405-1625 others(13): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68572001 | |||||||
| chr17:68572001 | TATATATA others(4): Show |
T | 4 | a0001c0001t0002g0229 a0002c0002t0001g0224 a0002c0003t0001g0230 others(1): Show |
4 | HG00280.hp1 HG01256.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.405-16269_405-1625 others(15): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68572001 | |||||||
| chr17:68572003 | T | C | 3 | a0001c0001t0001g0189 a0001c0005t0002g0083 a0001c0005t0002g0084 |
3 | NA18522.hp1 NA18960.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.405-16260A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68572003 | |||||||
| chr17:68572011 | T | C | 1 | a0001c0005t0002g0121 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.405-16268A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68572011 | |||||||
| chr17:68572045 | G | T | 2 | a0002c0002t0001g0197 a0002c0002t0001g0198 |
2 | HG02055.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.405-16302C>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68572045 | |||||||
| chr17:68572158 | G | A | 2 | a0002c0003t0001g0249 a0003c0012t0001g0227 |
2 | NA18977.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.405-16415C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68572158 | |||||||
| chr17:68572460 | A | G | 1 | a0002c0003t0001g0174 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.405-16717T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68572460 | |||||||
| chr17:68572659 | A | G | 79 | a0001c0001t0001g0003 a0001c0001t0001g0151 a0001c0001t0001g0155 others(76): Show |
82 | HG00280.hp2 HG00673.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.405-16916T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68572659 | |||||||
| chr17:68572693 | G | A | 1 | a0001c0001t0001g0157 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.405-16950C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68572693 | |||||||
| chr17:68572807 | G | T | 1 | a0001c0001t0003g0206 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.405-17064C>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68572807 | |||||||
| chr17:68572857 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.405-17114G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68572857 | |||||||
| chr17:68573004 | C | A | 2 | a0002c0002t0001g0197 a0002c0002t0001g0198 |
2 | HG02055.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.405-17261G>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68573004 | |||||||
| chr17:68573008 | C | T | 1 | a0003c0009t0001g0079 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.405-17265G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68573008 | |||||||
| chr17:68573434 | CTCTT | C | 64 | a0001c0001t0001g0189 a0001c0001t0001g0212 a0001c0001t0001g0216 others(61): Show |
64 | HG00408.hp1 HG00609.hp2 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.405-17695_405-1769 others(8): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68573434 | |||||||
| chr17:68573434 | CTCTTTCT others(1): Show |
C | 3 | a0002c0002t0001g0197 a0002c0002t0001g0198 a0003c0013t0001g0047 |
3 | HG02055.hp1 HG02602.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.405-17699_405-1769 others(12): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68573434 | |||||||
| chr17:68573438 | T | C | 1 | a0003c0015t0001g0113 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.405-17695A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68573438 | |||||||
| chr17:68573452 | CTTTCTTC others(1): Show |
C | 75 | a0001c0001t0001g0003 a0001c0001t0001g0151 a0001c0001t0001g0155 others(72): Show |
78 | HG00280.hp2 HG00673.hp2 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.405-17717_405-1771 others(12): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68573452 | |||||||
| chr17:68573452 | CTTTCTTC others(5): Show |
C | 6 | a0001c0001t0001g0348 a0001c0001t0002g0350 a0001c0017t0005g0014 others(3): Show |
6 | HG02647.hp1 HG02809.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.405-17721_405-1771 others(16): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68573452 | |||||||
| chr17:68573456 | CTTCT | C | 49 | a0001c0001t0001g0213 a0001c0001t0001g0220 a0001c0001t0001g0222 others(46): Show |
49 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(46): Show |
intron_variant | MODIFIER | c.405-17717_405-1771 others(8): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68573456 | |||||||
| chr17:68573473 | T | C | 1 | a0001c0001t0002g0211 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.405-17730A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68573473 | |||||||
| chr17:68573598 | TTC | T | 5 | a0001c0001t0002g0209 a0001c0001t0002g0254 a0001c0001t0005g0201 others(2): Show |
5 | HG01361.hp2 HG02630.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.405-17857_405-1785 others(6): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68573598 | |||||||
| chr17:68573723 | A | G | 79 | a0001c0001t0001g0003 a0001c0001t0001g0151 a0001c0001t0001g0155 others(76): Show |
82 | HG00280.hp2 HG00673.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.405-17980T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68573723 | |||||||
| chr17:68573749 | G | T | 38 | a0001c0001t0001g0250 a0001c0001t0001g0261 a0001c0001t0001g0264 others(35): Show |
39 | HG00558.hp1 HG00597.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.405-18006C>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68573749 | |||||||
| chr17:68574210 | G | A | 1 | a0001c0005t0004g0081 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.405-18467C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68574210 | |||||||
| chr17:68574238 | TTATTTTT others(5): Show |
T | 1 | a0001c0004t0001g0021 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.405-18507_405-1849 others(16): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68574238 | |||||||
| chr17:68574330 | C | T | 1 | a0003c0006t0001g0203 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.405-18587G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68574330 | |||||||
| chr17:68574535 | A | T | 15 | a0001c0001t0001g0189 a0001c0001t0001g0212 a0001c0001t0001g0216 others(12): Show |
15 | HG01884.hp2 HG02145.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.405-18792T>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68574535 | |||||||
| chr17:68574578 | C | T | 2 | a0004c0011t0002g0061 a0004c0011t0005g0060 |
2 | HG01884.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.405-18835G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68574578 | |||||||
| chr17:68575046 | G | A | 2 | a0001c0001t0002g0237 a0002c0003t0001g0232 |
2 | HG01074.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.405-19303C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575046 | |||||||
| chr17:68575255 | T | C | 1 | a0002c0003t0001g0298 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.405-19512A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575255 | |||||||
| chr17:68575382 | C | CAT | 86 | a0001c0001t0001g0130 a0001c0001t0001g0133 a0001c0001t0001g0134 others(83): Show |
88 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.405-19641_405-1964 others(6): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575382 | |||||||
| chr17:68575395 | A | T | 5 | a0001c0001t0002g0209 a0001c0001t0002g0254 a0001c0001t0005g0201 others(2): Show |
5 | HG01361.hp2 HG02630.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.405-19652T>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575395 | |||||||
| chr17:68575421 | A | ATATATAT others(25): Show |
1 | a0001c0004t0003g0033 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.405-19710_405-1967 others(36): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575421 | |||||||
| chr17:68575421 | ATATATAT others(9): Show |
A | 10 | a0001c0001t0001g0281 a0001c0001t0001g0287 a0001c0001t0002g0279 others(7): Show |
11 | HG01069.hp2 HG01071.hp1 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.405-19694_405-1967 others(20): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575421 | |||||||
| chr17:68575445 | T | TATATATA others(23): Show |
65 | a0001c0001t0001g0003 a0001c0001t0001g0151 a0001c0001t0001g0155 others(62): Show |
68 | HG00673.hp2 HG00735.hp1 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.405-19703_405-1970 others(34): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575445 | |||||||
| chr17:68575445 | T | TATATATA others(46): Show |
6 | a0001c0001t0002g0154 a0001c0001t0002g0184 a0001c0001t0002g0186 others(3): Show |
6 | HG00738.hp1 HG01167.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.405-19703_405-1970 others(57): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575445 | |||||||
| chr17:68575445 | T | TATATATA others(69): Show |
1 | a0002c0002t0001g0185 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.405-19703_405-1970 others(80): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575445 | |||||||
| chr17:68575445 | T | TATATATT others(46): Show |
1 | a0001c0001t0001g0161 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.405-19703_405-1970 others(57): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575445 | |||||||
| chr17:68575446 | A | ATATATTT others(23): Show |
1 | a0001c0001t0006g0275 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.405-19733_405-1970 others(34): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575446 | |||||||
| chr17:68575461 | T | A | 2 | a0001c0005t0001g0088 a0001c0005t0001g0099 |
2 | HG01361.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.405-19718A>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575461 | |||||||
| chr17:68575463 | TATATA | T | 3 | a0001c0001t0012g0013 a0002c0003t0001g0297 a0002c0003t0001g0298 |
3 | HG01358.hp1 HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.405-19725_405-1972 others(9): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575463 | |||||||
| chr17:68575486 | T | TATATTTT others(48): Show |
2 | a0001c0001t0001g0269 a0002c0002t0001g0219 |
2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.405-19744_405-1974 others(59): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575486 | |||||||
| chr17:68575495 | G | T | 2 | a0001c0001t0001g0269 a0002c0002t0001g0219 |
2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.405-19752C>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575495 | |||||||
| chr17:68575498 | A | T | 2 | a0001c0001t0001g0269 a0002c0002t0001g0219 |
2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.405-19755T>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575498 | |||||||
| chr17:68575502 | G | GATATATA others(6): Show |
2 | a0004c0011t0002g0061 a0004c0011t0005g0060 |
2 | HG01884.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.405-19760_405-1975 others(17): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575502 | |||||||
| chr17:68575502 | G | GATATTAT others(9): Show |
128 | a0001c0001t0001g0003 a0001c0001t0001g0151 a0001c0001t0001g0155 others(125): Show |
131 | HG00280.hp2 HG00408.hp1 HG00609.hp2 others(128): Show |
intron_variant | MODIFIER | c.405-19775_405-1976 others(20): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575502 | |||||||
| chr17:68575502 | G | T | 2 | a0001c0001t0001g0269 a0002c0002t0001g0219 |
2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.405-19759C>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575502 | |||||||
| chr17:68575506 | T | TTATATAT others(16): Show |
2 | a0001c0001t0001g0268 a0002c0002t0001g0296 |
2 | HG01346.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.405-19786_405-1976 others(27): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575506 | |||||||
| chr17:68575506 | T | TTATATAT others(32): Show |
1 | a0001c0001t0001g0212 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.405-19764_405-1976 others(43): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575506 | |||||||
| chr17:68575522 | TTATATAA | T | 12 | a0001c0001t0001g0182 a0001c0001t0001g0252 a0001c0001t0001g0253 others(9): Show |
12 | HG01884.hp1 HG02109.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.405-19786_405-1978 others(11): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575522 | |||||||
| chr17:68575554 | ATATATTT others(21): Show |
A | 1 | a0002c0003t0001g0232 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.405-19839_405-1981 others(32): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575554 | |||||||
| chr17:68575576 | T | C | 2 | a0001c0001t0001g0274 a0001c0001t0002g0273 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.405-19833A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575576 | |||||||
| chr17:68575577 | ATATTC | A | 8 | a0001c0001t0001g0213 a0001c0001t0002g0204 a0001c0001t0002g0231 others(5): Show |
8 | HG00099.hp2 HG01070.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.405-19839_405-1983 others(9): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575577 | |||||||
| chr17:68575617 | T | TTATTATA others(210): Show |
1 | a0002c0003t0010g0282 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.405-19875_405-1987 others(221): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575617 | |||||||
| chr17:68575626 | A | G | 1 | a0002c0003t0010g0282 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.405-19883T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575626 | |||||||
| chr17:68575630 | A | G | 2 | a0001c0001t0001g0189 a0001c0001t0002g0188 |
2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.405-19887T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575630 | |||||||
| chr17:68575631 | T | A | 1 | a0002c0003t0010g0282 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.405-19888A>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575631 | |||||||
| chr17:68575631 | TA | T | 35 | a0001c0004t0001g0034 a0001c0004t0001g0037 a0001c0004t0001g0043 others(32): Show |
35 | HG00408.hp1 HG00609.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.405-19889delT | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575631 | |||||||
| chr17:68575709 | ATTATATA others(9): Show |
A | 4 | a0001c0001t0001g0213 a0001c0001t0002g0244 a0001c0001t0002g0319 others(1): Show |
4 | HG01070.hp2 HG02738.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.405-19982_405-1996 others(20): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575709 | |||||||
| chr17:68575719 | TTATATTT others(9): Show |
T | 1 | a0002c0003t0001g0230 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.405-19992_405-1997 others(20): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575719 | |||||||
| chr17:68575725 | TTTATATA | T | 5 | a0001c0001t0001g0295 a0001c0001t0001g0323 a0002c0002t0001g0296 others(2): Show |
5 | HG01496.hp2 HG01928.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.405-19989_405-1998 others(11): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575725 | |||||||
