Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| 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 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and 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 | copy fasta | chr17 | 68530116 | 68606367 |
| a0002 | 0/0 | 541 | 132 | 18 | 28 | 72 | 5 | 9 | 57 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0003 | 1/1 | 541 | 44 | 5 | 17 | 9 | 3 | 8 | 5 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0004 | 0/0 | 541 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0005 | 0/0 | 541 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0006 | 0/0 | 541 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0007 | 0/0 | 541 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0008 | 0/0 | 541 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0009 | 0/0 | 541 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0010 | 0/0 | 541 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0011 | 0/0 | 541 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0012 | 0/0 | 541 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 1626 | 127 | 47 | 19 | 35 | 7 | 19 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| c0002 | 0/0 | 1626 | 55 | 7 | 12 | 28 | 4 | 4 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| c0003 | 0/0 | 1626 | 35 | 11 | 5 | 16 | 1 | 2 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| c0004 | 0/0 | 1626 | 33 | 3 | 1 | 24 | 1 | 4 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| c0005 | 0/0 | 1626 | 31 | 4 | 3 | 21 | 0 | 3 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| c0006 | 1/0 | 1626 | 31 | 3 | 13 | 4 | 3 | 7 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| c0007 | 0/0 | 1626 | 28 | 0 | 10 | 17 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| c0008 | 0/0 | 1626 | 8 | 0 | 0 | 6 | 0 | 2 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| c0009 | 0/1 | 1626 | 5 | 1 | 3 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| c0010 | 0/0 | 1626 | 4 | 0 | 1 | 3 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| c0011 | 0/0 | 1626 | 3 | 3 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| c0012 | 0/0 | 1626 | 3 | 0 | 0 | 3 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| c0013 | 0/0 | 1626 | 2 | 0 | 1 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| c0014 | 0/0 | 1626 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| c0015 | 0/0 | 1626 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| c0016 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| c0017 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| c0018 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| c0019 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| c0020 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| c0021 | 0/0 | 1626 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| c0022 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| c0023 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| c0024 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| c0025 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| c0026 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 3063 | 231 | 41 | 51 | 98 | 11 | 28 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| t0002 | 0/0 | 3063 | 68 | 15 | 9 | 29 | 5 | 10 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| t0003 | 0/0 | 3063 | 18 | 0 | 0 | 13 | 0 | 5 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| t0004 | 0/0 | 3063 | 15 | 0 | 0 | 15 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| t0005 | 0/0 | 3063 | 13 | 9 | 4 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| t0006 | 0/0 | 3063 | 7 | 7 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| t0007 | 0/0 | 3063 | 5 | 0 | 0 | 5 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| t0008 | 0/0 | 3063 | 3 | 2 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| t0009 | 0/0 | 3063 | 2 | 1 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| t0010 | 0/0 | 3063 | 2 | 2 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| t0011 | 0/0 | 3063 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| t0012 | 0/0 | 3063 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| t0013 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| t0014 | 0/0 | 3063 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| t0015 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| t0016 | 0/0 | 3063 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| t0017 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| t0018 | 0/0 | 3063 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| t0019 | 0/0 | 3063 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| t0020 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| t0021 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| t0022 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| t0023 | 0/0 | 3063 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| t0024 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| t0025 | 0/0 | 3063 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0074 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0324 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0345 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1626 | 127 | 47 | 19 | 35 | 7 | 19 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0001c0004 | 0/0 | 1626 | 33 | 3 | 1 | 24 | 1 | 4 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0001c0005 | 0/0 | 1626 | 31 | 4 | 3 | 21 | 0 | 3 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0001c0017 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0002c0002 | 0/0 | 1626 | 55 | 7 | 12 | 28 | 4 | 4 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0002c0003 | 0/0 | 1626 | 35 | 11 | 5 | 16 | 1 | 2 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0002c0007 | 0/0 | 1626 | 28 | 0 | 10 | 17 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0002c0008 | 0/0 | 1626 | 8 | 0 | 0 | 6 | 0 | 2 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0002c0010 | 0/0 | 1626 | 4 | 0 | 1 | 3 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0002c0014 | 0/0 | 1626 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0003c0006 | 1/0 | 1626 | 31 | 3 | 13 | 4 | 3 | 7 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0003c0009 | 0/1 | 1626 | 5 | 1 | 3 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0003c0012 | 0/0 | 1626 | 3 | 0 | 0 | 3 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0003c0013 | 0/0 | 1626 | 2 | 0 | 1 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0003c0015 | 0/0 | 1626 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0003c0018 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0004c0011 | 0/0 | 1626 | 3 | 3 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0005c0024 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0005c0025 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0006c0020 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0007c0016 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0008c0021 | 0/0 | 1626 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0009c0022 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0010c0019 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0011c0023 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0012c0026 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | 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 | copy fasta | chr17 | 68530116 | 68606367 |
| a0001c0001t0002 | 0/0 | 4688 | 41 | 10 | 8 | 12 | 5 | 6 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0001c0001t0003 | 0/0 | 4688 | 10 | 0 | 0 | 5 | 0 | 5 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0001c0001t0004 | 0/0 | 4688 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0001c0001t0005 | 0/0 | 4688 | 10 | 6 | 4 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0001c0001t0006 | 0/0 | 4688 | 6 | 6 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0001c0001t0012 | 0/0 | 4688 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0001c0001t0020 | 0/0 | 4688 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0001c0001t0021 | 0/0 | 4688 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0001c0001t0022 | 0/0 | 4688 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0001c0001t0023 | 0/0 | 4688 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0001c0001t0025 | 0/0 | 4688 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0001c0004t0001 | 0/0 | 4688 | 7 | 0 | 0 | 4 | 1 | 2 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0001c0004t0002 | 0/0 | 4688 | 9 | 0 | 0 | 7 | 0 | 2 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0001c0004t0003 | 0/0 | 4688 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0001c0004t0004 | 0/0 | 4688 | 12 | 0 | 0 | 12 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0001c0004t0008 | 0/0 | 4688 | 3 | 2 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0001c0004t0013 | 0/0 | 4688 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0001c0005t0001 | 0/0 | 4688 | 6 | 0 | 2 | 3 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0001c0005t0002 | 0/0 | 4688 | 16 | 3 | 1 | 10 | 0 | 2 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0001c0005t0003 | 0/0 | 4688 | 7 | 0 | 0 | 7 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0001c0005t0004 | 0/0 | 4688 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0001c0005t0006 | 0/0 | 4688 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0001c0017t0005 | 0/0 | 4688 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0002c0002t0001 | 0/0 | 4688 | 46 | 6 | 11 | 21 | 4 | 4 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0002c0002t0007 | 0/0 | 4688 | 5 | 0 | 0 | 5 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0002c0002t0014 | 0/0 | 4688 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0002c0002t0018 | 0/0 | 4688 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0002c0002t0019 | 0/0 | 4688 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0002c0002t0024 | 0/0 | 4688 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0002c0003t0001 | 0/0 | 4688 | 28 | 8 | 4 | 14 | 1 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0002c0003t0009 | 0/0 | 4688 | 2 | 1 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0002c0003t0010 | 0/0 | 4688 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0002c0003t0011 | 0/0 | 4688 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0002c0003t0016 | 0/0 | 4688 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0002c0003t0017 | 0/0 | 4688 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0002c0007t0001 | 0/0 | 4688 | 28 | 0 | 10 | 17 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0002c0008t0001 | 0/0 | 4688 | 8 | 0 | 0 | 6 | 0 | 2 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0002c0010t0001 | 0/0 | 4688 | 4 | 0 | 1 | 3 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0002c0014t0001 | 0/0 | 4688 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0003c0006t0001 | 1/0 | 4688 | 31 | 3 | 13 | 4 | 3 | 7 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0003c0009t0001 | 0/1 | 4688 | 5 | 1 | 3 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0003c0012t0001 | 0/0 | 4688 | 3 | 0 | 0 | 3 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0003c0013t0001 | 0/0 | 4688 | 2 | 0 | 1 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0003c0015t0001 | 0/0 | 4688 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0003c0018t0001 | 0/0 | 4688 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0004c0011t0002 | 0/0 | 4688 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0004c0011t0005 | 0/0 | 4688 | 2 | 2 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0005c0024t0001 | 0/0 | 4688 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0005c0025t0001 | 0/0 | 4688 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0006c0020t0001 | 0/0 | 4688 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0007c0016t0015 | 0/0 | 4688 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0008c0021t0001 | 0/0 | 4688 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0009c0022t0002 | 0/0 | 4688 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0010c0019t0010 | 0/0 | 4688 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0011c0023t0001 | 0/0 | 4688 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| a0012c0026t0001 | 0/0 | 4688 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | copy fasta | chr17 | 68530116 | 68606367 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0148 | 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 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 |
| a0001c0001t0001g0192 | 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 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0254 | 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 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0350 | 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 |
| a0001c0001t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0002g0274 | 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 |
| a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0002g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0003g0194 | 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 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0003g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0005g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0005g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0005g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0005g0282 | 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 |
| a0001c0001t0005g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0005g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0005g0357 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0006g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0006g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0006g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0006g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0006g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0012g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0020g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0021g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0022g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0023g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0001t0025g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0002g0024 | 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 |
| a0001c0004t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0004g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0004g0019 | 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 |
| a0001c0004t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0004g0045 | 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 |
| a0001c0004t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0008g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0004t0008g0008 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0004t0013g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0002g0068 | 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 |
| a0001c0005t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0002g0101 | 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 |
| a0001c0005t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0005t0006g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0001c0017t0005g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0149 | 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 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 | 0 | 1 | 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 |
| a0002c0002t0001g0179 | 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 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0002c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0259 | 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 |
| a0002c0002t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0001g0342 | 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 |
| a0002c0002t0007g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0007g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0007g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0014g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0018g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0019g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0002t0024g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0147 | 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 |
| a0002c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0002c0003t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0002c0003t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0291 | 0/0 | 1 | 0 | 1 | 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 |
| a0002c0003t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0009g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0009g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0010g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0011g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0003t0011g0367 | 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 |
| a0002c0003t0017g0138 | 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 |
| a0002c0007t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0007t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0007t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0007t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0007t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0007t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0007t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0007t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0007t0001g0085 | 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 |
| a0002c0007t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0007t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0007t0001g0090 | 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 |
| a0002c0007t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0007t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0007t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0007t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0007t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0007t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0002c0007t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0007t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0007t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0007t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0002c0008t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0008t0001g0028 | 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 |
| a0002c0008t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0008t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0008t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0008t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0002c0010t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0010t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0010t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0010t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0014t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0002c0014t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0272 | 0/0 | 1 | 1 | 0 | 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 |
| a0003c0006t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0324 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0345 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0006t0001g0348 | 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 |
