Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 652991 |
| ensemblid | ENSG00000215474.8 |
| hgncid | 32695 |
| symbol | SKOR2 |
| name | SKI family transcriptional corepressor 2 |
| refseq_nuc | NM_001278063.4 |
| refseq_prot | NP_001264992.1 |
| ensembl_nuc | ENST00000425639.3 |
| ensembl_prot | ENSP00000414750.3 |
| mane_status | MANE Select |
| chr | chr18 |
| start | 47206169 |
| end | 47251660 |
| strand | - |
| ver | v1.2 |
| region | chr18:47206169-47251660 |
| region5000 | chr18:47201169-47256660 |
| regionname0 | SKOR2_chr18_47206169_47251660 |
| regionname5000 | SKOR2_chr18_47201169_47256660 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 1015 | 188 | 54 | 26 | 81 | 7 | 19 | 53 | SKOR2_chr18_47201169_47256660 | SKOR2 | MASSP others(1010): Show |
chr18 | 47201169 | 47256660 |
| a0002 | 0/1 | 1015 | 130 | 25 | 26 | 65 | 7 | 6 | 51 | SKOR2_chr18_47201169_47256660 | SKOR2 | MASSP others(1010): Show |
chr18 | 47201169 | 47256660 |
| a0003 | 0/0 | 1016 | 9 | 6 | 0 | 3 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | MASSP others(1011): Show |
chr18 | 47201169 | 47256660 |
| a0004 | 0/0 | 1015 | 5 | 0 | 0 | 0 | 0 | 5 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | MASSP others(1010): Show |
chr18 | 47201169 | 47256660 |
| a0005 | 0/0 | 1015 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | MASSP others(1010): Show |
chr18 | 47201169 | 47256660 |
| a0006 | 0/0 | 1015 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SKOR2_chr18_47201169_47256660 | SKOR2 | MASSP others(1010): Show |
chr18 | 47201169 | 47256660 |
| a0007 | 0/0 | 1015 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | MASSP others(1010): Show |
chr18 | 47201169 | 47256660 |
| a0008 | 0/0 | 1015 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | MASSP others(1010): Show |
chr18 | 47201169 | 47256660 |
| a0009 | 0/0 | 1015 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | MASSP others(1010): Show |
chr18 | 47201169 | 47256660 |
| a0010 | 0/0 | 1015 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | MASSP others(1010): Show |
chr18 | 47201169 | 47256660 |
| a0011 | 0/0 | 1015 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | MASSP others(1010): Show |
chr18 | 47201169 | 47256660 |
| a0012 | 0/0 | 1015 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | MASSP others(1010): Show |
chr18 | 47201169 | 47256660 |
| a0013 | 0/0 | 1015 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | MASSP others(1010): Show |
chr18 | 47201169 | 47256660 |
| a0014 | 0/0 | 1015 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | MASSP others(1010): Show |
chr18 | 47201169 | 47256660 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 3045 | 175 | 47 | 24 | 79 | 6 | 18 | SKOR2_chr18_47201169_47256660 | SKOR2 | ATGGC others(3040): Show |
chr18 | 47201169 | 47256660 | ||
| a0001c0003 | 0/0 | 3045 | 7 | 7 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | ATGGC others(3040): Show |
chr18 | 47201169 | 47256660 | ||
| a0001c0006 | 0/0 | 3045 | 3 | 0 | 1 | 0 | 1 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | ATGGC others(3040): Show |
chr18 | 47201169 | 47256660 | ||
| a0001c0014 | 0/0 | 3045 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | ATGGC others(3040): Show |
chr18 | 47201169 | 47256660 | ||
| a0001c0020 | 0/0 | 3045 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | ATGGC others(3040): Show |
chr18 | 47201169 | 47256660 | ||
| a0001c0021 | 0/0 | 3045 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | ATGGC others(3040): Show |
chr18 | 47201169 | 47256660 | ||
| a0002c0002 | 0/1 | 3045 | 127 | 25 | 26 | 64 | 7 | 4 | SKOR2_chr18_47201169_47256660 | SKOR2 | ATGGC others(3040): Show |
chr18 | 47201169 | 47256660 | ||
| a0002c0008 | 0/0 | 3045 | 2 | 0 | 0 | 0 | 0 | 2 | SKOR2_chr18_47201169_47256660 | SKOR2 | ATGGC others(3040): Show |
chr18 | 47201169 | 47256660 | ||
| a0002c0012 | 0/0 | 3045 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | ATGGC others(3040): Show |
chr18 | 47201169 | 47256660 | ||
| a0003c0005 | 0/0 | 3048 | 4 | 4 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | ATGGC others(3043): Show |
chr18 | 47201169 | 47256660 | ||
| a0003c0007 | 0/0 | 3048 | 3 | 0 | 0 | 3 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | ATGGC others(3043): Show |
chr18 | 47201169 | 47256660 | ||
| a0003c0010 | 0/0 | 3048 | 2 | 2 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | ATGGC others(3043): Show |
chr18 | 47201169 | 47256660 | ||
| a0004c0004 | 0/0 | 3045 | 5 | 0 | 0 | 0 | 0 | 5 | SKOR2_chr18_47201169_47256660 | SKOR2 | ATGGC others(3040): Show |
chr18 | 47201169 | 47256660 | ||
| a0005c0011 | 0/0 | 3045 | 2 | 2 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | ATGGC others(3040): Show |