| chr17:68575789 | T | TAC | 10 | a0001c0001t0005g0007 a0001c0001t0005g0283 a0001c0001t0005g0284 others(7): Show |
11 | HG01069.hp2 HG01071.hp1 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.405-20047_405-2004 others(6): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575789 | |||||||
| chr17:68575789 | T | TACAC | 15 | a0001c0001t0001g0250 a0001c0001t0001g0261 a0001c0001t0001g0264 others(12): Show |
15 | HG00558.hp1 HG00597.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.405-20047_405-2004 others(8): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575789 | |||||||
| chr17:68575789 | T | TACACACA others(1): Show |
4 | a0001c0001t0002g0209 a0001c0001t0006g0207 a0001c0001t0006g0208 others(1): Show |
4 | HG02129.hp1 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.405-20047_405-2004 others(12): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575789 | |||||||
| chr17:68575789 | T | TACACACA others(3): Show |
2 | a0001c0001t0002g0254 a0001c0001t0005g0201 |
2 | HG01361.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.405-20047_405-2004 others(14): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575789 | |||||||
| chr17:68575789 | T | TACACACA others(9): Show |
2 | a0002c0007t0001g0066 a0002c0007t0001g0067 |
2 | HG01099.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.405-20047_405-2004 others(20): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575789 | |||||||
| chr17:68575791 | T | C | 37 | a0001c0001t0001g0250 a0001c0001t0001g0261 a0001c0001t0001g0264 others(34): Show |
38 | HG00558.hp1 HG00597.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.405-20048A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575791 | |||||||
| chr17:68575791 | T | TAC | 21 | a0001c0001t0001g0189 a0001c0001t0001g0213 a0001c0001t0001g0236 others(18): Show |
21 | HG00140.hp1 HG00597.hp2 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.405-20050_405-2004 others(6): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575791 | |||||||
| chr17:68575791 | T | TACAC | 24 | a0001c0001t0001g0220 a0001c0001t0001g0222 a0001c0001t0001g0233 others(21): Show |
24 | HG00609.hp1 HG01346.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.405-20052_405-2004 others(8): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575791 | |||||||
| chr17:68575791 | T | TACACAC | 29 | a0001c0001t0001g0157 a0001c0001t0001g0182 a0001c0001t0001g0252 others(26): Show |
31 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.405-20054_405-2004 others(10): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575791 | |||||||
| chr17:68575791 | T | TACACACA others(1): Show |
21 | a0001c0001t0001g0190 a0001c0001t0001g0348 a0001c0001t0002g0350 others(18): Show |
21 | HG01109.hp2 HG01123.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.405-20056_405-2004 others(12): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575791 | |||||||
| chr17:68575791 | T | TACACACA others(3): Show |
29 | a0001c0001t0001g0003 a0001c0001t0001g0165 a0001c0001t0001g0191 others(26): Show |
30 | HG00735.hp1 HG00735.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.405-20058_405-2004 others(14): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575791 | |||||||
| chr17:68575791 | T | TACACACA others(5): Show |
25 | a0001c0001t0001g0130 a0001c0001t0001g0137 a0001c0001t0001g0151 others(22): Show |
25 | HG00140.hp2 HG00673.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.405-20060_405-2004 others(16): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575791 | |||||||
| chr17:68575791 | T | TACACACA others(7): Show |
18 | a0001c0001t0001g0269 a0001c0001t0002g0146 a0001c0001t0003g0255 others(15): Show |
18 | HG00621.hp1 HG01891.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.405-20062_405-2004 others(18): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575791 | |||||||
| chr17:68575791 | T | TACACACA others(9): Show |
33 | a0001c0001t0001g0134 a0001c0001t0001g0195 a0001c0001t0001g0295 others(30): Show |
34 | HG00741.hp2 HG01074.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.405-20064_405-2004 others(20): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575791 | |||||||
| chr17:68575791 | T | TACACACA others(11): Show |
21 | a0001c0001t0001g0133 a0001c0001t0001g0346 a0001c0001t0001g0347 others(18): Show |
22 | HG00323.hp1 HG00544.hp2 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.405-20066_405-2004 others(22): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575791 | |||||||
| chr17:68575791 | T | TACACACA others(13): Show |
7 | a0001c0001t0002g0289 a0002c0002t0001g0139 a0002c0002t0001g0148 others(4): Show |
7 | HG00099.hp1 NA18961.hp1 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.405-20068_405-2004 others(24): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575791 | |||||||
| chr17:68575791 | T | TACACACA others(15): Show |
5 | a0001c0005t0002g0085 a0002c0002t0001g0173 a0002c0002t0001g0305 others(2): Show |
5 | HG01981.hp2 HG02004.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.405-20070_405-2004 others(26): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575791 | |||||||
| chr17:68575791 | T | TACACACA others(17): Show |
4 | a0001c0001t0006g0218 a0001c0005t0001g0088 a0001c0005t0001g0099 others(1): Show |
4 | HG01361.hp1 HG01433.hp2 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.405-20072_405-2004 others(28): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575791 | |||||||
| chr17:68575791 | T | TACACACA others(19): Show |
1 | a0001c0005t0003g0118 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.405-20074_405-2004 others(30): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575791 | |||||||
| chr17:68575791 | T | TACACACA others(21): Show |
3 | a0001c0005t0002g0106 a0002c0007t0001g0097 a0002c0014t0001g0117 |
3 | HG02293.hp1 HG02523.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.405-20076_405-2004 others(32): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575791 | |||||||
| chr17:68575791 | T | TACACACA others(23): Show |
1 | a0001c0001t0001g0352 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.405-20078_405-2004 others(34): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575791 | |||||||
| chr17:68575791 | TAC | T | 4 | a0001c0001t0001g0330 a0001c0001t0002g0204 a0001c0001t0002g0231 others(1): Show |
4 | HG00099.hp2 HG02486.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.405-20050_405-2004 others(6): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575791 | |||||||
| chr17:68575791 | TACACACA others(3): Show |
T | 7 | a0001c0001t0001g0216 a0001c0001t0001g0270 a0001c0001t0002g0272 others(4): Show |
7 | HG02145.hp2 HG02572.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.405-20058_405-2004 others(14): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575791 | |||||||
| chr17:68575815 | C | T | 1 | a0001c0001t0002g0292 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.405-20072G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575815 | |||||||
| chr17:68575832 | A | ACAC | 27 | a0001c0004t0001g0037 a0001c0004t0001g0043 a0001c0004t0001g0045 others(24): Show |
27 | HG00408.hp1 HG00609.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.405-20090_405-2008 others(7): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575832 | |||||||
| chr17:68575832 | A | ACACAC | 5 | a0001c0004t0002g0057 a0001c0004t0004g0027 a0001c0004t0004g0036 others(2): Show |
5 | HG02074.hp1 NA18997.hp2 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.405-20090_405-2008 others(9): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575832 | |||||||
| chr17:68575833 | T | A | 35 | a0001c0004t0001g0034 a0001c0004t0001g0037 a0001c0004t0001g0043 others(32): Show |
35 | HG00408.hp1 HG00609.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.405-20090A>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575833 | |||||||
| chr17:68575833 | T | C | 107 | a0001c0001t0001g0003 a0001c0001t0001g0151 a0001c0001t0001g0155 others(104): Show |
111 | HG00280.hp2 HG00558.hp1 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.405-20090A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575833 | |||||||
| chr17:68575873 | G | A | 1 | a0001c0001t0003g0192 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.405-20130C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575873 | |||||||
| chr17:68575917 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.405-20174G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575917 | |||||||
| chr17:68575918 | G | A | 3 | a0001c0001t0006g0275 a0001c0001t0020g0327 a0002c0002t0001g0328 |
3 | HG02451.hp2 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.405-20175C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575918 | |||||||
| chr17:68575918 | G | T | 35 | a0001c0004t0001g0034 a0001c0004t0001g0037 a0001c0004t0001g0043 others(32): Show |
35 | HG00408.hp1 HG00609.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.405-20175C>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575918 | |||||||
| chr17:68575937 | TC | T | 4 | a0001c0001t0001g0270 a0001c0001t0002g0272 a0001c0005t0002g0121 others(1): Show |
4 | HG02572.hp1 HG03041.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.405-20195delG | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68575937 | |||||||
| chr17:68576089 | G | A | 2 | a0001c0001t0002g0217 a0002c0002t0001g0215 |
2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.405-20346C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68576089 | |||||||
| chr17:68576244 | C | G | 1 | a0002c0007t0001g0086 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.405-20501G>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68576244 | |||||||
| chr17:68576255 | C | A | 1 | a0001c0001t0006g0275 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.405-20512G>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68576255 | |||||||
| chr17:68576506 | G | T | 6 | a0001c0001t0002g0279 a0001c0001t0002g0280 a0001c0001t0005g0283 others(3): Show |
6 | HG01891.hp2 HG02451.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.405-20763C>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68576506 | |||||||
| chr17:68576507 | C | T | 22 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0269 others(19): Show |
22 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.405-20764G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68576507 | |||||||
| chr17:68576522 | G | A | 14 | a0001c0005t0003g0107 a0001c0005t0003g0118 a0002c0002t0001g0139 others(11): Show |
14 | HG00544.hp1 HG00621.hp2 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.405-20779C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68576522 | |||||||
| chr17:68576552 | C | T | 1 | a0002c0008t0001g0032 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.405-20809G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68576552 | |||||||
| chr17:68576605 | C | T | 4 | a0001c0005t0002g0071 a0001c0005t0003g0065 a0001c0005t0003g0069 others(1): Show |
4 | NA18954.hp2 NA18957.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.405-20862G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68576605 | |||||||
| chr17:68576617 | C | G | 8 | a0001c0001t0001g0212 a0001c0001t0001g0216 a0001c0001t0001g0270 others(5): Show |
8 | HG02145.hp2 HG02572.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.405-20874G>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68576617 | |||||||
| chr17:68576618 | G | A | 1 | a0002c0002t0001g0305 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.405-20875C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68576618 | |||||||
| chr17:68576633 | CA | C | 3 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0002c0003t0001g0251 |
3 | HG02717.hp1 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.405-20891delT | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68576633 | |||||||
| chr17:68576658 | G | A | 2 | a0002c0007t0001g0093 a0002c0007t0001g0094 |
2 | NA18952.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.405-20915C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68576658 | |||||||
| chr17:68576718 | G | A | 1 | a0001c0005t0002g0074 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.405-20975C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68576718 | |||||||
| chr17:68576863 | C | G | 1 | a0001c0001t0002g0209 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.405-21120G>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68576863 | |||||||
| chr17:68577335 | T | C | 2 | a0001c0001t0002g0334 a0001c0001t0002g0341 |
2 | NA18939.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.405-21592A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68577335 | |||||||
| chr17:68577725 | C | T | 2 | a0001c0001t0006g0275 a0002c0002t0001g0328 |
2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.405-21982G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68577725 | |||||||
| chr17:68577750 | C | A | 1 | a0001c0001t0002g0211 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.405-22007G>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68577750 | |||||||
| chr17:68577751 | T | C | 1 | a0001c0001t0022g0362 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.405-22008A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68577751 | |||||||
| chr17:68577797 | C | T | 1 | a0001c0001t0001g0347 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.405-22054G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68577797 | |||||||
| chr17:68577877 | T | A | 3 | a0001c0001t0012g0013 a0002c0003t0001g0297 a0002c0003t0001g0298 |
3 | HG01358.hp1 HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.405-22134A>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68577877 | |||||||
| chr17:68578005 | C | CCA | 5 | a0001c0001t0001g0268 a0001c0001t0001g0330 a0001c0001t0006g0278 others(2): Show |
5 | HG01346.hp2 HG02572.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.404+22256_404+2225 others(6): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68578005 | |||||||
| chr17:68578024 | C | T | 35 | a0001c0004t0001g0034 a0001c0004t0001g0037 a0001c0004t0001g0043 others(32): Show |
35 | HG00408.hp1 HG00609.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.404+22239G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68578024 | |||||||
| chr17:68578062 | C | T | 5 | a0001c0001t0005g0283 a0001c0001t0005g0284 a0001c0001t0005g0285 others(2): Show |
5 | HG01891.hp2 HG02451.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.404+22201G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68578062 | |||||||
| chr17:68578257 | G | C | 1 | a0002c0002t0001g0325 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.404+22006C>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68578257 | |||||||