| a0003c0009t0001g0074 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0009t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0009t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0012t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0012t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0012t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0013t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0013t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0015t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0015t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0003c0018t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0004c0011t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0004c0011t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0004c0011t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0005c0024t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0005c0025t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0006c0020t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0007c0016t0015g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0008c0021t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0009c0022t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0010c0019t0010g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0011c0023t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| a0012c0026t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 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 | g0290 | EUR | GBR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0235 | EUR | GBR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00140 | hp1 | a0002 | c0003 | t0001 | g0211 | EUR | GBR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0134 | EUR | GBR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0230 | 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 | g0041 | EUR | FIN | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0229 | EUR | FIN | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00408 | hp1 | a0001 | c0004 | t0004 | g0017 | EAS | CHS | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0328 | EAS | CHS | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00544 | hp1 | a0001 | c0005 | t0003 | g0115 | EAS | CHS | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00544 | hp2 | a0001 | c0005 | t0003 | g0075 | EAS | CHS | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0263 | EAS | CHS | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0308 | EAS | CHS | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00597 | hp1 | a0011 | c0023 | t0001 | g0361 | EAS | CHS | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00597 | hp2 | a0003 | c0006 | t0001 | g0204 | EAS | CHS | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00609 | hp1 | a0005 | c0024 | t0001 | g0362 | EAS | CHS | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00609 | hp2 | a0001 | c0004 | t0003 | g0031 | EAS | CHS | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00621 | hp1 | a0001 | c0005 | t0001 | g0100 | EAS | CHS | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00621 | hp2 | a0002 | c0007 | t0001 | g0085 | EAS | CHS | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00673 | hp1 | a0002 | c0008 | t0001 | g0040 | EAS | CHS | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00673 | hp2 | a0003 | c0006 | t0001 | g0152 | EAS | CHS | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0145 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00735 | hp2 | a0002 | c0003 | t0001 | g0291 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0186 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00738 | hp2 | a0003 | c0006 | t0001 | g0323 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00741 | hp1 | a0003 | c0006 | t0001 | g0278 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG00741 | hp2 | a0002 | c0007 | t0001 | g0121 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01069 | hp2 | a0001 | c0001 | t0005 | g0287 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01070 | hp1 | a0003 | c0006 | t0001 | g0314 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0245 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01071 | hp1 | a0001 | c0001 | t0005 | g0005 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01071 | hp2 | a0003 | c0006 | t0001 | g0312 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0335 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01074 | hp2 | a0002 | c0003 | t0001 | g0240 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0289 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01099 | hp1 | a0002 | c0007 | t0001 | g0064 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01099 | hp2 | a0001 | c0001 | t0005 | g0357 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0242 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01106 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0309 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01109 | hp2 | a0001 | c0004 | t0008 | g0008 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0188 | 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 | g0050 | 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 | g0063 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01192 | hp2 | a0003 | c0006 | t0001 | g0318 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01243 | hp2 | a0002 | c0003 | t0009 | g0322 | AMR | PUR | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01255 | hp2 | a0002 | c0003 | t0001 | g0181 | AMR | CLM | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01256 | hp1 | a0003 | c0006 | t0001 | g0003 | AMR | CLM | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01256 | hp2 | a0003 | c0006 | t0001 | g0141 | 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 | g0320 | 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 | g0003 | AMR | CLM | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01261 | hp1 | a0001 | c0005 | t0002 | g0123 | AMR | CLM | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01261 | hp2 | a0002 | c0010 | t0001 | g0053 | AMR | CLM | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01346 | hp1 | a0002 | c0007 | t0001 | g0065 | AMR | CLM | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01358 | hp1 | a0001 | c0001 | t0012 | g0010 | AMR | CLM | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01358 | hp2 | a0003 | c0006 | t0001 | g0317 | AMR | CLM | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01361 | hp1 | a0001 | c0005 | t0001 | g0089 | AMR | CLM | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0255 | AMR | CLM | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01433 | hp1 | a0003 | c0006 | t0001 | g0348 | AMR | CLM | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01433 | hp2 | a0001 | c0005 | t0001 | g0096 | AMR | CLM | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01496 | hp1 | a0003 | c0006 | t0001 | g0347 | AMR | CLM | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0306 | AMR | CLM | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01515 | hp1 | a0003 | c0006 | t0001 | g0224 | EUR | IBS | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0177 | EUR | IBS | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0176 | EUR | IBS | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01517 | hp2 | a0003 | c0006 | t0001 | g0236 | EUR | IBS | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01884 | hp1 | a0003 | c0006 | t0001 | g0215 | AFR | ACB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01884 | hp2 | a0004 | c0011 | t0002 | g0058 | AFR | ACB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | ACB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0282 | AFR | ACB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | PEL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | PEL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01934 | hp1 | a0002 | c0007 | t0001 | g0122 | AMR | PEL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0311 | AMR | PEL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0153 | AMR | PEL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0295 | AMR | PEL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0326 | AMR | PEL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01981 | hp2 | a0003 | c0009 | t0001 | g0083 | AMR | PEL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02004 | hp1 | a0003 | c0006 | t0001 | g0319 | AMR | PEL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02004 | hp2 | a0002 | c0007 | t0001 | g0095 | AMR | PEL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0340 | EAS | KHV | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02040 | hp2 | a0003 | c0012 | t0001 | g0169 | EAS | KHV | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0198 | AFR | ACB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0350 | AFR | ACB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0342 | EAS | KHV | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02071 | hp2 | a0002 | c0007 | t0001 | g0108 | EAS | KHV | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02074 | hp1 | a0001 | c0005 | t0002 | g0098 | EAS | KHV | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0339 | EAS | KHV | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02080 | hp1 | a0002 | c0007 | t0001 | g0084 | EAS | KHV | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02080 | hp2 | a0002 | c0003 | t0001 | g0150 | EAS | KHV | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02129 | hp1 | a0002 | c0007 | t0001 | g0061 | EAS | KHV | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0337 | EAS | KHV | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0226 | AFR | ACB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02145 | hp2 | a0001 | c0001 | t0021 | g0203 | AFR | ACB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0307 | AMR | PEL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02148 | hp2 | a0003 | c0006 | t0001 | g0277 | AMR | PEL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02155 | hp1 | a0002 | c0007 | t0001 | g0103 | EAS | CDX | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02155 | hp2 | a0002 | c0003 | t0001 | g0303 | EAS | CDX | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02258 | hp1 | a0001 | c0001 | t0022 | g0365 | AFR | ACB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0274 | AFR | ACB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02280 | hp1 | a0001 | c0005 | t0002 | g0101 | AFR | ACB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0329 | AFR | ACB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02293 | hp1 | a0002 | c0007 | t0001 | g0094 | AMR | PEL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0234 | AMR | PEL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02300 | hp1 | a0002 | c0002 | t0019 | g0297 | AMR | PEL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02300 | hp2 | a0002 | c0007 | t0001 | g0124 | 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 | g0276 | AFR | ACB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02523 | hp1 | a0002 | c0014 | t0001 | g0114 | EAS | KHV | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02523 | hp2 | a0002 | c0002 | t0018 | g0133 | EAS | KHV | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0279 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02602 | hp1 | a0003 | c0013 | t0001 | g0044 | SAS | PJL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0216 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02630 | hp1 | a0001 | c0004 | t0008 | g0009 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0210 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02647 | hp1 | a0007 | c0016 | t0015 | g0012 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0355 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02683 | hp1 | a0003 | c0006 | t0001 | g0164 | SAS | PJL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02717 | hp2 | a0001 | c0005 | t0006 | g0113 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0189 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0313 | SAS | PJL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02735 | hp2 | a0003 | c0006 | t0001 | g0249 | SAS | PJL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02738 | hp1 | a0002 | c0007 | t0001 | g0104 | SAS | PJL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02809 | hp1 | a0002 | c0003 | t0001 | g0353 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0139 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0202 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0281 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02895 | hp2 | a0003 | c0006 | t0001 | g0325 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02922 | hp1 | a0002 | c0003 | t0001 | g0244 | AFR | ESN | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0332 | AFR | ESN | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02965 | hp1 | a0001 | c0004 | t0008 | g0006 | AFR | ESN | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | ESN | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02976 | hp1 | a0002 | c0003 | t0001 | g0201 | AFR | ESN | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0349 | AFR | ESN | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03017 | hp1 | a0003 | c0006 | t0001 | g0232 | SAS | PJL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03041 | hp1 | a0003 | c0006 | t0001 | g0272 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0315 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0352 | 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 | g0217 | AFR | ESN | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0199 | AFR | ESN | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03139 | hp1 | a0001 | c0001 | t0006 | g0209 | AFR | ESN | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03139 | hp2 | a0002 | c0003 | t0001 | g0299 | AFR | ESN | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03195 | hp1 | a0003 | c0009 | t0001 | g0076 | AFR | ESN | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0208 | AFR | ESN | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0285 | AFR | MSL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03225 | hp2 | a0002 | c0002 | t0024 | g0374 | 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 | g0029 | SAS | PJL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0356 | AFR | MSL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03453 | hp2 | a0002 | c0003 | t0017 | g0138 | AFR | MSL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0273 | AFR | MSL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03486 | hp2 | a0002 | c0003 | t0001 | g0252 | AFR | MSL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0321 | SAS | PJL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03491 | hp2 | a0003 | c0006 | t0001 | g0004 | SAS | PJL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03492 | hp1 | a0003 | c0006 | t0001 | g0004 | SAS | PJL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03492 | hp2 | a0001 | c0005 | t0001 | g0102 | SAS | PJL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03516 | hp1 | a0001 | c0005 | t0002 | g0079 | AFR | ESN | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0331 | AFR | ESN | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03540 | hp1 | a0001 | c0017 | t0005 | g0011 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03540 | hp2 | a0002 | c0003 | t0010 | g0283 | AFR | GWD | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0333 | AFR | MSL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03579 | hp2 | a0009 | c0022 | t0002 | g0334 | AFR | MSL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03654 | hp1 | a0002 | c0008 | t0001 | g0039 | SAS | PJL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0194 | SAS | PJL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0243 | SAS | PJL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03688 | hp1 | a0001 | c0005 | t0002 | g0109 | SAS | STU | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0227 | SAS | STU | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0327 | SAS | PJL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0246 | SAS | PJL | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | BEB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03831 | hp2 | a0002 | c0008 | t0001 | g0028 | SAS | BEB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0180 | SAS | BEB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03834 | hp2 | a0001 | c0005 | t0002 | g0112 | SAS | BEB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0158 | SAS | BEB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | BEB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03942 | hp1 | a0003 | c0006 | t0001 | g0304 | SAS | BEB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0187 | SAS | BEB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG04115 | hp1 | a0001 | c0004 | t0001 | g0043 | 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 | g0042 | SAS | BEB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0267 | SAS | BEB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0268 | SAS | STU | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG04199 | hp2 | a0001 | c0004 | t0002 | g0014 | SAS | STU | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | STU | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG04204 | hp2 | a0002 | c0003 | t0001 | g0302 | SAS | STU | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG04228 | hp1 | a0008 | c0021 | t0001 | g0300 | SAS | STU | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG04228 | hp2 | a0003 | c0006 | t0001 | g0207 | SAS | STU | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | YRI | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0351 | 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 | g0370 | EAS | CHB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18747 | hp1 | a0001 | c0004 | t0002 | g0047 | EAS | CHB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18747 | hp2 | a0003 | c0006 | t0001 | g0173 | EAS | CHB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18906 | hp1 | a0001 | c0004 | t0013 | g0007 | AFR | YRI | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18906 | hp2 | a0002 | c0003 | t0001 | g0231 | AFR | YRI | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0338 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18939 | hp2 | a0002 | c0007 | t0001 | g0107 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18942 | hp1 | a0005 | c0025 | t0001 | g0364 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0128 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0359 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18944 | hp1 | a0001 | c0005 | t0002 | g0071 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18944 | hp2 | a0002 | c0007 | t0001 | g0097 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18945 | hp1 | a0003 | c0006 | t0001 | g0258 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18945 | hp2 | a0001 | c0001 | t0023 | g0368 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18947 | hp1 | a0001 | c0004 | t0004 | g0020 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18948 | hp1 | a0002 | c0003 | t0011 | g0366 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18948 | hp2 | a0002 | c0008 | t0001 | g0033 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18950 | hp1 | a0001 | c0004 | t0004 | g0022 | 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 | g0239 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18952 | hp2 | a0002 | c0007 | t0001 | g0086 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18954 | hp2 | a0001 | c0005 | t0003 | g0066 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18956 | hp1 | a0002 | c0002 | t0014 | g0140 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18956 | hp2 | a0001 | c0005 | t0002 | g0082 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18957 | hp1 | a0001 | c0005 | t0003 | g0062 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0144 | 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 | g0034 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18960 | hp1 | a0001 | c0005 | t0002 | g0081 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18960 | hp2 | a0002 | c0002 | t0007 | g0372 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18961 | hp1 | a0002 | c0007 | t0001 | g0088 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18961 | hp2 | a0001 | c0004 | t0001 | g0018 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18962 | hp1 | a0002 | c0007 | t0001 | g0087 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18962 | hp2 | a0001 | c0005 | t0002 | g0073 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18964 | hp1 | a0001 | c0005 | t0002 | g0080 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18966 | hp1 | a0002 | c0003 | t0001 | g0341 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0179 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18967 | hp1 | a0001 | c0004 | t0004 | g0052 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18967 | hp2 | a0001 | c0005 | t0002 | g0072 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18969 | hp1 | a0003 | c0015 | t0001 | g0110 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18969 | hp2 | a0001 | c0001 | t0025 | g0375 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18970 | hp1 | a0001 | c0004 | t0001 | g0036 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18970 | hp2 | a0002 | c0007 | t0001 | g0077 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18971 | hp1 | a0002 | c0008 | t0001 | g0015 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18974 | hp1 | a0001 | c0005 | t0001 | g0099 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18977 | hp2 | a0003 | c0012 | t0001 | g0228 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18978 | hp1 | a0001 | c0005 | t0002 | g0068 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18978 | hp2 | a0002 | c0002 | t0007 | g0371 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18979 | hp1 | a0003 | c0015 | t0001 | g0111 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0259 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18981 | hp1 | a0001 | c0005 | t0003 | g0116 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18981 | hp2 | a0003 | c0012 | t0001 | g0310 | 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 | g0129 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18983 | hp1 | a0002 | c0003 | t0011 | g0367 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0336 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18984 | hp2 | a0002 | c0003 | t0001 | g0264 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18986 | hp1 | a0002 | c0007 | t0001 | g0093 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0344 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18987 | hp1 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18987 | hp2 | a0002 | c0010 | t0001 | g0049 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18989 | hp1 | a0001 | c0004 | t0002 | g0056 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0178 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18992 | hp1 | a0002 | c0002 | t0001 | g0248 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18994 | hp1 | a0001 | c0001 | t0004 | g0135 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18994 | hp2 | a0001 | c0005 | t0001 | g0117 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18997 | hp1 | a0002 | c0003 | t0001 | g0343 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18997 | hp2 | a0001 | c0004 | t0002 | g0054 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18998 | hp1 | a0001 | c0004 | t0001 | g0038 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA18998 | hp2 | a0001 | c0001 | t0004 | g0167 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19002 | hp2 | a0001 | c0004 | t0004 | g0025 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19005 | hp2 | a0002 | c0003 | t0001 | g0360 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19006 | hp1 | a0001 | c0004 | t0004 | g0051 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19006 | hp2 | a0002 | c0007 | t0001 | g0069 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19007 | hp1 | a0002 | c0007 | t0001 | g0070 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19007 | hp2 | a0001 | c0005 | t0003 | g0067 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19010 | hp1 | a0001 | c0004 | t0002 | g0046 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19010 | hp2 | a0002 | c0003 | t0001 | g0184 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19011 | hp2 | a0001 | c0004 | t0001 | g0035 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0225 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0354 | AFR | LWK | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0294 | 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 | g0330 | AFR | LWK | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19055 | hp1 | a0002 | c0003 | t0001 | g0250 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19055 | hp2 | a0002 | c0002 | t0001 | g0195 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19056 | hp1 | a0002 | c0003 | t0001 | g0132 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19056 | hp2 | a0002 | c0008 | t0001 | g0032 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19057 | hp1 | a0001 | c0004 | t0004 | g0019 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19057 | hp2 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19059 | hp1 | a0001 | c0004 | t0004 | g0048 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19059 | hp2 | a0002 | c0010 | t0001 | g0055 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19062 | hp1 | a0001 | c0004 | t0004 | g0023 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19062 | hp2 | a0002 | c0014 | t0001 | g0119 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19063 | hp2 | a0001 | c0004 | t0004 | g0027 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19064 | hp1 | a0001 | c0004 | t0004 | g0045 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19065 | hp1 | a0001 | c0005 | t0004 | g0078 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19065 | hp2 | a0002 | c0002 | t0007 | g0369 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0260 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19066 | hp2 | a0012 | c0026 | t0001 | g0363 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19067 | hp2 | a0001 | c0004 | t0002 | g0016 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19068 | hp1 | a0006 | c0020 | t0001 | g0136 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19068 | hp2 | a0002 | c0008 | t0001 | g0037 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0358 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19070 | hp2 | a0001 | c0005 | t0003 | g0092 | 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 | g0161 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19079 | hp1 | a0002 | c0007 | t0001 | g0091 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19079 | hp2 | a0001 | c0004 | t0002 | g0024 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19080 | hp1 | a0002 | c0002 | t0007 | g0373 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19083 | hp1 | a0001 | c0004 | t0004 | g0030 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19084 | hp1 | a0002 | c0003 | t0001 | g0146 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19084 | hp2 | a0001 | c0004 | t0002 | g0026 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0127 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0256 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19088 | hp2 | a0002 | c0010 | t0001 | g0021 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19090 | hp1 | a0002 | c0003 | t0001 | g0147 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19090 | hp2 | a0001 | c0005 | t0002 | g0120 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19091 | hp2 | a0002 | c0007 | t0001 | g0090 | EAS | JPT | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19240 | hp1 | a0010 | c0019 | t0010 | g0060 | AFR | YRI | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA19240 | hp2 | a0001 | c0005 | t0002 | g0118 | AFR | YRI | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ASW | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA20129 | hp2 | a0002 | c0003 | t0009 | g0346 | AFR | ASW | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA20752 | hp1 | a0003 | c0006 | t0001 | g0345 | EUR | TSI | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0237 | EUR | TSI | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0247 | EUR | TSI | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0174 | EUR | TSI | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0305 | SAS | GIH | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0293 | SAS | GIH | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0292 | AMR | CLM | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG01123 | hp2 | a0002 | c0003 | t0001 | g0175 | AMR | CLM | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | ACB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02486 | hp1 | a0004 | c0011 | t0005 | g0059 | AFR | ACB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0205 | AFR | ACB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02559 | hp1 | a0002 | c0003 | t0001 | g0200 | AFR | ACB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG02559 | hp2 | a0004 | c0011 | t0005 | g0057 | AFR | ACB | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | USA | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0220 | AFR | USA | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0316 | AFR | USA | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| NA20300 | hp2 | a0003 | c0018 | t0001 | g0013 | AFR | USA | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| homoSapiens_chm13v2 | hp1 | a0003 | c0009 | t0001 | g0074 | REF | REF | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| homoSapiens_grch38 | hp1 | a0003 | c0006 | t0001 | g0324 | REF | REF | FAM20A_chr17_68530116_68606367 | FAM20A | chr17 | 68530116 | 68606367 |
| 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 | a0008 | 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 | a0001a0002a0004others(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 | a0009 | 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 | a0002a0005a0007others(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 | a0006 | 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 | a0004a0010 | 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 | a0011 | 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 | a0005a0012 | 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 |
| 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 | a0003c0012a0003c0015a0006c0020others(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 | a0002c0002a0002c0007a0002c0008others(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 | a0001c0005a0002c0007a0002c0014others(2): Show | 68 | HG00544.hp1 HG00544.hp2 HG00621.hp1 others(65): 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 | a0001c0004a0002c0008a0002c0010others(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 | a0001c0017a0003c0018a0007c0016 | 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 |
| 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 | a0002c0003t0010a0010c0019t0010 | 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 | a0001c0001t0005a0001c0017t0005a0002c0002t0018others(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 | a0001c0001t0004a0001c0004t0004a0001c0005t0004 | 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 | a0002c0003t0017a0007c0016t0015 | 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 | a0001c0001t0002a0001c0001t0003a0001c0001t0023others(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 | a0001c0001t0020a0001c0004t0013 | 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 | a0001c0001t0006a0001c0005t0006 | 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 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(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 | a0001c0001t0003a0001c0004t0003a0001c0005t0003 | 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 | a0001c0001t0023a0002c0002t0007 | 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 | a0001c0001t0012a0001c0004t0008a0001c0004t0013 | 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 |
| 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 | a0002c0002t0001g0126a0002c0002t0001g0127a0002c0002t0001g0128others(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 | a0003c0006t0001g0325 | 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 | 84 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(81): 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 | a0002c0002t0001g0305 | 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 | a0001c0001t0002g0189 | 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 | a0002c0010t0001g0049 | 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 | 83 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(80): 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 | a0001c0001t0001g0355 | 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 | a0002c0002t0001g0220 | 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 | a0001c0001t0012g0010 | 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 | a0001c0001t0001g0213a0001c0001t0001g0354a0001c0001t0021g0203others(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 | 99 | a0001c0001t0002g0125a0001c0001t0002g0143a0001c0001t0002g0155others(96): 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 | a0002c0002t0001g0144 | 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 | a0005c0024t0001g0362 | 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 | a0002c0002t0001g0126a0002c0002t0001g0127a0002c0002t0001g0128others(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 | 94 | a0001c0001t0001g0183a0001c0001t0001g0190a0001c0001t0001g0288others(91): 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 | 332 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(329): 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 | a0004c0011t0005g0059 | 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 | a0001c0001t0005g0005a0001c0001t0005g0139a0001c0001t0005g0202others(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 | a0002c0007t0001g0104 | 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 | a0001c0001t0005g0005a0001c0001t0005g0287 | 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 | a0001c0001t0001g0142a0001c0001t0001g0166 | 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 | a0007c0016t0015g0012 | 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 | 79 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(76): 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0005g0005a0001c0001t0005g0139a0001c0001t0005g0202others(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 | a0007c0016t0015g0012 | 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 | a0003c0006t0001g0304 | 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 | a0001c0001t0001g0253a0001c0001t0005g0005a0001c0001t0005g0139others(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 | a0002c0002t0001g0126a0002c0002t0001g0127a0002c0002t0001g0128others(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 | a0003c0006t0001g0003 | 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 | a0002c0002t0001g0126a0002c0002t0001g0127a0002c0002t0001g0128others(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 | a0002c0002t0001g0336a0002c0002t0019g0297 | 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 | a0002c0003t0001g0240 | 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 | a0001c0001t0006g0217a0001c0001t0006g0315a0001c0005t0006g0113 | 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 | a0001c0001t0001g0237 | 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 | 86 | a0001c0001t0002g0125a0001c0001t0002g0143a0001c0001t0002g0155others(83): 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 | a0001c0005t0002g0080 | 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 | 76 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(73): 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 | a0001c0001t0001g0269a0001c0001t0001g0286a0001c0001t0001g0349others(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 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(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 | a0002c0002t0001g0127a0002c0002t0001g0128a0002c0002t0001g0225others(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 | a0001c0001t0001g0183a0001c0001t0001g0190a0001c0001t0001g0288others(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 | a0001c0001t0005g0005a0001c0001t0005g0139a0001c0001t0005g0202others(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 | a0002c0002t0001g0256a0002c0002t0001g0328a0002c0007t0001g0070others(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 | a0001c0001t0002g0280a0001c0001t0012g0010 | 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 | a0001c0001t0012g0010 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.813-155T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 5/10 | chr17 | 68542964 | ||||||
| chr17:68543034
|
G | A | 1 | a0003c0009t0001g0074 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.813-225C>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 5/10 | chr17 | 68543034 | ||||||
| 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 | 46 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(43): 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 | a0002c0007t0001g0077 | 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 | 83 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(80): 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 | a0001c0001t0002g0174 | 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 | a0003c0006t0001g0207 | 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 | a0001c0001t0002g0280a0001c0001t0012g0010a0002c0002t0001g0126others(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 | a0001c0001t0002g0165 | 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 | a0001c0001t0002g0229 | 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 | a0001c0001t0002g0293a0001c0001t0002g0327a0001c0004t0002g0014 | 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 | a0001c0001t0012g0010a0002c0002t0001g0126a0002c0002t0001g0127others(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 | 5 | a0001c0001t0001g0134a0001c0001t0001g0154a0001c0001t0001g0156others(2): 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 | 178 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(175): 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 | a0001c0001t0006g0208a0001c0001t0006g0209a0001c0001t0006g0217others(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 | 77 | a0001c0001t0001g0261a0001c0001t0002g0125a0001c0001t0002g0143others(74): 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 | a0002c0002t0024g0374 | 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 | a0001c0001t0001g0233a0001c0001t0001g0254 | 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 | a0001c0001t0001g0237a0001c0001t0012g0010a0002c0002t0001g0126others(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 | a0002c0002t0001g0168a0002c0007t0001g0061a0002c0008t0001g0034others(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 | 78 | a0001c0001t0001g0148a0001c0001t0001g0191a0001c0001t0001g0192others(75): 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 | a0001c0001t0001g0219 | 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 | a0001c0001t0002g0218 | 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 | a0001c0005t0002g0118 | 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 | a0001c0001t0003g0308 | 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 | a0001c0001t0001g0219a0001c0001t0002g0205a0001c0001t0002g0222others(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
