Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8027 |
| ensemblid | ENSG00000136738.15 |
| hgncid | 11357 |
| symbol | STAM |
| name | signal transducing adaptor molecule |
| refseq_nuc | NM_003473.4 |
| refseq_prot | NP_003464.1 |
| ensembl_nuc | ENST00000377524.8 |
| ensembl_prot | ENSP00000366746.3 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 17644151 |
| end | 17716824 |
| strand | + |
| ver | v1.2 |
| region | chr10:17644151-17716824 |
| region5000 | chr10:17639151-17721824 |
| regionname0 | STAM_chr10_17644151_17716824 |
| regionname5000 | STAM_chr10_17639151_17721824 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 540 | 422 | 92 | 80 | 197 | 16 | 35 | 161 | STAM_chr10_17639151_17721824 | STAM | MPLFA others(535): Show |
chr10 | 17639151 | 17721824 |
| a0002 | 0/0 | 540 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | STAM_chr10_17639151_17721824 | STAM | MPLFA others(535): Show |
chr10 | 17639151 | 17721824 |
| a0003 | 0/0 | 540 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | MPLFA others(535): Show |
chr10 | 17639151 | 17721824 |
| a0004 | 0/0 | 540 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | MPLFA others(535): Show |
chr10 | 17639151 | 17721824 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1620 | 330 | 81 | 69 | 140 | 13 | 25 | STAM_chr10_17639151_17721824 | STAM | ATGCC others(1615): Show |
chr10 | 17639151 | 17721824 | ||
| a0001c0002 | 0/0 | 1620 | 82 | 9 | 11 | 51 | 3 | 8 | STAM_chr10_17639151_17721824 | STAM | ATGCC others(1615): Show |
chr10 | 17639151 | 17721824 | ||
| a0001c0003 | 0/0 | 1620 | 4 | 0 | 0 | 4 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | ATGCC others(1615): Show |
chr10 | 17639151 | 17721824 | ||
| a0001c0005 | 0/0 | 1620 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | ATGCC others(1615): Show |
chr10 | 17639151 | 17721824 | ||
| a0001c0006 | 0/0 | 1620 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | ATGCC others(1615): Show |
chr10 | 17639151 | 17721824 | ||
| a0001c0008 | 0/0 | 1620 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | ATGCC others(1615): Show |
chr10 | 17639151 | 17721824 | ||
| a0001c0009 | 0/0 | 1620 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | ATGCC others(1615): Show |
chr10 | 17639151 | 17721824 | ||
| a0001c0010 | 0/0 | 1620 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | ATGCC others(1615): Show |
chr10 | 17639151 | 17721824 | ||
| a0001c0012 | 0/0 | 1620 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | ATGCC others(1615): Show |
chr10 | 17639151 | 17721824 | ||
| a0002c0004 | 0/0 | 1620 | 2 | 0 | 0 | 2 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | ATGCC others(1615): Show |
chr10 | 17639151 | 17721824 | ||
| a0003c0007 | 0/0 | 1620 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | ATGCC others(1615): Show |
chr10 | 17639151 | 17721824 | ||
| a0004c0011 | 0/0 | 1620 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | ATGCC others(1615): Show |
chr10 | 17639151 | 17721824 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3856 | 116 | 23 | 13 | 69 | 3 | 8 | STAM_chr10_17639151_17721824 | STAM | CCTTG others(3851): Show |
chr10 | 17639151 | 17721824 |
| a0001c0001t0002 | 1/0 | 3856 | 120 | 11 | 31 | 61 | 5 | 11 | STAM_chr10_17639151_17721824 | STAM | CCTTG others(3851): Show |
chr10 | 17639151 | 17721824 |
| a0001c0001t0003 | 0/0 | 3858 | 7 | 7 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | CCTTG others(3853): Show |
chr10 | 17639151 | 17721824 |
| a0001c0001t0004 | 0/0 | 3858 | 28 | 18 | 5 | 1 | 2 | 2 | STAM_chr10_17639151_17721824 | STAM | CCTTG others(3853): Show |
chr10 | 17639151 | 17721824 |
| a0001c0001t0005 | 0/1 | 3859 | 20 | 1 | 12 | 4 | 2 | 0 | STAM_chr10_17639151_17721824 | STAM | CCTTG others(3854): Show |
chr10 | 17639151 | 17721824 |
| a0001c0001t0006 | 0/0 | 3858 | 5 | 5 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | CCTTG others(3853): Show |
chr10 | 17639151 | 17721824 |
| a0001c0001t0007 | 0/0 | 3856 | 5 | 0 | 1 | 0 | 1 | 3 | STAM_chr10_17639151_17721824 | STAM | CCTTG others(3851): Show |
chr10 | 17639151 | 17721824 |
| a0001c0001t0008 | 0/0 | 3857 | 3 | 0 | 1 | 2 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | CCTTG others(3852): Show |
chr10 | 17639151 | 17721824 |
| a0001c0001t0009 | 0/0 | 3859 | 3 | 1 | 0 | 2 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | CCTTG others(3854): Show |
chr10 | 17639151 | 17721824 |
| a0001c0001t0010 | 0/0 | 3856 | 3 | 2 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | CCTTG others(3851): Show |
chr10 | 17639151 | 17721824 |
| a0001c0001t0012 | 0/0 | 3858 | 2 | 2 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | CCTTG others(3853): Show |
chr10 | 17639151 | 17721824 |
| a0001c0001t0014 | 0/0 | 3856 | 2 | 0 | 2 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | CCTTG others(3851): Show |
chr10 | 17639151 | 17721824 |
| a0001c0001t0015 | 0/0 | 3856 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | CCTTG others(3851): Show |
chr10 | 17639151 | 17721824 |
| a0001c0001t0016 | 0/0 | 3856 | 2 | 2 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | CCTTG others(3851): Show |
chr10 | 17639151 | 17721824 |
| a0001c0001t0017 | 0/0 | 3857 | 2 | 2 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | CCTTG others(3852): Show |
chr10 | 17639151 | 17721824 |
| a0001c0001t0018 | 0/0 | 3858 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | CCTTG others(3853): Show |
chr10 | 17639151 | 17721824 |
| a0001c0001t0019 | 0/0 | 3856 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | CCTTG others(3851): Show |
chr10 | 17639151 | 17721824 |
| a0001c0001t0023 | 0/0 | 3856 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | CCTTG others(3851): Show |
chr10 | 17639151 | 17721824 |
| a0001c0001t0024 | 0/0 | 3856 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | CCTTG others(3851): Show |
chr10 | 17639151 | 17721824 |
| a0001c0001t0025 | 0/0 | 3856 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | CCTTG others(3851): Show |
chr10 | 17639151 | 17721824 |
| a0001c0001t0026 | 0/0 | 3856 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | CCTTG others(3851): Show |
chr10 | 17639151 | 17721824 |
| a0001c0001t0027 | 0/0 | 3856 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | CCTTG others(3851): Show |
chr10 | 17639151 | 17721824 |
| a0001c0001t0029 | 0/0 | 3858 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | CCTTG others(3853): Show |
chr10 | 17639151 | 17721824 |
| a0001c0001t0030 | 0/0 | 3856 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | CCTTG others(3851): Show |
chr10 | 17639151 | 17721824 |
| a0001c0001t0031 | 0/0 | 3856 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | CCTTG others(3851): Show |
chr10 | 17639151 | 17721824 |
| a0001c0001t0032 | 0/0 | 3856 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | CCTTG others(3851): Show |
chr10 | 17639151 | 17721824 |
| a0001c0002t0003 | 0/0 | 3858 | 68 | 2 | 10 | 45 | 3 | 8 | STAM_chr10_17639151_17721824 | STAM | CCTTG others(3853): Show |
chr10 | 17639151 | 17721824 |
| a0001c0002t0004 | 0/0 | 3858 | 6 | 6 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | CCTTG others(3853): Show |
chr10 | 17639151 | 17721824 |
| a0001c0002t0011 | 0/0 | 3858 | 3 | 0 | 0 | 3 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | CCTTG others(3853): Show |
chr10 | 17639151 | 17721824 |
| a0001c0002t0013 | 0/0 | 3858 | 2 | 0 | 0 | 2 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | CCTTG others(3853): Show |
chr10 | 17639151 | 17721824 |
| a0001c0002t0020 | 0/0 | 3858 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | CCTTG others(3853): Show |
chr10 | 17639151 | 17721824 |
| a0001c0002t0021 | 0/0 | 3858 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | CCTTG others(3853): Show |
chr10 | 17639151 | 17721824 |
| a0001c0002t0022 | 0/0 | 3858 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | CCTTG others(3853): Show |
chr10 | 17639151 | 17721824 |
| a0001c0003t0001 | 0/0 | 3856 | 4 | 0 | 0 | 4 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | CCTTG others(3851): Show |
chr10 | 17639151 | 17721824 |
| a0001c0005t0001 | 0/0 | 3856 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | CCTTG others(3851): Show |
chr10 | 17639151 | 17721824 |
| a0001c0006t0028 | 0/0 | 3858 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | CCTTG others(3853): Show |
chr10 | 17639151 | 17721824 |
| a0001c0008t0001 | 0/0 | 3856 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | CCTTG others(3851): Show |
chr10 | 17639151 | 17721824 |
| a0001c0009t0015 | 0/0 | 3856 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | CCTTG others(3851): Show |
chr10 | 17639151 | 17721824 |
| a0001c0010t0001 | 0/0 | 3856 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | CCTTG others(3851): Show |
chr10 | 17639151 | 17721824 |
| a0001c0012t0002 | 0/0 | 3856 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | CCTTG others(3851): Show |
chr10 | 17639151 | 17721824 |
| a0002c0004t0001 | 0/0 | 3856 | 2 | 0 | 0 | 2 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | CCTTG others(3851): Show |
chr10 | 17639151 | 17721824 |
| a0003c0007t0001 | 0/0 | 3856 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | CCTTG others(3851): Show |
chr10 | 17639151 | 17721824 |
| a0004c0011t0001 | 0/0 | 3856 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | CCTTG others(3851): Show |
chr10 | 17639151 | 17721824 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0001g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0001 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0002 | 0/0 | 5 | 0 | 3 | 1 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0233 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0002g0387 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0004g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0004g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0004g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0004g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0004g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0004g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0005g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0005g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0005g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0005g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0005g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0005g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0005g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0005g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0005g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0005g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0005g0048 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0005g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0005g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0005g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0005g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0005g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0005g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0006g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0006g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0006g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0006g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0006g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0007g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0007g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0007g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0007g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0007g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0008g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0008g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0008g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0009g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0009g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0009g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0010g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0010g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0010g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0012g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0012g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0014g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0014g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0015g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0016g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0017g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0017g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0018g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0019g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0023g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0024g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0025g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0026g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0027g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0029g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0030g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0031g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0001t0032g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0350 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0003g0388 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0004g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0004g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0004g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0004g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0004g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0004g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0011g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0011g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0011g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0013g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0013g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0020g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0021g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0002t0022g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0005t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0006t0028g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0008t0001g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0009t0015g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0010t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0001c0012t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0002c0004t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0002c0004t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0003c0007t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| a0004c0011t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0189 | EUR | GBR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG00099 | hp2 | a0001 | c0002 | t0003 | g0168 | EUR | GBR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0117 | EUR | GBR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG00280 | hp1 | a0001 | c0001 | t0007 | g0239 | EUR | FIN | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG00280 | hp2 | a0001 | c0001 | t0005 | g0045 | EUR | FIN | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG00323 | hp1 | a0001 | c0002 | t0003 | g0350 | EUR | FIN | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG00323 | hp2 | a0001 | c0001 | t0005 | g0055 | EUR | FIN | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | CHS | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | CHS | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG00558 | hp1 | a0001 | c0002 | t0003 | g0310 | EAS | CHS | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | CHS | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | CHS | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG00609 | hp1 | a0001 | c0001 | t0008 | g0050 | EAS | CHS | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | CHS | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0242 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG00639 | hp2 | a0001 | c0001 | t0005 | g0004 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG00642 | hp1 | a0001 | c0001 | t0007 | g0006 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0199 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG00673 | hp1 | a0001 | c0002 | t0003 | g0345 | EAS | CHS | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | CHS | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG00735 | hp1 | a0001 | c0001 | t0032 | g0225 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0262 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0275 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0282 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0356 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01069 | hp2 | a0001 | c0002 | t0003 | g0349 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0232 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0362 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01074 | hp1 | a0001 | c0002 | t0021 | g0172 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0303 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0274 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01081 | hp2 | a0001 | c0001 | t0005 | g0043 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01106 | hp1 | a0001 | c0002 | t0003 | g0169 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0360 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0052 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01167 | hp2 | a0001 | c0001 | t0005 | g0053 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01168 | hp1 | a0001 | c0001 | t0024 | g0292 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01168 | hp2 | a0001 | c0002 | t0003 | g0161 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01169 | hp1 | a0001 | c0001 | t0005 | g0047 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01169 | hp2 | a0001 | c0002 | t0003 | g0159 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0294 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01175 | hp2 | a0001 | c0001 | t0005 | g0046 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01192 | hp1 | a0001 | c0001 | t0010 | g0109 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0236 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01243 | hp2 | a0001 | c0002 | t0003 | g0036 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0176 | AMR | CLM | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0178 | AMR | CLM | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | CLM | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01257 | hp1 | a0001 | c0001 | t0005 | g0004 | AMR | CLM | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0024 | AMR | CLM | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01258 | hp2 | a0001 | c0001 | t0005 | g0004 | AMR | CLM | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01261 | hp2 | a0001 | c0001 | t0005 | g0044 | AMR | CLM | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01346 | hp1 | a0001 | c0001 | t0014 | g0140 | AMR | CLM | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01358 | hp2 | a0001 | c0001 | t0008 | g0011 | AMR | CLM | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01361 | hp1 | a0001 | c0002 | t0003 | g0165 | AMR | CLM | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01361 | hp2 | a0001 | c0001 | t0025 | g0223 | AMR | CLM | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01433 | hp1 | a0001 | c0002 | t0003 | g0160 | AMR | CLM | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01433 | hp2 | a0001 | c0001 | t0014 | g0131 | AMR | CLM | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01496 | hp1 | a0001 | c0002 | t0003 | g0163 | AMR | CLM | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0177 | EUR | IBS | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0230 | EUR | IBS | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0175 | EUR | IBS | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0306 | EUR | IBS | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0206 | AFR | ACB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01884 | hp2 | a0001 | c0001 | t0015 | g0386 | AFR | ACB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0264 | AFR | ACB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0179 | AFR | ACB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01928 | hp1 | a0001 | c0002 | t0003 | g0167 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0263 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01934 | hp1 | a0001 | c0001 | t0005 | g0042 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0281 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01943 | hp1 | a0001 | c0002 | t0003 | g0162 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0240 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0278 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0302 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0354 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0251 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0181 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0293 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0180 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02004 | hp2 | a0001 | c0001 | t0005 | g0011 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | KHV | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | KHV | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02055 | hp1 | a0001 | c0009 | t0015 | g0385 | AFR | ACB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02055 | hp2 | a0001 | c0001 | t0018 | g0173 | AFR | ACB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | KHV | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0368 | EAS | KHV | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0367 | EAS | KHV | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | KHV | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02129 | hp1 | a0001 | c0001 | t0005 | g0049 | EAS | KHV | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0357 | EAS | KHV | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | KHV | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02132 | hp2 | a0001 | c0010 | t0001 | g0003 | EAS | KHV | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | ACB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02145 | hp2 | a0001 | c0002 | t0004 | g0334 | AFR | ACB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02155 | hp1 | a0001 | c0002 | t0003 | g0320 | EAS | CDX | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | CDX | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02165 | hp1 | a0001 | c0002 | t0003 | g0319 | EAS | CDX | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | CDX | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0363 | AFR | ACB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02258 | hp1 | a0001 | c0001 | t0017 | g0377 | AFR | ACB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0365 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02280 | hp2 | a0001 | c0001 | t0017 | g0378 | AFR | ACB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0258 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0370 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0252 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0214 | AFR | ACB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | KHV | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02572 | hp1 | a0001 | c0001 | t0010 | g0111 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0290 | SAS | PJL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02602 | hp2 | a0001 | c0001 | t0007 | g0257 | SAS | PJL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02615 | hp1 | a0001 | c0002 | t0004 | g0332 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0210 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0305 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0355 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0157 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0243 | SAS | PJL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02717 | hp2 | a0001 | c0001 | t0031 | g0381 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0359 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02738 | hp1 | a0001 | c0002 | t0003 | g0171 | SAS | PJL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0220 | SAS | PJL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0188 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0155 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02895 | hp2 | a0001 | c0001 | t0016 | g0014 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0054 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02896 | hp2 | a0001 | c0002 | t0004 | g0347 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02922 | hp1 | a0001 | c0001 | t0006 | g0207 | AFR | ESN | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0215 | AFR | ESN | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02965 | hp1 | a0001 | c0002 | t0004 | g0323 | AFR | ESN | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02965 | hp2 | a0001 | c0001 | t0009 | g0380 | AFR | ESN | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02970 | hp1 | a0001 | c0001 | t0023 | g0187 | AFR | ESN | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | ESN | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03017 | hp1 | a0001 | c0002 | t0003 | g0164 | SAS | PJL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0211 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0194 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0195 | AFR | MSL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0204 | AFR | MSL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0025 | AFR | ESN | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ESN | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | ESN | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0387 | AFR | ESN | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0209 | AFR | ESN | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03209 | hp1 | a0001 | c0001 | t0029 | g0376 | AFR | MSL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03209 | hp2 | a0001 | c0002 | t0004 | g0330 | AFR | MSL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0150 | AFR | MSL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0018 | AFR | MSL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0231 | SAS | PJL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03239 | hp2 | a0001 | c0008 | t0001 | g0371 | SAS | PJL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0156 | AFR | MSL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0192 | AFR | MSL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03486 | hp1 | a0001 | c0002 | t0022 | g0183 | AFR | MSL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0017 | SAS | PJL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0266 | SAS | PJL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0017 | SAS | PJL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03516 | hp1 | a0001 | c0002 | t0003 | g0035 | AFR | ESN | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | ESN | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0184 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03540 | hp2 | a0001 | c0001 | t0019 | g0110 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03579 | hp1 | a0001 | c0006 | t0028 | g0379 | AFR | MSL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0208 | AFR | MSL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03669 | hp1 | a0001 | c0002 | t0003 | g0032 | SAS | PJL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03669 | hp2 | a0001 | c0002 | t0003 | g0346 | SAS | PJL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0234 | SAS | STU | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | STU | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03704 | hp1 | a0001 | c0002 | t0003 | g0340 | SAS | PJL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0358 | SAS | PJL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0364 | SAS | BEB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03834 | hp2 | a0001 | c0001 | t0007 | g0256 | SAS | BEB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03927 | hp1 | a0001 | c0002 | t0003 | g0341 | SAS | BEB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0235 | SAS | BEB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0250 | SAS | BEB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03942 | hp2 | a0003 | c0007 | t0001 | g0099 | SAS | BEB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0265 | SAS | BEB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG04184 | hp2 | a0001 | c0002 | t0003 | g0216 | SAS | BEB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | STU | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0286 | SAS | STU | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG04204 | hp1 | a0001 | c0002 | t0003 | g0170 | SAS | STU | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | STU | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG04228 | hp1 | a0001 | c0005 | t0001 | g0080 | SAS | STU | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | STU | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18522 | hp1 | a0001 | c0001 | t0010 | g0212 | AFR | YRI | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0200 | AFR | YRI | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | CHB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0174 | EAS | CHB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0198 | AFR | YRI | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18906 | hp2 | a0001 | c0001 | t0012 | g0383 | AFR | YRI | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18939 | hp2 | a0001 | c0002 | t0003 | g0008 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18940 | hp1 | a0001 | c0002 | t0003 | g0312 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18941 | hp1 | a0001 | c0002 | t0003 | g0337 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18941 | hp2 | a0001 | c0002 | t0003 | g0105 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18945 | hp2 | a0001 | c0002 | t0003 | g0022 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18948 | hp1 | a0001 | c0002 | t0003 | g0316 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18949 | hp2 | a0001 | c0002 | t0003 | g0326 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18951 | hp2 | a0001 | c0002 | t0003 | g0315 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18954 | hp2 | a0001 | c0002 | t0003 | g0388 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0366 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18956 | hp2 | a0001 | c0002 | t0003 | g0327 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18957 | hp1 | a0001 | c0002 | t0020 | g0373 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18959 | hp1 | a0001 | c0001 | t0009 | g0308 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18960 | hp2 | a0001 | c0002 | t0003 | g0008 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18962 | hp2 | a0001 | c0002 | t0003 | g0328 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18963 | hp2 | a0001 | c0002 | t0011 | g0247 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18965 | hp2 | a0001 | c0002 | t0003 | g0023 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18966 | hp1 | a0001 | c0003 | t0001 | g0122 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18967 | hp1 | a0001 | c0002 | t0003 | g0374 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18968 | hp2 | a0001 | c0002 | t0003 | g0335 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18971 | hp1 | a0001 | c0002 | t0003 | g0009 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18973 | hp2 | a0001 | c0002 | t0003 | g0375 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18974 | hp2 | a0001 | c0002 | t0003 | g0009 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18977 | hp1 | a0001 | c0002 | t0003 | g0325 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18977 | hp2 | a0001 | c0012 | t0002 | g0280 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18978 | hp1 | a0001 | c0002 | t0003 | g0202 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18978 | hp2 | a0002 | c0004 | t0001 | g0112 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18979 | hp1 | a0001 | c0002 | t0003 | g0318 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18981 | hp1 | a0001 | c0002 | t0003 | g0331 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18983 | hp1 | a0001 | c0001 | t0005 | g0010 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18983 | hp2 | a0001 | c0003 | t0001 | g0123 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18984 | hp2 | a0001 | c0002 | t0003 | g0322 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18985 | hp2 | a0001 | c0001 | t0009 | g0309 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18988 | hp1 | a0001 | c0002 | t0003 | g0343 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18989 | hp2 | a0001 | c0002 | t0003 | g0022 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18993 | hp2 | a0001 | c0001 | t0005 | g0041 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18995 | hp1 | a0001 | c0002 | t0003 | g0321 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18998 | hp2 | a0001 | c0002 | t0003 | g0009 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19000 | hp1 | a0001 | c0001 | t0008 | g0040 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19001 | hp1 | a0001 | c0002 | t0003 | g0311 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19002 | hp1 | a0002 | c0004 | t0001 | g0114 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19003 | hp2 | a0004 | c0011 | t0001 | g0058 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19004 | hp1 | a0001 | c0002 | t0003 | g0336 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19007 | hp2 | a0001 | c0002 | t0003 | g0154 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19009 | hp1 | a0001 | c0002 | t0013 | g0329 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19010 | hp1 | a0001 | c0002 | t0003 | g0342 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0033 | AFR | LWK | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0205 | AFR | LWK | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0361 | AFR | LWK | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0197 | AFR | LWK | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0353 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19058 | hp1 | a0001 | c0002 | t0011 | g0351 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19058 | hp2 | a0001 | c0001 | t0026 | g0019 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19062 | hp2 | a0001 | c0002 | t0003 | g0314 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19063 | hp1 | a0001 | c0002 | t0013 | g0023 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19065 | hp1 | a0001 | c0002 | t0003 | g0317 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19065 | hp2 | a0001 | c0001 | t0005 | g0010 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19068 | hp2 | a0001 | c0002 | t0003 | g0339 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19070 | hp1 | a0001 | c0002 | t0011 | g0352 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19070 | hp2 | a0001 | c0003 | t0001 | g0118 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19072 | hp2 | a0001 | c0002 | t0003 | g0338 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19074 | hp2 | a0001 | c0002 | t0003 | g0344 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19076 | hp1 | a0001 | c0002 | t0003 | g0008 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19076 | hp2 | a0001 | c0003 | t0001 | g0151 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19078 | hp2 | a0001 | c0002 | t0003 | g0218 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19086 | hp2 | a0001 | c0002 | t0003 | g0348 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19087 | hp1 | a0001 | c0002 | t0003 | g0372 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19091 | hp1 | a0001 | c0002 | t0003 | g0324 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19240 | hp1 | a0001 | c0001 | t0006 | g0203 | AFR | YRI | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | YRI | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA20129 | hp1 | a0001 | c0002 | t0003 | g0166 | AFR | ASW | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ASW | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA20752 | hp1 | a0001 | c0002 | t0003 | g0029 | EUR | TSI | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0124 | EUR | TSI | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0241 | EUR | TSI | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0088 | EUR | TSI | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA20905 | hp1 | a0001 | c0001 | t0027 | g0113 | SAS | GIH | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA20905 | hp2 | a0001 | c0001 | t0007 | g0147 | SAS | GIH | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0226 | AMR | CLM | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG01123 | hp2 | a0001 | c0001 | t0005 | g0051 | AMR | CLM | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0193 | AFR | ACB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02109 | hp2 | a0001 | c0001 | t0016 | g0014 | AFR | ACB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02559 | hp1 | a0001 | c0002 | t0004 | g0333 | AFR | ACB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0384 | AFR | ACB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03471 | hp1 | a0001 | c0001 | t0012 | g0182 | AFR | MSL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0056 | AFR | USA | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0273 | AFR | USA | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0213 | AFR | USA | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0369 | AFR | USA | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0201 | AFR | LWK | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| NA21309 | hp2 | a0001 | c0001 | t0030 | g0382 | AFR | LWK | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0005 | g0048 | REF | REF | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0233 | REF | REF | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:17688135 | A | C | 1 | a0004 | 1 | NA19003.hp2 | missense_variant | MODERATE | c.406A>C | p.Lys136Gln | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/14 | 595/3856 | 406/1623 | 136/540 | chr10 | 17688135 | |||