| chr17:68578429 | G | C | 35 | a0001c0004t0001g0034 a0001c0004t0001g0037 a0001c0004t0001g0043 others(32): Show |
35 | HG00408.hp1 HG00609.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.404+21834C>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68578429 | |||||||
| chr17:68578468 | T | C | 2 | a0001c0005t0001g0088 a0001c0005t0001g0099 |
2 | HG01361.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.404+21795A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68578468 | |||||||
| chr17:68578541 | A | C | 85 | a0001c0001t0001g0003 a0001c0001t0001g0151 a0001c0001t0001g0155 others(82): Show |
88 | HG00280.hp2 HG00673.hp2 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.404+21722T>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68578541 | |||||||
| chr17:68578649 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.404+21614T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68578649 | |||||||
| chr17:68578690 | A | T | 2 | a0004c0011t0002g0061 a0004c0011t0005g0060 |
2 | HG01884.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.404+21573T>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68578690 | |||||||
| chr17:68578769 | G | A | 35 | a0001c0004t0001g0034 a0001c0004t0001g0037 a0001c0004t0001g0043 others(32): Show |
35 | HG00408.hp1 HG00609.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.404+21494C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68578769 | |||||||
| chr17:68578838 | C | CA | 61 | a0001c0001t0001g0213 a0001c0001t0001g0220 a0001c0001t0001g0222 others(58): Show |
61 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.404+21424dupT | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68578838 | |||||||
| chr17:68578838 | C | CAA | 19 | a0001c0001t0001g0236 a0001c0001t0001g0240 a0001c0001t0001g0347 others(16): Show |
19 | HG00597.hp2 HG00609.hp1 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.404+21423_404+2142 others(6): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68578838 | |||||||
| chr17:68578838 | C | CAAA | 12 | a0001c0001t0002g0319 a0001c0001t0002g0350 a0001c0001t0012g0013 others(9): Show |
12 | HG00140.hp1 HG01358.hp1 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.404+21422_404+2142 others(7): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68578838 | |||||||
| chr17:68578838 | CAA | C | 11 | a0001c0001t0001g0165 a0001c0001t0001g0252 a0001c0001t0002g0211 others(8): Show |
11 | HG01243.hp1 HG01943.hp1 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.404+21423_404+2142 others(6): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68578838 | |||||||
| chr17:68578866 | A | T | 109 | a0001c0001t0001g0003 a0001c0001t0001g0151 a0001c0001t0001g0155 others(106): Show |
112 | HG00280.hp2 HG00408.hp1 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.404+21397T>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68578866 | |||||||
| chr17:68578868 | T | A | 109 | a0001c0001t0001g0003 a0001c0001t0001g0151 a0001c0001t0001g0155 others(106): Show |
112 | HG00280.hp2 HG00408.hp1 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.404+21395A>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68578868 | |||||||
| chr17:68578869 | A | G | 109 | a0001c0001t0001g0003 a0001c0001t0001g0151 a0001c0001t0001g0155 others(106): Show |
112 | HG00280.hp2 HG00408.hp1 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.404+21394T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68578869 | |||||||
| chr17:68578976 | C | T | 11 | a0001c0005t0001g0088 a0001c0005t0001g0099 a0001c0005t0002g0125 others(8): Show |
12 | HG00741.hp2 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.404+21287G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68578976 | |||||||
| chr17:68579000 | C | T | 1 | a0001c0001t0002g0211 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.404+21263G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68579000 | |||||||
| chr17:68579001 | G | A | 1 | a0002c0003t0001g0152 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.404+21262C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68579001 | |||||||
| chr17:68579013 | C | CA | 17 | a0001c0001t0001g0182 a0001c0001t0001g0269 a0001c0001t0001g0270 others(14): Show |
17 | HG01243.hp1 HG01891.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.404+21249dupT | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68579013 | |||||||
| chr17:68579013 | C | CAA | 72 | a0001c0001t0001g0003 a0001c0001t0001g0151 a0001c0001t0001g0155 others(69): Show |
75 | HG00280.hp2 HG00673.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.404+21248_404+2124 others(6): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68579013 | |||||||
| chr17:68579013 | CA | C | 7 | a0001c0001t0001g0145 a0001c0001t0002g0334 a0001c0001t0012g0013 others(4): Show |
8 | HG01257.hp1 HG01258.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.404+21249delT | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68579013 | |||||||
| chr17:68579024 | A | C | 5 | a0001c0001t0001g0189 a0001c0001t0001g0330 a0001c0001t0002g0188 others(2): Show |
5 | HG02572.hp2 HG02723.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.404+21239T>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68579024 | |||||||
| chr17:68579097 | A | C | 1 | a0003c0009t0001g0002 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.404+21166T>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68579097 | |||||||
| chr17:68579343 | A | C | 4 | a0001c0001t0001g0003 a0001c0001t0001g0155 a0001c0001t0002g0154 others(1): Show |
5 | HG01069.hp1 HG01081.hp1 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.404+20920T>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68579343 | |||||||
| chr17:68579353 | C | T | 1 | a0003c0009t0001g0079 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.404+20910G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68579353 | |||||||
| chr17:68579405 | G | C | 1 | a0001c0001t0001g0193 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.404+20858C>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68579405 | |||||||
| chr17:68579504 | C | A | 2 | a0001c0001t0001g0189 a0001c0001t0002g0188 |
2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.404+20759G>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68579504 | |||||||
| chr17:68579524 | T | A | 5 | a0001c0001t0002g0209 a0001c0001t0002g0254 a0001c0001t0005g0201 others(2): Show |
5 | HG01361.hp2 HG02630.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.404+20739A>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68579524 | |||||||
| chr17:68579580 | A | G | 8 | a0001c0001t0001g0348 a0001c0001t0002g0350 a0001c0017t0005g0014 others(5): Show |
8 | HG02055.hp1 HG02647.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.404+20683T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68579580 | |||||||
| chr17:68579598 | G | A | 21 | a0001c0001t0001g0212 a0001c0001t0001g0216 a0001c0001t0001g0270 others(18): Show |
21 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.404+20665C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68579598 | |||||||
| chr17:68579604 | G | A | 126 | a0001c0001t0001g0003 a0001c0001t0001g0151 a0001c0001t0001g0155 others(123): Show |
129 | HG00280.hp2 HG00408.hp1 HG00609.hp2 others(126): Show |
intron_variant | MODIFIER | c.404+20659C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68579604 | |||||||
| chr17:68579620 | G | A | 75 | a0001c0001t0001g0003 a0001c0001t0001g0151 a0001c0001t0001g0155 others(72): Show |
78 | HG00280.hp2 HG00673.hp2 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.404+20643C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68579620 | |||||||
| chr17:68579756 | A | G | 11 | a0001c0001t0001g0216 a0001c0001t0001g0252 a0001c0001t0001g0253 others(8): Show |
11 | HG02055.hp2 HG02109.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.404+20507T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68579756 | |||||||
| chr17:68579819 | G | C | 8 | a0001c0001t0001g0348 a0001c0001t0002g0350 a0001c0017t0005g0014 others(5): Show |
8 | HG02055.hp1 HG02647.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.404+20444C>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68579819 | |||||||
| chr17:68580008 | T | A | 78 | a0001c0001t0001g0003 a0001c0001t0001g0151 a0001c0001t0001g0155 others(75): Show |
81 | HG00280.hp2 HG00673.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.404+20255A>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68580008 | |||||||
| chr17:68580009 | T | TTAA | 78 | a0001c0001t0001g0003 a0001c0001t0001g0151 a0001c0001t0001g0155 others(75): Show |
81 | HG00280.hp2 HG00673.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.404+20253_404+2025 others(7): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68580009 | |||||||
| chr17:68580010 | G | A | 78 | a0001c0001t0001g0003 a0001c0001t0001g0151 a0001c0001t0001g0155 others(75): Show |
81 | HG00280.hp2 HG00673.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.404+20253C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68580010 | |||||||
| chr17:68580181 | T | A | 1 | a0001c0001t0002g0211 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.404+20082A>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68580181 | |||||||
| chr17:68580298 | G | T | 37 | a0001c0001t0001g0213 a0001c0001t0001g0220 a0001c0001t0001g0233 others(34): Show |
38 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.404+19965C>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68580298 | |||||||
| chr17:68580349 | C | T | 78 | a0001c0001t0001g0003 a0001c0001t0001g0151 a0001c0001t0001g0155 others(75): Show |
81 | HG00280.hp2 HG00673.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.404+19914G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68580349 | |||||||
| chr17:68580394 | C | T | 1 | a0010c0026t0001g0360 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.404+19869G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68580394 | |||||||
| chr17:68580407 | C | T | 1 | a0002c0007t0001g0097 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.404+19856G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68580407 | |||||||
| chr17:68580417 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.404+19846G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68580417 | |||||||
| chr17:68580639 | C | A | 2 | a0004c0011t0002g0061 a0004c0011t0005g0060 |
2 | HG01884.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.404+19624G>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68580639 | |||||||
| chr17:68580758 | T | A | 3 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0002c0003t0001g0251 |
3 | HG02717.hp1 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.404+19505A>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68580758 | |||||||
| chr17:68580860 | C | T | 1 | a0001c0001t0022g0362 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.404+19403G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68580860 | |||||||
| chr17:68580902 | C | T | 82 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(79): Show |
85 | HG00280.hp2 HG00673.hp2 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.404+19361G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68580902 | |||||||
| chr17:68581048 | A | G | 3 | a0001c0001t0001g0330 a0001c0001t0006g0278 a0008c0022t0002g0331 |
3 | HG02572.hp2 HG03579.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.404+19215T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581048 | |||||||
| chr17:68581112 | C | T | 2 | a0001c0004t0002g0057 a0001c0004t0002g0059 |
2 | NA18989.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.404+19151G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581112 | |||||||
| chr17:68581347 | A | G | 1 | a0001c0001t0001g0281 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.404+18916T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581347 | |||||||
| chr17:68581348 | GTTTTTCT others(3): Show |
G | 1 | a0001c0001t0001g0348 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.404+18905_404+1891 others(14): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581348 | |||||||
| chr17:68581350 | T | TTTCTTTC others(4): Show |
1 | a0002c0007t0001g0093 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.404+18912_404+1891 others(15): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581350 | |||||||
| chr17:68581350 | T | TTTCTTTC others(8): Show |
1 | a0002c0007t0001g0094 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.404+18912_404+1891 others(19): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581350 | |||||||
| chr17:68581350 | T | TTTTC | 41 | a0001c0001t0001g0151 a0001c0001t0001g0161 a0001c0001t0001g0182 others(38): Show |
43 | HG00280.hp1 HG00558.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.404+18909_404+1891 others(8): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581350 | |||||||
| chr17:68581350 | T | TTTTCTTT others(1): Show |
29 | a0001c0001t0001g0003 a0001c0001t0001g0165 a0001c0001t0001g0216 others(26): Show |
29 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.404+18905_404+1891 others(12): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581350 | |||||||
| chr17:68581350 | T | TTTTCTTT others(5): Show |
53 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0261 others(50): Show |
53 | HG00099.hp1 HG00609.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.404+18901_404+1891 others(16): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581350 | |||||||
| chr17:68581350 | T | TTTTCTTT others(9): Show |
56 | a0001c0001t0001g0157 a0001c0001t0001g0250 a0001c0001t0001g0268 others(53): Show |
57 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.404+18897_404+1891 others(20): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581350 | |||||||
| chr17:68581350 | T | TTTTCTTT others(13): Show |
39 | a0001c0001t0001g0189 a0001c0001t0001g0351 a0001c0001t0001g0352 others(36): Show |
39 | HG01070.hp1 HG01071.hp2 HG01433.hp2 others(36): Show |
intron_variant | MODIFIER | c.404+18893_404+1891 others(24): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581350 | |||||||
| chr17:68581350 | T | TTTTCTTT others(17): Show |
22 | a0001c0001t0001g0145 a0001c0001t0003g0181 a0001c0001t0003g0245 others(19): Show |
23 | HG00408.hp1 HG01167.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.404+18889_404+1891 others(28): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581350 | |||||||
| chr17:68581350 | T | TTTTCTTT others(21): Show |
14 | a0001c0001t0002g0184 a0001c0001t0002g0324 a0001c0001t0006g0208 others(11): Show |
14 | HG00738.hp1 HG01496.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.404+18885_404+1891 others(32): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581350 | |||||||
| chr17:68581350 | T | TTTTCTTT others(25): Show |
4 | a0001c0001t0005g0354 a0002c0003t0001g0340 a0002c0008t0001g0032 others(1): Show |