chr18 | 47201169 | 47256660 | ||
| a0006c0009 | 0/0 | 3045 | 2 | 0 | 0 | 2 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | ATGGC others(3040): Show |
chr18 | 47201169 | 47256660 | ||
| a0007c0019 | 0/0 | 3045 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | ATGGC others(3040): Show |
chr18 | 47201169 | 47256660 | ||
| a0008c0013 | 0/0 | 3045 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | ATGGC others(3040): Show |
chr18 | 47201169 | 47256660 | ||
| a0009c0016 | 0/0 | 3045 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | ATGGC others(3040): Show |
chr18 | 47201169 | 47256660 | ||
| a0010c0022 | 0/0 | 3045 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | ATGGC others(3040): Show |
chr18 | 47201169 | 47256660 | ||
| a0011c0018 | 0/0 | 3045 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | ATGGC others(3040): Show |
chr18 | 47201169 | 47256660 | ||
| a0012c0015 | 0/0 | 3045 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | ATGGC others(3040): Show |
chr18 | 47201169 | 47256660 | ||
| a0013c0023 | 0/0 | 3045 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | ATGGC others(3040): Show |
chr18 | 47201169 | 47256660 | ||
| a0014c0017 | 0/0 | 3045 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | ATGGC others(3040): Show |
chr18 | 47201169 | 47256660 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4109 | 124 | 32 | 19 | 52 | 5 | 15 | SKOR2_chr18_47201169_47256660 | SKOR2 | AGAGA others(4104): Show |
chr18 | 47201169 | 47256660 |
| a0001c0001t0002 | 0/0 | 4109 | 39 | 8 | 2 | 26 | 0 | 3 | SKOR2_chr18_47201169_47256660 | SKOR2 | AGAGA others(4104): Show |
chr18 | 47201169 | 47256660 |
| a0001c0001t0003 | 0/0 | 4109 | 6 | 3 | 2 | 0 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | AGAGA others(4104): Show |
chr18 | 47201169 | 47256660 |
| a0001c0001t0004 | 0/0 | 4109 | 2 | 2 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | AGAGA others(4104): Show |
chr18 | 47201169 | 47256660 |
| a0001c0001t0006 | 0/0 | 4109 | 2 | 2 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | AGAGA others(4104): Show |
chr18 | 47201169 | 47256660 |
| a0001c0001t0007 | 0/0 | 4109 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | AGAGA others(4104): Show |
chr18 | 47201169 | 47256660 |
| a0001c0001t0009 | 0/0 | 4109 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | AGAGA others(4104): Show |
chr18 | 47201169 | 47256660 |
| a0001c0003t0001 | 0/0 | 4109 | 7 | 7 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | AGAGA others(4104): Show |
chr18 | 47201169 | 47256660 |
| a0001c0006t0003 | 0/0 | 4109 | 3 | 0 | 1 | 0 | 1 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | AGAGA others(4104): Show |
chr18 | 47201169 | 47256660 |
| a0001c0014t0001 | 0/0 | 4109 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | AGAGA others(4104): Show |
chr18 | 47201169 | 47256660 |
| a0001c0020t0001 | 0/0 | 4109 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | AGAGA others(4104): Show |
chr18 | 47201169 | 47256660 |
| a0001c0021t0001 | 0/0 | 4109 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | AGAGA others(4104): Show |
chr18 | 47201169 | 47256660 |
| a0002c0002t0001 | 0/1 | 4109 | 9 | 1 | 4 | 0 | 3 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | AGAGA others(4104): Show |
chr18 | 47201169 | 47256660 |
| a0002c0002t0002 | 0/0 | 4109 | 78 | 21 | 17 | 33 | 3 | 4 | SKOR2_chr18_47201169_47256660 | SKOR2 | AGAGA others(4104): Show |
chr18 | 47201169 | 47256660 |
| a0002c0002t0003 | 0/0 | 4109 | 39 | 3 | 5 | 30 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | AGAGA others(4104): Show |
chr18 | 47201169 | 47256660 |
| a0002c0002t0008 | 0/0 | 4109 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | AGAGA others(4104): Show |
chr18 | 47201169 | 47256660 |
| a0002c0008t0002 | 0/0 | 4109 | 2 | 0 | 0 | 0 | 0 | 2 | SKOR2_chr18_47201169_47256660 | SKOR2 | AGAGA others(4104): Show |
chr18 | 47201169 | 47256660 |
| a0002c0012t0003 | 0/0 | 4109 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | AGAGA others(4104): Show |
chr18 | 47201169 | 47256660 |
| a0003c0005t0001 | 0/0 | 4112 | 4 | 4 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | AGAGA others(4107): Show |
chr18 | 47201169 | 47256660 |
| a0003c0007t0002 | 0/0 | 4112 | 3 | 0 | 0 | 3 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | AGAGA others(4107): Show |
chr18 | 47201169 | 47256660 |
| a0003c0010t0005 | 0/0 | 4112 | 2 | 2 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | AGAGA others(4107): Show |
chr18 | 47201169 | 47256660 |
| a0004c0004t0002 | 0/0 | 4109 | 5 | 0 | 0 | 0 | 0 | 5 | SKOR2_chr18_47201169_47256660 | SKOR2 | AGAGA others(4104): Show |
chr18 | 47201169 | 47256660 |