|
CA | C | 6 | a0001c0001t0002g0280a0002c0002t0001g0198a0003c0006t0001g0317others(3): Show | 6 | HG01169.hp1 HG01358.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.720-2448delT | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 4/10 | chr17 | 68546168 | ||||||
| chr17:68546168
|
CAA | C | 31 | a0001c0001t0001g0350a0001c0001t0002g0157a0001c0001t0002g0159others(28): 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 | a0001c0001t0001g0183a0001c0001t0001g0190a0001c0001t0001g0269others(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 | a0001c0001t0001g0196a0001c0004t0004g0051a0001c0005t0002g0073others(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 | 243 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(240): 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 | a0001c0001t0002g0229a0001c0004t0004g0048a0001c0005t0003g0092others(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 | 255 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(252): 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 | a0002c0002t0001g0198a0002c0002t0001g0199 | 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 | a0003c0006t0001g0277 | 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 | a0002c0008t0001g0039 | 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 | a0001c0001t0001g0269a0001c0001t0001g0271a0001c0001t0001g0286others(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 | a0001c0001t0005g0005a0001c0001t0005g0139a0001c0001t0005g0202others(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 | a0002c0002t0001g0198a0002c0002t0001g0199 | 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 | a0001c0001t0002g0189a0003c0006t0001g0272a0003c0018t0001g0013 | 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 | a0001c0001t0001g0131a0001c0001t0001g0191a0001c0001t0001g0192others(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 | a0001c0001t0001g0148a0001c0001t0001g0160a0001c0001t0001g0237others(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 | a0001c0001t0001g0253a0001c0001t0021g0203a0001c0001t0022g0365others(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 | a0001c0004t0002g0046 | 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 | a0001c0001t0001g0358 | 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 | a0001c0001t0001g0183a0001c0001t0001g0190a0001c0001t0001g0191others(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 | a0001c0001t0001g0163 | 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 | 184 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(181): 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 | a0001c0001t0002g0212a0001c0001t0002g0274 | 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 | a0002c0002t0001g0256 | 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 | a0001c0001t0012g0010 | 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 | a0001c0001t0001g0183a0001c0001t0001g0190a0001c0001t0001g0191others(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 | a0001c0001t0001g0183a0001c0001t0001g0190a0001c0001t0001g0191others(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 | a0001c0001t0001g0349a0001c0001t0005g0282a0001c0001t0005g0284others(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 | 216 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(213): 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 | a0001c0001t0001g0183a0001c0001t0001g0190a0001c0001t0001g0191others(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 | a0001c0001t0001g0213a0001c0001t0001g0219a0001c0001t0001g0354 | 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 | a0001c0001t0006g0217a0001c0001t0006g0315a0001c0005t0006g0113 | 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 | a0001c0001t0001g0355 | 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 | a0001c0001t0001g0213a0001c0001t0001g0219a0001c0001t0001g0253others(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 | a0002c0003t0017g0138 | 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 | a0001c0001t0002g0186 | 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 | a0002c0002t0001g0144a0002c0002t0001g0170a0002c0002t0001g0336others(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 | a0001c0001t0001g0183a0001c0001t0001g0190a0001c0001t0001g0191others(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 | a0001c0001t0001g0196a0001c0001t0001g0265a0001c0001t0001g0266others(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 | a0002c0002t0001g0168 | 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 | a0001c0004t0001g0041 | 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 | a0001c0001t0001g0183a0001c0001t0001g0190a0001c0001t0001g0214others(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 | a0001c0001t0002g0210a0001c0001t0002g0273a0001c0001t0002g0274others(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 | a0001c0001t0001g0191a0001c0001t0001g0193a0001c0001t0001g0214others(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 | a0001c0001t0001g0192a0001c0001t0002g0242a0001c0001t0002g0311others(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 | 103 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(100): 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 | a0001c0001t0001g0196a0001c0001t0001g0271a0001c0001t0001g0350others(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 | a0001c0001t0001g0183a0001c0001t0001g0190a0001c0001t0001g0191others(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 | a0001c0001t0001g0213a0001c0001t0001g0219a0001c0001t0001g0354others(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 | a0001c0001t0001g0349a0001c0001t0005g0282a0001c0001t0005g0284others(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 | a0002c0002t0001g0316 | 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 | a0001c0001t0002g0180a0001c0001t0002g0229a0001c0001t0002g0230others(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 | a0003c0006t0001g0004 | 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 | a0001c0001t0001g0223 | 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 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0219others(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 | 312 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(309): 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 | a0001c0001t0021g0203a0001c0001t0022g0365a0003c0009t0001g0076 | 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 | a0001c0001t0002g0280a0001c0005t0002g0106a0002c0003t0011g0367others(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 | a0001c0001t0001g0214a0001c0001t0001g0261a0001c0001t0001g0270others(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 | a0001c0001t0001g0214a0001c0001t0001g0261a0001c0001t0001g0270others(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 | a0002c0002t0001g0336a0002c0002t0019g0297 | 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 | a0002c0002t0001g0220 | 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 | a0001c0001t0002g0218 | 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 | a0002c0003t0009g0322 | 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 | a0001c0001t0001g0214a0001c0001t0001g0261a0001c0001t0001g0270others(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 | a0001c0001t0001g0214a0001c0001t0001g0261a0001c0001t0001g0270others(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 | a0001c0001t0001g0142a0001c0001t0001g0163a0001c0001t0001g0166 | 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 | a0001c0001t0001g0214a0001c0001t0001g0261a0001c0001t0001g0270others(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 | a0002c0003t0017g0138 | 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 | a0001c0001t0012g0010 | 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 | a0001c0001t0002g0187 | 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 | a0001c0001t0001g0151a0001c0001t0003g0171a0001c0001t0003g0257others(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 | a0001c0001t0001g0214a0001c0001t0002g0280a0001c0001t0002g0281others(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 | 49 | a0001c0001t0001g0183a0001c0001t0001g0190a0001c0001t0001g0269others(46): 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 | 143 | a0001c0001t0001g0134a0001c0001t0001g0142a0001c0001t0001g0148others(140): 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 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(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 | a0001c0001t0001g0349a0001c0001t0005g0282a0001c0001t0005g0284others(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 | a0002c0002t0001g0179a0002c0002t0001g0195a0002c0002t0007g0370others(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 | a0001c0001t0001g0213a0001c0001t0001g0219a0001c0001t0001g0261others(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 | a0001c0001t0001g0214a0001c0001t0001g0270a0001c0001t0002g0125others(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 | a0001c0001t0001g0349a0001c0001t0005g0282a0001c0001t0005g0284others(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 | a0001c0001t0001g0148 | 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 | a0002c0002t0007g0369 | 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 | a0001c0001t0001g0213a0001c0001t0001g0219a0001c0001t0001g0349others(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 | a0001c0001t0001g0213a0001c0001t0001g0219a0001c0001t0001g0349others(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 | a0002c0007t0001g0107 | 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 | a0001c0001t0001g0131 | 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 | a0001c0001t0012g0010 | 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 | a0001c0001t0001g0214a0001c0001t0001g0261a0001c0001t0001g0270others(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 | a0001c0001t0001g0214a0001c0001t0001g0261a0001c0001t0002g0125others(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 | a0003c0006t0001g0236 | 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 | 124 | a0001c0001t0001g0148a0001c0001t0001g0151a0001c0001t0001g0160others(121): 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 | a0001c0001t0001g0129a0001c0001t0001g0190a0001c0001t0001g0193others(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 | a0001c0001t0001g0130a0001c0001t0001g0134a0001c0001t0001g0142others(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 | a0001c0001t0001g0251a0002c0002t0001g0127a0002c0014t0001g0114 | 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 | 51 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0238others(48): Show | 52 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(49): 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 | a0001c0001t0002g0218 | 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 | a0001c0001t0001g0349a0001c0001t0005g0282a0001c0001t0005g0284others(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 | a0001c0001t0001g0213a0001c0001t0001g0219a0001c0001t0001g0354 | 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 | a0001c0001t0002g0212a0001c0005t0002g0118a0001c0005t0003g0092others(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 | a0001c0001t0022g0365a0002c0002t0001g0198a0002c0002t0001g0199 | 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 | a0001c0001t0001g0270a0001c0001t0002g0155a0001c0001t0002g0242others(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 | a0001c0001t0021g0203a0003c0009t0001g0076 | 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 |
26 | a0001c0001t0001g0154a0001c0001t0001g0156a0001c0001t0001g0162others(23): 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 | a0001c0001t0001g0261a0001c0001t0002g0229a0001c0001t0002g0235others(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 | a0001c0001t0002g0337a0001c0001t0002g0340 | 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 | a0002c0003t0001g0200a0002c0003t0001g0201a0002c0003t0001g0298 | 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 | a0001c0001t0002g0339 | 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 | a0001c0001t0001g0349a0001c0001t0005g0282a0001c0001t0005g0284others(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 | 237 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(234): 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 | a0001c0001t0001g0350a0001c0004t0008g0006 | 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 | a0001c0001t0001g0261a0001c0001t0001g0270a0001c0001t0002g0125others(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 | a0001c0001t0001g0214a0001c0001t0002g0245a0001c0001t0002g0321 | 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 | a0001c0001t0006g0276a0002c0002t0001g0198a0002c0002t0001g0199 | 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 | a0001c0001t0001g0219a0001c0001t0001g0349a0001c0001t0001g0354others(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 | a0001c0001t0001g0213a0001c0001t0022g0365a0004c0011t0005g0059 | 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 | a0001c0001t0001g0253 | 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 | a0001c0004t0008g0008 | 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 | a0001c0001t0001g0241a0001c0001t0001g0265a0001c0001t0001g0294others(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 | a0001c0001t0001g0148a0001c0001t0001g0191a0001c0001t0001g0193others(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 | a0001c0001t0001g0160a0001c0001t0001g0192a0001c0001t0002g0143others(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 | a0001c0001t0001g0213a0001c0001t0001g0219a0001c0001t0001g0253others(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 | a0002c0003t0001g0181 | 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 | a0001c0001t0001g0183a0009c0022t0002g0334 | 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 | a0002c0003t0001g0200a0002c0003t0001g0201a0002c0003t0001g0298 | 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 | a0002c0002t0001g0198a0002c0002t0001g0199 | 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 | a0001c0001t0003g0308 | 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 | a0001c0001t0001g0253a0001c0001t0001g0349a0001c0001t0005g0282others(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 | a0001c0001t0001g0213a0001c0001t0001g0219a0001c0001t0001g0354 | 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 | a0001c0005t0002g0123 | 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 | a0002c0003t0001g0200a0002c0003t0001g0201a0002c0003t0001g0298 | 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 | a0001c0001t0001g0253a0001c0001t0001g0349a0001c0001t0002g0280others(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 | a0001c0001t0001g0163 | 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 | a0001c0001t0001g0213a0001c0001t0001g0219a0001c0001t0001g0354 | 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 | a0001c0001t0001g0214a0001c0001t0001g0261a0001c0001t0001g0270others(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 | a0001c0001t0001g0214a0001c0001t0001g0261a0001c0001t0001g0270others(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 | a0002c0007t0001g0103a0003c0006t0001g0152 | 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 | a0001c0001t0001g0219 | 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 | 34 | a0001c0001t0001g0269a0001c0001t0001g0271a0001c0001t0001g0275others(31): 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 | a0001c0001t0001g0214a0001c0001t0001g0253a0001c0001t0001g0261others(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 | a0001c0001t0001g0142a0001c0001t0001g0163a0001c0001t0001g0166others(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 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0261others(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 | a0001c0001t0002g0205a0001c0001t0002g0222a0001c0001t0002g0280others(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 | a0002c0003t0001g0132 | 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 | a0001c0001t0001g0253a0001c0001t0001g0349a0001c0001t0002g0280others(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 | a0001c0001t0002g0155a0001c0001t0002g0311 | 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 | a0002c0002t0001g0216a0002c0002t0001g0331 | 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 | a0001c0001t0003g0246 | 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 | a0001c0001t0003g0267 | 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 | a0002c0002t0001g0292a0002c0002t0001g0320 | 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 | a0003c0006t0001g0003a0003c0006t0001g0164 | 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 | a0002c0002t0001g0263 | 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 | a0001c0001t0006g0217a0001c0001t0006g0315a0001c0005t0006g0113 | 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 | a0001c0001t0001g0183a0001c0001t0001g0190a0001c0001t0001g0288others(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 | a0001c0001t0001g0213a0001c0001t0001g0354a0002c0002t0001g0335 | 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 | 30 | a0001c0001t0001g0269a0001c0001t0001g0271a0001c0001t0001g0286others(27): 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 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0261others(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 | a0001c0001t0001g0214a0001c0001t0001g0261a0001c0001t0001g0270others(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 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0261others(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 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0261others(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 | a0001c0001t0001g0253a0001c0001t0001g0349a0001c0001t0002g0280others(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 | a0001c0001t0012g0010 | 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 |