4 | HG00673.hp1 HG01099.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.404+18881_404+1891 others(36): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581350 | |||||||
| chr17:68581350 | T | TTTTCTTT others(18): Show |
1 | a0001c0001t0001g0134 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.404+18912_404+1891 others(29): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581350 | |||||||
| chr17:68581350 | T | TTTTTTCT others(5): Show |
1 | a0002c0002t0001g0198 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.404+18912_404+1891 others(16): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581350 | |||||||
| chr17:68581350 | T | TTTTTTCT others(13): Show |
1 | a0002c0002t0001g0197 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.404+18912_404+1891 others(24): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581350 | |||||||
| chr17:68581350 | TTTTC | T | 18 | a0001c0001t0002g0211 a0001c0001t0002g0228 a0001c0001t0002g0292 others(15): Show |
19 | HG00140.hp1 HG00323.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.404+18909_404+1891 others(8): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581350 | |||||||
| chr17:68581350 | TTTTCTTT others(1): Show |
T | 9 | a0001c0001t0001g0213 a0001c0001t0001g0240 a0001c0001t0001g0287 others(6): Show |
9 | HG01257.hp2 HG01884.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.404+18905_404+1891 others(12): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581350 | |||||||
| chr17:68581350 | TTTTCTTT others(5): Show |
T | 5 | a0001c0001t0001g0281 a0001c0001t0001g0330 a0001c0001t0002g0350 others(2): Show |
5 | HG02615.hp1 HG03017.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.404+18901_404+1891 others(16): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581350 | |||||||
| chr17:68581350 | TTTTCTTT others(9): Show |
T | 3 | a0001c0001t0006g0278 a0002c0003t0017g0142 a0008c0022t0002g0331 |
3 | HG02572.hp2 HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.404+18897_404+1891 others(20): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581350 | |||||||
| chr17:68581350 | TTTTCTTT others(21): Show |
T | 2 | a0001c0001t0001g0274 a0001c0001t0002g0273 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.404+18885_404+1891 others(32): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581350 | |||||||
| chr17:68581354 | C | CTTTCTTT others(6): Show |
1 | a0001c0001t0001g0130 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.404+18896_404+1890 others(17): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581354 | |||||||
| chr17:68581357 | T | C | 1 | a0002c0008t0001g0031 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.404+18906A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581357 | |||||||
| chr17:68581358 | C | CTTTCTTT others(2): Show |
3 | a0001c0001t0001g0133 a0002c0002t0001g0131 a0002c0002t0001g0132 |
3 | NA18942.hp2 NA18982.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.404+18896_404+1890 others(13): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581358 | |||||||
| chr17:68581368 | T | TTCTTTCT others(3): Show |
1 | a0001c0001t0023g0365 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.404+18885_404+1889 others(14): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581368 | |||||||
| chr17:68581382 | C | CTTTCTTT others(27): Show |
1 | a0002c0003t0001g0251 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.404+18847_404+1888 others(38): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581382 | |||||||
| chr17:68581382 | C | CTTTCTTT others(35): Show |
1 | a0001c0001t0001g0253 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.404+18880_404+1888 others(46): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581382 | |||||||
| chr17:68581382 | C | CTTTCTTT others(39): Show |
1 | a0001c0001t0001g0252 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.404+18880_404+1888 others(50): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581382 | |||||||
| chr17:68581388 | T | TTCTTTCT others(27): Show |
1 | a0001c0001t0001g0212 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.404+18874_404+1887 others(38): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581388 | |||||||
| chr17:68581402 | C | CTTTCTTT others(10): Show |
1 | a0002c0008t0001g0031 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.404+18860_404+1886 others(21): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581402 | |||||||
| chr17:68581402 | C | CTTTCTTT others(14): Show |
1 | a0001c0001t0002g0324 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.404+18840_404+1886 others(25): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581402 | |||||||
| chr17:68581414 | C | CTTTCTTT others(10): Show |
1 | a0001c0001t0002g0196 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.404+18848_404+1884 others(21): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581414 | |||||||
| chr17:68581415 | T | TTTCTTTC others(4): Show |
1 | a0003c0006t0001g0203 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.404+18847_404+1884 others(15): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581415 | |||||||
| chr17:68581415 | T | TTTCTTTC others(12): Show |
3 | a0001c0001t0005g0326 a0002c0002t0001g0291 a0003c0018t0001g0016 |
3 | HG01123.hp1 HG02280.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.404+18847_404+1884 others(23): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581415 | |||||||
| chr17:68581415 | T | TTTCTTTC others(16): Show |
2 | a0002c0002t0001g0305 a0003c0009t0001g0112 |
2 | HG01981.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.404+18847_404+1884 others(27): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581415 | |||||||
| chr17:68581416 | T | TTCTTTCT others(3): Show |
2 | a0001c0001t0002g0209 a0002c0014t0001g0122 |
2 | HG02630.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.404+18846_404+1884 others(14): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581416 | |||||||
| chr17:68581416 | T | TTCTTTCT others(15): Show |
1 | a0003c0015t0001g0113 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.404+18846_404+1884 others(26): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581416 | |||||||
| chr17:68581417 | T | TCTTTCTT others(2): Show |
3 | a0001c0001t0003g0168 a0001c0004t0001g0046 a0004c0011t0002g0061 |
3 | HG01884.hp2 HG04115.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.404+18845_404+1884 others(13): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581417 | |||||||
| chr17:68581417 | T | TCTTTCTT others(13): Show |
1 | a0003c0006t0001g0306 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.404+18845_404+1884 others(24): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581417 | |||||||
| chr17:68581417 | T | TCTTTCTT others(8): Show |
1 | a0001c0004t0004g0054 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.404+18845_404+1884 others(19): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581417 | |||||||
| chr17:68581418 | T | C | 10 | a0001c0001t0001g0169 a0001c0001t0001g0270 a0001c0001t0002g0272 others(7): Show |
10 | HG00673.hp2 HG00735.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.404+18845A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581418 | |||||||
| chr17:68581419 | T | C | 1 | a0001c0001t0002g0196 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.404+18844A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581419 | |||||||
| chr17:68581420 | C | T | 10 | a0001c0001t0001g0169 a0001c0001t0001g0270 a0001c0001t0002g0272 others(7): Show |
10 | HG00673.hp2 HG00735.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.404+18843G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581420 | |||||||
| chr17:68581423 | T | TTTC | 4 | a0001c0001t0001g0270 a0001c0001t0002g0272 a0002c0002t0001g0173 others(1): Show |
4 | HG02572.hp1 HG03225.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.404+18839_404+1884 others(7): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581423 | |||||||
| chr17:68581423 | T | TTTCTTTC others(4): Show |
1 | a0003c0006t0001g0170 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.404+18839_404+1884 others(15): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581423 | |||||||
| chr17:68581425 | T | C | 1 | a0002c0010t0001g0058 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.404+18838A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581425 | |||||||
| chr17:68581431 | C | T | 2 | a0001c0005t0002g0096 a0002c0002t0024g0371 |
2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.404+18832G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581431 | |||||||
| chr17:68581433 | T | C | 1 | a0002c0002t0024g0371 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.404+18830A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581433 | |||||||
| chr17:68581435 | CTTTTCTT others(23): Show |
C | 2 | a0002c0002t0001g0197 a0002c0002t0001g0198 |
2 | HG02055.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.404+18798_404+1882 others(34): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581435 | |||||||
| chr17:68581439 | TCTTTTTT others(134): Show |
T | 1 | a0009c0021t0001g0304 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.404+18683_404+1882 others(4): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581439 | |||||||
| chr17:68581440 | C | T | 1 | a0002c0010t0001g0058 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.404+18823G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581440 | |||||||
| chr17:68581443 | T | C | 1 | a0002c0010t0001g0058 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.404+18820A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581443 | |||||||
| chr17:68581444 | T | C | 6 | a0001c0001t0001g0169 a0001c0005t0002g0096 a0002c0002t0001g0153 others(3): Show |
6 | HG00673.hp2 HG00735.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.404+18819A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581444 | |||||||
| chr17:68581448 | CTTTTCTT others(14): Show |
C | 1 | a0003c0009t0001g0079 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.404+18794_404+1881 others(25): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581448 | |||||||
| chr17:68581453 | C | T | 3 | a0001c0001t0001g0270 a0001c0001t0002g0272 a0002c0002t0024g0371 |
3 | HG02572.hp1 HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.404+18810G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581453 | |||||||
| chr17:68581457 | C | T | 5 | a0001c0001t0001g0169 a0001c0005t0002g0096 a0002c0002t0001g0153 others(2): Show |
5 | HG00673.hp2 HG00735.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.404+18806G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581457 | |||||||
| chr17:68581457 | CTTTCCTT others(5): Show |
C | 4 | a0001c0001t0001g0268 a0001c0001t0001g0329 a0002c0003t0001g0230 others(1): Show |
4 | HG01346.hp2 HG02922.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.404+18794_404+1880 others(16): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581457 | |||||||
| chr17:68581461 | C | CCTTT | 3 | a0001c0001t0002g0335 a0002c0003t0016g0301 a0002c0010t0001g0052 |
3 | HG02129.hp2 HG03239.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.404+18798_404+1880 others(8): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581461 | |||||||
| chr17:68581461 | C | T | 1 | a0002c0010t0001g0058 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.404+18802G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581461 | |||||||
| chr17:68581461 | CCTTT | C | 97 | a0001c0001t0001g0137 a0001c0001t0001g0274 a0001c0001t0001g0295 others(94): Show |
99 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.404+18798_404+1880 others(8): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581461 | |||||||
| chr17:68581461 | CCTTTCTT others(1): Show |
C | 164 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(161): Show |
169 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.404+18794_404+1880 others(12): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581461 | |||||||
| chr17:68581461 | CCTTTCTT others(5): Show |
C | 5 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0002g0279 others(2): Show |
5 | HG02258.hp1 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.404+18790_404+1880 others(16): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581461 | |||||||
| chr17:68581462 | C | T | 8 | a0001c0001t0001g0169 a0001c0001t0001g0270 a0001c0001t0002g0272 others(5): Show |
8 | HG00673.hp2 HG00735.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.404+18801G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581462 | |||||||
| chr17:68581465 | T | C | 3 | a0001c0001t0001g0270 a0001c0001t0002g0272 a0002c0002t0024g0371 |
3 | HG02572.hp1 HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.404+18798A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581465 | |||||||
| chr17:68581469 | T | TCTTTC | 5 | a0001c0001t0001g0169 a0001c0005t0002g0096 a0002c0002t0001g0153 others(2): Show |
5 | HG00673.hp2 HG00735.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.404+18789_404+1879 others(9): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581469 | |||||||
| chr17:68581489 | T | C | 1 | a0002c0010t0001g0058 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.404+18774A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581489 | |||||||
| chr17:68581490 | T | C | 1 | a0001c0005t0002g0096 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.404+18773A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581490 | |||||||
| chr17:68581492 | C | T | 1 | a0001c0005t0002g0096 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.404+18771G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581492 | |||||||
| chr17:68581496 | C | A | 1 | a0001c0001t0001g0222 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.404+18767G>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581496 | |||||||
| chr17:68581500 | CTTCT | C | 84 | a0001c0001t0001g0137 a0001c0001t0002g0196 a0001c0001t0002g0221 others(81): Show |
87 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.404+18759_404+1876 others(8): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581500 | |||||||
| chr17:68581503 | C | T | 2 | a0001c0005t0002g0096 a0002c0010t0001g0058 |
2 | HG02280.hp1 NA19059.hp2 |
intron_variant | MODIFIER | c.404+18760G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581503 | |||||||
| chr17:68581504 | T | C | 2 | a0001c0005t0002g0096 a0002c0010t0001g0058 |
2 | HG02280.hp1 NA19059.hp2 |
intron_variant | MODIFIER | c.404+18759A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581504 | |||||||
| chr17:68581581 | CT | C | 254 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(251): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.404+18681delA | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581581 | |||||||