| chr10:17696848 | C | A | 1 | a0003 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.802C>A | p.Leu268Ile | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/14 | 991/3856 | 802/1623 | 268/540 | chr10 | 17696848 | |||
| chr10:17700271 | A | T | 1 | a0002 | 2 | NA18978.hp2 NA19002.hp1 |
missense_variant | MODERATE | c.904A>T | p.Ile302Phe | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/14 | 1093/3856 | 904/1623 | 302/540 | chr10 | 17700271 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:17660546 | T | C | 1 | a0001c0005 | 1 | HG04228.hp1 | splice_region_variant&synonymous_variant | LOW | c.123T>C | p.Thr41Thr | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/14 | 312/3856 | 123/1623 | 41/540 | chr10 | 17660546 | |||
| chr10:17684855 | C | T | 1 | a0001c0012 | 1 | NA18977.hp2 | synonymous_variant | LOW | c.225C>T | p.Asn75Asn | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/14 | 414/3856 | 225/1623 | 75/540 | chr10 | 17684855 | |||
| chr10:17688140 | A | G | 1 | a0001c0003 | 4 | NA18966.hp1 NA18983.hp2 NA19070.hp2 others(1): Show |
synonymous_variant | LOW | c.411A>G | p.Glu137Glu | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/14 | 600/3856 | 411/1623 | 137/540 | chr10 | 17688140 | |||
| chr10:17688164 | T | C | 1 | a0001c0006 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.435T>C | p.Ile145Ile | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/14 | 624/3856 | 435/1623 | 145/540 | chr10 | 17688164 | |||
| chr10:17695134 | C | T | 1 | a0001c0010 | 1 | HG02132.hp2 | synonymous_variant | LOW | c.621C>T | p.Asn207Asn | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 7/14 | 810/3856 | 621/1623 | 207/540 | chr10 | 17695134 | |||
| chr10:17695209 | A | G | 1 | a0001c0009 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.696A>G | p.Lys232Lys | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 7/14 | 885/3856 | 696/1623 | 232/540 | chr10 | 17695209 | |||
| chr10:17714597 | T | C | 1 | a0001c0002 | 82 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(79): Show |
synonymous_variant | LOW | c.1440T>C | p.Tyr480Tyr | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 1629/3856 | 1440/1623 | 480/540 | chr10 | 17714597 | |||
| chr10:17714775 | C | T | 1 | a0001c0008 | 1 | HG03239.hp2 | synonymous_variant | LOW | c.1618C>T | p.Leu540Leu | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 1807/3856 | 1618/1623 | 540/540 | chr10 | 17714775 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:17644183 | C | T | 1 | a0001c0001t0032 | 1 | HG00735.hp1 | 5_prime_UTR_variant | MODIFIER | c.-157C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/14 | 157 | chr10 | 17644183 | ||||||
| chr10:17644235 | G | A | 2 | a0001c0001t0005 a0001c0001t0008 |
22 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(19): Show |
5_prime_UTR_variant | MODIFIER | c.-105G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/14 | 105 | chr10 | 17644235 | ||||||
| chr10:17644335 | C | T | 7 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0017 others(4): Show |
28 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(25): Show |
5_prime_UTR_variant | MODIFIER | c.-5C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/14 | 5 | chr10 | 17644335 | ||||||
| chr10:17714830 | T | C | 1 | a0001c0001t0018 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*50T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 50 | chr10 | 17714830 | ||||||
| chr10:17714959 | T | TCC | 2 | a0001c0001t0005 a0001c0001t0009 |
22 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*186_*187dupCC | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 188 | INFO_REALIGN_3_PRIME | chr10 | 17714959 | |||||
| chr10:17714967 | C | T | 1 | a0001c0001t0027 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*187C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 187 | chr10 | 17714967 | ||||||
| chr10:17714976 | A | T | 1 | a0001c0001t0007 | 5 | HG00280.hp1 HG00642.hp1 HG02602.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*196A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 196 | chr10 | 17714976 | ||||||
| chr10:17715079 | C | A | 1 | a0001c0006t0028 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*299C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 299 | chr10 | 17715079 | ||||||
| chr10:17715197 | G | A | 2 | a0001c0001t0010 a0001c0001t0019 |
4 | HG01192.hp1 HG02572.hp1 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*417G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 417 | chr10 | 17715197 | ||||||
| chr10:17715297 | G | A | 4 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0009 others(1): Show |
27 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*517G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 517 | chr10 | 17715297 | ||||||
| chr10:17715384 | A | AAG | 14 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(11): Show |
127 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*608_*609dupGA | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 610 | INFO_REALIGN_3_PRIME | chr10 | 17715384 | |||||
| chr10:17715411 | A | G | 1 | a0001c0002t0022 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*631A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 631 | chr10 | 17715411 | ||||||
| chr10:17715474 | G | A | 1 | a0001c0002t0020 | 1 | NA18957.hp1 | 3_prime_UTR_variant | MODIFIER | c.*694G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 694 | chr10 | 17715474 | ||||||
| chr10:17715491 | T | G | 1 | a0001c0001t0014 | 2 | HG01346.hp1 HG01433.hp2 |
3_prime_UTR_variant | MODIFIER | c.*711T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 711 | chr10 | 17715491 | ||||||
| chr10:17715502 | A | AT | 4 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0009 others(1): Show |
27 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*723dupT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 724 | INFO_REALIGN_3_PRIME | chr10 | 17715502 | |||||
| chr10:17715734 | A | C | 1 | a0001c0001t0026 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*954A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 954 | chr10 | 17715734 | ||||||
| chr10:17715770 | G | A | 1 | a0001c0001t0019 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*990G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 990 | chr10 | 17715770 | ||||||
| chr10:17715813 | G | A | 1 | a0001c0001t0019 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1033G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 1033 | chr10 | 17715813 | ||||||
| chr10:17715863 | T | C | 5 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0018 others(2): Show |
41 | HG00642.hp2 HG01255.hp2 HG01256.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1083T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 1083 | chr10 | 17715863 | ||||||
| chr10:17715961 | C | A | 34 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(31): Show |
291 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(288): Show |
3_prime_UTR_variant | MODIFIER | c.*1181C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 1181 | chr10 | 17715961 | ||||||
| chr10:17715968 | T | G | 1 | a0001c0001t0006 | 5 | HG02615.hp2 HG02922.hp1 HG03195.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1188T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 1188 | chr10 | 17715968 | ||||||
| chr10:17716014 | T | C | 1 | a0001c0001t0024 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1234T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 1234 | chr10 | 17716014 | ||||||
| chr10:17716109 | C | T | 1 | a0001c0002t0021 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1329C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 1329 | chr10 | 17716109 | ||||||
| chr10:17716220 | A | C | 1 | a0001c0001t0016 | 2 | HG02109.hp2 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1440A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 1440 | chr10 | 17716220 | ||||||
| chr10:17716255 | C | G | 1 | a0001c0001t0031 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1475C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 1475 | chr10 | 17716255 | ||||||
| chr10:17716282 | G | T | 1 | a0001c0001t0025 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1502G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 1502 | chr10 | 17716282 | ||||||
| chr10:17716417 | C | T | 1 | a0001c0002t0022 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1637C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 1637 | chr10 | 17716417 | ||||||
| chr10:17716489 | T | G | 2 | a0001c0001t0012 a0001c0001t0023 |
3 | HG02970.hp1 HG03471.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1709T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 1709 | chr10 | 17716489 | ||||||
| chr10:17716497 | A | G | 1 | a0001c0002t0013 | 2 | NA19009.hp1 NA19063.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1717A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 1717 | chr10 | 17716497 | ||||||
| chr10:17716521 | T | C | 4 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0009 others(1): Show |
27 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1741T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 1741 | chr10 | 17716521 | ||||||
| chr10:17716525 | G | A | 4 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0009 others(1): Show |
27 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1745G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 1745 | chr10 | 17716525 | ||||||
| chr10:17716548 | A | G | 4 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0009 others(1): Show |
27 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1768A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 1768 | chr10 | 17716548 | ||||||
| chr10:17716612 | C | G | 2 | a0001c0001t0012 a0001c0001t0023 |
3 | HG02970.hp1 HG03471.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1832C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 1832 | chr10 | 17716612 | ||||||
| chr10:17716623 | T | C | 1 | a0001c0002t0022 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1843T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 1843 | chr10 | 17716623 | ||||||
| chr10:17716740 | C | A | 2 | a0001c0001t0015 a0001c0009t0015 |
2 | HG01884.hp2 HG02055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1960C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 1960 | chr10 | 17716740 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:17644392 | G | C | 4 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(1): Show |
4 | HG02145.hp1 HG03130.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.40+13G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17644392 | |||||||
| chr10:17644430 | C | G | 1 | a0001c0002t0003g0388 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.40+51C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17644430 | |||||||
| chr10:17644450 | A | C | 1 | a0001c0001t0002g0387 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.40+71A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17644450 | |||||||
| chr10:17644665 | G | A | 1 | a0001c0002t0003g0029 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.40+286G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17644665 | |||||||
| chr10:17644946 | C | A | 1 | a0001c0001t0001g0030 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.40+567C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17644946 | |||||||
| chr10:17645072 | C | G | 2 | a0001c0001t0015g0386 a0001c0009t0015g0385 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.40+693C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17645072 | |||||||
| chr10:17645101 | A | G | 1 | a0001c0001t0015g0386 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.40+722A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17645101 | |||||||
| chr10:17645128 | T | A | 29 | a0001c0001t0001g0031 a0001c0001t0002g0034 a0001c0001t0002g0037 others(26): Show |
32 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.40+749T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17645128 | |||||||
| chr10:17645149 | G | C | 1 | a0001c0001t0001g0030 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.40+770G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17645149 | |||||||
| chr10:17645219 | A | G | 1 | a0001c0001t0004g0384 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.40+840A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17645219 | |||||||
| chr10:17645554 | T | C | 105 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(102): Show |
114 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.40+1175T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17645554 | |||||||
| chr10:17645776 | G | A | 60 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(57): Show |
68 | HG00597.hp1 HG00609.hp2 HG01255.hp1 others(65): Show |
intron_variant | MODIFIER | c.40+1397G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17645776 | |||||||
| chr10:17645862 | GCTT | G | 3 | a0001c0001t0010g0109 a0001c0001t0010g0111 a0001c0001t0019g0110 |
3 | HG01192.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.40+1487_40+1489del others(3): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 17645862 | ||||||
| chr10:17645960 | A | G | 1 | a0001c0001t0004g0056 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.40+1581A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17645960 | |||||||
| chr10:17646071 | T | C | 1 | a0001c0001t0002g0153 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.40+1692T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17646071 | |||||||
| chr10:17646110 | C | T | 1 | a0001c0001t0012g0383 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.40+1731C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17646110 | |||||||
| chr10:17646279 | T | C | 1 | a0001c0002t0003g0154 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.40+1900T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17646279 | |||||||
| chr10:17646376 | A | C | 1 | a0001c0001t0001g0030 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.40+1997A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17646376 | |||||||
| chr10:17646490 | A | T | 1 | a0001c0001t0001g0152 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.40+2111A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17646490 | |||||||
| chr10:17646511 | A | T | 29 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(26): Show |
32 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.40+2132A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17646511 | |||||||
| chr10:17646607 | G | A | 8 | a0001c0001t0001g0158 a0001c0001t0003g0025 a0001c0001t0003g0026 others(5): Show |
8 | HG02145.hp1 HG02630.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.40+2228G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17646607 | |||||||
| chr10:17646759 | A | T | 1 | a0001c0001t0010g0111 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.40+2380A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17646759 | |||||||
| chr10:17647117 | C | T | 29 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(26): Show |
32 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.40+2738C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17647117 | |||||||
| chr10:17647118 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.40+2739G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17647118 | |||||||
| chr10:17647167 | A | G | 2 | a0001c0001t0030g0382 a0001c0001t0031g0381 |
2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.40+2788A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17647167 | |||||||
| chr10:17647302 | T | G | 16 | a0001c0002t0003g0029 a0001c0002t0003g0032 a0001c0002t0003g0159 others(13): Show |
16 | HG00099.hp2 HG01074.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.40+2923T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17647302 | |||||||
| chr10:17647389 | A | G | 20 | a0001c0001t0001g0356 a0001c0001t0001g0357 a0001c0001t0001g0359 others(17): Show |
20 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.40+3010A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17647389 | |||||||
| chr10:17647423 | A | C | 1 | a0001c0001t0001g0355 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.40+3044A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17647423 | |||||||
| chr10:17647462 | A | G | 16 | a0001c0002t0003g0029 a0001c0002t0003g0032 a0001c0002t0003g0159 others(13): Show |
16 | HG00099.hp2 HG01074.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.40+3083A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17647462 | |||||||
| chr10:17647578 | T | G | 20 | a0001c0001t0001g0356 a0001c0001t0001g0357 a0001c0001t0001g0359 others(17): Show |
20 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.40+3199T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17647578 | |||||||
| chr10:17647612 | T | C | 11 | a0001c0001t0002g0387 a0001c0001t0004g0017 a0001c0001t0004g0174 others(8): Show |
12 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.40+3233T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17647612 | |||||||
| chr10:17647652 | G | A | 2 | a0001c0001t0012g0182 a0001c0001t0012g0383 |
2 | HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.40+3273G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17647652 | |||||||
| chr10:17647821 | C | A | 14 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(11): Show |
16 | HG02132.hp2 NA18940.hp2 NA18943.hp1 others(13): Show |
intron_variant | MODIFIER | c.40+3442C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17647821 | |||||||
| chr10:17647822 | G | A | 9 | a0001c0001t0001g0158 a0001c0001t0003g0025 a0001c0001t0003g0026 others(6): Show |
9 | HG02145.hp1 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.40+3443G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17647822 | |||||||
| chr10:17647829 | G | C | 1 | a0001c0001t0029g0376 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.40+3450G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17647829 | |||||||
| chr10:17647854 | C | T | 3 | a0001c0001t0001g0005 a0001c0001t0001g0107 a0001c0001t0001g0108 |
5 | NA18952.hp1 NA18961.hp2 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.40+3475C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17647854 | |||||||
| chr10:17648012 | AGAC | A | 29 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(26): Show |
32 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.40+3637_40+3639del others(3): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 17648012 | ||||||
| chr10:17648052 | A | G | 2 | a0001c0001t0002g0024 a0001c0001t0002g0354 |
3 | HG01256.hp2 HG01258.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.40+3673A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17648052 | |||||||
| chr10:17648239 | C | T | 29 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(26): Show |
32 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.40+3860C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17648239 | |||||||
| chr10:17648350 | A | G | 1 | a0001c0001t0002g0353 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.40+3971A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17648350 | |||||||
| chr10:17648405 | G | T | 1 | a0001c0001t0001g0106 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.40+4026G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17648405 | |||||||
| chr10:17648462 | C | T | 51 | a0001c0001t0002g0313 a0001c0002t0003g0008 a0001c0002t0003g0009 others(48): Show |
56 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.40+4083C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17648462 | |||||||
| chr10:17648558 | A | G | 3 | a0001c0001t0002g0307 a0001c0001t0009g0308 a0001c0001t0009g0309 |
3 | NA18954.hp1 NA18959.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.40+4179A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17648558 | |||||||
| chr10:17648582 | G | A | 3 | a0001c0001t0017g0377 a0001c0001t0017g0378 a0001c0001t0029g0376 |
3 | HG02258.hp1 HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.40+4203G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17648582 | |||||||
| chr10:17648587 | C | CTAGACGC others(50): Show |
1 | a0001c0001t0002g0306 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.40+4208_40+4209ins others(57): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17648587 | |||||||
| chr10:17648588 | G | A | 2 | a0001c0001t0002g0306 a0001c0009t0015g0385 |
2 | HG01517.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.40+4209G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17648588 | |||||||
| chr10:17648670 | C | G | 1 | a0001c0001t0004g0305 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.40+4291C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17648670 | |||||||
| chr10:17648683 | T | C | 283 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(280): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.40+4304T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17648683 | |||||||
| chr10:17648842 | A | G | 8 | a0001c0001t0001g0158 a0001c0001t0003g0025 a0001c0001t0003g0026 others(5): Show |
8 | HG02145.hp1 HG02630.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.40+4463A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17648842 | |||||||
| chr10:17648963 | A | G | 1 | a0001c0003t0001g0151 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.40+4584A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17648963 | |||||||
| chr10:17648980 | T | C | 1 | a0001c0001t0002g0184 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.40+4601T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17648980 | |||||||
| chr10:17649141 | C | T | 29 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(26): Show |
32 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.40+4762C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17649141 | |||||||
| chr10:17649393 | TA | T | 238 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(235): Show |
253 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.40+5030delA | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 17649393 | ||||||
| chr10:17649427 | T | G | 1 | a0001c0001t0001g0115 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.40+5048T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17649427 | |||||||
| chr10:17649502 | T | G | 11 | a0001c0001t0002g0387 a0001c0001t0004g0017 a0001c0001t0004g0174 others(8): Show |
12 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.40+5123T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17649502 | |||||||
| chr10:17649523 | A | G | 29 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(26): Show |
32 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.40+5144A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17649523 | |||||||
| chr10:17649636 | G | A | 259 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(256): Show |
275 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.40+5257G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17649636 | |||||||
| chr10:17649673 | G | C | 29 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(26): Show |
32 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.40+5294G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17649673 | |||||||
| chr10:17649715 | G | A | 1 | a0001c0001t0001g0012 | 2 | NA18947.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.40+5336G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17649715 | |||||||
| chr10:17649904 | G | A | 1 | a0001c0001t0002g0217 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.40+5525G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17649904 | |||||||
| chr10:17649944 | C | G | 2 | a0001c0001t0015g0386 a0001c0009t0015g0385 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.40+5565C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17649944 | |||||||
| chr10:17650168 | G | A | 2 | a0001c0001t0030g0382 a0001c0001t0031g0381 |
2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.40+5789G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17650168 | |||||||
| chr10:17650189 | A | G | 1 | a0001c0001t0004g0305 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.40+5810A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17650189 | |||||||
| chr10:17650311 | C | A | 259 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(256): Show |
275 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.40+5932C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17650311 | |||||||
| chr10:17650451 | A | G | 102 | a0001c0001t0001g0158 a0001c0001t0002g0387 a0001c0001t0003g0025 others(99): Show |
106 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.40+6072A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17650451 | |||||||
| chr10:17650453 | T | G | 4 | a0001c0001t0004g0033 a0001c0001t0004g0056 a0001c0002t0003g0035 others(1): Show |
4 | HG01243.hp2 HG03516.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.40+6074T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17650453 | |||||||
| chr10:17650472 | G | C | 1 | a0001c0001t0001g0116 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.40+6093G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17650472 | |||||||
| chr10:17650505 | A | G | 3 | a0001c0001t0012g0182 a0001c0001t0012g0383 a0001c0001t0023g0187 |
3 | HG02970.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.40+6126A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17650505 | |||||||
| chr10:17650527 | C | G | 2 | a0001c0001t0001g0185 a0001c0001t0001g0186 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.40+6148C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17650527 | |||||||
| chr10:17650544 | T | C | 1 | a0001c0001t0031g0381 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.40+6165T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17650544 | |||||||
| chr10:17650606 | C | T | 1 | a0001c0001t0004g0305 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.40+6227C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17650606 | |||||||
| chr10:17650607 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.40+6228G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17650607 | |||||||
| chr10:17650699 | C | G | 4 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(1): Show |
4 | HG02145.hp1 HG03130.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.40+6320C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17650699 | |||||||
| chr10:17650759 | C | T | 31 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(28): Show |
34 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.40+6380C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17650759 | |||||||
| chr10:17650866 | C | T | 4 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(1): Show |
4 | HG02145.hp1 HG03130.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.40+6487C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17650866 | |||||||
| chr10:17650867 | C | G | 1 | a0001c0001t0002g0195 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.40+6488C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17650867 | |||||||
| chr10:17650917 | T | A | 104 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(101): Show |
113 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.40+6538T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17650917 | |||||||
| chr10:17650924 | G | A | 2 | a0001c0001t0004g0033 a0001c0001t0004g0056 |
2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.40+6545G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17650924 | |||||||
| chr10:17650925 | C | T | 4 | a0001c0001t0004g0033 a0001c0001t0004g0056 a0001c0002t0003g0035 others(1): Show |
4 | HG01243.hp2 HG03516.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.40+6546C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17650925 | |||||||
| chr10:17650926 | G | A | 1 | a0001c0002t0003g0372 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.40+6547G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17650926 | |||||||
| chr10:17650958 | A | G | 31 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(28): Show |
34 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.40+6579A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17650958 | |||||||
| chr10:17650982 | G | A | 2 | a0001c0001t0015g0386 a0001c0009t0015g0385 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.40+6603G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17650982 | |||||||
| chr10:17651035 | A | G | 31 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(28): Show |
34 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.40+6656A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17651035 | |||||||
| chr10:17651060 | G | A | 1 | a0001c0001t0004g0305 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.40+6681G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17651060 | |||||||
| chr10:17651060 | G | C | 1 | a0001c0001t0004g0033 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.40+6681G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17651060 | |||||||
| chr10:17651064 | C | CA | 24 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0119 others(21): Show |
24 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(21): Show |
intron_variant | MODIFIER | c.40+6712dupA | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 17651064 | ||||||
| chr10:17651064 | CA | C | 87 | a0001c0001t0001g0031 a0001c0001t0001g0059 a0001c0001t0001g0070 others(84): Show |
89 | HG00099.hp2 HG00558.hp1 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.40+6712delA | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 17651064 | ||||||
| chr10:17651064 | CAA | C | 127 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(124): Show |
139 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(136): Show |
intron_variant | MODIFIER | c.40+6711_40+6712del others(2): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 17651064 | ||||||
| chr10:17651064 | CAAA | C | 11 | a0001c0001t0001g0030 a0001c0001t0004g0215 a0001c0001t0005g0055 others(8): Show |
11 | HG00323.hp2 HG01884.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.40+6710_40+6712del others(3): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 17651064 | ||||||
| chr10:17651536 | A | G | 31 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(28): Show |
34 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.40+7157A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17651536 | |||||||
| chr10:17651563 | T | C | 31 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(28): Show |
34 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.40+7184T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17651563 | |||||||
| chr10:17651581 | A | G | 1 | a0001c0001t0009g0380 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.40+7202A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17651581 | |||||||
| chr10:17651625 | G | A | 1 | a0001c0001t0018g0173 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.40+7246G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17651625 | |||||||
| chr10:17651649 | C | G | 1 | a0001c0001t0001g0196 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.40+7270C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17651649 | |||||||
| chr10:17651804 | T | C | 1 | a0001c0001t0002g0217 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.40+7425T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17651804 | |||||||
| chr10:17651873 | C | A | 31 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(28): Show |
34 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.40+7494C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17651873 | |||||||
| chr10:17651913 | G | C | 253 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(250): Show |
269 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.40+7534G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17651913 | |||||||
| chr10:17651974 | A | G | 1 | a0001c0001t0004g0305 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.40+7595A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17651974 | |||||||
| chr10:17652041 | A | C | 1 | a0001c0001t0001g0146 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.40+7662A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17652041 | |||||||
| chr10:17652042 | A | G | 2 | a0002c0004t0001g0112 a0002c0004t0001g0114 |
2 | NA18978.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.40+7663A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17652042 | |||||||
| chr10:17652098 | A | G | 4 | a0001c0001t0004g0033 a0001c0001t0004g0056 a0001c0002t0003g0035 others(1): Show |
4 | HG01243.hp2 HG03516.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.40+7719A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17652098 | |||||||