| a0005c0011t0002 | 0/0 | 4109 | 2 | 2 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | AGAGA others(4104): Show |
chr18 | 47201169 | 47256660 |
| a0006c0009t0002 | 0/0 | 4109 | 2 | 0 | 0 | 2 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | AGAGA others(4104): Show |
chr18 | 47201169 | 47256660 |
| a0007c0019t0002 | 0/0 | 4109 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | AGAGA others(4104): Show |
chr18 | 47201169 | 47256660 |
| a0008c0013t0003 | 0/0 | 4109 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | AGAGA others(4104): Show |
chr18 | 47201169 | 47256660 |
| a0009c0016t0002 | 0/0 | 4109 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | AGAGA others(4104): Show |
chr18 | 47201169 | 47256660 |
| a0010c0022t0001 | 0/0 | 4109 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | AGAGA others(4104): Show |
chr18 | 47201169 | 47256660 |
| a0011c0018t0001 | 0/0 | 4109 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | AGAGA others(4104): Show |
chr18 | 47201169 | 47256660 |
| a0012c0015t0002 | 0/0 | 4109 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | AGAGA others(4104): Show |
chr18 | 47201169 | 47256660 |
| a0013c0023t0002 | 0/0 | 4109 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | AGAGA others(4104): Show |
chr18 | 47201169 | 47256660 |
| a0014c0017t0001 | 0/0 | 4109 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | AGAGA others(4104): Show |
chr18 | 47201169 | 47256660 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 1/0 | 8 | 0 | 3 | 1 | 0 | 3 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0003 | 0/0 | 8 | 0 | 1 | 6 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0003g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0006g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0006g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0007g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0001t0009g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0003t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0003t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0003t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0003t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0003t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0006t0003g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0006t0003g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0006t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0014t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0020t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0001c0021t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0001g0119 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0001 | 0/0 | 10 | 2 | 5 | 2 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0014 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0003g0004 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0003g0007 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0003g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0003g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0003g0025 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0003g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0002t0008g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0008t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0008t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0002c0012t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0003c0005t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0003c0005t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0003c0005t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0003c0005t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0003c0007t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0003c0007t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0003c0007t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0003c0010t0005g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0003c0010t0005g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0004c0004t0002g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0004c0004t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0004c0004t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0004c0004t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0005c0011t0002g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0006c0009t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0006c0009t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0007c0019t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0008c0013t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0009c0016t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0010c0022t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0011c0018t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0012c0015t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0013c0023t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| a0014c0017t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0114 | EUR | GBR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0230 | EUR | GBR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0068 | EUR | GBR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG00140 | hp2 | a0002 | c0002 | t0003 | g0025 | EUR | GBR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG00280 | hp2 | a0002 | c0002 | t0002 | g0001 | EUR | FIN | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG00408 | hp2 | a0002 | c0002 | t0002 | g0168 | EAS | CHS | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG00438 | hp1 | a0001 | c0020 | t0001 | g0110 | EAS | CHS | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0026 | EAS | CHS | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG00544 | hp1 | a0003 | c0007 | t0002 | g0158 | EAS | CHS | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG00558 | hp1 | a0002 | c0002 | t0002 | g0192 | EAS | CHS | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG00597 | hp1 | a0002 | c0002 | t0003 | g0004 | EAS | CHS | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | CHS | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | CHS | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0026 | EAS | CHS | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG00639 | hp1 | a0002 | c0002 | t0002 | g0216 | AMR | PUR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG00639 | hp2 | a0002 | c0002 | t0003 | g0217 | AMR | PUR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG00642 | hp1 | a0002 | c0002 | t0002 | g0196 | AMR | PUR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG00642 | hp2 | a0002 | c0002 | t0002 | g0203 | AMR | PUR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | CHS | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG00733 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG00735 | hp2 | a0002 | c0002 | t0002 | g0194 | AMR | PUR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0022 | AMR | PUR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0022 | AMR | PUR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01168 | hp1 | a0002 | c0002 | t0002 | g0200 | AMR | PUR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | PUR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01255 | hp1 | a0002 | c0002 | t0002 | g0205 | AMR | CLM | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01255 | hp2 | a0001 | c0001 | t0009 | g0274 | AMR | CLM | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01257 | hp2 | a0007 | c0019 | t0002 | g0259 | AMR | CLM | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0118 | AMR | CLM | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01358 | hp2 | a0002 | c0002 | t0002 | g0014 | AMR | CLM | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01361 | hp1 | a0001 | c0006 | t0003 | g0154 | AMR | CLM | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01361 | hp2 | a0002 | c0002 | t0002 | g0199 | AMR | CLM | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01515 | hp1 | a0001 | c0006 | t0003 | g0155 | EUR | IBS | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0096 | EUR | IBS | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0097 | EUR | IBS | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0117 | EUR | IBS | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01884 | hp2 | a0008 | c0013 | t0003 | g0141 | AFR | ACB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01891 | hp1 | a0009 | c0016 | t0002 | g0207 | AFR | ACB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0123 | AFR | ACB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01934 | hp1 | a0001 | c0021 | t0001 | g0111 | AMR | PEL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01952 | hp1 | a0002 | c0002 | t0003 | g0169 | AMR | PEL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01952 | hp2 | a0002 | c0002 | t0002 | g0014 | AMR | PEL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01975 | hp1 | a0002 | c0002 | t0002 | g0189 | AMR | PEL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01981 | hp1 | a0002 | c0002 | t0002 | g0211 | AMR | PEL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01993 | hp1 | a0002 | c0002 | t0003 | g0025 | AMR | PEL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0115 | AMR | PEL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02004 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02015 | hp1 | a0002 | c0002 | t0008 | g0185 | EAS | KHV | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02040 | hp1 | a0002 | c0002 | t0003 | g0013 | EAS | KHV | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | KHV | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02071 | hp1 | a0002 | c0002 | t0003 | g0193 | EAS | KHV | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02074 | hp1 | a0002 | c0002 | t0002 | g0167 | EAS | KHV | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02074 | hp2 | a0002 | c0002 | t0002 | g0204 | EAS | KHV | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02080 | hp1 | a0002 | c0002 | t0002 | g0174 | EAS | KHV | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | KHV | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02132 | hp1 | a0002 | c0002 | t0002 | g0181 | EAS | KHV | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | KHV | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02145 | hp1 | a0002 | c0002 | t0002 | g0197 | AFR | ACB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0113 | AFR | ACB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | CDX | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02155 | hp2 | a0002 | c0002 | t0002 | g0176 | EAS | CDX | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | ACB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02258 | hp1 | a0002 | c0002 | t0003 | g0163 | AFR | ACB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0233 | AFR | ACB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0240 | AMR | PEL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02280 | hp1 | a0002 | c0002 | t0002 | g0219 | AFR | ACB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02293 | hp1 | a0010 | c0022 | t0001 | g0112 | AMR | PEL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02293 | hp2 | a0002 | c0002 | t0003 | g0170 | AMR | PEL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02300 | hp1 | a0002 | c0002 | t0003 | g0164 | AMR | PEL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02300 | hp2 | a0002 | c0002 | t0002 | g0027 | AMR | PEL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02451 | hp1 | a0001 | c0003 | t0001 | g0008 | AFR | ACB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | KHV | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02572 | hp2 | a0011 | c0018 | t0001 | g0105 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02602 | hp1 | a0002 | c0002 | t0002 | g0213 | SAS | PJL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02622 | hp1 | a0002 | c0002 | t0002 | g0220 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02630 | hp1 | a0003 | c0005 | t0001 | g0037 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02630 | hp2 | a0002 | c0002 | t0002 | g0001 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02647 | hp1 | a0002 | c0002 | t0002 | g0012 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0257 | SAS | PJL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02683 | hp2 | a0002 | c0002 | t0002 | g0214 | SAS | PJL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02698 | hp2 | a0002 | c0008 | t0002 | g0147 | SAS | PJL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02717 | hp2 | a0012 | c0015 | t0002 | g0215 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02818 | hp2 | a0001 | c0003 | t0001 | g0034 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02886 | hp2 | a0001 | c0003 | t0001 | g0008 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02895 | hp1 | a0002 | c0002 | t0002 | g0012 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02896 | hp2 | a0002 | c0002 | t0002 | g0227 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02897 | hp1 | a0002 | c0002 | t0002 | g0012 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0232 | AFR | ESN | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02965 | hp1 | a0005 | c0011 | t0002 | g0029 | AFR | ESN | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0124 | AFR | ESN | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02970 | hp1 | a0013 | c0023 | t0002 | g0260 | AFR | ESN | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02976 | hp2 | a0003 | c0005 | t0001 | g0038 | AFR | ESN | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG03041 | hp1 | a0002 | c0002 | t0003 | g0161 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0272 | AFR | MSL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG03130 | hp2 | a0002 | c0002 | t0002 | g0142 | AFR | ESN | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG03139 | hp1 | a0002 | c0002 | t0002 | g0162 | AFR | ESN | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG03139 | hp2 | a0003 | c0010 | t0005 | g0265 | AFR | ESN | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG03195 | hp1 | a0001 | c0003 | t0001 | g0031 | AFR | ESN | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG03195 | hp2 | a0002 | c0002 | t0002 | g0223 | AFR | ESN | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG03209 | hp1 | a0002 | c0002 | t0002 | g0224 | AFR | MSL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0263 | AFR | MSL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG03490 | hp2 | a0004 | c0004 | t0002 | g0153 | SAS | PJL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG03492 | hp1 | a0004 | c0004 | t0002 | g0023 | SAS | PJL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG03516 | hp2 | a0003 | c0010 | t0005 | g0264 | AFR | ESN | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG03540 | hp1 | a0002 | c0002 | t0002 | g0001 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG03540 | hp2 | a0003 | c0005 | t0001 | g0036 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG03579 | hp1 | a0002 | c0002 | t0002 | g0226 | AFR | MSL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0261 | AFR | MSL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG03654 | hp1 | a0002 | c0002 | t0002 | g0172 | SAS | PJL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0251 | SAS | PJL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG03704 | hp2 | a0001 | c0006 | t0003 | g0156 | SAS | PJL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG03710 | hp2 | a0002 | c0002 | t0002 | g0206 | SAS | PJL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0252 | SAS | BEB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG03942 | hp1 | a0004 | c0004 | t0002 | g0152 | SAS | BEB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG04204 | hp1 | a0004 | c0004 | t0002 | g0023 | SAS | STU | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | STU | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | STU | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0228 | AFR | YRI | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18522 | hp2 | a0005 | c0011 | t0002 | g0029 | AFR | YRI | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18612 | hp2 | a0002 | c0002 | t0003 | g0004 | EAS | CHB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18747 | hp1 | a0003 | c0007 | t0002 | g0157 | EAS | CHB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CHB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0033 | AFR | YRI | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | YRI | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18939 | hp2 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18940 | hp2 | a0002 | c0002 | t0003 | g0024 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18947 | hp1 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18947 | hp2 | a0001 | c0001 | t0007 | g0084 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18949 | hp1 | a0002 | c0002 | t0003 | g0271 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18950 | hp1 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18950 | hp2 | a0002 | c0002 | t0002 | g0184 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18953 | hp2 | a0002 | c0002 | t0002 | g0190 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18957 | hp1 | a0001 | c0014 | t0001 | g0051 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18957 | hp2 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18959 | hp1 | a0002 | c0002 | t0002 | g0222 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18962 | hp2 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18966 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18968 | hp2 | a0002 | c0002 | t0003 | g0024 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18969 | hp2 | a0002 | c0002 | t0003 | g0180 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18972 | hp1 | a0002 | c0002 | t0003 | g0209 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18972 | hp2 | a0002 | c0002 | t0002 | g0175 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18973 | hp2 | a0002 | c0002 | t0002 | g0201 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18974 | hp1 | a0014 | c0017 | t0001 | g0052 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18974 | hp2 | a0006 | c0009 | t0002 | g0150 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18975 | hp2 | a0002 | c0002 | t0003 | g0166 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18977 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0191 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18980 | hp1 | a0002 | c0002 | t0003 | g0013 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18980 | hp2 | a0002 | c0002 | t0003 | g0270 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18982 | hp1 | a0002 | c0002 | t0003 | g0013 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18984 | hp2 | a0002 | c0002 | t0002 | g0202 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18986 | hp1 | a0002 | c0002 | t0003 | g0182 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18986 | hp2 