| chr17:68581624 | G | A | 2 | a0001c0001t0002g0179 a0002c0003t0001g0180 |
2 | HG01255.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.404+18639C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581624 | |||||||
| chr17:68581649 | C | T | 1 | a0001c0001t0002g0228 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.404+18614G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581649 | |||||||
| chr17:68581661 | C | T | 31 | a0001c0001t0001g0250 a0001c0001t0001g0261 a0001c0001t0001g0264 others(28): Show |
32 | HG00558.hp1 HG00597.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.404+18602G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581661 | |||||||
| chr17:68581669 | G | A | 7 | a0001c0001t0002g0209 a0001c0001t0002g0254 a0001c0001t0005g0201 others(4): Show |
7 | HG01361.hp2 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.404+18594C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581669 | |||||||
| chr17:68581736 | C | T | 4 | a0001c0001t0001g0270 a0001c0001t0002g0272 a0002c0002t0024g0371 others(1): Show |
4 | HG02572.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.404+18527G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581736 | |||||||
| chr17:68581749 | T | A | 1 | a0002c0002t0024g0371 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.404+18514A>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581749 | |||||||
| chr17:68581757 | G | C | 2 | a0001c0001t0001g0264 a0001c0001t0001g0265 |
2 | NA19011.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.404+18506C>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581757 | |||||||
| chr17:68581856 | G | A | 1 | a0001c0001t0022g0362 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.404+18407C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581856 | |||||||
| chr17:68581947 | C | G | 1 | a0003c0006t0001g0322 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.404+18316G>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581947 | |||||||
| chr17:68582008 | T | C | 37 | a0001c0001t0001g0213 a0001c0001t0001g0220 a0001c0001t0001g0222 others(34): Show |
38 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(35): Show |
intron_variant | MODIFIER | c.404+18255A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68582008 | |||||||
| chr17:68582026 | C | T | 4 | a0001c0004t0008g0009 a0001c0004t0008g0011 a0001c0004t0008g0012 others(1): Show |
4 | HG01109.hp2 HG02630.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.404+18237G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68582026 | |||||||
| chr17:68582058 | C | T | 2 | a0001c0001t0002g0228 a0001c0001t0002g0229 |
2 | HG00280.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.404+18205G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68582058 | |||||||
| chr17:68582082 | A | G | 70 | a0001c0001t0001g0137 a0001c0001t0001g0274 a0001c0001t0002g0273 others(67): Show |
72 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.404+18181T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68582082 | |||||||
| chr17:68582137 | T | G | 1 | a0002c0003t0001g0174 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.404+18126A>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68582137 | |||||||
| chr17:68582147 | A | G | 34 | a0001c0001t0001g0250 a0001c0001t0001g0261 a0001c0001t0001g0264 others(31): Show |
35 | HG00558.hp1 HG00597.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.404+18116T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68582147 | |||||||
| chr17:68582417 | C | T | 2 | a0002c0003t0001g0297 a0002c0003t0001g0298 |
2 | HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.404+17846G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68582417 | |||||||
| chr17:68582580 | A | G | 1 | a0001c0001t0001g0212 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.404+17683T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68582580 | |||||||
| chr17:68582612 | G | A | 34 | a0001c0001t0001g0250 a0001c0001t0001g0261 a0001c0001t0001g0264 others(31): Show |
35 | HG00558.hp1 HG00597.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.404+17651C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68582612 | |||||||
| chr17:68582620 | C | G | 1 | a0001c0001t0022g0362 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.404+17643G>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68582620 | |||||||
| chr17:68582627 | C | T | 81 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(78): Show |
84 | HG00280.hp2 HG00673.hp2 HG00735.hp1 others(81): Show |
intron_variant | MODIFIER | c.404+17636G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68582627 | |||||||
| chr17:68582657 | A | G | 1 | a0002c0002t0001g0332 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.404+17606T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68582657 | |||||||
| chr17:68582747 | C | G | 3 | a0001c0001t0001g0348 a0001c0001t0002g0350 a0002c0003t0001g0349 |
3 | HG02809.hp1 HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.404+17516G>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68582747 | |||||||
| chr17:68582780 | A | AT | 33 | a0001c0001t0001g0182 a0001c0001t0001g0268 a0001c0001t0001g0293 others(30): Show |
33 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.404+17482dupA | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68582780 | |||||||
| chr17:68582780 | A | ATT | 74 | a0001c0001t0001g0137 a0001c0001t0001g0220 a0001c0001t0001g0222 others(71): Show |
77 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(74): Show |
intron_variant | MODIFIER | c.404+17481_404+1748 others(6): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68582780 | |||||||
| chr17:68582780 | A | ATTT | 21 | a0001c0001t0001g0213 a0001c0001t0002g0225 a0001c0001t0002g0226 others(18): Show |
21 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.404+17480_404+1748 others(7): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68582780 | |||||||
| chr17:68582780 | AT | A | 109 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(106): Show |
112 | HG00280.hp2 HG00408.hp1 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.404+17482delA | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68582780 | |||||||
| chr17:68582780 | ATT | A | 22 | a0001c0001t0001g0134 a0001c0001t0001g0250 a0001c0001t0001g0348 others(19): Show |
22 | HG00323.hp1 HG01884.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.404+17481_404+1748 others(6): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68582780 | |||||||
| chr17:68582780 | ATTT | A | 45 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0261 others(42): Show |
46 | HG00558.hp1 HG00597.hp1 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.404+17480_404+1748 others(7): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68582780 | |||||||
| chr17:68582780 | ATTTTTTT others(6): Show |
A | 4 | a0001c0004t0002g0049 a0001c0005t0004g0081 a0002c0007t0001g0080 others(1): Show |
4 | NA18970.hp2 NA19010.hp1 NA19059.hp2 others(1): Show |
intron_variant | MODIFIER | c.404+17470_404+1748 others(17): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68582780 | |||||||
| chr17:68582966 | A | AT | 8 | a0001c0001t0001g0270 a0001c0001t0001g0274 a0001c0001t0002g0272 others(5): Show |
8 | HG01884.hp2 HG02258.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.404+17296dupA | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68582966 | |||||||
| chr17:68582966 | AT | A | 284 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(281): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.404+17296delA | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68582966 | |||||||
| chr17:68583041 | C | T | 23 | a0001c0001t0001g0270 a0001c0001t0001g0274 a0001c0001t0001g0346 others(20): Show |
23 | HG01099.hp2 HG01884.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.404+17222G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68583041 | |||||||
| chr17:68583048 | C | T | 52 | a0001c0001t0001g0213 a0001c0001t0001g0220 a0001c0001t0001g0222 others(49): Show |
53 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.404+17215G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68583048 | |||||||
| chr17:68583353 | C | T | 1 | a0003c0006t0001g0214 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.404+16910G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68583353 | |||||||
| chr17:68583390 | GTT | G | 2 | a0001c0005t0002g0115 a0003c0009t0001g0002 |
3 | HG01257.hp1 HG01258.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.404+16871_404+1687 others(6): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68583390 | |||||||
| chr17:68583476 | C | T | 8 | a0001c0005t0001g0120 a0001c0005t0002g0071 a0001c0005t0002g0087 others(5): Show |
8 | HG00544.hp2 HG02074.hp1 NA18954.hp2 others(5): Show |
intron_variant | MODIFIER | c.404+16787G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68583476 | |||||||
| chr17:68583687 | C | T | 46 | a0001c0001t0001g0216 a0001c0001t0001g0269 a0001c0001t0002g0211 others(43): Show |
46 | HG00323.hp1 HG00408.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.404+16576G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68583687 | |||||||
| chr17:68583773 | C | G | 305 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(302): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.404+16490G>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68583773 | |||||||
| chr17:68583817 | G | A | 6 | a0001c0001t0001g0346 a0001c0001t0001g0347 a0001c0001t0001g0351 others(3): Show |
6 | HG01099.hp2 HG02055.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.404+16446C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68583817 | |||||||
| chr17:68584155 | A | G | 1 | a0003c0006t0001g0203 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.404+16108T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68584155 | |||||||
| chr17:68584197 | A | G | 17 | a0001c0001t0001g0346 a0001c0001t0001g0347 a0001c0001t0001g0348 others(14): Show |
17 | HG01099.hp2 HG01884.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.404+16066T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68584197 | |||||||
| chr17:68584317 | AAAAACAA others(8): Show |
A | 1 | a0001c0004t0002g0050 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.404+15931_404+1594 others(19): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68584317 | |||||||
| chr17:68584337 | CAAAACAA others(5): Show |
C | 88 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(85): Show |
91 | HG00280.hp2 HG00673.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.404+15914_404+1592 others(16): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68584337 | |||||||
| chr17:68584347 | CAA | C | 133 | a0001c0001t0001g0137 a0001c0001t0001g0212 a0001c0001t0001g0213 others(130): Show |
136 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.404+15914_404+1591 others(6): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68584347 | |||||||
| chr17:68584348 | A | AAAACAAA others(2): Show |
24 | a0001c0001t0001g0250 a0001c0001t0001g0261 a0001c0001t0001g0264 others(21): Show |
25 | HG00558.hp1 HG00597.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.404+15914_404+1591 others(13): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68584348 | |||||||
| chr17:68584348 | A | AAAACAAA others(7): Show |
7 | a0001c0001t0002g0279 a0001c0001t0002g0280 a0001c0001t0005g0283 others(4): Show |
7 | HG01891.hp2 HG02451.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.404+15914_404+1591 others(18): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68584348 | |||||||
| chr17:68584349 | A | AAAC | 11 | a0001c0001t0002g0272 a0001c0001t0012g0013 a0001c0001t0022g0362 others(8): Show |
11 | HG00741.hp2 HG01261.hp1 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.404+15913_404+1591 others(7): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68584349 | |||||||
| chr17:68584349 | A | AAACAAAA others(1): Show |
47 | a0001c0001t0001g0216 a0001c0001t0001g0269 a0001c0001t0002g0211 others(44): Show |
47 | HG00323.hp1 HG00408.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.404+15913_404+1591 others(12): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68584349 | |||||||
| chr17:68584354 | A | C | 68 | a0001c0001t0001g0137 a0001c0005t0001g0088 a0001c0005t0001g0089 others(65): Show |
70 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.404+15909T>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68584354 | |||||||
| chr17:68584496 | T | C | 1 | a0003c0006t0001g0214 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.404+15767A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68584496 | |||||||
| chr17:68584613 | C | T | 1 | a0002c0007t0001g0124 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.404+15650G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68584613 | |||||||
| chr17:68584707 | T | C | 88 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(85): Show |
91 | HG00280.hp2 HG00673.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.404+15556A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68584707 | |||||||
| chr17:68584752 | A | T | 2 | a0001c0001t0020g0327 a0002c0002t0001g0328 |
2 | HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.404+15511T>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68584752 | |||||||
| chr17:68584779 | A | G | 31 | a0001c0001t0001g0250 a0001c0001t0001g0261 a0001c0001t0001g0264 others(28): Show |
32 | HG00558.hp1 HG00597.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.404+15484T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68584779 | |||||||
| chr17:68584783 | G | C | 4 | a0001c0001t0001g0270 a0001c0001t0002g0272 a0002c0002t0024g0371 others(1): Show |
4 | HG02572.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.404+15480C>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68584783 | |||||||
| chr17:68585144 | G | A | 1 | a0002c0014t0001g0117 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.404+15119C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68585144 | |||||||
| chr17:68585164 | G | A | 78 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(75): Show |
81 | HG00280.hp2 HG00673.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.404+15099C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68585164 | |||||||
| chr17:68585262 | T | C | 2 | a0001c0001t0020g0327 a0002c0002t0001g0328 |
2 | HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.404+15001A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68585262 | |||||||
| chr17:68585272 | GTT | G | 3 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0002c0003t0001g0251 |
3 | HG02717.hp1 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.404+14989_404+1499 others(6): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68585272 | |||||||
| chr17:68585292 | CT | C | 52 | a0001c0001t0001g0250 a0001c0001t0001g0261 a0001c0001t0001g0264 others(49): Show |