| chr10:17652247 | TA | T | 16 | a0001c0001t0001g0030 a0001c0001t0001g0356 a0001c0001t0001g0359 others(13): Show |
16 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.40+7878delA | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 17652247 | ||||||
| chr10:17652286 | T | C | 1 | a0001c0001t0009g0380 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.40+7907T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17652286 | |||||||
| chr10:17652313 | A | G | 31 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(28): Show |
34 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.40+7934A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17652313 | |||||||
| chr10:17652336 | C | T | 2 | a0001c0001t0002g0297 a0001c0001t0002g0298 |
2 | HG02027.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.40+7957C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17652336 | |||||||
| chr10:17652450 | A | G | 31 | a0001c0001t0004g0017 a0001c0001t0004g0018 a0001c0001t0004g0174 others(28): Show |
33 | HG00642.hp2 HG01255.hp2 HG01256.hp1 others(30): Show |
intron_variant | MODIFIER | c.41-8014A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17652450 | |||||||
| chr10:17652508 | T | C | 31 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(28): Show |
34 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.41-7956T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17652508 | |||||||
| chr10:17652551 | C | G | 21 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(18): Show |
24 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.41-7913C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17652551 | |||||||
| chr10:17652596 | T | C | 1 | a0001c0001t0023g0187 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.41-7868T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17652596 | |||||||
| chr10:17652606 | G | A | 253 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(250): Show |
269 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.41-7858G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17652606 | |||||||
| chr10:17652654 | C | T | 1 | a0001c0002t0003g0346 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.41-7810C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17652654 | |||||||
| chr10:17652757 | T | C | 1 | a0001c0002t0022g0183 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.41-7707T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17652757 | |||||||
| chr10:17652865 | T | C | 2 | a0001c0001t0001g0185 a0001c0001t0001g0186 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.41-7599T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17652865 | |||||||
| chr10:17652957 | C | G | 7 | a0001c0001t0001g0149 a0001c0001t0001g0152 a0001c0001t0001g0355 others(4): Show |
7 | HG01192.hp1 HG02572.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.41-7507C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17652957 | |||||||
| chr10:17652997 | T | C | 1 | a0001c0002t0003g0312 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.41-7467T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17652997 | |||||||
| chr10:17653185 | A | G | 21 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(18): Show |
24 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.41-7279A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17653185 | |||||||
| chr10:17653284 | C | T | 1 | a0001c0001t0029g0376 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.41-7180C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17653284 | |||||||
| chr10:17653324 | T | A | 1 | a0001c0001t0002g0230 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.41-7140T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17653324 | |||||||
| chr10:17653337 | T | G | 1 | a0001c0001t0031g0381 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.41-7127T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17653337 | |||||||
| chr10:17653355 | A | T | 29 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(26): Show |
32 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.41-7109A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17653355 | |||||||
| chr10:17653395 | A | T | 18 | a0001c0001t0001g0356 a0001c0001t0001g0359 a0001c0001t0001g0360 others(15): Show |
18 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.41-7069A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17653395 | |||||||
| chr10:17653471 | T | C | 31 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(28): Show |
34 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.41-6993T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17653471 | |||||||
| chr10:17653524 | C | T | 7 | a0001c0001t0004g0175 a0001c0001t0004g0176 a0001c0001t0004g0177 others(4): Show |
7 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.41-6940C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17653524 | |||||||
| chr10:17653587 | C | A | 10 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0002g0034 others(7): Show |
10 | HG00099.hp1 HG02109.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.41-6877C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17653587 | |||||||
| chr10:17653618 | T | G | 1 | a0001c0001t0004g0204 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.41-6846T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17653618 | |||||||
| chr10:17653718 | G | A | 31 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(28): Show |
34 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.41-6746G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17653718 | |||||||
| chr10:17653773 | A | G | 35 | a0001c0001t0001g0016 a0001c0001t0001g0115 a0001c0001t0001g0116 others(32): Show |
36 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.41-6691A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17653773 | |||||||
| chr10:17653789 | G | A | 1 | a0001c0001t0004g0215 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.41-6675G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17653789 | |||||||
| chr10:17653938 | A | G | 1 | a0001c0001t0002g0192 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.41-6526A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17653938 | |||||||
| chr10:17654025 | C | T | 1 | a0001c0002t0003g0372 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.41-6439C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654025 | |||||||
| chr10:17654074 | G | T | 2 | a0001c0001t0015g0386 a0001c0009t0015g0385 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.41-6390G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654074 | |||||||
| chr10:17654105 | G | A | 31 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(28): Show |
34 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.41-6359G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654105 | |||||||
| chr10:17654214 | G | GTTA | 74 | a0001c0001t0002g0231 a0001c0001t0002g0313 a0001c0002t0003g0008 others(71): Show |
79 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.41-6229_41-6227dup others(3): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 17654214 | ||||||
| chr10:17654226 | A | G | 31 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(28): Show |
34 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.41-6238A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654226 | |||||||
| chr10:17654228 | T | C | 8 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(5): Show |
8 | HG02280.hp1 HG02451.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.41-6236T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654228 | |||||||
| chr10:17654229 | A | G | 1 | a0001c0001t0004g0181 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.41-6235A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654229 | |||||||
| chr10:17654246 | G | A | 2 | a0001c0001t0001g0117 a0001c0001t0001g0124 |
2 | HG00140.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.41-6218G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654246 | |||||||
| chr10:17654284 | A | G | 21 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(18): Show |
24 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.41-6180A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654284 | |||||||
| chr10:17654285 | T | C | 21 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(18): Show |
24 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.41-6179T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654285 | |||||||
| chr10:17654324 | G | A | 2 | a0001c0001t0001g0079 a0001c0001t0002g0232 |
2 | HG01071.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.41-6140G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654324 | |||||||
| chr10:17654359 | A | T | 3 | a0001c0001t0017g0377 a0001c0001t0017g0378 a0001c0001t0029g0376 |
3 | HG02258.hp1 HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.41-6105A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654359 | |||||||
| chr10:17654367 | C | T | 2 | a0001c0003t0001g0122 a0001c0003t0001g0123 |
2 | NA18966.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.41-6097C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654367 | |||||||
| chr10:17654373 | C | T | 2 | a0001c0001t0005g0054 a0001c0001t0005g0055 |
2 | HG00323.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.41-6091C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654373 | |||||||
| chr10:17654513 | C | T | 2 | a0001c0001t0015g0386 a0001c0009t0015g0385 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.41-5951C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654513 | |||||||
| chr10:17654517 | C | T | 6 | a0001c0001t0004g0204 a0001c0001t0004g0211 a0001c0001t0004g0213 others(3): Show |
6 | HG02451.hp1 HG02559.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.41-5947C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654517 | |||||||
| chr10:17654587 | T | A | 4 | a0001c0002t0003g0317 a0001c0002t0003g0318 a0001c0002t0003g0319 others(1): Show |
4 | HG02155.hp1 HG02165.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-5877T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654587 | |||||||
| chr10:17654702 | G | A | 4 | a0001c0001t0009g0380 a0001c0001t0017g0377 a0001c0001t0017g0378 others(1): Show |
4 | HG02258.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-5762G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654702 | |||||||
| chr10:17654709 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.41-5755T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654709 | |||||||
| chr10:17654725 | A | G | 2 | a0001c0001t0002g0295 a0001c0001t0002g0296 |
2 | NA18968.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.41-5739A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654725 | |||||||
| chr10:17654758 | T | G | 21 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(18): Show |
24 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.41-5706T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654758 | |||||||
| chr10:17654793 | G | A | 14 | a0001c0001t0001g0356 a0001c0001t0001g0359 a0001c0001t0001g0360 others(11): Show |
14 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.41-5671G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654793 | |||||||
| chr10:17654795 | C | G | 14 | a0001c0001t0001g0356 a0001c0001t0001g0359 a0001c0001t0001g0360 others(11): Show |
14 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.41-5669C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654795 | |||||||
| chr10:17654834 | G | A | 100 | a0001c0001t0001g0158 a0001c0001t0003g0025 a0001c0001t0003g0026 others(97): Show |
104 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.41-5630G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654834 | |||||||
| chr10:17655023 | T | A | 2 | a0001c0001t0004g0033 a0001c0001t0004g0056 |
2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.41-5441T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17655023 | |||||||
| chr10:17655052 | A | G | 29 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(26): Show |
32 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.41-5412A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17655052 | |||||||
| chr10:17655201 | T | C | 1 | a0001c0001t0002g0306 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.41-5263T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17655201 | |||||||
| chr10:17655324 | T | C | 1 | a0001c0001t0001g0030 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.41-5140T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17655324 | |||||||
| chr10:17655342 | T | C | 27 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(24): Show |
30 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.41-5122T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17655342 | |||||||
| chr10:17655346 | A | T | 31 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(28): Show |
34 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.41-5118A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17655346 | |||||||
| chr10:17655348 | G | T | 29 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(26): Show |
32 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.41-5116G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17655348 | |||||||
| chr10:17655358 | G | C | 1 | a0001c0001t0002g0358 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.41-5106G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17655358 | |||||||
| chr10:17655440 | T | C | 1 | a0001c0001t0001g0364 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.41-5024T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17655440 | |||||||
| chr10:17655487 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.41-4977C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17655487 | |||||||
| chr10:17655488 | G | A | 102 | a0001c0001t0001g0158 a0001c0001t0003g0025 a0001c0001t0003g0026 others(99): Show |
106 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.41-4976G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17655488 | |||||||
| chr10:17655516 | C | A | 2 | a0001c0001t0015g0386 a0001c0009t0015g0385 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.41-4948C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17655516 | |||||||
| chr10:17655526 | T | C | 2 | a0001c0003t0001g0118 a0001c0003t0001g0151 |
2 | NA19070.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.41-4938T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17655526 | |||||||
| chr10:17655534 | A | G | 6 | a0001c0001t0004g0018 a0001c0001t0004g0197 a0001c0001t0004g0198 others(3): Show |
7 | HG00642.hp2 HG02976.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.41-4930A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17655534 | |||||||
| chr10:17655603 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.41-4861G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17655603 | |||||||
| chr10:17655644 | T | G | 1 | a0001c0001t0002g0387 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.41-4820T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17655644 | |||||||
| chr10:17655707 | A | C | 9 | a0001c0001t0001g0158 a0001c0001t0003g0025 a0001c0001t0003g0026 others(6): Show |
9 | HG02145.hp1 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.41-4757A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17655707 | |||||||
| chr10:17655880 | C | T | 1 | a0001c0001t0002g0294 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.41-4584C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17655880 | |||||||
| chr10:17655938 | C | T | 1 | a0001c0008t0001g0371 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.41-4526C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17655938 | |||||||
| chr10:17655942 | CGT | C | 31 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(28): Show |
34 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.41-4517_41-4516del others(2): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 17655942 | ||||||
| chr10:17656074 | C | T | 29 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(26): Show |
32 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.41-4390C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17656074 | |||||||
| chr10:17656111 | A | G | 390 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(387): Show |
423 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(420): Show |
intron_variant | MODIFIER | c.41-4353A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17656111 | |||||||
| chr10:17656245 | G | A | 31 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(28): Show |
34 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.41-4219G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17656245 | |||||||
| chr10:17656280 | C | T | 53 | a0001c0002t0003g0009 a0001c0002t0003g0023 a0001c0002t0003g0029 others(50): Show |
55 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.41-4184C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17656280 | |||||||
| chr10:17656288 | C | T | 4 | a0001c0001t0009g0380 a0001c0001t0017g0377 a0001c0001t0017g0378 others(1): Show |
4 | HG02258.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-4176C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17656288 | |||||||
| chr10:17656292 | T | TC | 4 | a0001c0001t0017g0377 a0001c0001t0017g0378 a0001c0001t0029g0376 others(1): Show |
4 | HG02258.hp1 HG02280.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-4172_41-4171ins others(1): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17656292 | |||||||
| chr10:17656293 | T | A | 4 | a0001c0001t0017g0377 a0001c0001t0017g0378 a0001c0001t0029g0376 others(1): Show |
4 | HG02258.hp1 HG02280.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-4171T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17656293 | |||||||
| chr10:17656293 | T | C | 25 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(22): Show |
28 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.41-4171T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17656293 | |||||||
| chr10:17656293 | T | TA | 15 | a0001c0001t0001g0106 a0001c0001t0002g0295 a0001c0001t0004g0017 others(12): Show |
16 | HG01243.hp2 HG01255.hp2 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.41-4150dupA | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 17656293 | ||||||
| chr10:17656293 | TA | T | 92 | a0001c0001t0001g0016 a0001c0001t0001g0069 a0001c0001t0001g0115 others(89): Show |
95 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.41-4150delA | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 17656293 | ||||||
| chr10:17656294 | A | C | 2 | a0001c0001t0005g0053 a0001c0001t0005g0055 |
2 | HG00323.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.41-4170A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17656294 | |||||||
| chr10:17656495 | T | G | 1 | a0001c0001t0001g0126 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.41-3969T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17656495 | |||||||
| chr10:17656515 | C | G | 4 | a0001c0002t0003g0317 a0001c0002t0003g0318 a0001c0002t0003g0319 others(1): Show |
4 | HG02155.hp1 HG02165.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-3949C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17656515 | |||||||
| chr10:17656529 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.41-3935C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17656529 | |||||||
| chr10:17656563 | C | T | 3 | a0001c0001t0001g0030 a0001c0006t0028g0379 a0001c0009t0015g0385 |
3 | HG02055.hp1 HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.41-3901C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17656563 | |||||||
| chr10:17656564 | G | A | 1 | a0001c0001t0012g0182 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.41-3900G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17656564 | |||||||
| chr10:17656567 | A | T | 31 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(28): Show |
34 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.41-3897A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17656567 | |||||||
| chr10:17656614 | C | T | 104 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(101): Show |
113 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.41-3850C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17656614 | |||||||
| chr10:17656738 | C | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0104 |
3 | NA18944.hp1 NA18963.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.41-3726C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17656738 | |||||||
| chr10:17656857 | C | A | 31 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(28): Show |
34 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.41-3607C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17656857 | |||||||
| chr10:17656879 | T | C | 273 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(270): Show |
292 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(289): Show |
intron_variant | MODIFIER | c.41-3585T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17656879 | |||||||
| chr10:17656966 | C | T | 4 | a0001c0001t0001g0158 a0001c0001t0003g0155 a0001c0001t0003g0156 others(1): Show |
4 | HG02630.hp2 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-3498C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17656966 | |||||||
| chr10:17657044 | A | G | 4 | a0001c0001t0001g0355 a0001c0001t0012g0182 a0001c0001t0012g0383 others(1): Show |
4 | HG02630.hp1 HG02970.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-3420A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17657044 | |||||||
| chr10:17657049 | A | G | 4 | a0001c0001t0001g0355 a0001c0001t0012g0182 a0001c0001t0012g0383 others(1): Show |
4 | HG02630.hp1 HG02970.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-3415A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17657049 | |||||||
| chr10:17657056 | T | C | 31 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(28): Show |
34 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.41-3408T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17657056 | |||||||
| chr10:17657144 | C | G | 1 | a0001c0009t0015g0385 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.41-3320C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17657144 | |||||||
| chr10:17657196 | T | A | 267 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(264): Show |
286 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(283): Show |
intron_variant | MODIFIER | c.41-3268T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17657196 | |||||||
| chr10:17657223 | G | A | 31 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(28): Show |
34 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.41-3241G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17657223 | |||||||
| chr10:17657239 | C | T | 1 | a0001c0001t0002g0291 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.41-3225C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17657239 | |||||||
| chr10:17657343 | C | T | 1 | a0001c0001t0002g0290 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.41-3121C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17657343 | |||||||
| chr10:17657399 | T | C | 1 | a0001c0001t0002g0235 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.41-3065T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17657399 | |||||||
| chr10:17657471 | G | T | 2 | a0001c0002t0003g0319 a0001c0002t0003g0320 |
2 | HG02155.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.41-2993G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17657471 | |||||||
| chr10:17657593 | T | G | 29 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(26): Show |
32 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.41-2871T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17657593 | |||||||
| chr10:17657608 | A | G | 3 | a0001c0001t0012g0182 a0001c0001t0012g0383 a0001c0001t0023g0187 |
3 | HG02970.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.41-2856A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17657608 | |||||||
| chr10:17657660 | A | G | 1 | a0001c0001t0001g0144 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.41-2804A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17657660 | |||||||
| chr10:17657685 | A | G | 2 | a0001c0001t0001g0031 a0001c0001t0001g0070 |
2 | HG01975.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.41-2779A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17657685 | |||||||
| chr10:17657704 | G | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0104 |
3 | NA18944.hp1 NA18963.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.41-2760G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17657704 | |||||||
| chr10:17657841 | T | TTCTC | 3 | a0001c0001t0015g0386 a0001c0006t0028g0379 a0001c0009t0015g0385 |
3 | HG01884.hp2 HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.41-2617_41-2614dup others(4): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 17657841 | ||||||
| chr10:17657849 | C | CTCTCT | 28 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(25): Show |
31 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.41-2614_41-2613ins others(5): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 17657849 | ||||||
| chr10:17657890 | C | T | 4 | a0001c0001t0004g0033 a0001c0001t0004g0056 a0001c0002t0003g0035 others(1): Show |
4 | HG01243.hp2 HG03516.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-2574C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17657890 | |||||||
| chr10:17657903 | C | A | 1 | a0001c0001t0029g0376 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.41-2561C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17657903 | |||||||
| chr10:17658197 | GT | G | 31 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(28): Show |
34 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.41-2257delT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 17658197 | ||||||
| chr10:17658231 | T | G | 1 | a0001c0006t0028g0379 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.41-2233T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17658231 | |||||||
| chr10:17658246 | G | T | 1 | a0001c0001t0001g0149 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.41-2218G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17658246 | |||||||
| chr10:17658302 | A | G | 1 | a0001c0001t0023g0187 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.41-2162A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17658302 | |||||||
| chr10:17658308 | T | G | 1 | a0001c0002t0022g0183 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.41-2156T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17658308 | |||||||
| chr10:17658432 | A | G | 31 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(28): Show |
34 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.41-2032A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17658432 | |||||||
| chr10:17658446 | A | G | 2 | a0001c0001t0001g0152 a0001c0001t0002g0150 |
2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.41-2018A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17658446 | |||||||
| chr10:17658527 | TC | T | 31 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(28): Show |
34 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.41-1936delC | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17658527 | |||||||
| chr10:17658536 | G | A | 1 | a0001c0001t0004g0305 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.41-1928G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17658536 | |||||||
| chr10:17658539 | C | G | 4 | a0001c0001t0004g0033 a0001c0001t0004g0056 a0001c0002t0003g0035 others(1): Show |
4 | HG01243.hp2 HG03516.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-1925C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17658539 | |||||||
| chr10:17658573 | C | T | 1 | a0001c0002t0021g0172 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.41-1891C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17658573 | |||||||
| chr10:17658738 | C | G | 1 | a0001c0001t0001g0068 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.41-1726C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17658738 | |||||||
| chr10:17658738 | C | T | 2 | a0001c0001t0030g0382 a0001c0001t0031g0381 |
2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.41-1726C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17658738 | |||||||
| chr10:17658809 | T | G | 1 | a0001c0001t0005g0042 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.41-1655T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17658809 | |||||||
| chr10:17658853 | A | T | 2 | a0001c0001t0001g0152 a0001c0001t0002g0150 |
2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.41-1611A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17658853 | |||||||
| chr10:17658859 | G | A | 30 | a0001c0001t0001g0030 a0001c0001t0002g0236 a0001c0001t0005g0004 others(27): Show |
33 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.41-1605G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17658859 | |||||||
| chr10:17658925 | A | C | 1 | a0001c0001t0031g0381 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.41-1539A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17658925 | |||||||
| chr10:17658926 | T | A | 1 | a0001c0001t0018g0173 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.41-1538T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17658926 | |||||||
| chr10:17658965 | A | G | 2 | a0001c0001t0015g0386 a0001c0009t0015g0385 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.41-1499A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17658965 | |||||||
| chr10:17659115 | C | CT | 112 | a0001c0001t0001g0158 a0001c0001t0002g0313 a0001c0001t0003g0025 others(109): Show |
119 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.41-1339dupT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 17659115 | ||||||
| chr10:17659117 | T | C | 1 | a0001c0001t0002g0237 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.41-1347T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17659117 | |||||||
| chr10:17659265 | G | A | 30 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(27): Show |
33 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.41-1199G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17659265 | |||||||
| chr10:17659374 | C | T | 1 | a0001c0001t0030g0382 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.41-1090C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17659374 | |||||||
| chr10:17659463 | C | CT | 184 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(181): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.41-979dupT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 17659463 | ||||||
| chr10:17659463 | C | CTTTTT | 19 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(16): Show |
22 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.41-983_41-979dupTT others(3): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 17659463 | ||||||
| chr10:17659463 | CT | C | 14 | a0001c0001t0002g0230 a0001c0001t0002g0237 a0001c0001t0002g0238 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.41-979delT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 17659463 | ||||||
| chr10:17659560 | T | C | 31 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(28): Show |
34 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.41-904T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17659560 | |||||||
| chr10:17659595 | G | A | 1 | a0001c0009t0015g0385 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.41-869G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17659595 | |||||||
| chr10:17659614 | G | A | 1 | a0001c0001t0002g0236 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.41-850G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17659614 | |||||||
| chr10:17659631 | G | A | 2 | a0001c0001t0004g0033 a0001c0001t0004g0056 |
2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.41-833G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17659631 | |||||||
| chr10:17659768 | T | G | 1 | a0001c0001t0002g0387 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.41-696T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17659768 | |||||||
| chr10:17659948 | C | T | 4 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(1): Show |
4 | HG02145.hp1 HG03130.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-516C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17659948 | |||||||
| chr10:17660032 | T | G | 1 | a0001c0001t0004g0206 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.41-432T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17660032 | |||||||
| chr10:17660049 | C | A | 2 | a0001c0001t0015g0386 a0001c0009t0015g0385 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.41-415C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17660049 | |||||||
| chr10:17660049 | C | CA | 24 | a0001c0001t0001g0119 a0001c0001t0001g0364 a0001c0001t0001g0366 others(21): Show |
27 | HG02071.hp2 HG02074.hp1 HG02698.hp2 others(24): Show |
intron_variant | MODIFIER | c.41-405dupA | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 17660049 | ||||||
| chr10:17660049 | C | CAA | 29 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(26): Show |
32 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.41-406_41-405dupAA | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 17660049 | ||||||
| chr10:17660095 | T | C | 1 | a0001c0009t0015g0385 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.41-369T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17660095 | |||||||
| chr10:17660119 | T | C | 1 | a0001c0001t0004g0305 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.41-345T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17660119 | |||||||
| chr10:17660123 | A | G | 1 | a0001c0002t0022g0183 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.41-341A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17660123 | |||||||
| chr10:17660154 | A | G | 16 | a0001c0002t0003g0029 a0001c0002t0003g0032 a0001c0002t0003g0159 others(13): Show |
16 | HG00099.hp2 HG01074.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.41-310A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17660154 | |||||||
| chr10:17660264 | T | C | 29 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(26): Show |
32 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.41-200T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17660264 | |||||||
| chr10:17660337 | A | C | 1 | a0001c0001t0006g0210 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.41-127A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17660337 | |||||||
| chr10:17660599 | C | T | 1 | a0001c0001t0004g0305 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.125+51C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17660599 | |||||||
| chr10:17660617 | G | A | 2 | a0001c0001t0030g0382 a0001c0001t0031g0381 |
2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.125+69G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17660617 | |||||||
| chr10:17660641 | C | T | 105 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(102): Show |
114 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.125+93C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17660641 | |||||||
| chr10:17660658 | G | A | 1 | a0001c0001t0029g0376 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.125+110G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17660658 | |||||||
| chr10:17661293 | G | T | 1 | a0001c0001t0002g0286 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.125+745G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17661293 | |||||||
| chr10:17661480 | A | C | 2 | a0001c0001t0030g0382 a0001c0001t0031g0381 |