201 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(198): 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 | 84 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0261others(81): 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 | 253 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(250): 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 | a0001c0001t0002g0186a0001c0001t0002g0188a0001c0001t0002g0189others(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 | 55 | a0001c0001t0001g0253a0001c0001t0001g0269a0001c0001t0001g0271others(52): 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 | 257 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(254): 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 | a0003c0006t0001g0003 | 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 | 33 | a0001c0001t0001g0269a0001c0001t0001g0271a0001c0001t0001g0286others(30): 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 | a0001c0001t0001g0253a0001c0001t0001g0349a0001c0001t0002g0280others(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 | a0001c0001t0001g0214a0001c0001t0001g0261a0001c0001t0001g0270others(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 | 34 | a0001c0001t0001g0269a0001c0001t0001g0271a0001c0001t0001g0286others(31): 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 | a0001c0001t0001g0253a0001c0001t0001g0349a0001c0001t0005g0282others(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 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(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 | 110 | a0001c0001t0001g0196a0001c0001t0001g0213a0001c0001t0001g0214others(107): 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 | a0001c0001t0012g0010 | 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 | a0002c0002t0001g0256 | 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 | a0001c0001t0001g0214a0001c0001t0001g0261a0001c0001t0001g0270others(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 | a0001c0001t0002g0245 | 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 | a0002c0008t0001g0034 | 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 | a0001c0001t0001g0214a0001c0001t0001g0261a0001c0001t0001g0270others(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 | a0001c0001t0001g0183a0001c0001t0001g0190a0001c0001t0001g0288others(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 | a0001c0001t0001g0253a0001c0001t0001g0349a0001c0001t0005g0282others(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 | a0002c0003t0001g0231 | 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 | a0002c0002t0001g0306 | 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 | a0001c0001t0001g0349a0001c0001t0005g0282a0001c0001t0005g0284others(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 | a0001c0001t0001g0214a0001c0001t0001g0261a0001c0001t0001g0270others(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 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(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 | a0001c0001t0001g0214a0001c0001t0001g0261a0001c0001t0001g0270others(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 | a0001c0001t0001g0349a0001c0001t0005g0282a0001c0001t0005g0284others(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 | a0001c0004t0002g0026a0001c0004t0002g0054a0001c0004t0002g0056others(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 | a0003c0006t0001g0215 | 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 | a0001c0001t0001g0214a0001c0001t0001g0261a0001c0001t0001g0270others(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 | a0001c0001t0012g0010 | 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 | a0001c0005t0002g0082 | 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 | a0001c0001t0001g0214a0001c0001t0001g0261a0001c0001t0001g0270others(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 | a0001c0001t0001g0253 | 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 | a0001c0001t0002g0280a0001c0001t0021g0203a0001c0001t0022g0365others(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 | a0001c0001t0001g0214a0001c0001t0001g0261a0001c0001t0001g0270others(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 | a0002c0003t0017g0138 | 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 | a0002c0002t0001g0168 | 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 | a0001c0001t0001g0349a0001c0001t0005g0282a0001c0001t0005g0284others(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 | a0001c0001t0001g0183a0001c0001t0001g0190a0001c0001t0001g0213others(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 | a0001c0001t0002g0242a0004c0011t0002g0058 | 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 | a0001c0001t0001g0214a0001c0001t0001g0253a0001c0001t0001g0261others(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 | a0001c0001t0002g0188 | 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 | a0001c0001t0001g0350a0001c0004t0008g0006 | 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 | a0001c0001t0021g0203a0001c0001t0022g0365 | 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 | a0001c0001t0005g0282a0001c0001t0005g0284a0001c0001t0005g0285others(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 | a0001c0001t0012g0010 | 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 | a0001c0001t0001g0214a0001c0001t0001g0261a0001c0001t0001g0270others(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 | a0001c0001t0002g0229a0001c0001t0002g0230 | 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 | a0001c0001t0002g0218 | 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 | a0001c0001t0001g0183a0001c0001t0001g0190a0001c0001t0001g0288others(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 | a0001c0005t0002g0081 | 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 | a0001c0001t0002g0218 | 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 | 3 | a0003c0006t0001g0345a0003c0009t0001g0074a0003c0013t0001g0050 | 3 | HG01169.hp1 NA20752.hp1 homoSapiens_chm13v2.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 | a0010c0019t0010g0060 | 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 | a0003c0006t0001g0152 | 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 | a0001c0001t0001g0214a0001c0001t0001g0261a0001c0001t0001g0270others(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 | a0001c0001t0012g0010 | 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 | a0002c0002t0001g0185a0002c0002t0001g0247 | 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 | a0002c0003t0001g0231 | 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 | a0001c0001t0002g0218a0001c0001t0012g0010 | 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 | a0001c0001t0012g0010 | 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 | a0001c0001t0002g0218a0001c0001t0012g0010 | 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 | a0001c0001t0005g0202a0001c0017t0005g0011a0004c0011t0005g0057 | 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 | a0001c0001t0002g0218a0001c0001t0012g0010 | 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 | a0001c0001t0002g0187a0002c0003t0001g0252a0002c0003t0001g0353 | 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 | a0001c0001t0012g0010 | 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 | a0001c0001t0001g0213a0001c0001t0001g0354 | 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 | a0001c0001t0002g0180a0001c0001t0002g0227a0001c0001t0002g0229others(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 | a0004c0011t0005g0059 | 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 | a0001c0001t0001g0350a0001c0004t0008g0006 | 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 | a0001c0004t0002g0046 | 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 | a0001c0001t0001g0129a0001c0001t0025g0375 | 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 | a0001c0004t0004g0025 | 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 | a0001c0001t0001g0350a0001c0004t0008g0006a0001c0005t0002g0118others(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 | a0002c0007t0001g0107 | 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 | a0002c0003t0017g0138 | 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 | a0001c0004t0001g0041 | 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 | a0001c0004t0004g0030 | 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 | a0001c0001t0021g0203a0001c0001t0022g0365 | 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 | 276 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(273): 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 | a0002c0003t0017g0138 | 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 | a0001c0001t0001g0190a0001c0001t0001g0288a0001c0001t0001g0294others(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 | a0001c0001t0001g0190a0001c0001t0001g0219a0001c0001t0001g0288others(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 | a0001c0001t0001g0354 | 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 | a0001c0001t0002g0218 | 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 | a0001c0001t0001g0221a0001c0001t0001g0238a0001c0001t0001g0352others(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 | 204 | a0001c0001t0001g0148a0001c0001t0001g0154a0001c0001t0001g0156others(201): 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 | a0002c0003t0001g0200a0002c0003t0001g0201a0002c0003t0001g0298 | 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 | a0001c0005t0002g0079 | 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 | a0002c0002t0001g0198a0002c0002t0001g0199 | 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 | a0001c0004t0004g0045 | 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 | 155 | a0001c0001t0001g0148a0001c0001t0001g0154a0001c0001t0001g0156others(152): 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 | a0003c0015t0001g0110a0003c0015t0001g0111 | 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 | a0002c0007t0001g0085 | 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 | a0002c0010t0001g0055 | 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 | a0001c0001t0001g0275a0001c0001t0005g0139a0001c0001t0005g0202others(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 | a0001c0005t0006g0113 | 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 | 134 | a0001c0001t0001g0148a0001c0001t0001g0154a0001c0001t0001g0156others(131): 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 | a0001c0001t0001g0219a0002c0003t0017g0138 | 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 | a0001c0001t0001g0190a0001c0001t0001g0219a0001c0001t0001g0288others(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 | 168 | a0001c0001t0001g0148a0001c0001t0001g0151a0001c0001t0001g0154others(165): 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 | a0001c0001t0001g0350a0001c0001t0003g0206a0001c0001t0003g0246others(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 | a0002c0002t0001g0195 | 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 | a0003c0009t0001g0076 | 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 | a0001c0001t0001g0219a0002c0003t0017g0138 | 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 | a0003c0006t0001g0224 | 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 | 134 | a0001c0001t0001g0148a0001c0001t0001g0154a0001c0001t0001g0156others(131): 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 | a0001c0001t0001g0190a0001c0001t0001g0288a0001c0001t0001g0294others(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 | 130 | a0001c0001t0001g0148a0001c0001t0001g0154a0001c0001t0001g0156others(127): 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 | a0001c0001t0001g0190a0001c0001t0001g0288a0001c0001t0001g0332others(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 | 155 | a0001c0001t0001g0148a0001c0001t0001g0154a0001c0001t0001g0156others(152): 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 | a0001c0004t0002g0046 | 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 | a0001c0005t0001g0099a0002c0002t0001g0195a0002c0003t0001g0150others(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 | 77 | a0001c0001t0001g0190a0001c0001t0001g0269a0001c0001t0001g0270others(74): 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 | a0005c0025t0001g0364 | 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 | a0011c0023t0001g0361 | 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 | a0001c0001t0002g0218a0001c0001t0002g0280a0002c0002t0001g0198others(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 | a0002c0002t0001g0176a0002c0002t0001g0177a0002c0002t0001g0289 | 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 | a0001c0001t0001g0253a0001c0001t0006g0209a0001c0001t0006g0276others(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 | a0003c0006t0001g0141a0003c0006t0001g0249a0003c0006t0001g0277 | 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 | a0002c0007t0001g0063a0002c0007t0001g0064a0002c0007t0001g0065 | 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 | a0002c0002t0001g0328 | 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 | a0001c0001t0002g0188 | 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 | a0001c0001t0002g0189a0001c0005t0002g0118a0003c0006t0001g0272others(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 | 252 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(249): 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 | a0001c0001t0001g0214a0001c0001t0002g0188a0001c0005t0002g0079others(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 | 101 | a0001c0001t0001g0134a0001c0001t0001g0221a0001c0001t0001g0223others(98): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): 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 | a0002c0002t0024g0374 | 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 | a0001c0001t0001g0219a0001c0001t0002g0189a0001c0001t0002g0212others(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 | a0001c0001t0001g0213a0001c0001t0001g0253a0001c0001t0001g0269others(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 | a0001c0001t0002g0281 | 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 | a0001c0001t0001g0183a0001c0001t0001g0213a0001c0001t0001g0269others(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 | a0001c0001t0001g0214a0001c0001t0001g0221a0001c0001t0001g0269others(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 | a0001c0001t0001g0190a0001c0001t0001g0213a0001c0001t0001g0214others(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 | a0001c0001t0002g0281a0001c0001t0005g0139a0001c0005t0006g0113 | 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 | 304 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(301): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): 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 | a0001c0001t0001g0354a0001c0001t0001g0356 | 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 | a0001c0001t0001g0253a0001c0001t0001g0254a0002c0003t0001g0252 | 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 | a0004c0011t0005g0059a0010c0019t0010g0060 | 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 | a0002c0002t0001g0220 | 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 | 74 | a0001c0001t0001g0148a0001c0001t0001g0151a0001c0001t0001g0154others(71): 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 | 75 | a0001c0001t0001g0148a0001c0001t0001g0151a0001c0001t0001g0154others(72): 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 | a0001c0001t0001g0251a0001c0001t0001g0261a0001c0001t0001g0265others(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 | a0001c0001t0001g0275a0001c0001t0002g0274 | 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 | a0001c0001t0002g0337 | 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 | a0001c0001t0001g0270a0001c0001t0001g0352a0001c0001t0002g0189others(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 | 36 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(33): Show | 36 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.405-9513C>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68565256 | ||||||
| chr17:68565352
|
T | C | 374 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(371): Show | 379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.405-9609A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68565352 | ||||||
| chr17:68565383
|
C | CT | 27 | a0001c0001t0001g0221a0001c0001t0001g0294a0001c0001t0001g0326others(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 | a0001c0001t0002g0212a0001c0001t0006g0217a0001c0004t0008g0008others(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 | a0001c0004t0013g0007 | 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 | a0001c0001t0002g0189a0007c0016t0015g0012 | 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 | a0001c0017t0005g0011a0003c0018t0001g0013 | 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 | a0001c0001t0001g0131a0001c0001t0001g0253a0001c0001t0001g0254others(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 | 66 | a0001c0001t0001g0148a0001c0001t0001g0154a0001c0001t0001g0156others(63): 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 | a0001c0001t0001g0271a0001c0001t0002g0273a0001c0001t0003g0267others(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 | a0001c0001t0001g0213a0001c0001t0001g0219a0001c0001t0001g0251others(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 | a0001c0001t0005g0282 | 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 | a0001c0004t0002g0029 | 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 | a0001c0001t0001g0275a0001c0001t0002g0274 | 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 | a0004c0011t0002g0058a0004c0011t0005g0057 | 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 | a0002c0002t0001g0342 | 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 | a0001c0004t0001g0041 | 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 | 81 | a0001c0001t0001g0148a0001c0001t0001g0151a0001c0001t0001g0154others(78): 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 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0349others(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 | 76 | a0001c0001t0001g0148a0001c0001t0001g0151a0001c0001t0001g0154others(73): 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 | a0001c0001t0001g0270a0001c0001t0001g0352a0001c0001t0002g0189others(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 | a0002c0002t0001g0198a0002c0002t0001g0199 | 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 | 88 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(85): Show | 90 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(87): 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 | a0001c0001t0001g0190a0001c0001t0001g0213a0001c0001t0001g0219others(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 | a0001c0004t0001g0035a0001c0004t0001g0036a0001c0004t0001g0038others(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 | 74 | a0001c0001t0001g0148a0001c0001t0001g0151a0001c0001t0001g0154others(71): 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 | a0001c0001t0002g0226a0003c0006t0001g0141a0003c0006t0001g0232others(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 | a0002c0002t0001g0198a0002c0002t0001g0199 | 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 | a0001c0001t0001g0352a0001c0001t0002g0351a0002c0003t0001g0353 | 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 | a0001c0001t0001g0286a0001c0001t0001g0288a0001c0001t0002g0210others(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 | a0003c0015t0001g0110a0003c0015t0001g0111 | 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 | 72 | a0001c0001t0001g0148a0001c0001t0001g0151a0001c0001t0001g0154others(69): 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 | 75 | a0001c0001t0001g0148a0001c0001t0001g0151a0001c0001t0001g0154others(72): 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 | a0001c0001t0002g0157 | 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 | a0001c0005t0003g0115a0002c0002t0001g0342a0002c0007t0001g0084others(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 | a0001c0001t0006g0276a0001c0001t0020g0330a0002c0002t0001g0331 | 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 | a0001c0001t0001g0275a0001c0001t0002g0274a0004c0011t0002g0058others(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 | a0001c0001t0001g0275a0001c0001t0002g0274a0004c0011t0002g0058others(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 | 78 | a0001c0001t0001g0148a0001c0001t0001g0151a0001c0001t0001g0154others(75): 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 | a0002c0002t0024g0374 | 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 | a0001c0001t0003g0171 | 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 | a0002c0002t0001g0172 | 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 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0349others(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 | a0004c0011t0002g0058a0004c0011t0005g0057 | 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 | a0002c0010t0001g0049 | 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 | a0001c0001t0006g0276a0001c0001t0020g0330a0002c0002t0001g0331 | 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 | a0001c0001t0001g0275a0001c0001t0002g0274a0004c0011t0002g0058others(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 | 80 | a0001c0001t0001g0148a0001c0001t0001g0151a0001c0001t0001g0154others(77): 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 | 80 | a0001c0001t0001g0148a0001c0001t0001g0151a0001c0001t0001g0154others(77): 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 | a0002c0003t0009g0322 | 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 | a0004c0011t0005g0059a0010c0019t0010g0060 | 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 | a0001c0001t0022g0365 | 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 | a0001c0001t0001g0275a0001c0001t0002g0274 | 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 | a0001c0001t0001g0213 | 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 | a0001c0001t0001g0166a0001c0001t0003g0182a0002c0003t0001g0146others(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 | a0001c0001t0001g0213a0001c0001t0001g0219a0001c0001t0001g0271others(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 | a0001c0001t0002g0189a0001c0017t0005g0011a0003c0018t0001g0013others(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 | 80 | a0001c0001t0001g0148a0001c0001t0001g0151a0001c0001t0001g0154others(77): 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 | 239 | a0001c0001t0001g0148a0001c0001t0001g0151a0001c0001t0001g0154others(236): 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 | a0001c0005t0002g0080 | 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 | a0001c0001t0001g0333a0001c0001t0006g0279a0009c0022t0002g0334 | 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 | a0002c0002t0001g0225 | 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 | a0001c0001t0006g0276 | 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 | a0001c0004t0001g0035a0001c0004t0001g0036a0001c0004t0001g0038others(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 | a0001c0005t0002g0118 | 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 | a0001c0001t0006g0276a0001c0001t0020g0330a0002c0002t0001g0331 | 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 | a0002c0003t0001g0184 | 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 | a0001c0001t0002g0227 | 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 | a0002c0002t0001g0158a0002c0002t0001g0176a0002c0002t0001g0177 | 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 | a0001c0004t0001g0043a0001c0004t0004g0052 | 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 | a0001c0004t0001g0038a0001c0004t0001g0042a0001c0004t0002g0014others(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 | a0003c0013t0001g0044 | 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 | a0001c0004t0001g0035a0001c0004t0001g0036a0001c0004t0004g0020others(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 | a0001c0004t0002g0024a0001c0004t0002g0029a0001c0004t0002g0054others(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 | a0001c0004t0004g0045a0001c0004t0004g0048a0002c0008t0001g0034 | 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 | a0001c0004t0002g0016a0001c0004t0002g0026a0001c0004t0003g0031others(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 | 26 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0134others(23): 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 | 11 | a0001c0001t0002g0222a0001c0004t0002g0046a0002c0002t0001g0127others(8): Show | 11 | HG01943.hp1 HG02040.hp2 HG02683.hp1 others(8): 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 | a0001c0001t0001g0265a0001c0001t0001g0358a0001c0001t0002g0143others(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 | a0001c0001t0002g0159a0002c0002t0001g0179a0002c0003t0001g0303 | 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 | a0003c0006t0001g0325 | 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 | a0003c0006t0001g0003 | 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 | a0001c0001t0001g0193a0001c0001t0001g0266a0001c0001t0001g0275others(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 | a0001c0001t0001g0142a0001c0001t0001g0148a0001c0001t0001g0191others(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 | a0001c0001t0001g0129a0001c0001t0001g0183a0001c0001t0001g0253others(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 | a0001c0001t0001g0213a0001c0001t0001g0271a0001c0001t0002g0165others(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 | a0001c0001t0001g0269a0001c0001t0001g0294a0001c0001t0001g0350others(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 | a0001c0001t0001g0190a0001c0001t0001g0192a0001c0001t0001g0251others(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 | a0001c0001t0006g0209a0001c0005t0001g0100a0001c0005t0002g0071others(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 | a0001c0001t0002g0189a0001c0001t0002g0210a0001c0001t0002g0327others(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 | a0001c0001t0025g0375a0001c0005t0002g0123a0002c0002t0001g0137others(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 | a0001c0005t0002g0106a0001c0005t0002g0118a0001c0005t0003g0092others(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 | 15 | a0001c0001t0001g0154a0001c0001t0001g0156a0001c0001t0001g0162others(12): 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 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0005g0282others(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 | a0001c0001t0001g0286a0001c0001t0001g0333a0001c0001t0006g0279others(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 | a0003c0006t0001g0319 | 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 | a0001c0001t0002g0180a0002c0003t0001g0181a0003c0006t0001g0004 | 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 | a0001c0001t0005g0139a0004c0011t0005g0059a0010c0019t0010g0060 | 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 | a0001c0001t0001g0214a0001c0001t0001g0221a0001c0001t0001g0223others(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 | a0002c0002t0024g0374 | 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 | a0001c0001t0001g0254 | 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 | a0001c0001t0001g0253 | 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 | a0001c0001t0001g0271a0001c0001t0002g0273a0001c0001t0021g0203 | 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 | a0002c0002t0001g0199 | 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 | a0001c0001t0001g0269 | 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 | a0002c0002t0001g0198 | 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 | a0001c0001t0003g0206a0001c0004t0013g0007a0002c0002t0001g0234others(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 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0237others(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 | a0001c0001t0001g0214a0001c0001t0001g0233a0001c0001t0001g0241others(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 | a0001c0001t0002g0230a0002c0002t0001g0225a0002c0003t0001g0231others(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 | a0001c0001t0001g0190a0001c0005t0002g0080a0001c0005t0002g0081 | 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 | a0001c0005t0002g0118 | 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 | a0002c0002t0001g0198a0002c0002t0001g0199 | 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 | a0002c0003t0001g0250a0003c0012t0001g0228 | 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 | a0002c0003t0001g0175 | 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 | 81 | a0001c0001t0001g0148a0001c0001t0001g0151a0001c0001t0001g0154others(78): 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 | a0001c0001t0001g0166 | 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 | a0001c0001t0001g0196 | 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 | a0002c0002t0001g0198a0002c0002t0001g0199 | 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 | a0003c0009t0001g0076 | 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 | a0001c0001t0001g0190a0001c0001t0001g0213a0001c0001t0001g0219others(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 | a0002c0002t0001g0198a0002c0002t0001g0199a0003c0013t0001g0044 | 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 | a0003c0015t0001g0110 | 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 | 77 | a0001c0001t0001g0148a0001c0001t0001g0151a0001c0001t0001g0154others(74): 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 | a0001c0001t0001g0352a0001c0001t0002g0351a0001c0017t0005g0011others(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 | a0001c0001t0001g0214a0001c0001t0001g0221a0001c0001t0001g0223others(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 | a0001c0001t0002g0212 | 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 | a0001c0001t0002g0210a0001c0001t0002g0255a0001c0001t0005g0202others(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 | 81 | a0001c0001t0001g0148a0001c0001t0001g0151a0001c0001t0001g0154others(78): 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 | a0001c0001t0001g0251a0001c0001t0001g0261a0001c0001t0001g0265others(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 | a0001c0005t0004g0078 | 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 | a0001c0004t0001g0018 | 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 | a0003c0006t0001g0204 | 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 | a0001c0001t0001g0190a0001c0001t0001g0213a0001c0001t0001g0219others(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 | a0004c0011t0002g0058a0004c0011t0005g0057 | 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 | a0001c0001t0002g0242a0002c0003t0001g0240 | 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 | 87 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(84): Show | 89 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(86): 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 | a0001c0001t0002g0210a0001c0001t0002g0255a0001c0001t0005g0202others(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 | a0001c0004t0003g0031 | 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 | a0001c0001t0001g0286a0001c0001t0001g0288a0001c0001t0002g0280others(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 |
67 | a0001c0001t0001g0148a0001c0001t0001g0151a0001c0001t0001g0154others(64): 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 | a0001c0001t0002g0155a0001c0001t0002g0186a0001c0001t0002g0187others(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 | a0001c0001t0001g0160 | 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 | a0001c0001t0006g0276 | 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 | a0001c0005t0001g0089a0001c0005t0001g0096 | 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 | a0001c0001t0012g0010a0002c0003t0001g0298a0002c0003t0001g0299 | 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 | a0001c0001t0001g0270a0002c0002t0001g0220 | 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 | a0001c0001t0001g0270a0002c0002t0001g0220 | 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 | a0001c0001t0001g0270a0002c0002t0001g0220 | 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 | a0004c0011t0002g0058a0004c0011t0005g0057 | 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 |
130 | a0001c0001t0001g0148a0001c0001t0001g0151a0001c0001t0001g0154others(127): 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 | a0001c0001t0001g0270a0002c0002t0001g0220 | 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 | a0001c0001t0001g0269a0002c0002t0001g0295 | 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 | a0001c0001t0001g0213 | 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 | a0001c0001t0001g0183a0001c0001t0001g0253a0001c0001t0001g0254others(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 | a0002c0003t0001g0240 | 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 | a0001c0001t0001g0275a0001c0001t0002g0274 | 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 | a0001c0001t0001g0214a0001c0001t0002g0205a0001c0001t0002g0235others(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 | a0002c0003t0010g0283 | 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 | a0002c0003t0010g0283 | 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 | a0001c0001t0001g0190a0001c0001t0002g0189 | 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 | a0002c0003t0010g0283 | 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 | a0001c0004t0001g0035a0001c0004t0001g0036a0001c0004t0001g0038others(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 | a0001c0001t0001g0214a0001c0001t0002g0245a0001c0001t0002g0321others(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 | a0002c0003t0001g0231 | 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 | a0001c0001t0001g0296a0001c0001t0001g0326a0002c0002t0001g0295others(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 | a0001c0001t0005g0005a0001c0001t0005g0282a0001c0001t0005g0284others(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 | a0001c0001t0001g0251a0001c0001t0001g0261a0001c0001t0001g0265others(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 | a0001c0001t0002g0210a0001c0001t0006g0208a0001c0001t0006g0209others(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 | a0001c0001t0002g0255a0001c0001t0005g0202 | 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 | a0002c0007t0001g0063a0002c0007t0001g0064 | 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 | a0001c0001t0001g0251a0001c0001t0001g0261a0001c0001t0001g0265others(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 | a0001c0001t0001g0190a0001c0001t0001g0214a0001c0001t0001g0238others(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 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0233others(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 | 30 | a0001c0001t0001g0166a0001c0001t0001g0183a0001c0001t0001g0253others(27): 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 | a0001c0001t0001g0192a0001c0001t0001g0352a0001c0001t0002g0351others(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 |
30 | a0001c0001t0001g0154a0001c0001t0001g0162a0001c0001t0001g0163others(27): 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 | a0001c0001t0001g0130a0001c0001t0001g0134a0001c0001t0001g0148others(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 |
19 | a0001c0001t0001g0270a0001c0001t0002g0143a0001c0001t0003g0257others(16): Show | 19 | HG00621.hp1 HG01891.hp1 HG02280.hp1 others(16): 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 | a0001c0001t0001g0131a0001c0001t0001g0196a0001c0001t0001g0296others(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 | a0001c0001t0001g0129a0001c0001t0001g0349a0001c0001t0001g0350others(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 | a0001c0001t0002g0290a0002c0002t0001g0137a0002c0002t0001g0149others(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 | a0001c0005t0002g0082a0002c0002t0001g0172a0002c0002t0001g0307others(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 | a0001c0001t0006g0217a0001c0005t0001g0089a0001c0005t0001g0096others(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 | a0001c0005t0003g0115 | 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 | a0001c0005t0002g0106a0002c0007t0001g0094a0002c0014t0001g0114 | 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 | a0001c0001t0001g0355 | 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 | a0001c0001t0001g0333a0001c0001t0002g0205a0001c0001t0002g0235others(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 | a0001c0001t0001g0219a0001c0001t0001g0271a0001c0001t0002g0273others(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 | a0001c0001t0002g0293 | 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 | a0001c0004t0001g0035a0001c0004t0001g0036a0001c0004t0001g0042others(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 | a0001c0004t0002g0054a0001c0004t0004g0025a0001c0004t0004g0030others(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 | a0001c0004t0001g0035a0001c0004t0001g0036a0001c0004t0001g0038others(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 | 109 | a0001c0001t0001g0148a0001c0001t0001g0151a0001c0001t0001g0154others(106): 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 | a0001c0001t0003g0194 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0006g0276a0001c0001t0020g0330a0002c0002t0001g0331 | 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 | a0001c0004t0001g0035a0001c0004t0001g0036a0001c0004t0001g0038others(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 | a0001c0001t0001g0271a0001c0001t0002g0273a0001c0005t0002g0118others(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 | a0001c0001t0002g0218a0002c0002t0001g0216 | 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 | a0002c0007t0001g0097 | 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 | a0001c0001t0006g0276 | 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 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0005g0282others(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 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0270others(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 | a0001c0005t0003g0092a0001c0005t0003g0115a0002c0002t0001g0137others(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 | a0002c0008t0001g0040 | 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 | a0001c0005t0002g0068a0001c0005t0003g0062a0001c0005t0003g0066others(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 | a0001c0001t0001g0213a0001c0001t0001g0219a0001c0001t0001g0271others(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 | a0002c0002t0001g0307 | 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 | a0001c0001t0001g0253a0001c0001t0001g0254a0002c0003t0001g0252 | 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 | a0002c0007t0001g0086a0002c0007t0001g0087 | 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 | a0001c0005t0002g0071 | 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 | a0001c0001t0002g0210 | 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 | a0001c0001t0002g0338a0001c0001t0002g0344 | 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 | a0001c0001t0006g0276a0002c0002t0001g0331 | 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 | a0001c0001t0002g0212 | 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 | a0001c0001t0022g0365 | 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 | a0001c0001t0001g0350 | 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 | a0001c0001t0012g0010a0002c0003t0001g0298a0002c0003t0001g0299 | 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 | a0001c0001t0001g0269a0001c0001t0001g0333a0001c0001t0006g0279others(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 | a0001c0004t0001g0035a0001c0004t0001g0036a0001c0004t0001g0038others(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 | a0001c0001t0005g0282a0001c0001t0005g0284a0001c0001t0005g0285others(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 | a0002c0002t0001g0328 | 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 | a0001c0004t0001g0035a0001c0004t0001g0036a0001c0004t0001g0038others(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 | a0001c0005t0001g0089a0001c0005t0001g0096 | 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 | 87 | a0001c0001t0001g0148a0001c0001t0001g0151a0001c0001t0001g0154others(84): 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 | a0001c0001t0001g0183 | 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 | a0004c0011t0002g0058a0004c0011t0005g0057 | 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 | a0001c0004t0001g0035a0001c0004t0001g0036a0001c0004t0001g0038others(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 | a0001c0001t0001g0214a0001c0001t0001g0221a0001c0001t0001g0223others(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 | a0001c0001t0001g0233a0001c0001t0001g0238a0001c0001t0001g0350others(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 | a0001c0001t0002g0321a0001c0001t0002g0351a0001c0001t0012g0010others(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 | a0001c0001t0001g0163a0001c0001t0001g0253a0001c0001t0002g0212others(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 | 111 | a0001c0001t0001g0148a0001c0001t0001g0151a0001c0001t0001g0154others(108): 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 | 111 | a0001c0001t0001g0148a0001c0001t0001g0151a0001c0001t0001g0154others(108): 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 | AG | 263 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(260): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.404+21393_404+2139 others(5): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68578869 | ||||||