53 | HG00558.hp1 HG00597.hp1 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.404+14970delA | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68585292 | |||||||
| chr17:68585323 | T | TATTA | 312 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(309): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.404+14936_404+1493 others(8): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68585323 | |||||||
| chr17:68585365 | C | T | 80 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(77): Show |
83 | HG00280.hp2 HG00673.hp2 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.404+14898G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68585365 | |||||||
| chr17:68585394 | C | G | 2 | a0001c0001t0020g0327 a0002c0002t0001g0328 |
2 | HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.404+14869G>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68585394 | |||||||
| chr17:68585451 | AT | A | 313 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(310): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.404+14811delA | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68585451 | |||||||
| chr17:68585488 | T | A | 31 | a0001c0001t0001g0250 a0001c0001t0001g0261 a0001c0001t0001g0264 others(28): Show |
32 | HG00558.hp1 HG00597.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.404+14775A>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68585488 | |||||||
| chr17:68585568 | C | T | 1 | a0002c0002t0001g0147 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.404+14695G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68585568 | |||||||
| chr17:68585657 | G | A | 31 | a0001c0001t0001g0250 a0001c0001t0001g0261 a0001c0001t0001g0264 others(28): Show |
32 | HG00558.hp1 HG00597.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.404+14606C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68585657 | |||||||
| chr17:68585752 | C | T | 1 | a0001c0001t0002g0146 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.404+14511G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68585752 | |||||||
| chr17:68585759 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.404+14504C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68585759 | |||||||
| chr17:68585898 | T | C | 1 | a0001c0001t0002g0272 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.404+14365A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68585898 | |||||||
| chr17:68586247 | T | C | 1 | a0001c0001t0001g0212 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.404+14016A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68586247 | |||||||
| chr17:68586638 | G | A | 1 | a0003c0006t0001g0005 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.404+13625C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68586638 | |||||||
| chr17:68586719 | C | G | 2 | a0001c0001t0005g0007 a0001c0001t0005g0286 |
3 | HG01069.hp2 HG01071.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.404+13544G>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68586719 | |||||||
| chr17:68586750 | T | C | 1 | a0001c0005t0002g0082 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.404+13513A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68586750 | |||||||
| chr17:68587016 | G | A | 36 | a0001c0001t0001g0250 a0001c0001t0001g0261 a0001c0001t0001g0264 others(33): Show |
37 | HG00558.hp1 HG00597.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.404+13247C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68587016 | |||||||
| chr17:68587025 | G | A | 2 | a0002c0002t0001g0175 a0002c0002t0001g0176 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.404+13238C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68587025 | |||||||
| chr17:68587188 | G | A | 1 | a0001c0001t0022g0362 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.404+13075C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68587188 | |||||||
| chr17:68587312 | A | ATCCATCC others(5): Show |
1 | a0002c0010t0001g0058 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.404+12939_404+1295 others(16): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68587312 | |||||||
| chr17:68587405 | G | A | 1 | a0001c0001t0006g0314 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.404+12858C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68587405 | |||||||
| chr17:68588079 | C | T | 2 | a0001c0005t0002g0083 a0001c0005t0002g0084 |
2 | NA18960.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.404+12184G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68588079 | |||||||
| chr17:68588127 | T | TA | 36 | a0001c0001t0001g0216 a0001c0001t0001g0269 a0001c0001t0001g0348 others(33): Show |
36 | HG00323.hp1 HG00609.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.404+12135dupT | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68588127 | |||||||
| chr17:68588133 | A | C | 2 | a0001c0001t0002g0179 a0002c0003t0001g0180 |
2 | HG01255.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.404+12130T>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68588133 | |||||||
| chr17:68588139 | G | A | 274 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(271): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.404+12124C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68588139 | |||||||
| chr17:68588139 | G | T | 1 | a0002c0007t0001g0086 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.404+12124C>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68588139 | |||||||
| chr17:68588219 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.404+12044A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68588219 | |||||||
| chr17:68588290 | A | G | 47 | a0001c0001t0001g0216 a0001c0001t0001g0269 a0001c0001t0002g0211 others(44): Show |
47 | HG00323.hp1 HG00408.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.404+11973T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68588290 | |||||||
| chr17:68588301 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.404+11962C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68588301 | |||||||
| chr17:68588304 | C | T | 2 | a0001c0004t0001g0021 a0001c0004t0004g0022 |
2 | NA18961.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.404+11959G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68588304 | |||||||
| chr17:68588379 | A | G | 1 | a0003c0013t0001g0047 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.404+11884T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68588379 | |||||||
| chr17:68588736 | T | C | 1 | a0001c0001t0002g0341 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.404+11527A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68588736 | |||||||
| chr17:68588750 | C | T | 17 | a0001c0001t0001g0346 a0001c0001t0001g0347 a0001c0001t0001g0348 others(14): Show |
17 | HG01099.hp2 HG01884.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.404+11513G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68588750 | |||||||
| chr17:68588764 | A | ACATTCTG others(5): Show |
1 | a0001c0004t0004g0051 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.404+11498_404+1149 others(16): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68588764 | |||||||
| chr17:68588891 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.404+11372G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68588891 | |||||||
| chr17:68589046 | G | C | 1 | a0002c0003t0001g0180 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.404+11217C>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68589046 | |||||||
| chr17:68589057 | G | T | 1 | a0001c0001t0001g0220 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.404+11206C>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68589057 | |||||||
| chr17:68589064 | T | C | 1 | a0002c0003t0009g0343 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.404+11199A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68589064 | |||||||
| chr17:68589229 | C | G | 2 | a0002c0002t0001g0291 a0002c0010t0001g0056 |
2 | HG01123.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.404+11034G>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68589229 | |||||||
| chr17:68589269 | C | T | 2 | a0002c0002t0001g0197 a0002c0002t0001g0198 |
2 | HG02055.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.404+10994G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68589269 | |||||||
| chr17:68589270 | G | A | 1 | a0001c0001t0012g0013 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.404+10993C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68589270 | |||||||
| chr17:68589320 | C | T | 22 | a0001c0005t0001g0088 a0001c0005t0001g0099 a0001c0005t0002g0125 others(19): Show |
23 | HG00544.hp1 HG00621.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.404+10943G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68589320 | |||||||
| chr17:68589335 | A | G | 83 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(80): Show |
87 | HG00140.hp2 HG00280.hp2 HG00673.hp2 others(84): Show |
intron_variant | MODIFIER | c.404+10928T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68589335 | |||||||
| chr17:68589353 | G | A | 1 | a0002c0002t0001g0177 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.404+10910C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68589353 | |||||||
| chr17:68589370 | C | T | 3 | a0001c0005t0002g0083 a0001c0005t0002g0084 a0001c0005t0002g0085 |
3 | NA18956.hp2 NA18960.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.404+10893G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68589370 | |||||||
| chr17:68589660 | A | T | 1 | a0002c0010t0001g0058 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.404+10603T>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68589660 | |||||||
| chr17:68589681 | C | A | 315 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(312): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.404+10582G>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68589681 | |||||||
| chr17:68589700 | ATAT | A | 3 | a0002c0002t0001g0315 a0003c0006t0001g0008 a0003c0006t0001g0316 |
4 | HG01192.hp2 HG01358.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.404+10560_404+1056 others(7): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68589700 | |||||||
| chr17:68589807 | A | G | 2 | a0004c0011t0002g0061 a0004c0011t0005g0060 |
2 | HG01884.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.404+10456T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68589807 | |||||||
| chr17:68589924 | G | C | 4 | a0001c0001t0001g0189 a0001c0001t0002g0188 a0001c0001t0005g0141 others(1): Show |
4 | HG02723.hp1 HG02809.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.404+10339C>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68589924 | |||||||
| chr17:68589999 | A | G | 1 | a0002c0002t0007g0367 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.404+10264T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68589999 | |||||||
| chr17:68590001 | A | G | 288 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(285): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.404+10262T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68590001 | |||||||
| chr17:68590075 | G | A | 368 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(365): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.404+10188C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68590075 | |||||||
| chr17:68590088 | T | C | 4 | a0001c0001t0001g0329 a0001c0001t0001g0330 a0001c0001t0006g0278 others(1): Show |
4 | HG02572.hp2 HG02922.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.404+10175A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68590088 | |||||||
| chr17:68590268 | G | A | 1 | a0002c0002t0001g0246 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.404+9995C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68590268 | |||||||
| chr17:68590395 | C | T | 3 | a0001c0001t0001g0351 a0004c0011t0002g0061 a0004c0011t0005g0060 |
3 | HG01884.hp2 HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.404+9868G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68590395 | |||||||
| chr17:68590434 | GTGAACCC others(16): Show |
G | 2 | a0001c0001t0004g0138 a0002c0010t0001g0052 |
2 | NA18987.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.404+9806_404+9828d others(25): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68590434 | |||||||
| chr17:68590457 | A | G | 3 | a0001c0001t0001g0270 a0001c0001t0002g0272 a0003c0006t0001g0271 |
3 | HG02572.hp1 HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.404+9806T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68590457 | |||||||
| chr17:68590576 | C | G | 3 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0002c0003t0001g0251 |
3 | HG02717.hp1 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.404+9687G>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68590576 | |||||||
| chr17:68590696 | G | A | 2 | a0001c0004t0001g0045 a0001c0004t0001g0046 |
2 | HG04115.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.404+9567C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68590696 | |||||||
| chr17:68590741 | T | C | 1 | a0002c0002t0001g0178 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.404+9522A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68590741 | |||||||
| chr17:68590930 | GC | G | 169 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(166): Show |
174 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.404+9332delG | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68590930 | |||||||
| chr17:68590989 | T | C | 54 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0220 others(51): Show |
55 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.404+9274A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68590989 | |||||||
| chr17:68591093 | C | CT | 88 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(85): Show |
91 | HG00280.hp2 HG00673.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.404+9169dupA | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68591093 | |||||||
| chr17:68591093 | C | CTGTTT | 99 | a0001c0001t0001g0137 a0001c0001t0001g0216 a0001c0001t0001g0250 others(96): Show |
101 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.404+9165_404+9169d others(7): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68591093 | |||||||
| chr17:68591093 | C | CTGTTTTG others(3): Show |
52 | a0001c0001t0001g0252 a0001c0001t0002g0209 a0001c0001t0002g0211 others(49): Show |
52 | HG00323.hp1 HG00609.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.404+9160_404+9169d others(12): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68591093 | |||||||
| chr17:68591093 | C | CTGTTTTG others(8): Show |
6 | a0001c0001t0001g0212 a0001c0001t0001g0270 a0001c0001t0012g0013 others(3): Show |