2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.125+932A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17661480 | |||||||
| chr10:17661488 | G | A | 10 | a0001c0001t0005g0004 a0001c0001t0005g0042 a0001c0001t0005g0043 others(7): Show |
12 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.125+940G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17661488 | |||||||
| chr10:17661501 | G | T | 255 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(252): Show |
271 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(268): Show |
intron_variant | MODIFIER | c.125+953G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17661501 | |||||||
| chr10:17661556 | C | T | 1 | a0001c0002t0013g0329 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.125+1008C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17661556 | |||||||
| chr10:17661586 | A | G | 1 | a0001c0001t0002g0150 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.125+1038A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17661586 | |||||||
| chr10:17661613 | T | C | 31 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(28): Show |
34 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.125+1065T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17661613 | |||||||
| chr10:17661629 | T | C | 31 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(28): Show |
34 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.125+1081T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17661629 | |||||||
| chr10:17661695 | T | C | 31 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(28): Show |
34 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.125+1147T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17661695 | |||||||
| chr10:17661711 | A | G | 1 | a0001c0001t0001g0068 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.125+1163A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17661711 | |||||||
| chr10:17661742 | A | G | 2 | a0001c0001t0015g0386 a0001c0009t0015g0385 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.125+1194A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17661742 | |||||||
| chr10:17661784 | T | C | 31 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(28): Show |
34 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.125+1236T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17661784 | |||||||
| chr10:17661872 | C | T | 2 | a0001c0002t0003g0319 a0001c0002t0003g0320 |
2 | HG02155.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.125+1324C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17661872 | |||||||
| chr10:17661908 | T | TC | 269 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(266): Show |
288 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(285): Show |
intron_variant | MODIFIER | c.125+1363dupC | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17661908 | ||||||
| chr10:17661972 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.125+1424T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17661972 | |||||||
| chr10:17661995 | C | T | 105 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(102): Show |
114 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.125+1447C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17661995 | |||||||
| chr10:17662063 | G | A | 1 | a0001c0001t0002g0244 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.125+1515G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17662063 | |||||||
| chr10:17662256 | G | A | 4 | a0001c0001t0004g0033 a0001c0001t0004g0056 a0001c0002t0003g0035 others(1): Show |
4 | HG01243.hp2 HG03516.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.125+1708G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17662256 | |||||||
| chr10:17662373 | A | G | 31 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(28): Show |
34 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.125+1825A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17662373 | |||||||
| chr10:17662446 | C | T | 1 | a0001c0002t0003g0029 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.125+1898C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17662446 | |||||||
| chr10:17662543 | G | C | 1 | a0001c0001t0001g0071 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.125+1995G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17662543 | |||||||
| chr10:17662544 | A | G | 1 | a0001c0001t0001g0363 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.125+1996A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17662544 | |||||||
| chr10:17662634 | A | T | 257 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(254): Show |
273 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(270): Show |
intron_variant | MODIFIER | c.125+2086A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17662634 | |||||||
| chr10:17662889 | C | T | 4 | a0001c0001t0009g0380 a0001c0001t0017g0377 a0001c0001t0017g0378 others(1): Show |
4 | HG02258.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.125+2341C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17662889 | |||||||
| chr10:17662902 | C | G | 2 | a0001c0001t0015g0386 a0001c0009t0015g0385 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.125+2354C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17662902 | |||||||
| chr10:17662966 | C | G | 1 | a0001c0001t0015g0386 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.125+2418C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17662966 | |||||||
| chr10:17663025 | C | T | 1 | a0001c0001t0001g0357 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.125+2477C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17663025 | |||||||
| chr10:17663195 | T | C | 1 | a0001c0001t0009g0380 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.125+2647T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17663195 | |||||||
| chr10:17663214 | G | C | 1 | a0001c0001t0001g0072 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.125+2666G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17663214 | |||||||
| chr10:17663288 | A | T | 1 | a0001c0005t0001g0080 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.125+2740A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17663288 | |||||||
| chr10:17663288 | AT | A | 31 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(28): Show |
34 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.125+2746delT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17663288 | ||||||
| chr10:17663334 | A | G | 1 | a0001c0001t0002g0231 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.125+2786A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17663334 | |||||||
| chr10:17663340 | A | T | 1 | a0001c0002t0003g0345 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.125+2792A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17663340 | |||||||
| chr10:17663453 | G | A | 31 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(28): Show |
34 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.125+2905G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17663453 | |||||||
| chr10:17663508 | T | C | 3 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 |
3 | NA18970.hp1 NA18991.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.125+2960T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17663508 | |||||||
| chr10:17663653 | A | G | 4 | a0001c0001t0002g0034 a0001c0001t0002g0193 a0001c0001t0002g0194 others(1): Show |
4 | HG02109.hp1 HG03041.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.125+3105A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17663653 | |||||||
| chr10:17663898 | A | G | 2 | a0001c0001t0015g0386 a0001c0009t0015g0385 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.125+3350A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17663898 | |||||||
| chr10:17663909 | A | G | 2 | a0001c0001t0015g0386 a0001c0009t0015g0385 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.125+3361A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17663909 | |||||||
| chr10:17663921 | C | A | 31 | a0001c0001t0001g0030 a0001c0001t0005g0004 a0001c0001t0005g0010 others(28): Show |
34 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.125+3373C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17663921 | |||||||
| chr10:17663949 | G | T | 1 | a0001c0009t0015g0385 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.125+3401G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17663949 | |||||||
| chr10:17664009 | A | G | 1 | a0001c0001t0002g0387 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.125+3461A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17664009 | |||||||
| chr10:17664081 | AAT | A | 29 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(26): Show |
32 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.125+3535_125+3536d others(4): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17664081 | ||||||
| chr10:17664114 | G | T | 214 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(211): Show |
226 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.125+3566G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17664114 | |||||||
| chr10:17664137 | C | T | 41 | a0001c0002t0003g0009 a0001c0002t0003g0023 a0001c0002t0003g0154 others(38): Show |
43 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.125+3589C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17664137 | |||||||
| chr10:17664147 | C | T | 73 | a0001c0001t0001g0158 a0001c0001t0003g0025 a0001c0001t0003g0026 others(70): Show |
76 | HG00323.hp1 HG00558.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.125+3599C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17664147 | |||||||
| chr10:17664167 | A | G | 34 | a0001c0001t0001g0356 a0001c0001t0001g0359 a0001c0001t0001g0360 others(31): Show |
34 | HG00099.hp2 HG01069.hp1 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.125+3619A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17664167 | |||||||
| chr10:17664341 | T | C | 29 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(26): Show |
32 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.125+3793T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17664341 | |||||||
| chr10:17664354 | G | A | 1 | a0001c0002t0004g0330 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.125+3806G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17664354 | |||||||
| chr10:17664377 | C | T | 1 | a0001c0001t0002g0387 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.125+3829C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17664377 | |||||||
| chr10:17664387 | A | C | 3 | a0001c0001t0012g0182 a0001c0001t0012g0383 a0001c0001t0023g0187 |
3 | HG02970.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.125+3839A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17664387 | |||||||
| chr10:17664461 | C | T | 39 | a0001c0001t0004g0017 a0001c0001t0004g0174 a0001c0001t0004g0175 others(36): Show |
43 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.125+3913C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17664461 | |||||||
| chr10:17664594 | G | C | 1 | a0001c0006t0028g0379 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.125+4046G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17664594 | |||||||
| chr10:17664684 | T | C | 6 | a0001c0001t0004g0204 a0001c0001t0004g0211 a0001c0001t0004g0213 others(3): Show |
6 | HG02451.hp1 HG02559.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.125+4136T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17664684 | |||||||
| chr10:17664772 | C | A | 1 | a0001c0001t0005g0049 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.125+4224C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17664772 | |||||||
| chr10:17664799 | A | G | 6 | a0001c0001t0001g0285 a0001c0001t0002g0021 a0001c0001t0002g0039 others(3): Show |
7 | NA18943.hp2 NA18947.hp2 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.125+4251A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17664799 | |||||||
| chr10:17664840 | G | A | 2 | a0001c0001t0003g0026 a0001c0001t0003g0028 |
2 | HG02145.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.125+4292G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17664840 | |||||||
| chr10:17664843 | C | T | 1 | a0001c0001t0004g0305 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.125+4295C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17664843 | |||||||
| chr10:17664992 | T | C | 2 | a0001c0001t0001g0081 a0001c0001t0001g0088 |
2 | HG01255.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.125+4444T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17664992 | |||||||
| chr10:17665005 | T | G | 1 | a0001c0001t0005g0054 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.125+4457T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17665005 | |||||||
| chr10:17665100 | C | G | 102 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(99): Show |
111 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.125+4552C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17665100 | |||||||
| chr10:17665102 | A | G | 2 | a0001c0001t0004g0018 a0001c0001t0004g0201 |
3 | HG02976.hp1 HG03225.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.125+4554A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17665102 | |||||||
| chr10:17665150 | T | C | 1 | a0001c0001t0001g0129 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.125+4602T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17665150 | |||||||
| chr10:17665153 | CAGT | C | 103 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(100): Show |
112 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.125+4606_125+4608d others(5): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17665153 | |||||||
| chr10:17665226 | T | C | 29 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(26): Show |
32 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.125+4678T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17665226 | |||||||
| chr10:17665424 | A | G | 2 | a0001c0002t0003g0170 a0001c0002t0003g0171 |
2 | HG02738.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.125+4876A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17665424 | |||||||
| chr10:17665465 | T | A | 1 | a0001c0002t0003g0216 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.125+4917T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17665465 | |||||||
| chr10:17665554 | T | A | 1 | a0001c0002t0003g0331 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.125+5006T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17665554 | |||||||
| chr10:17665669 | C | T | 261 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(258): Show |
280 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(277): Show |
intron_variant | MODIFIER | c.125+5121C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17665669 | |||||||
| chr10:17665766 | G | A | 2 | a0001c0001t0004g0033 a0001c0001t0004g0056 |
2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.125+5218G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17665766 | |||||||
| chr10:17665872 | C | T | 29 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(26): Show |
32 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.125+5324C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17665872 | |||||||
| chr10:17665950 | T | C | 1 | a0001c0002t0004g0332 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.125+5402T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17665950 | |||||||
| chr10:17665983 | A | G | 1 | a0001c0001t0001g0067 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.125+5435A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17665983 | |||||||
| chr10:17665994 | C | A | 261 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(258): Show |
280 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(277): Show |
intron_variant | MODIFIER | c.125+5446C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17665994 | |||||||
| chr10:17666385 | G | GTTTTTTT others(5): Show |
1 | a0001c0001t0017g0378 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.125+5838_125+5839i others(14): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17666385 | ||||||
| chr10:17666387 | A | AT | 140 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0015 others(137): Show |
151 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.125+5864dupT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17666387 | ||||||
| chr10:17666387 | A | ATT | 58 | a0001c0001t0001g0003 a0001c0001t0001g0060 a0001c0001t0001g0061 others(55): Show |
60 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.125+5863_125+5864d others(4): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17666387 | ||||||
| chr10:17666387 | A | ATTT | 10 | a0001c0001t0001g0059 a0001c0001t0001g0065 a0001c0001t0001g0066 others(7): Show |
10 | HG00438.hp1 HG01346.hp1 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.125+5862_125+5864d others(5): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17666387 | ||||||
| chr10:17666387 | A | ATTTTTTT others(5): Show |
2 | a0001c0001t0017g0377 a0001c0001t0029g0376 |
2 | HG02258.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.125+5853_125+5864d others(14): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17666387 | ||||||
| chr10:17666387 | A | ATTTTTTT others(7): Show |
1 | a0001c0001t0009g0380 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.125+5851_125+5864d others(16): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17666387 | ||||||
| chr10:17666387 | A | T | 1 | a0001c0001t0017g0378 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.125+5839A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17666387 | |||||||
| chr10:17666387 | AT | A | 10 | a0001c0001t0002g0019 a0001c0001t0002g0237 a0001c0001t0002g0245 others(7): Show |
10 | NA18948.hp2 NA18963.hp2 NA18965.hp1 others(7): Show |
intron_variant | MODIFIER | c.125+5864delT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17666387 | ||||||
| chr10:17666387 | ATTTTTTT others(4): Show |
A | 23 | a0001c0001t0001g0081 a0001c0001t0001g0088 a0001c0001t0005g0004 others(20): Show |
26 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.125+5854_125+5864d others(13): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17666387 | ||||||
| chr10:17666443 | G | A | 93 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(90): Show |
100 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.125+5895G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17666443 | |||||||
| chr10:17666479 | C | G | 33 | a0001c0001t0001g0158 a0001c0001t0003g0155 a0001c0001t0003g0156 others(30): Show |
36 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.125+5931C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17666479 | |||||||
| chr10:17666507 | G | A | 1 | a0001c0006t0028g0379 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.125+5959G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17666507 | |||||||
| chr10:17666519 | T | C | 1 | a0001c0006t0028g0379 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.125+5971T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17666519 | |||||||
| chr10:17666551 | T | C | 1 | a0001c0001t0008g0050 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.125+6003T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17666551 | |||||||
| chr10:17666587 | C | T | 4 | a0001c0001t0004g0056 a0001c0001t0017g0377 a0001c0001t0017g0378 others(1): Show |
4 | HG02258.hp1 HG02280.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.125+6039C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17666587 | |||||||
| chr10:17666598 | C | T | 3 | a0001c0001t0017g0377 a0001c0001t0017g0378 a0001c0002t0003g0170 |
3 | HG02258.hp1 HG02280.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.125+6050C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17666598 | |||||||
| chr10:17666662 | G | A | 1 | a0001c0009t0015g0385 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.125+6114G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17666662 | |||||||
| chr10:17666677 | A | G | 2 | a0001c0002t0003g0170 a0001c0002t0003g0171 |
2 | HG02738.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.125+6129A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17666677 | |||||||
| chr10:17666729 | C | G | 1 | a0001c0002t0003g0331 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.125+6181C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17666729 | |||||||
| chr10:17666837 | A | G | 1 | a0001c0001t0002g0034 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.125+6289A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17666837 | |||||||
| chr10:17667103 | G | A | 2 | a0001c0001t0002g0249 a0001c0001t0002g0301 |
2 | NA18961.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.125+6555G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17667103 | |||||||
| chr10:17667112 | C | T | 14 | a0001c0001t0001g0356 a0001c0001t0001g0359 a0001c0001t0001g0360 others(11): Show |
14 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.125+6564C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17667112 | |||||||
| chr10:17667128 | A | AT | 143 | a0001c0001t0001g0149 a0001c0001t0001g0152 a0001c0001t0001g0185 others(140): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.125+6595dupT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17667128 | ||||||
| chr10:17667128 | ATT | A | 246 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(243): Show |
262 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.125+6594_125+6595d others(4): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17667128 | ||||||
| chr10:17667158 | C | G | 1 | a0001c0001t0023g0187 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.125+6610C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17667158 | |||||||
| chr10:17667163 | G | A | 14 | a0001c0001t0001g0356 a0001c0001t0001g0359 a0001c0001t0001g0360 others(11): Show |
14 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.125+6615G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17667163 | |||||||
| chr10:17667229 | C | T | 27 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(24): Show |
30 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.125+6681C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17667229 | |||||||
| chr10:17667312 | A | G | 1 | a0001c0001t0002g0217 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.125+6764A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17667312 | |||||||
| chr10:17667383 | A | T | 1 | a0001c0002t0003g0331 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.125+6835A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17667383 | |||||||
| chr10:17667402 | G | A | 1 | a0001c0002t0022g0183 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.125+6854G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17667402 | |||||||
| chr10:17667560 | A | G | 29 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(26): Show |
32 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.125+7012A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17667560 | |||||||
| chr10:17667580 | A | C | 1 | a0001c0001t0010g0111 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.125+7032A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17667580 | |||||||
| chr10:17667624 | A | G | 29 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(26): Show |
32 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.125+7076A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17667624 | |||||||
| chr10:17667677 | A | G | 2 | a0001c0001t0015g0386 a0001c0009t0015g0385 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.125+7129A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17667677 | |||||||
| chr10:17667757 | T | G | 2 | a0001c0001t0030g0382 a0001c0001t0031g0381 |
2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.125+7209T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17667757 | |||||||
| chr10:17667915 | GA | G | 8 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(5): Show |
8 | HG02145.hp1 HG02630.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.125+7369delA | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17667915 | ||||||
| chr10:17667928 | G | C | 2 | a0001c0001t0015g0386 a0001c0009t0015g0385 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.125+7380G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17667928 | |||||||
| chr10:17667965 | T | C | 18 | a0001c0001t0001g0356 a0001c0001t0001g0359 a0001c0001t0001g0360 others(15): Show |
18 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.125+7417T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17667965 | |||||||
| chr10:17668061 | T | G | 1 | a0001c0001t0001g0355 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.125+7513T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17668061 | |||||||
| chr10:17668089 | A | G | 29 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(26): Show |
32 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.125+7541A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17668089 | |||||||
| chr10:17668115 | T | A | 21 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(18): Show |
24 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.125+7567T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17668115 | |||||||
| chr10:17668178 | T | A | 1 | a0001c0001t0002g0250 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.125+7630T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17668178 | |||||||
| chr10:17668275 | G | A | 98 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(95): Show |
107 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.125+7727G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17668275 | |||||||
| chr10:17668488 | C | T | 29 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(26): Show |
32 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.125+7940C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17668488 | |||||||
| chr10:17668640 | C | T | 1 | a0001c0001t0001g0355 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.125+8092C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17668640 | |||||||
| chr10:17668906 | A | C | 18 | a0001c0001t0001g0356 a0001c0001t0001g0359 a0001c0001t0001g0360 others(15): Show |
18 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.125+8358A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17668906 | |||||||
| chr10:17669051 | A | G | 50 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0059 others(47): Show |
53 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.125+8503A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17669051 | |||||||
| chr10:17669216 | C | T | 2 | a0001c0001t0006g0203 a0001c0001t0006g0209 |
2 | HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.125+8668C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17669216 | |||||||
| chr10:17669340 | G | T | 2 | a0001c0001t0015g0386 a0001c0009t0015g0385 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.125+8792G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17669340 | |||||||
| chr10:17669354 | G | GT | 10 | a0001c0001t0002g0228 a0001c0001t0002g0230 a0001c0001t0002g0248 others(7): Show |
10 | HG01175.hp1 HG01243.hp2 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.125+8821dupT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17669354 | ||||||
| chr10:17669412 | A | C | 29 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(26): Show |
32 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.125+8864A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17669412 | |||||||
| chr10:17669438 | G | A | 259 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(256): Show |
275 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.125+8890G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17669438 | |||||||
| chr10:17669622 | G | A | 2 | a0001c0001t0030g0382 a0001c0001t0031g0381 |
2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.125+9074G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17669622 | |||||||
| chr10:17669732 | C | T | 3 | a0001c0002t0003g0342 a0001c0002t0003g0343 a0001c0002t0003g0344 |
3 | NA18988.hp1 NA19010.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.125+9184C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17669732 | |||||||
| chr10:17669774 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.125+9226C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17669774 | |||||||
| chr10:17669783 | C | T | 10 | a0001c0001t0004g0017 a0001c0001t0004g0174 a0001c0001t0004g0175 others(7): Show |
11 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.125+9235C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17669783 | |||||||
| chr10:17669801 | C | T | 1 | a0001c0001t0005g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.125+9253C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17669801 | |||||||
| chr10:17669811 | C | T | 2 | a0001c0001t0009g0308 a0001c0001t0009g0309 |
2 | NA18959.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.125+9263C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17669811 | |||||||
| chr10:17669825 | G | A | 3 | a0001c0001t0002g0238 a0001c0001t0002g0251 a0001c0001t0002g0252 |
3 | HG01981.hp1 HG02300.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.125+9277G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17669825 | |||||||
| chr10:17669848 | C | T | 27 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(24): Show |
30 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.125+9300C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17669848 | |||||||
| chr10:17669884 | C | CT | 66 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0013 others(63): Show |
73 | HG00597.hp1 HG00609.hp2 HG01255.hp1 others(70): Show |
intron_variant | MODIFIER | c.125+9355dupT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17669884 | ||||||
| chr10:17669884 | C | CTT | 56 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0059 others(53): Show |
59 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.125+9354_125+9355d others(4): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17669884 | ||||||
| chr10:17669884 | C | CTTTT | 20 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(17): Show |
23 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.125+9352_125+9355d others(6): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17669884 | ||||||
| chr10:17669884 | CT | C | 48 | a0001c0001t0001g0365 a0001c0001t0001g0369 a0001c0001t0001g0370 others(45): Show |
50 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.125+9355delT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17669884 | ||||||
| chr10:17669921 | G | A | 2 | a0001c0001t0015g0386 a0001c0009t0015g0385 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.125+9373G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17669921 | |||||||
| chr10:17669951 | C | G | 2 | a0001c0001t0015g0386 a0001c0009t0015g0385 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.125+9403C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17669951 | |||||||
| chr10:17669985 | C | T | 8 | a0001c0001t0002g0024 a0001c0001t0002g0273 a0001c0001t0002g0274 others(5): Show |
9 | HG00735.hp1 HG00738.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.125+9437C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17669985 | |||||||
| chr10:17670171 | A | G | 10 | a0001c0001t0004g0017 a0001c0001t0004g0174 a0001c0001t0004g0175 others(7): Show |
11 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.125+9623A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17670171 | |||||||
| chr10:17670191 | C | T | 3 | a0001c0001t0017g0377 a0001c0001t0017g0378 a0001c0001t0029g0376 |
3 | HG02258.hp1 HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.125+9643C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17670191 | |||||||
| chr10:17670232 | T | C | 1 | a0001c0001t0001g0355 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.125+9684T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17670232 | |||||||
| chr10:17670250 | A | T | 1 | a0001c0006t0028g0379 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.125+9702A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17670250 | |||||||
| chr10:17670298 | G | A | 29 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(26): Show |
32 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.125+9750G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17670298 | |||||||
| chr10:17670298 | G | T | 2 | a0001c0002t0003g0322 a0001c0002t0003g0328 |
2 | NA18962.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.125+9750G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17670298 | |||||||
| chr10:17670453 | A | C | 43 | a0001c0001t0001g0030 a0001c0002t0003g0009 a0001c0002t0003g0023 others(40): Show |
45 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.125+9905A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17670453 | |||||||
| chr10:17670735 | T | C | 1 | a0001c0001t0031g0381 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.125+10187T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17670735 | |||||||
| chr10:17670744 | A | G | 29 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(26): Show |
32 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.125+10196A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17670744 | |||||||
| chr10:17670758 | T | TTATC | 29 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(26): Show |
32 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.125+10213_125+1021 others(8): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17670758 | ||||||
| chr10:17670782 | T | TAAGAAAC others(798): Show |
1 | a0001c0001t0015g0386 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.125+10240_125+1024 others(809): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17670782 | ||||||
| chr10:17670782 | T | TAAGAAAC others(801): Show |
1 | a0001c0009t0015g0385 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.125+10240_125+1024 others(812): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17670782 | ||||||
| chr10:17670782 | T | TAAGAAAT others(800): Show |
1 | a0001c0001t0031g0381 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.125+10245_125+1024 others(811): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17670782 | ||||||
| chr10:17670782 | T | TAAGAAAT others(799): Show |
1 | a0001c0001t0030g0382 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.125+10245_125+1024 others(810): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17670782 | ||||||
| chr10:17670782 | T | TAAGAAAT others(800): Show |
1 | a0001c0001t0009g0380 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.125+10245_125+1024 others(811): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17670782 | ||||||
| chr10:17670782 | T | TAAGAAAT others(799): Show |
6 | a0001c0001t0005g0042 a0001c0001t0005g0043 a0001c0001t0005g0045 others(3): Show |
6 | HG00280.hp2 HG01081.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.125+10245_125+1024 others(810): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17670782 | ||||||
| chr10:17670782 | T | TAAGAAAT others(801): Show |
1 | a0001c0001t0008g0040 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.125+10245_125+1024 others(812): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17670782 | ||||||
| chr10:17670782 | T | TAAGAAAT others(800): Show |
15 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0041 others(12): Show |
16 | HG00323.hp2 HG00609.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.125+10245_125+1024 others(811): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17670782 | ||||||
| chr10:17670782 | T | TAAGAAAT others(799): Show |
1 | a0001c0001t0005g0004 | 3 | HG00639.hp2 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.125+10245_125+1024 others(810): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17670782 | ||||||