| chr17:68578869
|
A | G | 111 | a0001c0001t0001g0148a0001c0001t0001g0151a0001c0001t0001g0154others(108): 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 | a0001c0005t0001g0089a0001c0005t0001g0096a0001c0005t0002g0123others(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 | a0001c0001t0002g0212 | 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 | a0002c0003t0001g0150 | 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 | a0001c0001t0001g0183a0001c0001t0001g0270a0001c0001t0001g0271others(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 | 74 | a0001c0001t0001g0148a0001c0001t0001g0151a0001c0001t0001g0154others(71): 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 | a0001c0001t0001g0142a0001c0001t0002g0338a0001c0001t0012g0010others(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 | a0001c0001t0001g0190a0001c0001t0001g0333a0001c0001t0002g0189others(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 | 5 | a0001c0001t0001g0154a0001c0001t0001g0156a0001c0001t0001g0162others(2): 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 | a0003c0009t0001g0076 | 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 | a0001c0001t0001g0191 | 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 | a0001c0001t0001g0190a0001c0001t0002g0189 | 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 | a0001c0001t0002g0210a0001c0001t0002g0255a0001c0001t0005g0202others(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 | a0001c0001t0001g0352a0001c0001t0002g0351a0001c0017t0005g0011others(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 | a0001c0001t0001g0213a0001c0001t0001g0219a0001c0001t0001g0271others(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 | 128 | a0001c0001t0001g0148a0001c0001t0001g0151a0001c0001t0001g0154others(125): 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 | 77 | a0001c0001t0001g0148a0001c0001t0001g0151a0001c0001t0001g0154others(74): 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 | a0001c0001t0001g0219a0001c0001t0001g0253a0001c0001t0001g0254others(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 | a0001c0001t0001g0352a0001c0001t0002g0351a0001c0017t0005g0011others(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 | 80 | a0001c0001t0001g0148a0001c0001t0001g0151a0001c0001t0001g0154others(77): 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 | 80 | a0001c0001t0001g0148a0001c0001t0001g0151a0001c0001t0001g0154others(77): 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 | 80 | a0001c0001t0001g0148a0001c0001t0001g0151a0001c0001t0001g0154others(77): 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 | a0001c0001t0002g0212 | 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 | a0001c0001t0001g0214a0001c0001t0001g0221a0001c0001t0001g0233others(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 | 80 | a0001c0001t0001g0148a0001c0001t0001g0151a0001c0001t0001g0154others(77): 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 | a0012c0026t0001g0363 | 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 | a0002c0007t0001g0094 | 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 | a0001c0001t0001g0221 | 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 | a0004c0011t0002g0058a0004c0011t0005g0057 | 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 | a0001c0001t0001g0253a0001c0001t0001g0254a0002c0003t0001g0252 | 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 | a0001c0001t0022g0365 | 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 | 84 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(81): 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 | a0001c0001t0001g0333a0001c0001t0006g0279a0009c0022t0002g0334 | 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 | a0001c0004t0002g0054a0001c0004t0002g0056 | 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 | a0001c0001t0001g0286 | 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 | a0001c0001t0001g0352 | 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 | a0002c0007t0001g0086 | 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 | a0002c0007t0001g0087 | 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 | 42 | a0001c0001t0001g0148a0001c0001t0001g0160a0001c0001t0001g0183others(39): Show | 44 | HG00280.hp1 HG00558.hp2 HG00609.hp1 others(41): 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 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0219others(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 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0261others(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 | a0001c0001t0001g0166a0001c0001t0001g0251a0001c0001t0001g0269others(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 | a0001c0001t0001g0190a0001c0001t0001g0354a0001c0001t0001g0355others(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 | a0001c0001t0001g0142a0001c0001t0003g0182a0001c0001t0003g0246others(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 | a0001c0001t0002g0186a0001c0001t0002g0327a0001c0001t0006g0209others(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 | a0001c0001t0005g0357a0002c0003t0001g0343a0002c0008t0001g0040others(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 | a0001c0001t0001g0131 | 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 | a0002c0002t0001g0199 | 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 | a0002c0002t0001g0198 | 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 | a0001c0001t0002g0212a0001c0001t0002g0229a0001c0001t0002g0293others(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 | a0001c0001t0001g0214a0001c0001t0001g0233a0001c0001t0001g0288others(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 | a0001c0001t0001g0286a0001c0001t0001g0333a0001c0001t0002g0351others(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 | a0001c0001t0006g0279a0002c0003t0017g0138a0009c0022t0002g0334 | 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 | a0001c0001t0001g0275a0001c0001t0002g0274 | 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 | a0002c0008t0001g0028 | 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 | a0001c0001t0001g0129a0002c0002t0001g0127a0002c0002t0001g0128 | 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 | a0001c0001t0023g0368 | 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 | a0002c0003t0001g0252 | 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 | a0001c0001t0001g0254 | 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 | a0001c0001t0001g0253 | 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 | a0001c0001t0001g0213 | 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 | a0002c0008t0001g0028 | 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 | a0001c0001t0002g0327 | 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 | a0001c0001t0002g0197 | 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 | a0003c0006t0001g0204 | 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 | a0001c0001t0005g0329a0002c0002t0001g0292a0003c0018t0001g0013 | 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 | a0002c0002t0001g0307a0003c0009t0001g0083 | 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 | a0001c0001t0002g0210a0002c0014t0001g0119 | 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 | a0003c0015t0001g0110 | 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 | a0001c0001t0003g0171a0001c0004t0001g0043a0004c0011t0002g0058 | 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 | a0003c0006t0001g0304 | 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 | a0001c0004t0004g0051 | 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 | a0001c0001t0001g0151a0001c0001t0001g0271a0001c0001t0002g0273others(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 | a0001c0001t0002g0197 | 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 | a0001c0001t0001g0151a0001c0001t0001g0271a0001c0001t0002g0273others(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 | a0001c0001t0001g0271a0001c0001t0002g0273a0002c0002t0001g0172others(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 | a0003c0006t0001g0152 | 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 | a0002c0010t0001g0055 | 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 | a0001c0005t0002g0101a0002c0002t0024g0374 | 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 | a0002c0002t0024g0374 | 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 | a0002c0002t0001g0198a0002c0002t0001g0199 | 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 | a0008c0021t0001g0300 | 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 | a0002c0010t0001g0055 | 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 | a0002c0010t0001g0055 | 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 | a0001c0001t0001g0151a0001c0005t0002g0101a0002c0002t0001g0145others(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 | a0003c0009t0001g0076 | 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 | a0001c0001t0001g0271a0001c0001t0002g0273a0002c0002t0024g0374 | 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 | a0001c0001t0001g0151a0001c0005t0002g0101a0002c0002t0001g0145others(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 | a0001c0001t0001g0269a0001c0001t0001g0332a0002c0003t0001g0231others(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 | a0001c0001t0002g0337a0002c0003t0016g0301a0002c0010t0001g0049 | 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 | a0002c0010t0001g0055 | 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 | a0001c0001t0001g0134a0001c0001t0001g0275a0001c0001t0001g0296others(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 | 166 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0148others(163): 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 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0002g0281others(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 | a0001c0001t0001g0151a0001c0001t0001g0271a0001c0001t0002g0273others(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 | a0001c0001t0001g0271a0001c0001t0002g0273a0002c0002t0024g0374 | 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 | a0001c0001t0001g0151a0001c0005t0002g0101a0002c0002t0001g0145others(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 | a0002c0010t0001g0055 | 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 | a0001c0005t0002g0101 | 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 | a0001c0005t0002g0101 | 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 | a0001c0001t0001g0223 | 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 | 85 | a0001c0001t0001g0134a0001c0001t0002g0197a0001c0001t0002g0222others(82): 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 | a0001c0005t0002g0101a0002c0010t0001g0055 | 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 | a0001c0005t0002g0101a0002c0010t0001g0055 | 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 | 257 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(254): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.404+18681delA | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68581581 | ||||||
| chr17:68581624
|
G | A | 2 | a0001c0001t0002g0180a0002c0003t0001g0181 | 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 | a0001c0001t0002g0229 | 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 | a0001c0001t0001g0251a0001c0001t0001g0261a0001c0001t0001g0265others(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 | a0001c0001t0002g0210a0001c0001t0002g0255a0001c0001t0005g0202others(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 | a0001c0001t0001g0271a0001c0001t0002g0273a0002c0002t0024g0374others(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 | a0002c0002t0024g0374 | 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 | a0001c0001t0001g0265a0001c0001t0001g0266 | 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 | a0001c0001t0022g0365 | 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 | a0003c0006t0001g0325 | 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 | a0001c0001t0001g0214a0001c0001t0001g0221a0001c0001t0001g0223others(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 | a0001c0004t0008g0006a0001c0004t0008g0008a0001c0004t0008g0009others(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 | a0001c0001t0002g0229a0001c0001t0002g0230 | 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 | 71 | a0001c0001t0001g0134a0001c0001t0001g0275a0001c0001t0002g0274others(68): Show | 73 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(70): 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 | a0002c0003t0001g0175 | 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 | a0001c0001t0001g0251a0001c0001t0001g0261a0001c0001t0001g0265others(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 | a0002c0003t0001g0298a0002c0003t0001g0299 | 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 | a0001c0001t0001g0213 | 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 | a0001c0001t0001g0251a0001c0001t0001g0261a0001c0001t0001g0265others(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 | a0001c0001t0022g0365 | 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 | 83 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(80): 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 | a0002c0002t0001g0335 | 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 | a0001c0001t0001g0352a0001c0001t0002g0351a0002c0003t0001g0353 | 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 | a0001c0001t0001g0183a0001c0001t0001g0269a0001c0001t0001g0294others(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 | 75 | a0001c0001t0001g0134a0001c0001t0001g0221a0001c0001t0001g0223others(72): Show | 78 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(75): 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 | a0001c0001t0001g0214a0001c0001t0002g0226a0001c0001t0002g0227others(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 | 111 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0151others(108): 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 | a0001c0001t0001g0131a0001c0001t0001g0251a0001c0001t0001g0352others(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 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0261others(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 | a0001c0004t0002g0046a0001c0005t0004g0078a0002c0007t0001g0077others(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 | a0001c0001t0001g0271a0001c0001t0001g0275a0001c0001t0002g0273others(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 | 286 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(283): 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 | a0001c0001t0001g0271a0001c0001t0001g0275a0001c0001t0001g0349others(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 | a0001c0001t0001g0214a0001c0001t0001g0221a0001c0001t0001g0223others(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 | a0003c0006t0001g0215 | 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 | a0001c0005t0002g0112a0003c0009t0001g0002 | 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 | a0001c0005t0001g0117a0001c0005t0002g0068a0001c0005t0002g0098others(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 | a0001c0001t0001g0219a0001c0001t0001g0270a0001c0001t0002g0212others(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 | 308 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(305): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): 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 | a0001c0001t0001g0349a0001c0001t0001g0350a0001c0001t0001g0354others(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 | a0003c0006t0001g0204 | 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 | a0001c0001t0001g0349a0001c0001t0001g0350a0001c0001t0001g0352others(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 | a0001c0004t0002g0047 | 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 | 90 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(87): 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 | ||||||
| chr17:68584342
|
CAAAACAA others(5): Show |
C | 1 | a0003c0009t0001g0074 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.404+15909_404+1592 others(16): Show |
FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68584342 | ||||||
| chr17:68584347
|
CAA | C | 133 | a0001c0001t0001g0134a0001c0001t0001g0213a0001c0001t0001g0214others(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 | a0001c0001t0001g0251a0001c0001t0001g0261a0001c0001t0001g0265others(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 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0005g0282others(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 | a0001c0001t0002g0273a0001c0001t0012g0010a0001c0001t0022g0365others(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 | a0001c0001t0001g0219a0001c0001t0001g0270a0001c0001t0002g0212others(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 | a0001c0001t0001g0134a0001c0005t0001g0089a0001c0005t0001g0096others(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 | a0003c0006t0001g0215 | 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 | a0002c0007t0001g0121 | 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 | 90 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(87): 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 | a0001c0001t0020g0330a0002c0002t0001g0331 | 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 | a0001c0001t0001g0251a0001c0001t0001g0261a0001c0001t0001g0265others(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 | a0001c0001t0001g0271a0001c0001t0002g0273a0002c0002t0024g0374others(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 | a0002c0014t0001g0114 | 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 | 80 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(77): 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 | a0001c0001t0020g0330a0002c0002t0001g0331 | 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 | a0001c0001t0001g0253a0001c0001t0001g0254a0002c0003t0001g0252 | 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 | a0001c0001t0001g0251a0001c0001t0001g0261a0001c0001t0001g0265others(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 | 315 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(312): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): 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 | 82 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(79): 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 | a0001c0001t0020g0330a0002c0002t0001g0331 | 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 | 316 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(313): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.404+14811delA | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68585451 | ||||||
| chr17:68585488
|