6 | HG00408.hp1 HG01358.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.404+9155_404+9169d others(17): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68591093 | |||||||
| chr17:68591093 | C | CTTGTTT | 8 | a0001c0001t0006g0275 a0001c0001t0022g0362 a0001c0001t0023g0365 others(5): Show |
8 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.404+9169_404+9170i others(8): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68591093 | |||||||
| chr17:68591093 | C | CTTGTTTT others(4): Show |
7 | a0001c0001t0001g0329 a0001c0001t0001g0330 a0001c0001t0006g0278 others(4): Show |
7 | HG02572.hp2 HG02647.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.404+9169_404+9170i others(13): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68591093 | |||||||
| chr17:68591093 | CTGTTT | C | 47 | a0001c0001t0001g0213 a0001c0001t0001g0220 a0001c0001t0001g0222 others(44): Show |
48 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(45): Show |
intron_variant | MODIFIER | c.404+9165_404+9169d others(7): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68591093 | |||||||
| chr17:68591115 | G | GTTTTGTT others(3): Show |
2 | a0003c0006t0001g0344 a0003c0006t0001g0345 |
2 | HG01433.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.404+9147_404+9148i others(12): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68591115 | |||||||
| chr17:68591120 | G | GTTTTGTT others(4): Show |
1 | a0001c0004t0002g0019 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.404+9142_404+9143i others(13): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68591120 | |||||||
| chr17:68591176 | G | A | 4 | a0001c0004t0008g0009 a0001c0004t0008g0011 a0001c0004t0008g0012 others(1): Show |
4 | HG01109.hp2 HG02630.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.404+9087C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68591176 | |||||||
| chr17:68591195 | C | G | 2 | a0004c0011t0002g0061 a0004c0011t0005g0060 |
2 | HG01884.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.404+9068G>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68591195 | |||||||
| chr17:68591248 | G | T | 3 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0002c0003t0001g0251 |
3 | HG02717.hp1 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.404+9015C>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68591248 | |||||||
| chr17:68591262 | T | C | 1 | a0002c0007t0001g0072 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.404+9001A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68591262 | |||||||
| chr17:68591346 | G | A | 137 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(134): Show |
141 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.404+8917C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68591346 | |||||||
| chr17:68591403 | G | T | 1 | a0001c0001t0012g0013 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.404+8860C>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68591403 | |||||||
| chr17:68591444 | A | C | 1 | a0002c0002t0001g0215 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.404+8819T>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68591444 | |||||||
| chr17:68591557 | A | T | 34 | a0001c0001t0001g0250 a0001c0001t0001g0261 a0001c0001t0001g0264 others(31): Show |
35 | HG00558.hp1 HG00597.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.404+8706T>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68591557 | |||||||
| chr17:68591683 | T | A | 1 | a0001c0005t0006g0116 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.404+8580A>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68591683 | |||||||
| chr17:68591683 | T | G | 8 | a0001c0001t0001g0216 a0001c0001t0001g0269 a0001c0001t0002g0211 others(5): Show |
8 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.404+8580A>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68591683 | |||||||
| chr17:68591742 | T | TG | 130 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(127): Show |
134 | HG00280.hp2 HG00558.hp1 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.404+8520dupC | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68591742 | |||||||
| chr17:68591742 | T | TGG | 63 | a0001c0001t0001g0137 a0001c0001t0002g0289 a0001c0005t0001g0088 others(60): Show |
65 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.404+8519_404+8520d others(4): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68591742 | |||||||
| chr17:68591769 | C | T | 53 | a0001c0001t0001g0293 a0001c0001t0001g0295 a0001c0001t0001g0323 others(50): Show |
54 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.404+8494G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68591769 | |||||||
| chr17:68591817 | C | T | 4 | a0001c0001t0001g0270 a0001c0001t0002g0272 a0002c0002t0024g0371 others(1): Show |
4 | HG02572.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.404+8446G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68591817 | |||||||
| chr17:68591857 | C | T | 1 | a0010c0026t0001g0360 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.404+8406G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68591857 | |||||||
| chr17:68591858 | T | A | 3 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0002c0003t0001g0251 |
3 | HG02717.hp1 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.404+8405A>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68591858 | |||||||
| chr17:68591859 | C | A | 3 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0002c0003t0001g0251 |
3 | HG02717.hp1 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.404+8404G>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68591859 | |||||||
| chr17:68591887 | C | T | 8 | a0001c0001t0001g0216 a0001c0001t0001g0269 a0001c0001t0002g0211 others(5): Show |
8 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.404+8376G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68591887 | |||||||
| chr17:68591948 | A | C | 4 | a0001c0001t0002g0254 a0001c0001t0005g0201 a0002c0003t0001g0199 others(1): Show |
4 | HG01361.hp2 HG02559.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.404+8315T>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68591948 | |||||||
| chr17:68592078 | C | T | 1 | a0003c0006t0001g0223 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.404+8185G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68592078 | |||||||
| chr17:68592080 | A | G | 2 | a0001c0001t0022g0362 a0003c0006t0001g0214 |
2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.404+8183T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68592080 | |||||||
| chr17:68592138 | GT | G | 44 | a0001c0001t0001g0213 a0001c0001t0001g0220 a0001c0001t0001g0222 others(41): Show |
45 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(42): Show |
intron_variant | MODIFIER | c.404+8124delA | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68592138 | |||||||
| chr17:68592195 | C | T | 2 | a0001c0001t0020g0327 a0002c0002t0001g0328 |
2 | HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.404+8068G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68592195 | |||||||
| chr17:68592388 | T | A | 2 | a0001c0001t0001g0274 a0001c0001t0002g0273 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.404+7875A>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68592388 | |||||||
| chr17:68592686 | A | G | 32 | a0001c0001t0001g0250 a0001c0001t0001g0261 a0001c0001t0001g0264 others(29): Show |
33 | HG00558.hp1 HG00597.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.404+7577T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68592686 | |||||||
| chr17:68592720 | A | G | 1 | a0001c0001t0002g0128 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.404+7543T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68592720 | |||||||
| chr17:68592991 | T | C | 3 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0002c0003t0001g0251 |
3 | HG02717.hp1 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.404+7272A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68592991 | |||||||
| chr17:68593109 | A | G | 66 | a0001c0001t0002g0289 a0001c0005t0001g0088 a0001c0005t0001g0089 others(63): Show |
68 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.404+7154T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68593109 | |||||||
| chr17:68593147 | A | G | 81 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(78): Show |
84 | HG00140.hp2 HG00280.hp2 HG00673.hp2 others(81): Show |
intron_variant | MODIFIER | c.404+7116T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68593147 | |||||||
| chr17:68593640 | A | G | 1 | a0001c0005t0003g0078 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.404+6623T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68593640 | |||||||
| chr17:68594016 | C | T | 1 | a0001c0001t0012g0013 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.404+6247G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68594016 | |||||||
| chr17:68594129 | TG | T | 3 | a0002c0010t0001g0058 a0004c0011t0002g0061 a0004c0011t0005g0060 |
3 | HG01884.hp2 HG02559.hp2 NA19059.hp2 |
intron_variant | MODIFIER | c.404+6133delC | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68594129 | |||||||
| chr17:68594133 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.404+6130G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68594133 | |||||||
| chr17:68594150 | G | A | 1 | a0001c0001t0003g0181 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.404+6113C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68594150 | |||||||
| chr17:68594164 | C | T | 1 | a0001c0001t0001g0329 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.404+6099G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68594164 | |||||||
| chr17:68594255 | T | C | 45 | a0001c0001t0001g0351 a0001c0001t0001g0352 a0001c0001t0001g0353 others(42): Show |
45 | HG00323.hp1 HG00408.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.404+6008A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68594255 | |||||||
| chr17:68594261 | T | C | 3 | a0001c0001t0001g0348 a0001c0001t0002g0350 a0002c0003t0001g0349 |
3 | HG02809.hp1 HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.404+6002A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68594261 | |||||||
| chr17:68594262 | A | G | 3 | a0001c0001t0001g0351 a0001c0001t0001g0352 a0001c0001t0001g0353 |
3 | HG02647.hp2 HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.404+6001T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68594262 | |||||||
| chr17:68594265 | G | A | 3 | a0001c0001t0001g0351 a0001c0001t0001g0352 a0001c0001t0001g0353 |
3 | HG02647.hp2 HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.404+5998C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68594265 | |||||||
| chr17:68594294 | G | C | 1 | a0001c0001t0001g0182 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.404+5969C>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68594294 | |||||||
| chr17:68594353 | C | T | 180 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(177): Show |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.404+5910G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68594353 | |||||||
| chr17:68594355 | C | T | 180 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(177): Show |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.404+5908G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68594355 | |||||||
| chr17:68594398 | C | CA | 28 | a0001c0001t0001g0270 a0001c0001t0001g0274 a0001c0001t0001g0323 others(25): Show |
28 | HG00408.hp2 HG01099.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.404+5864dupT | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68594398 | |||||||
| chr17:68594398 | CA | C | 78 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(75): Show |
81 | HG00280.hp2 HG00673.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.404+5864delT | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68594398 | |||||||
| chr17:68594466 | A | G | 1 | a0003c0006t0001g0144 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.404+5797T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68594466 | |||||||
| chr17:68594533 | C | T | 14 | a0001c0001t0001g0250 a0001c0001t0001g0261 a0001c0001t0001g0264 others(11): Show |
14 | HG00558.hp1 HG00597.hp1 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.404+5730G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68594533 | |||||||
| chr17:68594689 | T | G | 1 | a0002c0003t0001g0183 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.404+5574A>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68594689 | |||||||
| chr17:68594693 | T | A | 1 | a0001c0005t0003g0118 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.404+5570A>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68594693 | |||||||
| chr17:68594698 | G | A | 8 | a0001c0001t0002g0334 a0001c0001t0002g0335 a0001c0001t0002g0336 others(5): Show |
8 | HG02040.hp1 HG02071.hp1 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.404+5565C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68594698 | |||||||
| chr17:68594710 | T | C | 182 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(179): Show |
187 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.404+5553A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68594710 | |||||||
| chr17:68594980 | G | A | 2 | a0001c0001t0002g0184 a0002c0002t0001g0185 |
2 | HG00280.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.404+5283C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68594980 | |||||||
| chr17:68595102 | A | T | 1 | a0002c0010t0001g0058 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.404+5161T>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68595102 | |||||||
| chr17:68595399 | CCT | C | 3 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0002c0003t0001g0251 |
3 | HG02717.hp1 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.404+4862_404+4863d others(4): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68595399 | |||||||
| chr17:68595582 | A | C | 3 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0002c0003t0001g0251 |
3 | HG02717.hp1 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.404+4681T>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68595582 | |||||||
| chr17:68595633 | TCTTAG | T | 27 | a0001c0001t0001g0250 a0001c0001t0001g0261 a0001c0001t0001g0264 others(24): Show |
28 | HG00558.hp1 HG00597.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.404+4625_404+4629d others(7): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68595633 | |||||||
| chr17:68595648 | G | A | 1 | a0001c0005t0003g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.404+4615C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68595648 | |||||||
| chr17:68595653 | C | T | 3 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0002c0003t0001g0251 |
3 | HG02717.hp1 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.404+4610G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68595653 | |||||||