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18988 | hp1 | a0003 | c0007 | t0002 | g0159 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18989 | hp1 | a0002 | c0002 | t0002 | g0187 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18990 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18993 | hp1 | a0002 | c0002 | t0002 | g0186 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18995 | hp2 | a0002 | c0002 | t0002 | g0210 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18998 | hp2 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18999 | hp1 | a0002 | c0002 | t0002 | g0177 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0195 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19007 | hp2 | a0002 | c0002 | t0003 | g0173 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19011 | hp2 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19012 | hp1 | a0002 | c0002 | t0003 | g0267 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19012 | hp2 | a0002 | c0002 | t0002 | g0178 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19030 | hp1 | a0002 | c0002 | t0002 | g0221 | AFR | LWK | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19030 | hp2 | a0002 | c0002 | t0002 | g0143 | AFR | LWK | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | LWK | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19043 | hp2 | a0002 | c0002 | t0002 | g0225 | AFR | LWK | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19055 | hp1 | a0002 | c0002 | t0003 | g0266 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19057 | hp1 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19057 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19060 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19060 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19062 | hp1 | a0002 | c0002 | t0003 | g0165 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0198 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19063 | hp2 | a0002 | c0002 | t0003 | g0269 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19064 | hp2 | a0002 | c0012 | t0003 | g0139 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19070 | hp2 | a0002 | c0002 | t0003 | g0268 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19077 | hp2 | a0002 | c0002 | t0002 | g0208 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19079 | hp1 | a0002 | c0002 | t0002 | g0160 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19082 | hp1 | a0002 | c0002 | t0002 | g0179 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19082 | hp2 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19083 | hp1 | a0002 | c0002 | t0003 | g0183 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19085 | hp2 | a0006 | c0009 | t0002 | g0149 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | YRI | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0262 | AFR | YRI | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ASW | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ASW | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA20752 | hp1 | a0002 | c0002 | t0002 | g0027 | EUR | TSI | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0067 | EUR | TSI | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0116 | EUR | TSI | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA20805 | hp2 | a0002 | c0002 | t0002 | g0218 | EUR | TSI | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA20905 | hp1 | a0004 | c0004 | t0002 | g0151 | SAS | GIH | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA20905 | hp2 | a0002 | c0008 | t0002 | g0148 | SAS | GIH | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0229 | AMR | CLM | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0234 | AMR | CLM | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0145 | AFR | ACB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0231 | AFR | ACB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02486 | hp2 | a0002 | c0002 | t0002 | g0138 | AFR | ACB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02559 | hp1 | a0001 | c0003 | t0001 | g0008 | AFR | ACB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG02559 | hp2 | a0003 | c0005 | t0001 | g0035 | AFR | ACB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0140 | AFR | MSL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0273 | AFR | MSL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG06807 | hp1 | a0001 | c0003 | t0001 | g0032 | AFR | USA | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| HG06807 | hp2 | a0002 | c0002 | t0003 | g0007 | AFR | USA | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA20300 | hp1 | a0002 | c0002 | t0002 | g0212 | AFR | USA | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA20300 | hp2 | a0002 | c0002 | t0002 | g0171 | AFR | USA | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | LWK | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| NA21309 | hp2 | a0002 | c0002 | t0002 | g0188 | AFR | LWK | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0119 | REF | REF | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0002 | REF | REF | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:47230518 | C | T | 1 | a0012 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.2858G>A | p.Arg953Gln | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/9 | 3192/4109 | 2858/3048 | 953/1015 | chr18 | 47230518 | |||