T | A | 31 | a0001c0001t0001g0251a0001c0001t0001g0261a0001c0001t0001g0265others(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 | a0002c0002t0001g0144 | 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 | a0001c0001t0001g0251a0001c0001t0001g0261a0001c0001t0001g0265others(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 | a0001c0001t0002g0143 | 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 | a0001c0001t0001g0134 | 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 | a0001c0001t0002g0273 | 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 | a0001c0001t0001g0213 | 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 | a0003c0006t0001g0003 | 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 | a0001c0001t0005g0005a0001c0001t0005g0287 | 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 | a0001c0005t0002g0079 | 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 | a0001c0001t0001g0251a0001c0001t0001g0261a0001c0001t0001g0265others(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 | a0002c0002t0001g0176a0002c0002t0001g0177 | 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 | a0001c0001t0022g0365 | 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 | a0002c0010t0001g0055 | 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 | a0001c0001t0006g0315 | 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 | a0001c0005t0002g0080a0001c0005t0002g0081 | 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 | a0001c0001t0001g0219a0001c0001t0001g0270a0001c0001t0001g0352others(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 | a0001c0001t0002g0180a0002c0003t0001g0181 | 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 | 277 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(274): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): 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 | a0002c0007t0001g0097 | 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 | a0001c0001t0001g0183 | 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 | a0001c0001t0001g0219a0001c0001t0001g0270a0001c0001t0002g0212others(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 | a0001c0001t0001g0253 | 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 | a0001c0004t0001g0018a0001c0004t0004g0019 | 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 | a0003c0013t0001g0044 | 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 | a0001c0001t0002g0344 | 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 | a0001c0001t0001g0349a0001c0001t0001g0350a0001c0001t0001g0352others(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 | a0001c0004t0004g0048 | 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 | a0001c0001t0001g0213 | 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 | a0002c0003t0001g0181 | 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 | a0001c0001t0001g0221 | 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 | a0002c0003t0009g0346 | 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 | a0002c0002t0001g0292a0002c0010t0001g0053 | 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 | a0002c0002t0001g0198a0002c0002t0001g0199 | 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 | a0001c0001t0012g0010 | 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 | a0001c0005t0001g0089a0001c0005t0001g0096a0001c0005t0002g0123others(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 | 85 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(82): 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 | a0002c0002t0001g0178 | 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 | a0001c0005t0002g0080a0001c0005t0002g0081a0001c0005t0002g0082 | 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 | a0002c0010t0001g0055 | 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 | 318 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(315): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.404+10582G>T | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68589681 | ||||||
| chr17:68589700
|
ATAT | A | 4 | a0002c0002t0001g0316a0003c0006t0001g0317a0003c0006t0001g0318others(1): Show | 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 | a0004c0011t0002g0058a0004c0011t0005g0057 | 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 | a0001c0001t0001g0190a0001c0001t0002g0189a0001c0001t0005g0139others(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 | a0002c0002t0007g0370 | 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 | 291 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(288): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.404+10262T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68590001 | ||||||
| chr17:68590075
|
G | A | 372 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(369): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): 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 | a0001c0001t0001g0332a0001c0001t0001g0333a0001c0001t0006g0279others(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 | a0002c0002t0001g0247 | 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 | a0001c0001t0001g0354a0004c0011t0002g0058a0004c0011t0005g0057 | 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 | a0001c0001t0004g0135a0002c0010t0001g0049 | 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 | a0001c0001t0001g0271a0001c0001t0002g0273a0003c0006t0001g0272 | 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 | a0001c0001t0001g0253a0001c0001t0001g0254a0002c0003t0001g0252 | 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 | a0001c0004t0001g0042a0001c0004t0001g0043 | 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 | a0002c0002t0001g0179 | 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 | 171 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(168): 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 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0221others(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 | 90 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(87): 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 | 100 | a0001c0001t0001g0134a0001c0001t0001g0219a0001c0001t0001g0251others(97): Show | 102 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(99): 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 | a0001c0001t0001g0253a0001c0001t0002g0210a0001c0001t0002g0212others(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 | a0001c0001t0001g0213a0001c0001t0001g0271a0001c0001t0012g0010others(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 | a0001c0001t0006g0276a0001c0001t0022g0365a0001c0001t0023g0368others(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 | a0001c0001t0001g0332a0001c0001t0001g0333a0001c0001t0006g0279others(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 | a0001c0001t0001g0214a0001c0001t0001g0221a0001c0001t0001g0223others(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 | a0003c0006t0001g0347a0003c0006t0001g0348 | 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 | a0001c0004t0002g0016 | 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 | a0001c0004t0008g0006a0001c0004t0008g0008a0001c0004t0008g0009others(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 | a0004c0011t0002g0058a0004c0011t0005g0057 | 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 | a0001c0001t0001g0253a0001c0001t0001g0254a0002c0003t0001g0252 | 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 | a0002c0007t0001g0069 | 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 | 139 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(136): 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 | a0001c0001t0012g0010 | 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 | a0002c0002t0001g0216 | 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 | a0001c0001t0001g0251a0001c0001t0001g0261a0001c0001t0001g0265others(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 | a0001c0005t0006g0113 | 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 | a0001c0001t0001g0219a0001c0001t0001g0270a0001c0001t0002g0212others(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 | 132 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(129): 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 | a0001c0001t0001g0134a0001c0001t0002g0290a0001c0005t0001g0089others(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 | 54 | a0001c0001t0001g0294a0001c0001t0001g0296a0001c0001t0001g0326others(51): 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 | a0001c0001t0001g0271a0001c0001t0002g0273a0002c0002t0024g0374others(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 | a0012c0026t0001g0363 | 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 | a0001c0001t0001g0253a0001c0001t0001g0254a0002c0003t0001g0252 | 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 | a0001c0001t0001g0253a0001c0001t0001g0254a0002c0003t0001g0252 | 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 | a0001c0001t0001g0219a0001c0001t0001g0270a0001c0001t0002g0212others(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 | a0001c0001t0002g0255a0001c0001t0005g0202a0002c0003t0001g0200others(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 | a0003c0006t0001g0224 | 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 | a0001c0001t0022g0365a0003c0006t0001g0215 | 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 | a0001c0001t0001g0214a0001c0001t0001g0221a0001c0001t0001g0223others(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 | a0001c0001t0020g0330a0002c0002t0001g0331 | 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 | a0001c0001t0001g0275a0001c0001t0002g0274 | 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 | a0001c0001t0001g0251a0001c0001t0001g0261a0001c0001t0001g0265others(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 | a0001c0001t0002g0125 | 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 | a0001c0001t0001g0253a0001c0001t0001g0254a0002c0003t0001g0252 | 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 | 67 | a0001c0001t0002g0290a0001c0005t0001g0089a0001c0005t0001g0096others(64): Show | 69 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.404+7154T>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68593109 | ||||||
| chr17:68593147
|
A | G | 83 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(80): 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 | a0001c0005t0003g0075 | 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 | a0001c0001t0012g0010 | 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 | a0002c0010t0001g0055a0004c0011t0002g0058a0004c0011t0005g0057 | 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 | a0001c0001t0001g0223 | 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 | a0001c0001t0003g0182 | 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 | a0001c0001t0001g0332 | 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 | a0001c0001t0001g0354a0001c0001t0001g0355a0001c0001t0001g0356others(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 | a0001c0001t0001g0352a0001c0001t0002g0351a0002c0003t0001g0353 | 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 | a0001c0001t0001g0354a0001c0001t0001g0355a0001c0001t0001g0356 | 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 | a0001c0001t0001g0354a0001c0001t0001g0355a0001c0001t0001g0356 | 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 | a0001c0001t0001g0183 | 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 | 182 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(179): 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 | 182 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(179): 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 | a0001c0001t0001g0271a0001c0001t0001g0275a0001c0001t0001g0326others(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 | 80 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(77): 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 | a0003c0006t0001g0141 | 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 | a0001c0001t0001g0251a0001c0001t0001g0261a0001c0001t0001g0265others(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 | a0002c0003t0001g0184 | 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 | a0001c0005t0003g0115 | 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 | a0001c0001t0002g0337a0001c0001t0002g0338a0001c0001t0002g0339others(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 | 184 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(181): 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 | a0001c0001t0002g0186a0002c0002t0001g0185 | 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 | a0002c0010t0001g0055 | 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 | a0001c0001t0001g0253a0001c0001t0001g0254a0002c0003t0001g0252 | 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 | a0001c0001t0001g0253a0001c0001t0001g0254a0002c0003t0001g0252 | 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 | a0001c0001t0001g0251a0001c0001t0001g0261a0001c0001t0001g0265others(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 | a0001c0005t0003g0116 | 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 | a0001c0001t0001g0253a0001c0001t0001g0254a0002c0003t0001g0252 | 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 | a0003c0006t0001g0249 | 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 | a0001c0005t0001g0117 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.404+4417A>G | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68595846 | ||||||
| chr17:68595955
|
C | G | 1 | a0003c0009t0001g0074 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.404+4308G>C | FAM20A | ENSG00000108950.12 | transcript | ENST00000592554.2 | protein_coding | 1/10 | chr17 | 68595955 | ||||||
| chr17:68596066
|
C | G | 3 | a0001c0005t0002g0071a0001c0005t0002g0072a0001c0005t0002g0073 | 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 | a0001c0001t0001g0221 | 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 | a0001c0001t0001g0219a0001c0001t0001g0270a0001c0001t0002g0212others(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 | a0001c0001t0001g0275a0001c0001t0001g0332a0001c0001t0002g0274others(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 | a0001c0001t0001g0333a0002c0002t0014g0140 | 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 |
68 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(65): 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 | a0001c0001t0001g0190a0001c0001t0002g0187a0001c0001t0002g0188others(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 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(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 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0286others(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 | a0009c0022t0002g0334 | 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 | a0001c0001t0001g0253a0001c0001t0001g0254a0002c0003t0001g0252 | 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 | a0002c0007t0001g0070 | 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 | a0002c0014t0001g0119 | 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 | a0001c0001t0021g0203 | 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 | a0001c0004t0001g0018a0001c0004t0001g0035a0001c0004t0001g0036others(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 | a0002c0010t0001g0049a0002c0010t0001g0055 | 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 | a0001c0001t0001g0332a0001c0001t0001g0333a0001c0001t0006g0279others(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 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0233others(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 | a0001c0001t0001g0349a0001c0001t0001g0350a0001c0001t0001g0352others(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 | a0001c0001t0001g0253a0001c0001t0001g0254a0002c0003t0001g0252 | 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 | 88 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(85): 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 | a0001c0005t0002g0120 | 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 | a0001c0004t0001g0018a0001c0004t0001g0035a0001c0004t0001g0036others(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 | a0002c0003t0001g0211 | 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 | a0001c0001t0001g0271a0001c0001t0002g0273a0002c0002t0024g0374others(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 | 93 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(90): 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 | a0001c0001t0002g0210a0001c0001t0002g0255a0001c0001t0005g0202others(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 | 96 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(93): 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 | a0003c0006t0001g0277 | 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 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0271others(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 | a0001c0001t0001g0251a0001c0004t0001g0018a0001c0004t0001g0035others(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 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0219others(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 | a0001c0001t0002g0205a0001c0001t0003g0206a0001c0001t0005g0202others(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 | a0001c0001t0002g0197a0001c0001t0002g0337a0001c0001t0002g0338others(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 | a0001c0001t0001g0196 | 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 | a0001c0001t0001g0269 | 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 | a0001c0001t0001g0270 | 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 | 67 | a0001c0001t0001g0134a0001c0005t0001g0089a0001c0005t0001g0096others(64): Show | 69 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(66): 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 | a0001c0005t0002g0123a0002c0007t0001g0121a0002c0007t0001g0122others(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 | a0002c0002t0001g0198a0002c0002t0001g0199 | 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 | a0001c0001t0006g0276a0002c0003t0011g0366 | 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 | a0001c0001t0001g0271a0001c0001t0001g0275a0001c0001t0002g0273others(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 | a0002c0002t0018g0133 | 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 | a0001c0004t0001g0018a0001c0004t0001g0035a0001c0004t0001g0036others(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 | a0001c0001t0001g0196 | 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 | a0001c0001t0002g0197 | 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 | a0001c0001t0001g0271a0001c0001t0002g0273a0003c0006t0001g0272 | 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 | a0001c0001t0001g0271a0001c0001t0002g0273a0003c0006t0001g0272 | 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 | a0001c0001t0001g0271a0001c0001t0002g0273a0003c0006t0001g0272 | 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 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0219others(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 | a0001c0001t0002g0197 | 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 | a0001c0004t0002g0054a0001c0004t0002g0056a0002c0010t0001g0055 | 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 | a0001c0004t0001g0018a0001c0004t0001g0035a0001c0004t0001g0036others(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 | a0001c0001t0001g0349a0001c0001t0001g0350a0001c0001t0001g0352others(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 | 86 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(83): 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 | a0001c0001t0001g0358a0001c0001t0003g0359a0002c0003t0001g0360 | 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 | a0001c0004t0002g0056 | 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 | a0002c0003t0001g0132 | 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 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(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 |