| chr10:17670782 | T | TAAGAAAT others(799): Show |
1 | a0001c0001t0029g0376 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.125+10245_125+1024 others(810): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17670782 | ||||||
| chr10:17670809 | C | A | 16 | a0001c0001t0001g0359 a0001c0001t0001g0360 a0001c0001t0001g0361 others(13): Show |
16 | HG01106.hp2 HG02071.hp2 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.125+10261C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17670809 | |||||||
| chr10:17670853 | T | G | 8 | a0001c0001t0002g0019 a0001c0001t0002g0219 a0001c0001t0002g0237 others(5): Show |
8 | NA18948.hp2 NA18965.hp1 NA19001.hp2 others(5): Show |
intron_variant | MODIFIER | c.125+10305T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17670853 | |||||||
| chr10:17671014 | T | C | 1 | a0001c0001t0001g0068 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.125+10466T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17671014 | |||||||
| chr10:17671102 | A | G | 6 | a0001c0001t0004g0018 a0001c0001t0004g0197 a0001c0001t0004g0198 others(3): Show |
7 | HG00642.hp2 HG02976.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.125+10554A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17671102 | |||||||
| chr10:17671246 | C | T | 1 | a0001c0001t0029g0376 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.125+10698C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17671246 | |||||||
| chr10:17671458 | A | T | 1 | a0001c0001t0001g0057 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.125+10910A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17671458 | |||||||
| chr10:17671578 | C | T | 21 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(18): Show |
24 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.125+11030C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17671578 | |||||||
| chr10:17671724 | C | G | 1 | a0001c0001t0004g0305 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.125+11176C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17671724 | |||||||
| chr10:17671968 | A | G | 1 | a0001c0001t0001g0355 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.125+11420A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17671968 | |||||||
| chr10:17671986 | G | A | 6 | a0001c0001t0009g0380 a0001c0001t0017g0377 a0001c0001t0017g0378 others(3): Show |
6 | HG02258.hp1 HG02280.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.125+11438G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17671986 | |||||||
| chr10:17672069 | A | G | 1 | a0001c0002t0003g0154 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.125+11521A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17672069 | |||||||
| chr10:17672183 | G | A | 1 | a0001c0001t0030g0382 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.125+11635G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17672183 | |||||||
| chr10:17672288 | A | G | 4 | a0001c0002t0003g0009 a0001c0002t0003g0216 a0001c0002t0003g0324 others(1): Show |
6 | HG04184.hp2 NA18971.hp1 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.125+11740A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17672288 | |||||||
| chr10:17672391 | A | G | 113 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(110): Show |
123 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.125+11843A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17672391 | |||||||
| chr10:17672423 | T | G | 1 | a0001c0001t0001g0125 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.125+11875T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17672423 | |||||||
| chr10:17672575 | C | T | 1 | a0001c0001t0023g0187 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.125+12027C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17672575 | |||||||
| chr10:17672674 | A | G | 1 | a0001c0001t0004g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.126-12001A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17672674 | |||||||
| chr10:17672818 | G | T | 32 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(29): Show |
33 | HG00642.hp2 HG01243.hp2 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.126-11857G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17672818 | |||||||
| chr10:17672833 | AGTGTGAT others(2): Show |
A | 27 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(24): Show |
30 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.126-11837_126-1182 others(13): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17672833 | ||||||
| chr10:17672867 | T | TAAGAG | 29 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(26): Show |
32 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.126-11805_126-1180 others(9): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17672867 | ||||||
| chr10:17672990 | G | A | 6 | a0001c0001t0001g0149 a0001c0001t0001g0152 a0001c0001t0002g0150 others(3): Show |
6 | HG01192.hp1 HG02572.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.126-11685G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17672990 | |||||||
| chr10:17673023 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.126-11652A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17673023 | |||||||
| chr10:17673156 | T | C | 3 | a0001c0001t0001g0005 a0001c0001t0001g0107 a0001c0001t0001g0108 |
5 | NA18952.hp1 NA18961.hp2 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.126-11519T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17673156 | |||||||
| chr10:17673279 | T | C | 2 | a0001c0002t0003g0311 a0001c0002t0003g0314 |
2 | NA19001.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.126-11396T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17673279 | |||||||
| chr10:17673289 | T | TTAG | 2 | a0001c0001t0001g0015 a0001c0001t0001g0104 |
3 | NA18944.hp1 NA18963.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.126-11385_126-1138 others(7): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17673289 | ||||||
| chr10:17673293 | C | T | 27 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(24): Show |
30 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.126-11382C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17673293 | |||||||
| chr10:17673294 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.126-11381G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17673294 | |||||||
| chr10:17673329 | A | G | 1 | a0001c0002t0003g0341 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.126-11346A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17673329 | |||||||
| chr10:17673398 | G | A | 3 | a0001c0001t0012g0182 a0001c0001t0012g0383 a0001c0001t0023g0187 |
3 | HG02970.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.126-11277G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17673398 | |||||||
| chr10:17673410 | G | T | 1 | a0001c0001t0002g0281 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.126-11265G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17673410 | |||||||
| chr10:17673463 | C | T | 9 | a0001c0001t0002g0275 a0001c0001t0004g0018 a0001c0001t0004g0033 others(6): Show |
10 | HG00642.hp2 HG00738.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.126-11212C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17673463 | |||||||
| chr10:17673603 | G | C | 1 | a0001c0001t0004g0056 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.126-11072G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17673603 | |||||||
| chr10:17673649 | G | A | 2 | a0001c0002t0003g0035 a0001c0002t0003g0036 |
2 | HG01243.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.126-11026G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17673649 | |||||||
| chr10:17673673 | C | A | 27 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(24): Show |
30 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.126-11002C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17673673 | |||||||
| chr10:17674014 | G | C | 2 | a0001c0002t0003g0035 a0001c0002t0003g0036 |
2 | HG01243.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.126-10661G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17674014 | |||||||
| chr10:17674014 | G | GC | 29 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(26): Show |
32 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.126-10661_126-1066 others(5): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17674014 | |||||||
| chr10:17674097 | T | C | 2 | a0001c0001t0015g0386 a0001c0009t0015g0385 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.126-10578T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17674097 | |||||||
| chr10:17674294 | T | G | 3 | a0001c0001t0017g0377 a0001c0001t0017g0378 a0001c0001t0029g0376 |
3 | HG02258.hp1 HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.126-10381T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17674294 | |||||||
| chr10:17674405 | C | T | 6 | a0001c0002t0004g0323 a0001c0002t0004g0330 a0001c0002t0004g0332 others(3): Show |
6 | HG02145.hp2 HG02559.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.126-10270C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17674405 | |||||||
| chr10:17674737 | G | A | 99 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(96): Show |
108 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.126-9938G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17674737 | |||||||
| chr10:17674870 | A | G | 2 | a0001c0001t0015g0386 a0001c0009t0015g0385 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.126-9805A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17674870 | |||||||
| chr10:17674872 | G | A | 242 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(239): Show |
258 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.126-9803G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17674872 | |||||||
| chr10:17674879 | T | C | 21 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(18): Show |
24 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.126-9796T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17674879 | |||||||
| chr10:17674909 | C | A | 1 | a0001c0001t0015g0386 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.126-9766C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17674909 | |||||||
| chr10:17674931 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.126-9744A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17674931 | |||||||
| chr10:17675099 | T | G | 1 | a0001c0001t0001g0359 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.126-9576T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17675099 | |||||||
| chr10:17675109 | T | G | 1 | a0001c0001t0001g0355 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.126-9566T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17675109 | |||||||
| chr10:17675503 | C | CA | 103 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(100): Show |
112 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.126-9158dupA | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17675503 | ||||||
| chr10:17675503 | C | CAA | 7 | a0001c0001t0015g0386 a0001c0001t0017g0377 a0001c0001t0017g0378 others(4): Show |
7 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.126-9159_126-9158d others(4): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17675503 | ||||||
| chr10:17675503 | C | CAAA | 21 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(18): Show |
24 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.126-9160_126-9158d others(5): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17675503 | ||||||
| chr10:17675579 | G | A | 1 | a0001c0001t0007g0239 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.126-9096G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17675579 | |||||||
| chr10:17675700 | T | G | 1 | a0001c0001t0004g0305 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.126-8975T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17675700 | |||||||
| chr10:17675799 | A | AT | 27 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(24): Show |
30 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.126-8867dupT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17675799 | ||||||
| chr10:17675862 | C | T | 1 | a0001c0002t0022g0183 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.126-8813C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17675862 | |||||||
| chr10:17675894 | T | G | 1 | a0001c0001t0001g0070 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.126-8781T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17675894 | |||||||
| chr10:17675960 | C | T | 1 | a0001c0001t0002g0039 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.126-8715C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17675960 | |||||||
| chr10:17676008 | G | C | 1 | a0001c0001t0001g0090 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.126-8667G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17676008 | |||||||
| chr10:17676068 | A | G | 10 | a0001c0001t0004g0017 a0001c0001t0004g0174 a0001c0001t0004g0175 others(7): Show |
11 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.126-8607A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17676068 | |||||||
| chr10:17676144 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.126-8531C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17676144 | |||||||
| chr10:17676283 | A | G | 29 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(26): Show |
32 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.126-8392A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17676283 | |||||||
| chr10:17676304 | G | A | 27 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(24): Show |
30 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.126-8371G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17676304 | |||||||
| chr10:17676334 | T | C | 1 | a0001c0001t0031g0381 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.126-8341T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17676334 | |||||||
| chr10:17676495 | G | A | 13 | a0001c0001t0001g0356 a0001c0001t0001g0359 a0001c0001t0001g0360 others(10): Show |
13 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.126-8180G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17676495 | |||||||
| chr10:17676557 | C | T | 1 | a0001c0001t0002g0153 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.126-8118C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17676557 | |||||||
| chr10:17676578 | A | G | 6 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(3): Show |
6 | HG00609.hp2 NA18970.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.126-8097A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17676578 | |||||||
| chr10:17676582 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.126-8093A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17676582 | |||||||
| chr10:17676699 | A | G | 5 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(2): Show |
5 | HG02145.hp1 HG03130.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.126-7976A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17676699 | |||||||
| chr10:17676700 | T | C | 178 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(175): Show |
191 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.126-7975T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17676700 | |||||||
| chr10:17676798 | A | G | 3 | a0001c0001t0002g0224 a0001c0001t0002g0295 a0001c0001t0002g0296 |
3 | HG00423.hp2 NA18968.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.126-7877A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17676798 | |||||||
| chr10:17676808 | C | A | 1 | a0001c0001t0015g0386 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.126-7867C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17676808 | |||||||
| chr10:17676896 | C | CAT | 19 | a0001c0001t0001g0356 a0001c0001t0001g0359 a0001c0001t0001g0360 others(16): Show |
19 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.126-7765_126-7764d others(4): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17676896 | ||||||
| chr10:17677001 | G | C | 3 | a0001c0001t0001g0364 a0001c0001t0002g0297 a0001c0001t0002g0298 |
3 | HG02027.hp2 HG02165.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.126-7674G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17677001 | |||||||
| chr10:17677078 | G | A | 3 | a0001c0001t0003g0155 a0001c0001t0003g0156 a0001c0001t0003g0157 |
3 | HG02630.hp2 HG02818.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.126-7597G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17677078 | |||||||
| chr10:17677089 | C | T | 1 | a0001c0001t0002g0244 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.126-7586C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17677089 | |||||||
| chr10:17677135 | G | T | 7 | a0001c0001t0002g0034 a0001c0001t0002g0184 a0001c0001t0002g0188 others(4): Show |
7 | HG00099.hp1 HG02109.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.126-7540G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17677135 | |||||||
| chr10:17677243 | A | G | 16 | a0001c0002t0003g0029 a0001c0002t0003g0032 a0001c0002t0003g0159 others(13): Show |
16 | HG00099.hp2 HG01074.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.126-7432A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17677243 | |||||||
| chr10:17677247 | C | A | 29 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(26): Show |
32 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.126-7428C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17677247 | |||||||
| chr10:17677263 | C | A | 7 | a0001c0001t0004g0204 a0001c0001t0004g0205 a0001c0001t0004g0206 others(4): Show |
7 | HG01884.hp1 HG02451.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.126-7412C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17677263 | |||||||
| chr10:17677283 | T | C | 1 | a0001c0001t0001g0061 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.126-7392T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17677283 | |||||||
| chr10:17677391 | G | A | 2 | a0001c0001t0004g0033 a0001c0001t0004g0056 |
2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.126-7284G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17677391 | |||||||
| chr10:17677495 | G | A | 1 | a0001c0001t0012g0182 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.126-7180G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17677495 | |||||||
| chr10:17677797 | A | G | 8 | a0001c0001t0002g0226 a0001c0001t0002g0270 a0001c0001t0002g0271 others(5): Show |
8 | HG01123.hp1 HG01993.hp1 NA18612.hp1 others(5): Show |
intron_variant | MODIFIER | c.126-6878A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17677797 | |||||||
| chr10:17677808 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.126-6867C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17677808 | |||||||
| chr10:17677849 | A | G | 2 | a0001c0001t0015g0386 a0001c0009t0015g0385 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.126-6826A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17677849 | |||||||
| chr10:17677873 | G | A | 101 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(98): Show |
110 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.126-6802G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17677873 | |||||||
| chr10:17677947 | G | A | 1 | a0001c0001t0001g0357 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.126-6728G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17677947 | |||||||
| chr10:17677951 | G | A | 13 | a0001c0001t0001g0356 a0001c0001t0001g0359 a0001c0001t0001g0360 others(10): Show |
13 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.126-6724G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17677951 | |||||||
| chr10:17677965 | C | CT | 101 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(98): Show |
110 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.126-6706dupT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17677965 | ||||||
| chr10:17678049 | A | C | 2 | a0001c0001t0015g0386 a0001c0009t0015g0385 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.126-6626A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17678049 | |||||||
| chr10:17678049 | A | G | 1 | a0001c0002t0003g0340 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.126-6626A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17678049 | |||||||
| chr10:17678073 | C | A | 1 | a0001c0001t0029g0376 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.126-6602C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17678073 | |||||||
| chr10:17678219 | A | G | 2 | a0001c0001t0015g0386 a0001c0009t0015g0385 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.126-6456A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17678219 | |||||||
| chr10:17678260 | A | ATTTTTTT others(1): Show |
20 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(17): Show |
23 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.126-6412_126-6405d others(10): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17678260 | ||||||
| chr10:17678260 | A | ATTTTTTT others(3): Show |
9 | a0001c0001t0004g0017 a0001c0001t0004g0174 a0001c0001t0004g0175 others(6): Show |
10 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.126-6414_126-6405d others(12): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17678260 | ||||||
| chr10:17678260 | AT | A | 110 | a0001c0001t0001g0030 a0001c0001t0001g0355 a0001c0001t0001g0356 others(107): Show |
113 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.126-6405delT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17678260 | ||||||
| chr10:17678337 | C | G | 19 | a0001c0001t0001g0356 a0001c0001t0001g0359 a0001c0001t0001g0360 others(16): Show |
19 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.126-6338C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17678337 | |||||||
| chr10:17678366 | T | C | 25 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(22): Show |
28 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.126-6309T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17678366 | |||||||
| chr10:17678496 | C | T | 16 | a0001c0002t0003g0029 a0001c0002t0003g0032 a0001c0002t0003g0159 others(13): Show |
16 | HG00099.hp2 HG01074.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.126-6179C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17678496 | |||||||
| chr10:17678534 | G | A | 12 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0057 others(9): Show |
13 | HG00609.hp2 HG02129.hp2 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.126-6141G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17678534 | |||||||
| chr10:17678581 | G | A | 1 | a0001c0006t0028g0379 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.126-6094G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17678581 | |||||||
| chr10:17678750 | C | T | 2 | a0001c0001t0015g0386 a0001c0009t0015g0385 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.126-5925C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17678750 | |||||||
| chr10:17678938 | T | A | 1 | a0001c0001t0004g0017 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.126-5737T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17678938 | |||||||
| chr10:17678985 | C | G | 21 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(18): Show |
24 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.126-5690C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17678985 | |||||||
| chr10:17679028 | A | G | 1 | a0001c0001t0002g0296 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.126-5647A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17679028 | |||||||
| chr10:17679037 | T | C | 1 | a0001c0001t0002g0273 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.126-5638T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17679037 | |||||||
| chr10:17679043 | G | T | 4 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(1): Show |
4 | HG02145.hp1 HG03130.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.126-5632G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17679043 | |||||||
| chr10:17679089 | A | G | 1 | a0001c0002t0003g0345 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.126-5586A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17679089 | |||||||
| chr10:17679317 | C | T | 34 | a0001c0001t0004g0017 a0001c0001t0004g0174 a0001c0001t0004g0175 others(31): Show |
38 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.126-5358C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17679317 | |||||||
| chr10:17679379 | A | T | 3 | a0001c0001t0001g0005 a0001c0001t0001g0107 a0001c0001t0001g0108 |
5 | NA18952.hp1 NA18961.hp2 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.126-5296A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17679379 | |||||||
| chr10:17679491 | T | G | 1 | a0001c0001t0002g0254 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.126-5184T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17679491 | |||||||
| chr10:17679502 | C | G | 34 | a0001c0001t0004g0017 a0001c0001t0004g0174 a0001c0001t0004g0175 others(31): Show |
38 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.126-5173C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17679502 | |||||||
| chr10:17679574 | C | T | 1 | a0001c0001t0009g0380 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.126-5101C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17679574 | |||||||
| chr10:17679575 | G | A | 1 | a0001c0001t0002g0255 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.126-5100G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17679575 | |||||||
| chr10:17679579 | G | GT | 6 | a0001c0001t0001g0108 a0001c0001t0004g0033 a0001c0001t0004g0056 others(3): Show |
6 | HG01243.hp2 HG02145.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.126-5084dupT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17679579 | ||||||
| chr10:17679579 | GT | G | 27 | a0001c0001t0001g0124 a0001c0001t0005g0004 a0001c0001t0005g0010 others(24): Show |
30 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.126-5084delT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17679579 | ||||||
| chr10:17679579 | GTT | G | 9 | a0001c0001t0004g0017 a0001c0001t0004g0174 a0001c0001t0004g0175 others(6): Show |
10 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.126-5085_126-5084d others(4): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17679579 | ||||||
| chr10:17679669 | G | A | 1 | a0001c0001t0015g0386 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.126-5006G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17679669 | |||||||
| chr10:17679751 | GTTTCTTT others(5): Show |
G | 9 | a0001c0001t0004g0017 a0001c0001t0004g0174 a0001c0001t0004g0175 others(6): Show |
10 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.126-4915_126-4904d others(14): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17679751 | ||||||
| chr10:17680027 | A | T | 1 | a0001c0001t0005g0049 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.126-4648A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17680027 | |||||||
| chr10:17680038 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.126-4637A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17680038 | |||||||
| chr10:17680053 | T | C | 2 | a0001c0001t0015g0386 a0001c0009t0015g0385 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.126-4622T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17680053 | |||||||
| chr10:17680146 | G | A | 1 | a0001c0001t0002g0234 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.126-4529G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17680146 | |||||||
| chr10:17680163 | C | A | 6 | a0001c0001t0004g0215 a0001c0001t0006g0203 a0001c0001t0006g0207 others(3): Show |
6 | HG02615.hp2 HG02922.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.126-4512C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17680163 | |||||||
| chr10:17680210 | G | A | 8 | a0001c0001t0002g0006 a0001c0001t0002g0220 a0001c0001t0002g0258 others(5): Show |
9 | HG00280.hp1 HG00642.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.126-4465G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17680210 | |||||||
| chr10:17680265 | AT | A | 102 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(99): Show |
111 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.126-4409delT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17680265 | |||||||
| chr10:17680379 | A | G | 102 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(99): Show |
111 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.126-4296A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17680379 | |||||||
| chr10:17680416 | C | CT | 8 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(5): Show |
8 | HG00280.hp1 HG02145.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.126-4244dupT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17680416 | ||||||
| chr10:17680416 | CT | C | 8 | a0001c0001t0001g0030 a0001c0001t0001g0127 a0001c0001t0001g0152 others(5): Show |
8 | HG00099.hp1 HG02630.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.126-4244delT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17680416 | ||||||
| chr10:17680416 | CTT | C | 25 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(22): Show |
28 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.126-4245_126-4244d others(4): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17680416 | ||||||
| chr10:17680416 | CTTT | C | 9 | a0001c0001t0004g0017 a0001c0001t0004g0174 a0001c0001t0004g0175 others(6): Show |
10 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.126-4246_126-4244d others(5): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17680416 | ||||||
| chr10:17680541 | G | T | 8 | a0001c0001t0002g0034 a0001c0001t0002g0184 a0001c0001t0002g0188 others(5): Show |
8 | HG00099.hp1 HG02109.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.126-4134G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17680541 | |||||||
| chr10:17680768 | G | C | 2 | a0001c0001t0017g0377 a0001c0001t0017g0378 |
2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.126-3907G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17680768 | |||||||
| chr10:17680817 | T | C | 4 | a0001c0001t0009g0380 a0001c0001t0017g0377 a0001c0001t0017g0378 others(1): Show |
4 | HG02258.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.126-3858T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17680817 | |||||||
| chr10:17680835 | T | C | 9 | a0001c0001t0004g0017 a0001c0001t0004g0174 a0001c0001t0004g0175 others(6): Show |
10 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.126-3840T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17680835 | |||||||
| chr10:17680865 | C | T | 1 | a0001c0001t0001g0355 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.126-3810C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17680865 | |||||||
| chr10:17681060 | G | A | 1 | a0001c0001t0009g0380 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.126-3615G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17681060 | |||||||
| chr10:17681071 | G | A | 2 | a0001c0001t0001g0116 a0001c0001t0001g0145 |
2 | NA19082.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.126-3604G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17681071 | |||||||
| chr10:17681090 | A | G | 21 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(18): Show |
24 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.126-3585A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17681090 | |||||||
| chr10:17681134 | C | G | 4 | a0001c0001t0004g0033 a0001c0001t0004g0056 a0001c0002t0003g0035 others(1): Show |
4 | HG01243.hp2 HG03516.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.126-3541C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17681134 | |||||||
| chr10:17681134 | C | T | 34 | a0001c0001t0004g0017 a0001c0001t0004g0174 a0001c0001t0004g0175 others(31): Show |
38 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.126-3541C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17681134 | |||||||
| chr10:17681146 | T | A | 9 | a0001c0001t0004g0017 a0001c0001t0004g0174 a0001c0001t0004g0175 others(6): Show |
10 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.126-3529T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17681146 | |||||||
| chr10:17681169 | G | A | 1 | a0001c0001t0004g0384 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.126-3506G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17681169 | |||||||
| chr10:17681197 | C | CT | 144 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(141): Show |
156 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.126-3460dupT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17681197 | ||||||
| chr10:17681197 | C | CTT | 15 | a0001c0001t0001g0030 a0001c0001t0001g0102 a0001c0001t0001g0108 others(12): Show |
16 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.126-3461_126-3460d others(4): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17681197 | ||||||
| chr10:17681217 | A | C | 1 | a0001c0001t0029g0376 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.126-3458A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17681217 | |||||||
| chr10:17681218 | T | C | 50 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0013 others(47): Show |
56 | HG00597.hp1 HG00609.hp2 HG01255.hp1 others(53): Show |
intron_variant | MODIFIER | c.126-3457T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17681218 | |||||||
| chr10:17681225 | G | T | 1 | a0001c0001t0009g0380 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.126-3450G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17681225 | |||||||
| chr10:17681253 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.126-3422G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17681253 | |||||||
| chr10:17681276 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.126-3399C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17681276 | |||||||
| chr10:17681379 | C | T | 1 | a0001c0001t0001g0059 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.126-3296C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17681379 | |||||||
| chr10:17681395 | A | G | 1 | a0001c0001t0012g0383 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.126-3280A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17681395 | |||||||
| chr10:17681441 | C | T | 1 | a0001c0001t0002g0224 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.126-3234C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17681441 | |||||||
| chr10:17681641 | G | A | 2 | a0001c0002t0003g0335 a0001c0002t0003g0336 |
2 | NA18968.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.126-3034G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17681641 | |||||||
| chr10:17681715 | A | G | 1 | a0001c0001t0002g0286 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.126-2960A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17681715 | |||||||
| chr10:17681737 | C | G | 2 | a0001c0001t0015g0386 a0001c0009t0015g0385 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.126-2938C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17681737 | |||||||
| chr10:17681842 | A | G | 9 | a0001c0001t0004g0017 a0001c0001t0004g0174 a0001c0001t0004g0175 others(6): Show |
10 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.126-2833A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17681842 | |||||||
| chr10:17681867 | A | G | 2 | a0001c0001t0005g0047 a0001c0001t0005g0053 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.126-2808A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17681867 | |||||||
| chr10:17681892 | A | G | 1 | a0001c0001t0015g0386 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.126-2783A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17681892 | |||||||