| chr17:68595839 | G | A | 1 | a0003c0006t0001g0248 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.404+4424C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68595839 | |||||||
| chr17:68595846 | T | C | 1 | a0001c0005t0001g0120 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.404+4417A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68595846 | |||||||
| chr17:68596066 | C | G | 3 | a0001c0005t0002g0074 a0001c0005t0002g0075 a0001c0005t0002g0076 |
3 | NA18944.hp1 NA18962.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.404+4197G>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68596066 | |||||||
| chr17:68596095 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.404+4168G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68596095 | |||||||
| chr17:68596201 | C | CCA | 11 | a0001c0001t0001g0216 a0001c0001t0001g0269 a0001c0001t0002g0211 others(8): Show |
11 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.404+4060_404+4061d others(4): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68596201 | |||||||
| chr17:68596201 | C | CCACA | 7 | a0001c0001t0001g0274 a0001c0001t0001g0329 a0001c0001t0002g0273 others(4): Show |
7 | HG02258.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.404+4058_404+4061d others(6): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68596201 | |||||||
| chr17:68596201 | C | CCACACAC others(3): Show |
2 | a0001c0001t0001g0330 a0002c0002t0014g0143 |
2 | HG03579.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.404+4052_404+4061d others(12): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68596201 | |||||||
| chr17:68596201 | C | CCACACAC others(5): Show |
66 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(63): Show |
69 | HG00280.hp2 HG00673.hp2 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.404+4050_404+4061d others(14): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68596201 | |||||||
| chr17:68596201 | C | CCACACAC others(7): Show |
11 | a0001c0001t0001g0189 a0001c0001t0002g0186 a0001c0001t0002g0187 others(8): Show |
11 | HG01167.hp1 HG02723.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.404+4048_404+4061d others(16): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68596201 | |||||||
| chr17:68596201 | C | CCACACAC others(9): Show |
4 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0193 others(1): Show |
4 | HG02602.hp2 HG03654.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.404+4046_404+4061d others(18): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68596201 | |||||||
| chr17:68596201 | CCA | C | 14 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0281 others(11): Show |
15 | HG01069.hp2 HG01071.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.404+4060_404+4061d others(4): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68596201 | |||||||
| chr17:68596224 | C | A | 1 | a0008c0022t0002g0331 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.404+4039G>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68596224 | |||||||
| chr17:68596274 | T | G | 3 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0002c0003t0001g0251 |
3 | HG02717.hp1 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.404+3989A>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68596274 | |||||||
| chr17:68596553 | C | T | 1 | a0002c0007t0001g0073 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.404+3710G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68596553 | |||||||
| chr17:68596721 | T | G | 1 | a0002c0014t0001g0122 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.404+3542A>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68596721 | |||||||
| chr17:68596748 | A | T | 1 | a0001c0001t0021g0202 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.404+3515T>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68596748 | |||||||
| chr17:68596872 | AAAAG | A | 44 | a0001c0004t0001g0021 a0001c0004t0001g0034 a0001c0004t0001g0037 others(41): Show |
44 | HG00323.hp1 HG00408.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.404+3387_404+3390d others(6): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68596872 | |||||||
| chr17:68596876 | G | A | 2 | a0002c0010t0001g0052 a0002c0010t0001g0058 |
2 | NA18987.hp2 NA19059.hp2 |
intron_variant | MODIFIER | c.404+3387C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68596876 | |||||||
| chr17:68597027 | T | C | 5 | a0001c0001t0001g0329 a0001c0001t0001g0330 a0001c0001t0006g0278 others(2): Show |
5 | HG02258.hp1 HG02572.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.404+3236A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68597027 | |||||||
| chr17:68597221 | C | CA | 91 | a0001c0001t0001g0220 a0001c0001t0001g0222 a0001c0001t0001g0233 others(88): Show |
92 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.404+3041dupT | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68597221 | |||||||
| chr17:68597221 | CA | C | 16 | a0001c0001t0001g0346 a0001c0001t0001g0347 a0001c0001t0001g0348 others(13): Show |
16 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.404+3041delT | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68597221 | |||||||
| chr17:68597309 | TCTC | T | 3 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0002c0003t0001g0251 |
3 | HG02717.hp1 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.404+2951_404+2953d others(5): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68597309 | |||||||
| chr17:68597390 | AT | A | 86 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(83): Show |
89 | HG00140.hp2 HG00280.hp2 HG00673.hp2 others(86): Show |
intron_variant | MODIFIER | c.404+2872delA | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68597390 | |||||||
| chr17:68597486 | G | C | 1 | a0001c0005t0002g0123 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.404+2777C>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68597486 | |||||||
| chr17:68597500 | G | A | 46 | a0001c0004t0001g0021 a0001c0004t0001g0034 a0001c0004t0001g0037 others(43): Show |
46 | HG00323.hp1 HG00408.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.404+2763C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68597500 | |||||||
| chr17:68597568 | A | T | 1 | a0002c0003t0001g0210 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.404+2695T>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68597568 | |||||||
| chr17:68597758 | A | G | 6 | a0001c0001t0001g0270 a0001c0001t0002g0272 a0002c0002t0024g0371 others(3): Show |
6 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.404+2505T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68597758 | |||||||
| chr17:68597772 | A | G | 91 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(88): Show |
94 | HG00140.hp2 HG00280.hp2 HG00673.hp2 others(91): Show |
intron_variant | MODIFIER | c.404+2491T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68597772 | |||||||
| chr17:68597878 | A | T | 7 | a0001c0001t0002g0209 a0001c0001t0002g0254 a0001c0001t0005g0201 others(4): Show |
7 | HG01361.hp2 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.404+2385T>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68597878 | |||||||
| chr17:68597903 | T | C | 94 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(91): Show |
97 | HG00140.hp2 HG00280.hp2 HG00673.hp2 others(94): Show |
intron_variant | MODIFIER | c.404+2360A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68597903 | |||||||
| chr17:68597940 | C | G | 1 | a0003c0006t0001g0276 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.404+2323G>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68597940 | |||||||
| chr17:68598003 | G | GT | 20 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0270 others(17): Show |
20 | HG00741.hp1 HG01099.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.404+2259dupA | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68598003 | |||||||
| chr17:68598003 | G | GTT | 44 | a0001c0001t0001g0250 a0001c0004t0001g0021 a0001c0004t0001g0034 others(41): Show |
44 | HG00323.hp1 HG00408.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.404+2258_404+2259d others(4): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68598003 | |||||||
| chr17:68598003 | G | GTTTT | 48 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0216 others(45): Show |
49 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(46): Show |
intron_variant | MODIFIER | c.404+2256_404+2259d others(6): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68598003 | |||||||
| chr17:68598003 | G | GTTTTT | 8 | a0001c0001t0002g0204 a0001c0001t0003g0206 a0001c0001t0005g0201 others(5): Show |
8 | HG00597.hp2 HG02145.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.404+2255_404+2259d others(7): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68598003 | |||||||
| chr17:68598003 | GT | G | 14 | a0001c0001t0002g0196 a0001c0001t0002g0334 a0001c0001t0002g0335 others(11): Show |
14 | HG01099.hp2 HG02040.hp1 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.404+2259delA | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68598003 | |||||||
| chr17:68598099 | G | C | 1 | a0001c0001t0001g0195 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.404+2164C>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68598099 | |||||||
| chr17:68598301 | G | C | 1 | a0001c0001t0001g0268 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.404+1962C>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68598301 | |||||||
| chr17:68598603 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.404+1660C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68598603 | |||||||
| chr17:68598826 | A | C | 66 | a0001c0001t0001g0137 a0001c0005t0001g0088 a0001c0005t0001g0089 others(63): Show |
68 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.404+1437T>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68598826 | |||||||
| chr17:68598874 | G | A | 4 | a0001c0005t0002g0125 a0002c0007t0001g0124 a0002c0007t0001g0126 others(1): Show |
4 | HG00741.hp2 HG01261.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.404+1389C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68598874 | |||||||
| chr17:68598909 | A | G | 2 | a0002c0002t0001g0197 a0002c0002t0001g0198 |
2 | HG02055.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.404+1354T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68598909 | |||||||
| chr17:68598919 | C | T | 2 | a0001c0001t0006g0275 a0002c0003t0011g0363 |
2 | HG02451.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.404+1344G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68598919 | |||||||
| chr17:68599115 | G | GT | 8 | a0001c0001t0001g0270 a0001c0001t0001g0274 a0001c0001t0002g0272 others(5): Show |
8 | HG02055.hp1 HG02258.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.404+1147dupA | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68599115 | |||||||
| chr17:68599163 | A | T | 1 | a0002c0002t0018g0136 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.404+1100T>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68599163 | |||||||
| chr17:68599354 | T | A | 46 | a0001c0004t0001g0021 a0001c0004t0001g0034 a0001c0004t0001g0037 others(43): Show |
46 | HG00323.hp1 HG00408.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.404+909A>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68599354 | |||||||
| chr17:68599364 | G | C | 1 | a0001c0001t0001g0195 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.404+899C>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68599364 | |||||||
| chr17:68599442 | G | T | 1 | a0001c0001t0002g0196 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.404+821C>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68599442 | |||||||
| chr17:68599503 | A | T | 3 | a0001c0001t0001g0270 a0001c0001t0002g0272 a0003c0006t0001g0271 |
3 | HG02572.hp1 HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.404+760T>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68599503 | |||||||
| chr17:68599511 | C | T | 3 | a0001c0001t0001g0270 a0001c0001t0002g0272 a0003c0006t0001g0271 |
3 | HG02572.hp1 HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.404+752G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68599511 | |||||||
| chr17:68599512 | C | T | 3 | a0001c0001t0001g0270 a0001c0001t0002g0272 a0003c0006t0001g0271 |
3 | HG02572.hp1 HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.404+751G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68599512 | |||||||
| chr17:68599591 | C | T | 141 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0216 others(138): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.404+672G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68599591 | |||||||
| chr17:68599617 | A | G | 1 | a0001c0001t0002g0196 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.404+646T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68599617 | |||||||
| chr17:68599665 | G | A | 3 | a0001c0004t0002g0057 a0001c0004t0002g0059 a0002c0010t0001g0058 |
3 | NA18989.hp1 NA18997.hp2 NA19059.hp2 |
intron_variant | MODIFIER | c.404+598C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68599665 | |||||||
| chr17:68599697 | C | A | 47 | a0001c0004t0001g0021 a0001c0004t0001g0034 a0001c0004t0001g0037 others(44): Show |
47 | HG00323.hp1 HG00408.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.404+566G>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68599697 | |||||||
| chr17:68599805 | C | A | 12 | a0001c0001t0001g0346 a0001c0001t0001g0347 a0001c0001t0001g0348 others(9): Show |
12 | HG01099.hp2 HG02055.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.404+458G>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68599805 | |||||||
| chr17:68599845 | A | G | 84 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0133 others(81): Show |
87 | HG00140.hp2 HG00280.hp2 HG00673.hp2 others(84): Show |
intron_variant | MODIFIER | c.404+418T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68599845 | |||||||
| chr17:68599991 | G | A | 3 | a0001c0001t0001g0355 a0001c0001t0003g0356 a0002c0003t0001g0357 |
3 | NA18943.hp2 NA19005.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.404+272C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68599991 | |||||||
| chr17:68600052 | T | C | 1 | a0001c0004t0002g0059 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.404+211A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68600052 | |||||||
| chr17:68600238 | C | G | 1 | a0002c0003t0001g0135 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.404+25G>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68600238 | |||||||
| chr17:68600260 | C | T | 8 | a0001c0001t0001g0130 a0001c0001t0001g0133 a0001c0001t0001g0134 others(5): Show |
8 | NA18942.hp2 NA18950.hp2 NA18969.hp2 others(5): Show |
splice_region_variant&intron_variant | LOW | c.404+3G>A | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68600260 |