| chr10:17682004 | T | C | 90 | a0001c0001t0001g0356 a0001c0001t0001g0359 a0001c0001t0001g0360 others(87): Show |
95 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.126-2671T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17682004 | |||||||
| chr10:17682123 | C | A | 84 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0013 others(81): Show |
91 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.126-2552C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17682123 | |||||||
| chr10:17682178 | T | G | 3 | a0001c0001t0003g0155 a0001c0001t0003g0156 a0001c0001t0003g0157 |
3 | HG02630.hp2 HG02818.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.126-2497T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17682178 | |||||||
| chr10:17682184 | T | G | 1 | a0001c0001t0002g0255 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.126-2491T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17682184 | |||||||
| chr10:17682234 | G | C | 1 | a0001c0001t0029g0376 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.126-2441G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17682234 | |||||||
| chr10:17682241 | C | T | 1 | a0001c0001t0002g0246 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.126-2434C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17682241 | |||||||
| chr10:17682435 | A | G | 49 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0013 others(46): Show |
55 | HG00597.hp1 HG00609.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.126-2240A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17682435 | |||||||
| chr10:17682452 | A | G | 1 | a0001c0001t0001g0061 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.126-2223A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17682452 | |||||||
| chr10:17682504 | G | A | 9 | a0001c0001t0004g0017 a0001c0001t0004g0174 a0001c0001t0004g0175 others(6): Show |
10 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.126-2171G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17682504 | |||||||
| chr10:17682529 | T | G | 1 | a0001c0001t0001g0355 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.126-2146T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17682529 | |||||||
| chr10:17682909 | T | C | 1 | a0001c0002t0003g0036 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.126-1766T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17682909 | |||||||
| chr10:17682925 | T | G | 36 | a0001c0001t0004g0017 a0001c0001t0004g0174 a0001c0001t0004g0175 others(33): Show |
40 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.126-1750T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17682925 | |||||||
| chr10:17683110 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.126-1565T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17683110 | |||||||
| chr10:17683236 | T | G | 2 | a0001c0001t0001g0185 a0001c0001t0001g0186 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.126-1439T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17683236 | |||||||
| chr10:17683239 | C | T | 16 | a0001c0002t0003g0029 a0001c0002t0003g0032 a0001c0002t0003g0159 others(13): Show |
16 | HG00099.hp2 HG01074.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.126-1436C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17683239 | |||||||
| chr10:17683250 | A | G | 1 | a0001c0001t0002g0268 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.126-1425A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17683250 | |||||||
| chr10:17683307 | T | C | 35 | a0001c0001t0004g0017 a0001c0001t0004g0174 a0001c0001t0004g0175 others(32): Show |
39 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.126-1368T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17683307 | |||||||
| chr10:17683367 | G | T | 34 | a0001c0001t0004g0017 a0001c0001t0004g0174 a0001c0001t0004g0175 others(31): Show |
38 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.126-1308G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17683367 | |||||||
| chr10:17683389 | C | G | 1 | a0001c0001t0018g0173 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.126-1286C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17683389 | |||||||
| chr10:17683410 | C | T | 60 | a0001c0002t0003g0009 a0001c0002t0003g0023 a0001c0002t0003g0029 others(57): Show |
62 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.126-1265C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17683410 | |||||||
| chr10:17683432 | A | G | 37 | a0001c0001t0004g0017 a0001c0001t0004g0174 a0001c0001t0004g0175 others(34): Show |
41 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.126-1243A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17683432 | |||||||
| chr10:17683504 | G | A | 7 | a0001c0001t0004g0204 a0001c0001t0004g0205 a0001c0001t0004g0206 others(4): Show |
7 | HG01884.hp1 HG02451.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.126-1171G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17683504 | |||||||
| chr10:17683689 | T | C | 35 | a0001c0001t0004g0017 a0001c0001t0004g0174 a0001c0001t0004g0175 others(32): Show |
39 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.126-986T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17683689 | |||||||
| chr10:17683712 | A | C | 18 | a0001c0001t0001g0356 a0001c0001t0001g0359 a0001c0001t0001g0360 others(15): Show |
18 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.126-963A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17683712 | |||||||
| chr10:17683787 | C | T | 3 | a0001c0001t0017g0377 a0001c0001t0017g0378 a0001c0001t0029g0376 |
3 | HG02258.hp1 HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.126-888C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17683787 | |||||||
| chr10:17683856 | C | T | 248 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(245): Show |
264 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.126-819C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17683856 | |||||||
| chr10:17683913 | C | G | 1 | a0001c0002t0003g0336 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.126-762C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17683913 | |||||||
| chr10:17683940 | C | T | 34 | a0001c0001t0004g0017 a0001c0001t0004g0174 a0001c0001t0004g0175 others(31): Show |
38 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.126-735C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17683940 | |||||||
| chr10:17684048 | T | C | 2 | a0001c0001t0015g0386 a0001c0009t0015g0385 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.126-627T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17684048 | |||||||
| chr10:17684071 | G | A | 243 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(240): Show |
259 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.126-604G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17684071 | |||||||
| chr10:17684155 | G | A | 2 | a0001c0001t0015g0386 a0001c0009t0015g0385 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.126-520G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17684155 | |||||||
| chr10:17684306 | G | A | 1 | a0001c0006t0028g0379 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.126-369G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17684306 | |||||||
| chr10:17684422 | CT | C | 20 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0015 others(17): Show |
24 | HG00597.hp1 HG01496.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.126-242delT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17684422 | ||||||
| chr10:17684538 | G | A | 22 | a0001c0002t0003g0009 a0001c0002t0003g0023 a0001c0002t0003g0154 others(19): Show |
24 | HG00673.hp1 NA18941.hp1 NA18949.hp2 others(21): Show |
intron_variant | MODIFIER | c.126-137G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17684538 | |||||||
| chr10:17684574 | A | G | 60 | a0001c0002t0003g0009 a0001c0002t0003g0023 a0001c0002t0003g0029 others(57): Show |
62 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.126-101A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17684574 | |||||||
| chr10:17684649 | A | G | 6 | a0001c0001t0002g0273 a0001c0001t0002g0274 a0001c0001t0002g0275 others(3): Show |
6 | HG00735.hp1 HG00738.hp2 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.126-26A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17684649 | |||||||
| chr10:17685091 | C | T | 1 | a0001c0001t0001g0116 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.297+164C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17685091 | |||||||
| chr10:17685209 | A | G | 4 | a0001c0001t0002g0242 a0001c0001t0002g0306 a0001c0001t0024g0292 others(1): Show |
4 | HG00639.hp1 HG01168.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.297+282A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17685209 | |||||||
| chr10:17685242 | C | T | 2 | a0001c0001t0015g0386 a0001c0009t0015g0385 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.297+315C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17685242 | |||||||
| chr10:17685494 | G | C | 2 | a0001c0001t0001g0185 a0001c0001t0001g0186 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.297+567G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17685494 | |||||||
| chr10:17685507 | G | T | 1 | a0001c0001t0005g0052 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.297+580G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17685507 | |||||||
| chr10:17685515 | G | C | 33 | a0001c0001t0004g0017 a0001c0001t0004g0174 a0001c0001t0004g0175 others(30): Show |
37 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.297+588G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17685515 | |||||||
| chr10:17685609 | A | G | 1 | a0001c0002t0003g0341 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.297+682A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17685609 | |||||||
| chr10:17685614 | A | C | 5 | a0001c0001t0001g0152 a0001c0001t0001g0355 a0001c0001t0002g0387 others(2): Show |
5 | HG02630.hp1 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.297+687A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17685614 | |||||||
| chr10:17685648 | A | G | 2 | a0001c0002t0003g0335 a0001c0002t0003g0336 |
2 | NA18968.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.297+721A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17685648 | |||||||
| chr10:17685815 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.297+888A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17685815 | |||||||
| chr10:17685965 | T | C | 1 | a0001c0001t0002g0270 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.297+1038T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17685965 | |||||||
| chr10:17685993 | T | A | 1 | a0001c0002t0003g0202 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.297+1066T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17685993 | |||||||
| chr10:17686099 | C | T | 1 | a0001c0001t0023g0187 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.297+1172C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17686099 | |||||||
| chr10:17686118 | T | C | 35 | a0001c0001t0004g0017 a0001c0001t0004g0174 a0001c0001t0004g0175 others(32): Show |
39 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.297+1191T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17686118 | |||||||
| chr10:17686181 | C | T | 99 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(96): Show |
108 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.297+1254C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17686181 | |||||||
| chr10:17686200 | G | A | 1 | a0001c0001t0018g0173 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.297+1273G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17686200 | |||||||
| chr10:17686217 | A | G | 1 | a0001c0001t0002g0252 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.297+1290A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17686217 | |||||||
| chr10:17686279 | C | G | 27 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(24): Show |
30 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.297+1352C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17686279 | |||||||
| chr10:17686295 | C | T | 2 | a0001c0001t0001g0152 a0001c0001t0001g0355 |
2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.297+1368C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17686295 | |||||||
| chr10:17686315 | TTC | T | 7 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(4): Show |
7 | HG02145.hp1 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.297+1392_297+1393d others(4): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr10 | 17686315 | ||||||
| chr10:17686355 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.297+1428T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17686355 | |||||||
| chr10:17686374 | C | T | 3 | a0001c0001t0012g0182 a0001c0001t0012g0383 a0001c0001t0023g0187 |
3 | HG02970.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.297+1447C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17686374 | |||||||
| chr10:17686378 | C | CT | 39 | a0001c0001t0001g0096 a0001c0001t0001g0138 a0001c0001t0001g0186 others(36): Show |
42 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.297+1467dupT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr10 | 17686378 | ||||||
| chr10:17686378 | C | CTTT | 10 | a0001c0001t0004g0017 a0001c0001t0004g0174 a0001c0001t0004g0175 others(7): Show |
11 | HG01255.hp2 HG01256.hp1 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.297+1465_297+1467d others(5): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr10 | 17686378 | ||||||
| chr10:17686413 | G | T | 2 | a0001c0001t0001g0095 a0001c0001t0001g0098 |
2 | HG01496.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.297+1486G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17686413 | |||||||
| chr10:17686496 | C | T | 1 | a0001c0001t0009g0380 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.298-1531C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17686496 | |||||||
| chr10:17686518 | A | C | 18 | a0001c0001t0001g0356 a0001c0001t0001g0359 a0001c0001t0001g0360 others(15): Show |
18 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.298-1509A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17686518 | |||||||
| chr10:17686746 | G | A | 2 | a0001c0002t0003g0170 a0001c0002t0003g0171 |
2 | HG02738.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.298-1281G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17686746 | |||||||
| chr10:17686929 | T | C | 6 | a0001c0001t0001g0149 a0001c0001t0002g0150 a0001c0001t0010g0109 others(3): Show |
6 | HG01192.hp1 HG02572.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.298-1098T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17686929 | |||||||
| chr10:17686968 | C | G | 3 | a0001c0001t0012g0182 a0001c0001t0012g0383 a0001c0001t0023g0187 |
3 | HG02970.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.298-1059C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17686968 | |||||||
| chr10:17687202 | C | T | 9 | a0001c0001t0004g0017 a0001c0001t0004g0174 a0001c0001t0004g0175 others(6): Show |
10 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.298-825C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17687202 | |||||||
| chr10:17687292 | T | C | 104 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(101): Show |
113 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.298-735T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17687292 | |||||||
| chr10:17687327 | T | C | 2 | a0001c0001t0001g0102 a0001c0005t0001g0080 |
2 | HG02027.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.298-700T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17687327 | |||||||
| chr10:17687350 | C | T | 1 | a0001c0001t0001g0064 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.298-677C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17687350 | |||||||
| chr10:17687373 | A | T | 2 | a0001c0001t0017g0377 a0001c0001t0017g0378 |
2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.298-654A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17687373 | |||||||
| chr10:17687394 | C | T | 1 | a0001c0001t0002g0265 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.298-633C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17687394 | |||||||
| chr10:17687421 | G | A | 97 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(94): Show |
106 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.298-606G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17687421 | |||||||
| chr10:17687495 | C | T | 1 | a0001c0001t0002g0250 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.298-532C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17687495 | |||||||
| chr10:17687500 | CA | C | 242 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(239): Show |
258 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.298-518delA | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr10 | 17687500 | ||||||
| chr10:17687519 | A | G | 9 | a0001c0001t0004g0017 a0001c0001t0004g0174 a0001c0001t0004g0175 others(6): Show |
10 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.298-508A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17687519 | |||||||
| chr10:17687533 | G | A | 1 | a0004c0011t0001g0058 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.298-494G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17687533 | |||||||
| chr10:17687534 | T | G | 1 | a0004c0011t0001g0058 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.298-493T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17687534 | |||||||
| chr10:17687731 | T | A | 3 | a0001c0001t0017g0377 a0001c0001t0017g0378 a0001c0001t0029g0376 |
3 | HG02258.hp1 HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.298-296T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17687731 | |||||||
| chr10:17687733 | CT | C | 3 | a0001c0001t0001g0005 a0001c0001t0001g0107 a0001c0001t0001g0108 |
5 | NA18952.hp1 NA18961.hp2 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.298-292delT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr10 | 17687733 | ||||||
| chr10:17687738 | C | G | 3 | a0001c0001t0003g0155 a0001c0001t0003g0156 a0001c0001t0003g0157 |
3 | HG02630.hp2 HG02818.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.298-289C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17687738 | |||||||
| chr10:17687833 | A | C | 9 | a0001c0001t0004g0017 a0001c0001t0004g0174 a0001c0001t0004g0175 others(6): Show |
10 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.298-194A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17687833 | |||||||
| chr10:17687965 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.298-62T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17687965 | |||||||
| chr10:17688246 | T | G | 3 | a0001c0001t0001g0355 a0001c0001t0030g0382 a0001c0001t0031g0381 |
3 | HG02630.hp1 HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.444+73T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17688246 | |||||||
| chr10:17688259 | G | A | 1 | a0001c0001t0009g0380 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.444+86G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17688259 | |||||||
| chr10:17688313 | G | A | 2 | a0001c0001t0002g0265 a0001c0001t0002g0266 |
2 | HG03492.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.444+140G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17688313 | |||||||
| chr10:17688417 | C | T | 27 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(24): Show |
30 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.444+244C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17688417 | |||||||
| chr10:17688485 | C | T | 1 | a0001c0001t0005g0004 | 3 | HG00639.hp2 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.444+312C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17688485 | |||||||
| chr10:17688510 | T | A | 1 | a0001c0002t0004g0347 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.444+337T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17688510 | |||||||
| chr10:17688514 | G | C | 1 | a0001c0002t0004g0347 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.444+341G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17688514 | |||||||
| chr10:17688520 | T | G | 1 | a0001c0002t0004g0347 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.444+347T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17688520 | |||||||
| chr10:17688530 | T | C | 1 | a0001c0002t0004g0347 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.444+357T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17688530 | |||||||
| chr10:17688562 | A | G | 1 | a0001c0001t0002g0189 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.444+389A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17688562 | |||||||
| chr10:17688573 | C | A | 5 | a0001c0001t0004g0204 a0001c0001t0004g0211 a0001c0001t0004g0213 others(2): Show |
5 | HG02451.hp1 HG02559.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.444+400C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17688573 | |||||||
| chr10:17688582 | C | T | 3 | a0001c0001t0012g0182 a0001c0001t0012g0383 a0001c0001t0023g0187 |
3 | HG02970.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.444+409C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17688582 | |||||||
| chr10:17688628 | AT | A | 40 | a0001c0001t0005g0047 a0001c0002t0003g0009 a0001c0002t0003g0023 others(37): Show |
42 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.444+469delT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 17688628 | ||||||
| chr10:17688682 | C | T | 1 | a0001c0001t0002g0264 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.444+509C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17688682 | |||||||
| chr10:17688730 | T | C | 1 | a0001c0002t0022g0183 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.444+557T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17688730 | |||||||
| chr10:17688888 | T | A | 7 | a0001c0001t0004g0175 a0001c0001t0004g0176 a0001c0001t0004g0177 others(4): Show |
7 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.444+715T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17688888 | |||||||
| chr10:17688939 | A | G | 1 | a0001c0001t0027g0113 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.444+766A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17688939 | |||||||
| chr10:17689026 | A | T | 15 | a0001c0002t0003g0029 a0001c0002t0003g0032 a0001c0002t0003g0159 others(12): Show |
15 | HG00099.hp2 HG01074.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.444+853A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17689026 | |||||||
| chr10:17689178 | C | T | 6 | a0001c0002t0004g0323 a0001c0002t0004g0330 a0001c0002t0004g0332 others(3): Show |
6 | HG02145.hp2 HG02559.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.444+1005C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17689178 | |||||||
| chr10:17689220 | G | C | 1 | a0001c0001t0018g0173 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.444+1047G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17689220 | |||||||
| chr10:17689273 | T | C | 25 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(22): Show |
28 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.444+1100T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17689273 | |||||||
| chr10:17689295 | A | G | 1 | a0001c0001t0004g0384 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.444+1122A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17689295 | |||||||
| chr10:17689387 | A | G | 3 | a0001c0001t0017g0377 a0001c0001t0017g0378 a0001c0001t0029g0376 |
3 | HG02258.hp1 HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.444+1214A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17689387 | |||||||
| chr10:17689389 | G | A | 6 | a0001c0001t0002g0273 a0001c0001t0002g0274 a0001c0001t0002g0275 others(3): Show |
6 | HG00735.hp1 HG00738.hp2 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.444+1216G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17689389 | |||||||
| chr10:17689391 | C | T | 25 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(22): Show |
28 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.444+1218C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17689391 | |||||||
| chr10:17689566 | A | C | 14 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0057 others(11): Show |
15 | HG00609.hp2 HG02129.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.444+1393A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17689566 | |||||||
| chr10:17689643 | A | G | 1 | a0001c0006t0028g0379 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.444+1470A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17689643 | |||||||
| chr10:17689748 | T | A | 1 | a0001c0002t0003g0105 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.444+1575T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17689748 | |||||||
| chr10:17689758 | A | G | 42 | a0001c0002t0003g0009 a0001c0002t0003g0023 a0001c0002t0003g0154 others(39): Show |
44 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.444+1585A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17689758 | |||||||
| chr10:17689971 | C | A | 25 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(22): Show |
28 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.444+1798C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17689971 | |||||||
| chr10:17690077 | C | T | 1 | a0001c0002t0022g0183 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.444+1904C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17690077 | |||||||
| chr10:17690423 | T | C | 1 | a0001c0001t0005g0049 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.444+2250T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17690423 | |||||||
| chr10:17690463 | C | T | 25 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(22): Show |
28 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.444+2290C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17690463 | |||||||
| chr10:17690476 | A | G | 2 | a0001c0001t0015g0386 a0001c0009t0015g0385 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.444+2303A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17690476 | |||||||
| chr10:17690795 | G | A | 2 | a0001c0001t0014g0131 a0001c0001t0014g0140 |
2 | HG01346.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.445-2427G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17690795 | |||||||
| chr10:17690822 | A | G | 2 | a0001c0001t0015g0386 a0001c0009t0015g0385 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.445-2400A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17690822 | |||||||
| chr10:17690827 | T | C | 1 | a0001c0001t0002g0252 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.445-2395T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17690827 | |||||||
| chr10:17691010 | A | C | 1 | a0001c0001t0001g0030 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.445-2212A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17691010 | |||||||
| chr10:17691015 | G | A | 163 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(160): Show |
175 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.445-2207G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17691015 | |||||||
| chr10:17691086 | A | G | 2 | a0001c0002t0003g0035 a0001c0002t0003g0036 |
2 | HG01243.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.445-2136A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17691086 | |||||||
| chr10:17691104 | A | C | 1 | a0001c0001t0002g0269 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.445-2118A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17691104 | |||||||
| chr10:17691170 | T | C | 2 | a0001c0001t0015g0386 a0001c0009t0015g0385 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.445-2052T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17691170 | |||||||
| chr10:17691185 | T | C | 161 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(158): Show |
174 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.445-2037T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17691185 | |||||||
| chr10:17691202 | T | G | 2 | a0001c0001t0015g0386 a0001c0009t0015g0385 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.445-2020T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17691202 | |||||||
| chr10:17691247 | G | A | 1 | a0001c0001t0004g0017 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.445-1975G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17691247 | |||||||
| chr10:17691337 | T | C | 24 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0015 others(21): Show |
28 | HG00597.hp1 HG01255.hp1 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.445-1885T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17691337 | |||||||
| chr10:17691385 | G | A | 2 | a0001c0001t0001g0102 a0001c0005t0001g0080 |
2 | HG02027.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.445-1837G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17691385 | |||||||
| chr10:17691504 | C | T | 1 | a0001c0001t0029g0376 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.445-1718C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17691504 | |||||||
| chr10:17691511 | C | CTGTCTCA others(1): Show |
25 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(22): Show |
28 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.445-1711_445-1710i others(10): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17691511 | |||||||
| chr10:17691513 | A | C | 2 | a0001c0001t0015g0386 a0001c0009t0015g0385 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.445-1709A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17691513 | |||||||
| chr10:17691828 | G | A | 3 | a0001c0001t0012g0182 a0001c0001t0012g0383 a0001c0001t0023g0187 |
3 | HG02970.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.445-1394G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17691828 | |||||||
| chr10:17691850 | T | C | 25 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(22): Show |
28 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.445-1372T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17691850 | |||||||
| chr10:17691928 | G | A | 25 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(22): Show |
28 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.445-1294G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17691928 | |||||||
| chr10:17691963 | A | C | 3 | a0001c0001t0001g0128 a0001c0001t0001g0136 a0001c0001t0001g0142 |
3 | HG00438.hp1 HG00621.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.445-1259A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17691963 | |||||||
| chr10:17692085 | C | T | 3 | a0001c0001t0004g0211 a0001c0001t0004g0213 a0001c0001t0004g0214 |
3 | HG02451.hp1 HG03041.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.445-1137C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17692085 | |||||||
| chr10:17692154 | T | A | 1 | a0001c0001t0001g0355 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.445-1068T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17692154 | |||||||
| chr10:17692247 | G | A | 239 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(236): Show |
255 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.445-975G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17692247 | |||||||
| chr10:17692277 | T | G | 36 | a0001c0001t0004g0017 a0001c0001t0004g0174 a0001c0001t0004g0175 others(33): Show |
40 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.445-945T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17692277 | |||||||
| chr10:17692304 | AGGTTGAG | A | 3 | a0001c0001t0012g0182 a0001c0001t0012g0383 a0001c0001t0023g0187 |
3 | HG02970.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.445-915_445-909del others(7): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 17692304 | ||||||
| chr10:17692361 | C | G | 25 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(22): Show |
28 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.445-861C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17692361 | |||||||
| chr10:17692363 | A | G | 4 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(1): Show |
4 | HG02145.hp1 HG03130.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.445-859A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17692363 | |||||||
| chr10:17692374 | G | C | 2 | a0001c0001t0015g0386 a0001c0009t0015g0385 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.445-848G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17692374 | |||||||
| chr10:17692403 | G | A | 1 | a0001c0001t0001g0355 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.445-819G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17692403 | |||||||
| chr10:17692547 | G | A | 1 | a0001c0006t0028g0379 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.445-675G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17692547 | |||||||
| chr10:17692767 | T | C | 7 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(4): Show |
7 | HG02145.hp1 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.445-455T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17692767 | |||||||
| chr10:17693328 | C | T | 1 | a0001c0001t0002g0230 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.535+16C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | chr10 | 17693328 | |||||||
| chr10:17693392 | G | T | 1 | a0001c0009t0015g0385 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.535+80G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | chr10 | 17693392 | |||||||
| chr10:17693478 | G | A | 1 | a0001c0001t0002g0387 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.535+166G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | chr10 | 17693478 | |||||||
| chr10:17693479 | T | G | 2 | a0001c0001t0015g0386 a0001c0009t0015g0385 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.535+167T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | chr10 | 17693479 | |||||||
| chr10:17693508 | T | C | 34 | a0001c0001t0004g0204 a0001c0001t0004g0205 a0001c0001t0004g0206 others(31): Show |
37 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.535+196T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | chr10 | 17693508 | |||||||
| chr10:17693516 | T | C | 32 | a0001c0001t0004g0204 a0001c0001t0004g0205 a0001c0001t0004g0206 others(29): Show |
35 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.535+204T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | chr10 | 17693516 | |||||||
| chr10:17693588 | C | G | 1 | a0001c0001t0002g0387 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.535+276C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | chr10 | 17693588 | |||||||
| chr10:17693588 | C | T | 2 | a0001c0001t0030g0382 a0001c0001t0031g0381 |
2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.535+276C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | chr10 | 17693588 | |||||||
| chr10:17693621 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.535+309G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | chr10 | 17693621 | |||||||
| chr10:17693677 | T | C | 10 | a0001c0001t0004g0017 a0001c0001t0004g0174 a0001c0001t0004g0175 others(7): Show |
11 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.535+365T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | chr10 | 17693677 | |||||||
| chr10:17693720 | T | C | 3 | a0001c0001t0005g0010 a0001c0001t0005g0041 a0001c0001t0008g0040 |
4 | NA18983.hp1 NA18993.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.535+408T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | chr10 | 17693720 | |||||||
| chr10:17693889 | GT | G | 32 | a0001c0001t0004g0204 a0001c0001t0004g0205 a0001c0001t0004g0206 others(29): Show |
35 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.535+579delT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 17693889 | ||||||
| chr10:17693976 | A | G | 32 | a0001c0001t0004g0204 a0001c0001t0004g0205 a0001c0001t0004g0206 others(29): Show |
35 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.535+664A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | chr10 | 17693976 | |||||||
| chr10:17693985 | G | A | 32 | a0001c0001t0004g0204 a0001c0001t0004g0205 a0001c0001t0004g0206 others(29): Show |
35 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.535+673G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | chr10 | 17693985 | |||||||
| chr10:17694183 | A | T | 1 | a0001c0001t0002g0254 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.536-866A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | chr10 | 17694183 | |||||||
| chr10:17694248 | T | A | 32 | a0001c0001t0004g0204 a0001c0001t0004g0205 a0001c0001t0004g0206 others(29): Show |
35 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.536-801T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | chr10 | 17694248 | |||||||
| chr10:17694535 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.536-514T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | chr10 | 17694535 | |||||||
| chr10:17694555 | A | G | 10 | a0001c0001t0004g0204 a0001c0001t0004g0205 a0001c0001t0004g0206 others(7): Show |
10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.536-494A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | chr10 | 17694555 | |||||||
| chr10:17694586 | G | C | 38 | a0001c0002t0003g0008 a0001c0002t0003g0009 a0001c0002t0003g0022 others(35): Show |
43 | HG00323.hp1 HG00673.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.536-463G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | chr10 | 17694586 | |||||||
| chr10:17694841 | C | G | 1 | a0001c0001t0002g0039 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.536-208C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | chr10 | 17694841 | |||||||
| chr10:17694875 | G | A | 32 | a0001c0001t0004g0204 a0001c0001t0004g0205 a0001c0001t0004g0206 others(29): Show |
35 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.536-174G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | chr10 | 17694875 | |||||||
| chr10:17694884 | T | G | 23 | a0001c0001t0004g0017 a0001c0001t0004g0018 a0001c0001t0004g0174 others(20): Show |
25 | HG00642.hp2 HG01255.hp2 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.536-165T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | chr10 | 17694884 | |||||||
| chr10:17694889 | A | G | 2 | a0001c0001t0001g0117 a0001c0001t0001g0124 |
2 | HG00140.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.536-160A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | chr10 | 17694889 | |||||||
| chr10:17695245 | A | G | 2 | a0001c0001t0002g0024 a0001c0001t0002g0354 |
3 | HG01256.hp2 HG01258.hp1 HG01978.hp1 |
splice_region_variant&intron_variant | LOW | c.728+4A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 7/13 | chr10 | 17695245 | |||||||
| chr10:17695295 | T | C | 2 | a0001c0001t0015g0386 a0001c0009t0015g0385 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.728+54T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 7/13 | chr10 | 17695295 | |||||||
| chr10:17695362 | G | A | 21 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(18): Show |
24 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.728+121G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 7/13 | chr10 | 17695362 | |||||||
| chr10:17695570 | T | A | 1 | a0001c0001t0002g0244 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.728+329T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 7/13 | chr10 | 17695570 | |||||||
| chr10:17695661 | C | G | 34 | a0001c0001t0004g0204 a0001c0001t0004g0205 a0001c0001t0004g0206 others(31): Show |
37 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.728+420C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 7/13 | chr10 | 17695661 | |||||||
| chr10:17695718 | T | C | 1 | a0001c0001t0002g0217 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.728+477T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 7/13 | chr10 | 17695718 | |||||||
| chr10:17695869 | G | A | 13 | a0001c0001t0001g0356 a0001c0001t0001g0359 a0001c0001t0001g0360 others(10): Show |
13 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.728+628G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 7/13 | chr10 | 17695869 | |||||||
| chr10:17696023 | G | T | 1 | a0001c0001t0005g0044 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.729-752G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 7/13 | chr10 | 17696023 | |||||||
| chr10:17696066 | G | A | 2 | a0001c0001t0015g0386 a0001c0009t0015g0385 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.729-709G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 7/13 | chr10 | 17696066 | |||||||
| chr10:17696106 | G | T | 125 | a0001c0001t0001g0149 a0001c0001t0001g0152 a0001c0001t0001g0185 others(122): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.729-669G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 7/13 | chr10 | 17696106 | |||||||
| chr10:17696164 | A | AT | 18 | a0001c0001t0001g0152 a0001c0001t0001g0356 a0001c0001t0001g0359 others(15): Show |
18 | HG00099.hp2 HG01069.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.729-598dupT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 17696164 | ||||||
| chr10:17696199 | G | A | 2 | a0001c0001t0015g0386 a0001c0009t0015g0385 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.729-576G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 7/13 | chr10 | 17696199 | |||||||
| chr10:17696274 | T | C | 1 | a0001c0009t0015g0385 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.729-501T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 7/13 | chr10 | 17696274 | |||||||
| chr10:17696303 | G | A | 1 | a0001c0001t0001g0355 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.729-472G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 7/13 | chr10 | 17696303 | |||||||
| chr10:17696314 | G | T | 2 | a0001c0001t0002g0024 a0001c0001t0002g0354 |
3 | HG01256.hp2 HG01258.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.729-461G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 7/13 | chr10 | 17696314 | |||||||
| chr10:17696379 | T | G | 1 | a0001c0001t0004g0200 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.729-396T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 7/13 | chr10 | 17696379 | |||||||
| chr10:17696414 | A | G | 1 | a0001c0001t0001g0370 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.729-361A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 7/13 | chr10 | 17696414 | |||||||
| chr10:17696485 | A | G | 33 | a0001c0001t0004g0204 a0001c0001t0004g0205 a0001c0001t0004g0206 others(30): Show |
36 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.729-290A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 7/13 | chr10 | 17696485 | |||||||
| chr10:17696627 | T | C | 25 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(22): Show |
28 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.729-148T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 7/13 | chr10 | 17696627 | |||||||
| chr10:17696754 | A | G | 1 | a0001c0001t0001g0067 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.729-21A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 7/13 | chr10 | 17696754 | |||||||
| chr10:17696892 | A | G | 2 | a0001c0001t0001g0095 a0001c0001t0001g0098 |
2 | HG01496.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.823+23A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17696892 | |||||||
| chr10:17696982 | C | T | 1 | a0001c0001t0002g0293 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.823+113C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17696982 | |||||||
| chr10:17697076 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.823+207T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17697076 | |||||||
| chr10:17697097 | G | C | 1 | a0001c0001t0001g0355 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.823+228G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17697097 | |||||||
| chr10:17697175 | C | T | 1 | a0001c0002t0003g0216 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.823+306C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17697175 | |||||||
| chr10:17697220 | C | T | 1 | a0001c0001t0009g0380 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.823+351C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17697220 | |||||||
| chr10:17697244 | A | G | 1 | a0001c0001t0004g0213 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.823+375A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17697244 | |||||||
| chr10:17697284 | A | AT | 3 | a0001c0001t0001g0005 a0001c0001t0001g0107 a0001c0001t0001g0108 |
5 | NA18952.hp1 NA18961.hp2 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.823+417dupT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr10 | 17697284 | ||||||
| chr10:17697407 | T | A | 25 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(22): Show |
28 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.823+538T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17697407 | |||||||
| chr10:17697645 | A | C | 1 | a0001c0001t0009g0380 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.823+776A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17697645 | |||||||
| chr10:17697660 | T | G | 10 | a0001c0001t0002g0221 a0001c0001t0002g0235 a0001c0001t0002g0254 others(7): Show |
10 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(7): Show |
intron_variant | MODIFIER | c.823+791T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17697660 | |||||||
| chr10:17697722 | C | CTATT | 25 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(22): Show |
28 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.823+855_823+856ins others(4): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr10 | 17697722 | ||||||
| chr10:17697798 | T | A | 7 | a0001c0001t0001g0149 a0001c0001t0001g0152 a0001c0001t0002g0150 others(4): Show |
7 | HG01192.hp1 HG02572.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.823+929T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17697798 | |||||||
| chr10:17697804 | G | A | 348 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(345): Show |
378 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(375): Show |
intron_variant | MODIFIER | c.823+935G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17697804 | |||||||
| chr10:17697844 | A | G | 2 | a0001c0001t0010g0111 a0001c0001t0010g0212 |
2 | HG02572.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.823+975A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17697844 | |||||||
| chr10:17697850 | G | A | 1 | a0001c0001t0002g0387 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.823+981G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17697850 | |||||||
| chr10:17698093 | C | G | 3 | a0001c0001t0003g0155 a0001c0001t0003g0156 a0001c0001t0003g0157 |
3 | HG02630.hp2 HG02818.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.823+1224C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17698093 | |||||||
| chr10:17698125 | G | C | 1 | a0001c0001t0002g0234 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.823+1256G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17698125 | |||||||
| chr10:17698148 | G | A | 98 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(95): Show |
107 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.823+1279G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17698148 | |||||||
| chr10:17698260 | C | T | 1 | a0001c0001t0029g0376 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.823+1391C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17698260 | |||||||
| chr10:17698302 | T | C | 2 | a0001c0001t0002g0265 a0001c0001t0002g0266 |
2 | HG03492.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.823+1433T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17698302 | |||||||
| chr10:17698412 | C | T | 21 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(18): Show |
24 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.823+1543C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17698412 | |||||||
| chr10:17698421 | C | CT | 20 | a0001c0001t0001g0081 a0001c0001t0001g0088 a0001c0001t0001g0356 others(17): Show |
20 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.823+1565dupT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr10 | 17698421 | ||||||
| chr10:17698459 | A | G | 4 | a0001c0001t0004g0033 a0001c0001t0004g0056 a0001c0002t0003g0035 others(1): Show |
4 | HG01243.hp2 HG03516.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.823+1590A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17698459 | |||||||
| chr10:17698463 | G | A | 4 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(1): Show |
4 | HG02280.hp1 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.823+1594G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17698463 | |||||||
| chr10:17698494 | C | G | 4 | a0001c0001t0009g0380 a0001c0001t0017g0377 a0001c0001t0017g0378 others(1): Show |
4 | HG02258.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.823+1625C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17698494 | |||||||
| chr10:17698500 | G | A | 97 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(94): Show |
106 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.823+1631G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17698500 | |||||||
| chr10:17698507 | AAG | A | 3 | a0001c0001t0012g0182 a0001c0001t0012g0383 a0001c0001t0023g0187 |
3 | HG02970.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.823+1642_823+1643d others(4): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr10 | 17698507 | ||||||
| chr10:17698655 | G | A | 4 | a0001c0001t0004g0033 a0001c0001t0004g0056 a0001c0002t0003g0035 others(1): Show |
4 | HG01243.hp2 HG03516.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.824-1536G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17698655 | |||||||
| chr10:17698795 | G | A | 1 | a0001c0002t0022g0183 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.824-1396G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17698795 | |||||||
| chr10:17698865 | A | G | 2 | a0001c0001t0017g0377 a0001c0001t0017g0378 |
2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.824-1326A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17698865 | |||||||
| chr10:17698923 | C | G | 21 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(18): Show |
24 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.824-1268C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17698923 | |||||||
| chr10:17698974 | T | C | 3 | a0001c0001t0002g0193 a0001c0001t0002g0194 a0001c0001t0002g0195 |
3 | HG02109.hp1 HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.824-1217T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17698974 | |||||||
| chr10:17698989 | A | G | 11 | a0001c0001t0004g0017 a0001c0001t0004g0174 a0001c0001t0004g0175 others(8): Show |
12 | HG01255.hp2 HG01256.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.824-1202A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17698989 | |||||||
| chr10:17699047 | A | C | 8 | a0001c0001t0004g0204 a0001c0001t0004g0205 a0001c0001t0004g0206 others(5): Show |
8 | HG01884.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.824-1144A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17699047 | |||||||
| chr10:17699060 | T | G | 1 | a0001c0001t0032g0225 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.824-1131T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17699060 | |||||||
| chr10:17699108 | A | G | 1 | a0001c0001t0001g0101 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.824-1083A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17699108 | |||||||
| chr10:17699186 | A | G | 11 | a0001c0001t0004g0017 a0001c0001t0004g0174 a0001c0001t0004g0175 others(8): Show |
12 | HG01255.hp2 HG01256.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.824-1005A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17699186 | |||||||
| chr10:17699213 | A | G | 1 | a0001c0001t0002g0387 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.824-978A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17699213 | |||||||
| chr10:17699270 | T | C | 1 | a0001c0001t0001g0065 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.824-921T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17699270 | |||||||
| chr10:17699361 | T | A | 1 | a0001c0001t0005g0041 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.824-830T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17699361 | |||||||
| chr10:17699412 | G | A | 97 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(94): Show |
106 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.824-779G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17699412 | |||||||
| chr10:17699488 | T | C | 25 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(22): Show |
28 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.824-703T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17699488 | |||||||
| chr10:17699492 | T | C | 1 | a0001c0001t0006g0210 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.824-699T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17699492 | |||||||
| chr10:17699672 | C | T | 72 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(69): Show |
75 | HG00323.hp1 HG00558.hp1 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.824-519C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17699672 | |||||||
| chr10:17699691 | A | G | 13 | a0001c0001t0004g0017 a0001c0001t0004g0033 a0001c0001t0004g0056 others(10): Show |
14 | HG01243.hp2 HG01255.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.824-500A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17699691 | |||||||
| chr10:17699697 | C | T | 1 | a0001c0006t0028g0379 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.824-494C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17699697 | |||||||
| chr10:17699768 | A | AC | 3 | a0001c0001t0003g0155 a0001c0001t0003g0156 a0001c0001t0003g0157 |
3 | HG02630.hp2 HG02818.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.824-423_824-422ins others(1): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17699768 | |||||||
| chr10:17700348 | A | G | 1 | a0001c0001t0031g0381 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.912+69A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17700348 | |||||||
| chr10:17700351 | A | C | 3 | a0001c0001t0017g0377 a0001c0001t0017g0378 a0001c0001t0029g0376 |
3 | HG02258.hp1 HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.912+72A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17700351 | |||||||
| chr10:17700466 | G | A | 2 | a0001c0001t0001g0067 a0004c0011t0001g0058 |
2 | NA18940.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.912+187G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17700466 | |||||||
| chr10:17700563 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.912+284C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17700563 | |||||||
| chr10:17700570 | T | G | 14 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0057 others(11): Show |
16 | HG00609.hp2 HG02109.hp2 HG02129.hp2 others(13): Show |
intron_variant | MODIFIER | c.912+291T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17700570 | |||||||
| chr10:17700587 | A | AT | 34 | a0001c0001t0001g0355 a0001c0001t0002g0150 a0001c0001t0004g0033 others(31): Show |
37 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.912+322dupT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr10 | 17700587 | ||||||
| chr10:17700587 | AT | A | 118 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0285 others(115): Show |
132 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.912+322delT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr10 | 17700587 | ||||||
| chr10:17700606 | A | T | 1 | a0001c0001t0001g0096 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.912+327A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17700606 | |||||||
| chr10:17700611 | T | C | 2 | a0001c0001t0001g0356 a0001c0001t0001g0362 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.912+332T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17700611 | |||||||
| chr10:17700672 | A | G | 25 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(22): Show |
28 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.912+393A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17700672 | |||||||
| chr10:17700725 | C | G | 1 | a0001c0001t0009g0380 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.912+446C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17700725 | |||||||
| chr10:17700770 | A | C | 126 | a0001c0001t0001g0149 a0001c0001t0001g0152 a0001c0001t0001g0185 others(123): Show |
140 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.912+491A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17700770 | |||||||
| chr10:17700792 | CA | C | 14 | a0001c0001t0001g0356 a0001c0001t0001g0359 a0001c0001t0001g0360 others(11): Show |
14 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.912+514delA | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17700792 | |||||||
| chr10:17700813 | C | T | 2 | a0001c0001t0007g0256 a0001c0001t0007g0257 |
2 | HG02602.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.912+534C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17700813 | |||||||
| chr10:17700823 | A | G | 1 | a0001c0001t0009g0309 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.912+544A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17700823 | |||||||
| chr10:17700881 | A | T | 4 | a0001c0001t0004g0033 a0001c0001t0004g0056 a0001c0002t0003g0035 others(1): Show |
4 | HG01243.hp2 HG03516.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.912+602A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17700881 | |||||||
| chr10:17700925 | T | C | 4 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(1): Show |
4 | HG02145.hp1 HG03130.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.912+646T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17700925 | |||||||
| chr10:17700987 | C | A | 1 | a0001c0001t0002g0304 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.912+708C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17700987 | |||||||
| chr10:17700987 | C | T | 1 | a0001c0001t0001g0355 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.912+708C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17700987 | |||||||
| chr10:17701228 | G | T | 83 | a0001c0001t0002g0387 a0001c0001t0003g0025 a0001c0001t0003g0026 others(80): Show |
89 | HG00323.hp1 HG00558.hp1 HG00642.hp2 others(86): Show |
intron_variant | MODIFIER | c.912+949G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17701228 | |||||||
| chr10:17701273 | AAAT | A | 114 | a0001c0001t0001g0285 a0001c0001t0002g0001 a0001c0001t0002g0002 others(111): Show |
128 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.912+997_912+999del others(3): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr10 | 17701273 | ||||||
| chr10:17701319 | A | G | 9 | a0001c0001t0004g0017 a0001c0001t0004g0174 a0001c0001t0004g0175 others(6): Show |
10 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.912+1040A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17701319 | |||||||
| chr10:17701385 | A | G | 1 | a0001c0001t0002g0237 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.912+1106A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17701385 | |||||||
| chr10:17701727 | C | A | 4 | a0001c0001t0002g0228 a0001c0001t0002g0249 a0001c0001t0002g0287 others(1): Show |
4 | NA18952.hp2 NA18961.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.912+1448C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17701727 | |||||||
| chr10:17701727 | C | T | 1 | a0001c0001t0002g0289 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.912+1448C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17701727 | |||||||
| chr10:17701765 | G | A | 3 | a0001c0002t0003g0374 a0001c0002t0003g0375 a0001c0002t0020g0373 |
3 | NA18957.hp1 NA18967.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.912+1486G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17701765 | |||||||
| chr10:17701861 | G | C | 58 | a0001c0002t0003g0008 a0001c0002t0003g0009 a0001c0002t0003g0022 others(55): Show |
63 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.912+1582G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17701861 | |||||||
| chr10:17701890 | A | G | 2 | a0001c0001t0015g0386 a0001c0009t0015g0385 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.912+1611A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17701890 | |||||||
| chr10:17701894 | AAC | A | 24 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(21): Show |
27 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.912+1619_912+1620d others(4): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr10 | 17701894 | ||||||
| chr10:17702220 | A | C | 18 | a0001c0001t0001g0356 a0001c0001t0001g0359 a0001c0001t0001g0360 others(15): Show |
18 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.912+1941A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17702220 | |||||||
| chr10:17702303 | C | A | 2 | a0001c0001t0017g0377 a0001c0001t0017g0378 |
2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.912+2024C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17702303 | |||||||
| chr10:17702373 | A | C | 1 | a0001c0001t0015g0386 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.913-2058A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17702373 | |||||||
| chr10:17702454 | C | T | 2 | a0001c0002t0003g0035 a0001c0002t0003g0036 |
2 | HG01243.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.913-1977C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17702454 | |||||||
| chr10:17702585 | A | G | 7 | a0001c0001t0001g0119 a0001c0001t0001g0127 a0001c0001t0001g0130 others(4): Show |
7 | NA18944.hp2 NA19010.hp2 NA19056.hp1 others(4): Show |
intron_variant | MODIFIER | c.913-1846A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17702585 | |||||||
| chr10:17702748 | G | A | 9 | a0001c0001t0002g0387 a0001c0001t0003g0025 a0001c0001t0003g0026 others(6): Show |
9 | HG02145.hp1 HG02630.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.913-1683G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17702748 | |||||||
| chr10:17702776 | G | A | 1 | a0001c0001t0005g0044 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.913-1655G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17702776 | |||||||
| chr10:17702785 | A | G | 27 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(24): Show |
30 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.913-1646A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17702785 | |||||||
| chr10:17702802 | C | T | 1 | a0001c0001t0002g0298 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.913-1629C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17702802 | |||||||
| chr10:17702806 | G | C | 1 | a0001c0001t0001g0057 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.913-1625G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17702806 | |||||||
| chr10:17702823 | C | T | 3 | a0001c0001t0001g0005 a0001c0001t0001g0107 a0001c0001t0001g0108 |
5 | NA18952.hp1 NA18961.hp2 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.913-1608C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17702823 | |||||||
| chr10:17702829 | G | A | 3 | a0001c0001t0012g0182 a0001c0001t0012g0383 a0001c0001t0023g0187 |
3 | HG02970.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.913-1602G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17702829 | |||||||
| chr10:17702861 | C | T | 3 | a0001c0001t0003g0155 a0001c0001t0003g0156 a0001c0001t0003g0157 |
3 | HG02630.hp2 HG02818.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.913-1570C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17702861 | |||||||
| chr10:17702980 | G | A | 1 | a0001c0001t0002g0286 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.913-1451G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17702980 | |||||||
| chr10:17703008 | C | CA | 40 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(37): Show |
41 | HG00140.hp1 HG00673.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.913-1404dupA | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr10 | 17703008 | ||||||
| chr10:17703008 | C | CAAA | 9 | a0001c0001t0001g0149 a0001c0001t0001g0152 a0001c0001t0001g0185 others(6): Show |
9 | HG01192.hp1 HG02258.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.913-1406_913-1404d others(5): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr10 | 17703008 | ||||||
| chr10:17703008 | CA | C | 14 | a0001c0001t0001g0063 a0001c0001t0001g0104 a0001c0001t0001g0126 others(11): Show |
14 | HG00323.hp1 HG00558.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.913-1404delA | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr10 | 17703008 | ||||||
| chr10:17703015 | AAAAAAAA others(6): Show |
A | 25 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(22): Show |
28 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.913-1411_913-1399d others(15): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr10 | 17703015 | ||||||
| chr10:17703018 | AAAAAAAA others(3): Show |
A | 1 | a0001c0006t0028g0379 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.913-1408_913-1399d others(12): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr10 | 17703018 | ||||||
| chr10:17703023 | AAAAAG | A | 9 | a0001c0001t0001g0003 a0001c0001t0001g0068 a0001c0001t0001g0084 others(6): Show |
9 | HG02622.hp2 HG02970.hp1 HG03471.hp1 others(6): Show |
intron_variant | MODIFIER | c.913-1383_913-1379d others(7): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr10 | 17703023 | ||||||
| chr10:17703023 | AAAAAGAA others(3): Show |
A | 3 | a0001c0001t0001g0030 a0001c0001t0030g0382 a0001c0001t0031g0381 |
3 | HG02717.hp2 HG03195.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.913-1388_913-1379d others(12): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr10 | 17703023 | ||||||
| chr10:17703026 | AAG | A | 104 | a0001c0001t0001g0285 a0001c0001t0002g0001 a0001c0001t0002g0002 others(101): Show |
116 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.913-1403_913-1402d others(4): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr10 | 17703026 | ||||||
| chr10:17703027 | AG | A | 8 | a0001c0001t0002g0007 a0001c0001t0002g0021 a0001c0001t0002g0228 others(5): Show |
8 | NA18943.hp2 NA18952.hp2 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.913-1403delG | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17703027 | |||||||
| chr10:17703125 | A | G | 125 | a0001c0001t0001g0149 a0001c0001t0001g0152 a0001c0001t0001g0185 others(122): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.913-1306A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17703125 | |||||||
| chr10:17703198 | T | C | 3 | a0001c0002t0003g0335 a0001c0002t0003g0336 a0001c0002t0003g0348 |
3 | NA18968.hp2 NA19004.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.913-1233T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17703198 | |||||||
| chr10:17703231 | C | G | 2 | a0001c0002t0003g0162 a0001c0002t0003g0167 |
2 | HG01928.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.913-1200C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17703231 | |||||||
| chr10:17703331 | G | GT | 7 | a0001c0001t0001g0355 a0001c0001t0002g0219 a0001c0001t0002g0313 others(4): Show |
7 | HG00323.hp1 HG01175.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.913-1086dupT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr10 | 17703331 | ||||||
| chr10:17703331 | GT | G | 6 | a0001c0001t0001g0063 a0001c0001t0001g0089 a0001c0001t0001g0124 others(3): Show |
6 | HG02965.hp2 NA18987.hp2 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.913-1086delT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr10 | 17703331 | ||||||
| chr10:17703377 | A | G | 1 | a0001c0001t0004g0305 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.913-1054A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17703377 | |||||||
| chr10:17703481 | C | G | 3 | a0001c0001t0002g0275 a0001c0001t0002g0282 a0001c0001t0032g0225 |
3 | HG00735.hp1 HG00738.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.913-950C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17703481 | |||||||
| chr10:17703501 | A | T | 3 | a0001c0001t0012g0182 a0001c0001t0012g0383 a0001c0001t0023g0187 |
3 | HG02970.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.913-930A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17703501 | |||||||
| chr10:17703551 | A | G | 1 | a0001c0001t0001g0074 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.913-880A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17703551 | |||||||
| chr10:17703589 | A | T | 24 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(21): Show |
27 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.913-842A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17703589 | |||||||
| chr10:17703594 | C | A | 24 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(21): Show |
27 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.913-837C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17703594 | |||||||
| chr10:17703595 | A | G | 1 | a0001c0006t0028g0379 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.913-836A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17703595 | |||||||
| chr10:17703630 | A | C | 1 | a0001c0001t0002g0241 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.913-801A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17703630 | |||||||
| chr10:17703663 | A | C | 1 | a0001c0001t0004g0205 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.913-768A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17703663 | |||||||
| chr10:17703997 | G | A | 317 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(314): Show |
345 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(342): Show |
intron_variant | MODIFIER | c.913-434G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17703997 | |||||||
| chr10:17704001 | T | C | 2 | a0001c0001t0001g0152 a0001c0001t0002g0150 |
2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.913-430T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17704001 | |||||||
| chr10:17704074 | T | C | 7 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(4): Show |
7 | HG02145.hp1 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.913-357T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17704074 | |||||||
| chr10:17704088 | G | A | 2 | a0001c0001t0014g0131 a0001c0001t0014g0140 |
2 | HG01346.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.913-343G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17704088 | |||||||
| chr10:17704178 | G | T | 1 | a0001c0001t0023g0187 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.913-253G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17704178 | |||||||
| chr10:17704302 | C | A | 26 | a0001c0001t0004g0033 a0001c0001t0004g0056 a0001c0001t0005g0004 others(23): Show |
29 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.913-129C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17704302 | |||||||
| chr10:17704306 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.913-125A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17704306 | |||||||
| chr10:17704612 | A | C | 21 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(18): Show |
24 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.1000+94A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 10/13 | chr10 | 17704612 | |||||||
| chr10:17704697 | T | A | 1 | a0001c0009t0015g0385 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1000+179T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 10/13 | chr10 | 17704697 | |||||||
| chr10:17704719 | G | A | 2 | a0001c0001t0030g0382 a0001c0001t0031g0381 |
2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1000+201G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 10/13 | chr10 | 17704719 | |||||||
| chr10:17704752 | T | C | 17 | a0001c0001t0004g0018 a0001c0001t0004g0033 a0001c0001t0004g0056 others(14): Show |
18 | HG00642.hp2 HG01884.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.1001-218T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 10/13 | chr10 | 17704752 | |||||||
| chr10:17704754 | G | A | 2 | a0001c0001t0001g0030 a0001c0006t0028g0379 |
2 | HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1001-216G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 10/13 | chr10 | 17704754 | |||||||
| chr10:17704769 | C | T | 100 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(97): Show |
109 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1001-201C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 10/13 | chr10 | 17704769 | |||||||
| chr10:17704935 | A | G | 1 | a0001c0001t0015g0386 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1001-35A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 10/13 | chr10 | 17704935 | |||||||
| chr10:17705054 | G | C | 25 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(22): Show |
28 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.1055+30G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 11/13 | chr10 | 17705054 | |||||||
| chr10:17705109 | T | TA | 24 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(21): Show |
27 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.1055+95dupA | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr10 | 17705109 | ||||||
| chr10:17705122 | T | C | 8 | a0001c0001t0002g0034 a0001c0001t0002g0184 a0001c0001t0002g0188 others(5): Show |
8 | HG00099.hp1 HG02109.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1055+98T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 11/13 | chr10 | 17705122 | |||||||
| chr10:17705190 | T | C | 2 | a0001c0001t0017g0377 a0001c0001t0017g0378 |
2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1055+166T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 11/13 | chr10 | 17705190 | |||||||
| chr10:17705276 | A | G | 24 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(21): Show |
27 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.1055+252A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 11/13 | chr10 | 17705276 | |||||||
| chr10:17705390 | C | T | 1 | a0001c0006t0028g0379 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1056-198C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 11/13 | chr10 | 17705390 | |||||||
| chr10:17705449 | A | G | 3 | a0001c0001t0012g0182 a0001c0001t0012g0383 a0001c0001t0023g0187 |
3 | HG02970.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1056-139A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 11/13 | chr10 | 17705449 | |||||||
| chr10:17705501 | C | T | 24 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(21): Show |
27 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.1056-87C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 11/13 | chr10 | 17705501 | |||||||
| chr10:17705813 | A | G | 102 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(99): Show |
111 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.1209+72A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17705813 | |||||||
| chr10:17705880 | T | C | 24 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(21): Show |
27 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.1209+139T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17705880 | |||||||
| chr10:17705905 | C | CA | 27 | a0001c0001t0001g0059 a0001c0001t0001g0085 a0001c0001t0001g0356 others(24): Show |
27 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.1209+181dupA | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr10 | 17705905 | ||||||
| chr10:17705905 | CA | C | 21 | a0001c0001t0001g0063 a0001c0001t0005g0004 a0001c0001t0005g0010 others(18): Show |
24 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.1209+181delA | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr10 | 17705905 | ||||||
| chr10:17705909 | A | G | 1 | a0001c0001t0015g0386 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1209+168A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17705909 | |||||||
| chr10:17706052 | C | T | 1 | a0001c0009t0015g0385 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1209+311C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706052 | |||||||
| chr10:17706053 | G | A | 1 | a0001c0001t0002g0290 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1209+312G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706053 | |||||||
| chr10:17706064 | T | G | 2 | a0001c0001t0017g0377 a0001c0001t0017g0378 |
2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1209+323T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706064 | |||||||
| chr10:17706127 | T | G | 18 | a0001c0001t0001g0016 a0001c0001t0001g0115 a0001c0001t0001g0120 others(15): Show |
19 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.1209+386T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706127 | |||||||
| chr10:17706154 | A | T | 1 | a0001c0002t0003g0326 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1209+413A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706154 | |||||||
| chr10:17706173 | G | A | 285 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(282): Show |
314 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.1209+432G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706173 | |||||||
| chr10:17706199 | C | G | 1 | a0001c0001t0001g0106 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1209+458C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706199 | |||||||
| chr10:17706215 | T | G | 1 | a0001c0002t0003g0326 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1209+474T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706215 | |||||||
| chr10:17706223 | T | A | 24 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(21): Show |
27 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.1209+482T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706223 | |||||||
| chr10:17706229 | TTTG | T | 48 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0015 others(45): Show |
55 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.1209+503_1209+505d others(5): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr10 | 17706229 | ||||||
| chr10:17706232 | G | T | 1 | a0001c0002t0003g0326 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1209+491G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706232 | |||||||
| chr10:17706247 | T | G | 1 | a0001c0002t0003g0326 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1209+506T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706247 | |||||||
| chr10:17706256 | T | G | 1 | a0001c0002t0003g0326 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1209+515T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706256 | |||||||
| chr10:17706259 | C | G | 24 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(21): Show |
27 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.1209+518C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706259 | |||||||
| chr10:17706261 | T | G | 1 | a0001c0002t0003g0326 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1209+520T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706261 | |||||||
| chr10:17706264 | A | G | 1 | a0001c0002t0003g0326 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1209+523A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706264 | |||||||
| chr10:17706270 | G | T | 1 | a0001c0002t0003g0326 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1209+529G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706270 | |||||||
| chr10:17706272 | T | G | 1 | a0001c0002t0003g0326 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1209+531T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706272 | |||||||
| chr10:17706274 | A | G | 1 | a0001c0002t0003g0326 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1209+533A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706274 | |||||||
| chr10:17706285 | T | A | 102 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(99): Show |
111 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.1209+544T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706285 | |||||||
| chr10:17706308 | A | G | 1 | a0001c0002t0003g0326 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1209+567A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706308 | |||||||
| chr10:17706317 | T | G | 1 | a0001c0002t0003g0326 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1209+576T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706317 | |||||||
| chr10:17706369 | C | CT | 67 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0060 others(64): Show |
70 | HG00140.hp1 HG00621.hp1 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.1209+655dupT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr10 | 17706369 | ||||||
| chr10:17706369 | C | CTT | 95 | a0001c0001t0001g0030 a0001c0001t0001g0059 a0001c0001t0001g0062 others(92): Show |
105 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.1209+654_1209+655d others(4): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr10 | 17706369 | ||||||
| chr10:17706369 | C | CTTT | 33 | a0001c0001t0001g0125 a0001c0001t0002g0002 a0001c0001t0002g0006 others(30): Show |
38 | HG00140.hp2 HG00438.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.1209+653_1209+655d others(5): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr10 | 17706369 | ||||||
| chr10:17706369 | C | CTTTT | 14 | a0001c0001t0002g0024 a0001c0001t0002g0184 a0001c0001t0002g0226 others(11): Show |
16 | HG01123.hp1 HG01256.hp2 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1209+652_1209+655d others(6): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr10 | 17706369 | ||||||
| chr10:17706369 | CT | C | 67 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0015 others(64): Show |
73 | HG00609.hp2 HG01069.hp1 HG01071.hp2 others(70): Show |
intron_variant | MODIFIER | c.1209+655delT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr10 | 17706369 | ||||||
| chr10:17706369 | CTT | C | 14 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0057 others(11): Show |
15 | HG01884.hp2 HG02055.hp1 HG02129.hp2 others(12): Show |
intron_variant | MODIFIER | c.1209+654_1209+655d others(4): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr10 | 17706369 | ||||||
| chr10:17706369 | CTTTT | C | 20 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(17): Show |
23 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.1209+652_1209+655d others(6): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr10 | 17706369 | ||||||
| chr10:17706369 | CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0002g0224 a0001c0001t0002g0295 a0001c0001t0002g0296 |
3 | HG00423.hp2 NA18968.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.1209+644_1209+655d others(14): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr10 | 17706369 | ||||||
| chr10:17706373 | T | A | 1 | a0001c0002t0003g0326 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1209+632T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706373 | |||||||
| chr10:17706373 | T | C | 4 | a0001c0001t0005g0051 a0001c0001t0009g0309 a0001c0001t0017g0377 others(1): Show |
4 | HG01123.hp2 HG02258.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1209+632T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706373 | |||||||
| chr10:17706374 | T | C | 20 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(17): Show |
23 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.1209+633T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706374 | |||||||
| chr10:17706401 | C | T | 3 | a0001c0001t0012g0182 a0001c0001t0012g0383 a0001c0001t0023g0187 |
3 | HG02970.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1209+660C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706401 | |||||||
| chr10:17706402 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1209+661G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706402 | |||||||
| chr10:17706413 | C | T | 1 | a0001c0002t0003g0326 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1209+672C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706413 | |||||||
| chr10:17706417 | G | T | 1 | a0001c0002t0003g0326 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1209+676G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706417 | |||||||
| chr10:17706668 | C | G | 1 | a0001c0001t0001g0143 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1209+927C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706668 | |||||||
| chr10:17706701 | C | T | 1 | a0001c0009t0015g0385 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1209+960C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706701 | |||||||
| chr10:17706722 | G | T | 3 | a0001c0001t0012g0182 a0001c0001t0012g0383 a0001c0001t0023g0187 |
3 | HG02970.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1209+981G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706722 | |||||||
| chr10:17707029 | G | C | 3 | a0001c0001t0012g0182 a0001c0001t0012g0383 a0001c0001t0023g0187 |
3 | HG02970.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1209+1288G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17707029 | |||||||
| chr10:17707079 | A | G | 31 | a0001c0001t0004g0017 a0001c0001t0004g0018 a0001c0001t0004g0174 others(28): Show |
33 | HG00642.hp2 HG01255.hp2 HG01256.hp1 others(30): Show |
intron_variant | MODIFIER | c.1209+1338A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17707079 | |||||||
| chr10:17707175 | C | T | 99 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(96): Show |
108 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.1209+1434C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17707175 | |||||||
| chr10:17707308 | G | C | 230 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(227): Show |
253 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.1210-1468G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17707308 | |||||||
| chr10:17707334 | C | T | 1 | a0001c0001t0009g0380 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1210-1442C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17707334 | |||||||
| chr10:17707358 | C | G | 58 | a0001c0002t0003g0008 a0001c0002t0003g0009 a0001c0002t0003g0022 others(55): Show |
63 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.1210-1418C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17707358 | |||||||
| chr10:17707480 | G | A | 2 | a0001c0001t0005g0047 a0001c0001t0005g0053 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1210-1296G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17707480 | |||||||
| chr10:17707488 | G | A | 1 | a0001c0009t0015g0385 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1210-1288G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17707488 | |||||||
| chr10:17707585 | T | C | 1 | a0001c0002t0003g0339 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1210-1191T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17707585 | |||||||
| chr10:17707587 | G | T | 1 | a0001c0001t0001g0070 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1210-1189G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17707587 | |||||||
| chr10:17707915 | G | A | 1 | a0001c0001t0002g0290 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1210-861G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17707915 | |||||||
| chr10:17708035 | C | T | 2 | a0001c0002t0003g0310 a0001c0002t0003g0339 |
2 | HG00558.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1210-741C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17708035 | |||||||
| chr10:17708073 | G | T | 1 | a0001c0001t0009g0309 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1210-703G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17708073 | |||||||
| chr10:17708081 | G | A | 3 | a0001c0001t0009g0380 a0001c0001t0015g0386 a0001c0009t0015g0385 |
3 | HG01884.hp2 HG02055.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1210-695G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17708081 | |||||||
| chr10:17708096 | T | C | 1 | a0001c0001t0002g0295 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1210-680T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17708096 | |||||||
| chr10:17708162 | T | G | 13 | a0001c0001t0002g0221 a0001c0001t0002g0259 a0001c0001t0002g0261 others(10): Show |
16 | NA18939.hp2 NA18940.hp1 NA18941.hp2 others(13): Show |
intron_variant | MODIFIER | c.1210-614T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17708162 | |||||||
| chr10:17708171 | T | G | 1 | a0001c0001t0010g0212 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1210-605T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17708171 | |||||||
| chr10:17708261 | C | G | 5 | a0001c0001t0006g0203 a0001c0001t0006g0207 a0001c0001t0006g0208 others(2): Show |
5 | HG02615.hp2 HG02922.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1210-515C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17708261 | |||||||
| chr10:17708264 | C | T | 2 | a0001c0001t0017g0377 a0001c0001t0017g0378 |
2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1210-512C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17708264 | |||||||
| chr10:17708545 | A | C | 103 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(100): Show |
112 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.1210-231A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17708545 | |||||||
| chr10:17708594 | C | CATCA | 8 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(5): Show |
8 | HG02145.hp1 HG02630.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1210-180_1210-177d others(6): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr10 | 17708594 | ||||||
| chr10:17708636 | C | T | 133 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(130): Show |
142 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.1210-140C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17708636 | |||||||
| chr10:17708969 | T | G | 9 | a0001c0001t0004g0017 a0001c0001t0004g0174 a0001c0001t0004g0175 others(6): Show |
10 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.1385+18T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17708969 | |||||||
| chr10:17709003 | A | T | 24 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(21): Show |
27 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.1385+52A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17709003 | |||||||
| chr10:17709047 | T | C | 21 | a0001c0001t0001g0356 a0001c0001t0001g0359 a0001c0001t0001g0360 others(18): Show |
21 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.1385+96T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17709047 | |||||||
| chr10:17709055 | C | T | 9 | a0001c0001t0004g0017 a0001c0001t0004g0174 a0001c0001t0004g0175 others(6): Show |
10 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.1385+104C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17709055 | |||||||
| chr10:17709113 | A | G | 1 | a0001c0006t0028g0379 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1385+162A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17709113 | |||||||
| chr10:17709163 | A | C | 1 | a0001c0001t0001g0149 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1385+212A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17709163 | |||||||
| chr10:17709220 | T | A | 3 | a0001c0001t0001g0134 a0001c0003t0001g0118 a0001c0003t0001g0151 |
3 | NA18944.hp2 NA19070.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.1385+269T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17709220 | |||||||
| chr10:17709323 | C | T | 21 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(18): Show |
24 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.1385+372C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17709323 | |||||||
| chr10:17709342 | G | C | 1 | a0001c0001t0001g0130 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1385+391G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17709342 | |||||||
| chr10:17709354 | CTCTT | C | 2 | a0001c0001t0002g0020 a0001c0001t0002g0262 |
3 | HG00738.hp1 HG01346.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1385+405_1385+408d others(6): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr10 | 17709354 | ||||||
| chr10:17709477 | A | C | 44 | a0001c0002t0003g0009 a0001c0002t0003g0023 a0001c0002t0003g0154 others(41): Show |
46 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.1385+526A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17709477 | |||||||
| chr10:17709590 | G | A | 24 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(21): Show |
27 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.1385+639G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17709590 | |||||||
| chr10:17709682 | C | T | 1 | a0001c0006t0028g0379 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1385+731C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17709682 | |||||||
| chr10:17709731 | G | C | 5 | a0001c0001t0001g0356 a0001c0001t0001g0359 a0001c0001t0001g0361 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1385+780G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17709731 | |||||||
| chr10:17709776 | C | T | 2 | a0001c0001t0017g0377 a0001c0001t0017g0378 |
2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1385+825C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17709776 | |||||||
| chr10:17709798 | G | A | 92 | a0001c0001t0001g0356 a0001c0001t0001g0359 a0001c0001t0001g0360 others(89): Show |
95 | HG00323.hp1 HG00558.hp1 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.1385+847G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17709798 | |||||||
| chr10:17709963 | G | GCAGGATT others(309): Show |
7 | a0001c0001t0001g0030 a0001c0001t0001g0061 a0001c0001t0001g0070 others(4): Show |
7 | HG01257.hp2 HG01975.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.1385+1026_1385+102 others(320): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr10 | 17709963 | ||||||
| chr10:17709963 | G | GCAGGATT others(310): Show |
3 | a0001c0001t0001g0084 a0001c0001t0001g0086 a0001c0001t0001g0097 |
3 | NA18970.hp1 NA18982.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1385+1026_1385+102 others(321): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr10 | 17709963 | ||||||
| chr10:17709963 | G | GCAGGATT others(310): Show |
60 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(57): Show |
68 | HG00140.hp1 HG00423.hp1 HG01255.hp1 others(65): Show |
intron_variant | MODIFIER | c.1385+1026_1385+102 others(321): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr10 | 17709963 | ||||||
| chr10:17709963 | G | GCAGGATT others(310): Show |
1 | a0004c0011t0001g0058 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1385+1026_1385+102 others(321): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr10 | 17709963 | ||||||
| chr10:17709963 | G | GCAGGATT others(311): Show |
2 | a0001c0001t0001g0085 a0001c0001t0001g0087 |
2 | NA18991.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1385+1026_1385+102 others(322): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr10 | 17709963 | ||||||
| chr10:17709963 | G | GCAGGATT others(311): Show |
26 | a0001c0001t0001g0057 a0001c0001t0001g0059 a0001c0001t0001g0064 others(23): Show |
27 | HG00438.hp1 HG00597.hp1 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.1385+1026_1385+102 others(322): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr10 | 17709963 | ||||||
| chr10:17709963 | G | GCAGGATT others(311): Show |
1 | a0001c0001t0001g0067 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1385+1026_1385+102 others(322): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr10 | 17709963 | ||||||
| chr10:17709963 | G | GCAGGATT others(312): Show |
1 | a0001c0001t0001g0065 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1385+1026_1385+102 others(323): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr10 | 17709963 | ||||||
| chr10:17709963 | G | GCAGGATT others(313): Show |
1 | a0001c0001t0001g0090 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1385+1026_1385+102 others(324): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr10 | 17709963 | ||||||
| chr10:17709969 | T | TTTTTTTT others(308): Show |
1 | a0001c0001t0001g0062 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1385+1026_1385+102 others(319): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr10 | 17709969 | ||||||
| chr10:17710145 | G | A | 5 | a0001c0001t0006g0203 a0001c0001t0006g0207 a0001c0001t0006g0208 others(2): Show |
5 | HG02615.hp2 HG02922.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1385+1194G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17710145 | |||||||
| chr10:17710247 | G | A | 1 | a0001c0002t0003g0342 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1385+1296G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17710247 | |||||||
| chr10:17710443 | CAT | C | 24 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(21): Show |
27 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.1385+1493_1385+149 others(6): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17710443 | |||||||
| chr10:17710594 | C | T | 1 | a0001c0001t0003g0157 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1385+1643C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17710594 | |||||||
| chr10:17710746 | C | T | 9 | a0001c0001t0004g0017 a0001c0001t0004g0174 a0001c0001t0004g0175 others(6): Show |
10 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.1385+1795C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17710746 | |||||||
| chr10:17710855 | A | G | 1 | a0001c0001t0004g0204 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1385+1904A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17710855 | |||||||
| chr10:17710909 | A | G | 2 | a0001c0001t0015g0386 a0001c0009t0015g0385 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1385+1958A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17710909 | |||||||
| chr10:17710972 | G | T | 2 | a0001c0002t0003g0170 a0001c0002t0003g0171 |
2 | HG02738.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1385+2021G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17710972 | |||||||
| chr10:17711045 | A | G | 33 | a0001c0001t0004g0017 a0001c0001t0004g0174 a0001c0001t0004g0175 others(30): Show |
37 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1385+2094A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17711045 | |||||||
| chr10:17711159 | C | G | 35 | a0001c0001t0004g0017 a0001c0001t0004g0174 a0001c0001t0004g0175 others(32): Show |
39 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.1385+2208C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17711159 | |||||||
| chr10:17711271 | C | T | 7 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(4): Show |
7 | HG02145.hp1 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1385+2320C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17711271 | |||||||
| chr10:17711294 | C | T | 24 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(21): Show |
27 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.1385+2343C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17711294 | |||||||
| chr10:17711328 | A | G | 7 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(4): Show |
7 | HG02145.hp1 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1385+2377A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17711328 | |||||||
| chr10:17711701 | A | G | 1 | a0001c0001t0001g0138 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1385+2750A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17711701 | |||||||
| chr10:17711785 | C | G | 3 | a0001c0001t0023g0187 a0001c0001t0030g0382 a0001c0001t0031g0381 |
3 | HG02717.hp2 HG02970.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1386-2758C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17711785 | |||||||
| chr10:17711797 | G | A | 1 | a0001c0001t0005g0044 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1386-2746G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17711797 | |||||||
| chr10:17711857 | C | T | 2 | a0001c0001t0017g0377 a0001c0001t0017g0378 |
2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1386-2686C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17711857 | |||||||
| chr10:17711871 | T | C | 25 | a0001c0001t0004g0018 a0001c0001t0004g0033 a0001c0001t0004g0056 others(22): Show |
26 | HG00642.hp2 HG01884.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.1386-2672T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17711871 | |||||||
| chr10:17711942 | C | T | 24 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(21): Show |
27 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.1386-2601C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17711942 | |||||||
| chr10:17712150 | C | A | 54 | a0001c0002t0003g0008 a0001c0002t0003g0009 a0001c0002t0003g0022 others(51): Show |
59 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.1386-2393C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17712150 | |||||||
| chr10:17712183 | A | G | 1 | a0001c0001t0001g0360 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1386-2360A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17712183 | |||||||
| chr10:17712266 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1386-2277C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17712266 | |||||||
| chr10:17712526 | A | C | 2 | a0001c0001t0015g0386 a0001c0009t0015g0385 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1386-2017A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17712526 | |||||||
| chr10:17712538 | C | T | 249 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(246): Show |
265 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.1386-2005C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17712538 | |||||||
| chr10:17712555 | A | G | 1 | a0001c0001t0002g0284 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1386-1988A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17712555 | |||||||
| chr10:17712705 | T | C | 2 | a0001c0001t0001g0185 a0001c0001t0001g0186 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1386-1838T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17712705 | |||||||
| chr10:17712763 | G | C | 1 | a0001c0006t0028g0379 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1386-1780G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17712763 | |||||||
| chr10:17712810 | T | C | 24 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(21): Show |
27 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.1386-1733T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17712810 | |||||||
| chr10:17712813 | A | G | 114 | a0001c0001t0001g0356 a0001c0001t0001g0359 a0001c0001t0001g0360 others(111): Show |
120 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.1386-1730A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17712813 | |||||||
| chr10:17712861 | CGGAGCGG others(2): Show |
C | 17 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0015 others(14): Show |
21 | HG00597.hp1 NA18944.hp1 NA18945.hp1 others(18): Show |
intron_variant | MODIFIER | c.1386-1673_1386-166 others(13): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr10 | 17712861 | ||||||
| chr10:17712908 | T | G | 24 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(21): Show |
27 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.1386-1635T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17712908 | |||||||
| chr10:17712986 | C | T | 1 | a0001c0002t0003g0342 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1386-1557C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17712986 | |||||||
| chr10:17713004 | C | G | 4 | a0001c0001t0002g0242 a0001c0001t0002g0306 a0001c0001t0024g0292 others(1): Show |
4 | HG00639.hp1 HG01168.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.1386-1539C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17713004 | |||||||
| chr10:17713026 | A | G | 33 | a0001c0001t0004g0017 a0001c0001t0004g0174 a0001c0001t0004g0175 others(30): Show |
37 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1386-1517A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17713026 | |||||||
| chr10:17713155 | T | G | 1 | a0001c0001t0001g0090 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1386-1388T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17713155 | |||||||
| chr10:17713175 | C | T | 1 | a0001c0002t0003g0350 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1386-1368C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17713175 | |||||||
| chr10:17713189 | C | T | 24 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(21): Show |
27 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.1386-1354C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17713189 | |||||||
| chr10:17713291 | A | C | 26 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(23): Show |
29 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.1386-1252A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17713291 | |||||||
| chr10:17713389 | TTGCCTAT others(27): Show |
T | 2 | a0001c0001t0001g0185 a0001c0001t0001g0186 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1386-1143_1386-111 others(38): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr10 | 17713389 | ||||||
| chr10:17713668 | A | G | 3 | a0001c0001t0001g0356 a0001c0001t0001g0359 a0001c0001t0001g0362 |
3 | HG01069.hp1 HG01071.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1386-875A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17713668 | |||||||
| chr10:17713932 | C | T | 24 | a0001c0001t0004g0018 a0001c0001t0004g0033 a0001c0001t0004g0056 others(21): Show |
25 | HG00642.hp2 HG01884.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.1386-611C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17713932 | |||||||
| chr10:17713936 | G | T | 9 | a0001c0001t0004g0017 a0001c0001t0004g0174 a0001c0001t0004g0175 others(6): Show |
10 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.1386-607G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17713936 | |||||||
| chr10:17714059 | A | G | 1 | a0001c0001t0009g0380 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1386-484A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17714059 | |||||||
| chr10:17714312 | A | ACCC | 21 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0011 others(18): Show |
24 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.1386-225_1386-223d others(5): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr10 | 17714312 | ||||||
| chr10:17714336 | A | G | 1 | a0001c0002t0003g0166 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1386-207A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17714336 | |||||||
| chr10:17714405 | C | T | 1 | a0001c0006t0028g0379 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1386-138C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17714405 | |||||||
| chr10:17714448 | A | G | 2 | a0001c0001t0030g0382 a0001c0001t0031g0381 |
2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1386-95A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17714448 | |||||||
| chr10:17714452 | G | A | 2 | a0001c0002t0004g0332 a0001c0002t0004g0347 |
2 | HG02615.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1386-91G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17714452 | |||||||
| chr10:17714534 | C | A | 1 | a0001c0001t0001g0128 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1386-9C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17714534 |