| chr18:47230536 | A | C | 2 | a0003 a0011 |
5 | HG02559.hp2 HG02572.hp2 HG02630.hp1 others(2): Show |
missense_variant | MODERATE | c.2840T>G | p.Phe947Cys | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/9 | 3174/4109 | 2840/3048 | 947/1015 | chr18 | 47230536 | |||
| chr18:47230973 | G | A | 3 | a0003 a0009 a0012 |
5 | HG00544.hp1 HG01891.hp1 HG02717.hp2 others(2): Show |
missense_variant | MODERATE | c.2780C>T | p.Pro927Leu | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 5/9 | 3114/4109 | 2780/3048 | 927/1015 | chr18 | 47230973 | |||
| chr18:47244924 | A | C | 2 | a0005 a0013 |
3 | HG02965.hp1 HG02970.hp1 NA18522.hp2 |
missense_variant | MODERATE | c.2736T>G | p.Phe912Leu | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/9 | 3070/4109 | 2736/3048 | 912/1015 | chr18 | 47244924 | |||
| chr18:47246702 | C | G | 1 | a0014 | 1 | NA18974.hp1 | missense_variant | MODERATE | c.2482G>C | p.Asp828His | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/9 | 2816/4109 | 2482/3048 | 828/1015 | chr18 | 47246702 | |||
| chr18:47247011 | A | T | 6 | a0002 a0003 a0004 others(3): Show |
143 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(140): Show |
missense_variant | MODERATE | c.2173T>A | p.Cys725Ser | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/9 | 2507/4109 | 2173/3048 | 725/1015 | chr18 | 47247011 | |||
| chr18:47247103 | G | T | 1 | a0013 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.2081C>A | p.Ala694Asp | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/9 | 2415/4109 | 2081/3048 | 694/1015 | chr18 | 47247103 | |||
| chr18:47247178 | G | GGGT | 1 | a0003 | 9 | HG00544.hp1 HG02559.hp2 HG02630.hp1 others(6): Show |
conservative_inframe_insertion | MODERATE | c.2003_2005dupACC | p.His668dup | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/9 | 2339/4109 | 2005/3048 | 669/1015 | chr18 | 47247178 | |||
| chr18:47247638 | G | C | 1 | a0007 | 1 | HG01257.hp2 | missense_variant | MODERATE | c.1546C>G | p.Pro516Ala | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/9 | 1880/4109 | 1546/3048 | 516/1015 | chr18 | 47247638 | |||
| chr18:47247834 | C | G | 1 | a0004 | 5 | HG03490.hp2 HG03492.hp1 HG03942.hp1 others(2): Show |
missense_variant | MODERATE | c.1350G>C | p.Leu450Phe | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/9 | 1684/4109 | 1350/3048 | 450/1015 | chr18 | 47247834 | |||
| chr18:47247961 | G | T | 1 | a0008 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.1223C>A | p.Pro408His | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/9 | 1557/4109 | 1223/3048 | 408/1015 | chr18 | 47247961 | |||
| chr18:47247980 | C | T | 1 | a0006 | 2 | NA18974.hp2 NA19085.hp2 |
missense_variant | MODERATE | c.1204G>A | p.Gly402Ser | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/9 | 1538/4109 | 1204/3048 | 402/1015 | chr18 | 47247980 | |||
| chr18:47248802 | T | G | 1 | a0010 | 1 | HG02293.hp1 | missense_variant | MODERATE | c.382A>C | p.Lys128Gln | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/9 | 716/4109 | 382/3048 | 128/1015 | chr18 | 47248802 | |||
| chr18:47249152 | T | C | 1 | a0013 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.32A>G | p.Asp11Gly | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/9 | 366/4109 | 32/3048 | 11/1015 | chr18 | 47249152 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:47246703 | C | T | 1 | a0014c0017 | 1 | NA18974.hp1 | synonymous_variant | LOW | c.2481G>A | p.Gly827Gly | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/9 | 2815/4109 | 2481/3048 | 827/1015 | chr18 | 47246703 | |||
| chr18:47246838 | G | C | 1 | a0001c0003 | 7 | HG02451.hp1 HG02559.hp1 HG02818.hp2 others(4): Show |
synonymous_variant | LOW | c.2346C>G | p.Val782Val | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/9 | 2680/4109 | 2346/3048 | 782/1015 | chr18 | 47246838 | |||
| chr18:47247558 | G | C | 1 | a0003c0010 | 2 | HG03139.hp2 HG03516.hp2 |
synonymous_variant | LOW | c.1626C>G | p.Ser542Ser | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/9 | 1960/4109 | 1626/3048 | 542/1015 | chr18 | 47247558 | |||
| chr18:47247705 | C | T | 1 | a0001c0006 | 3 | HG01361.hp1 HG01515.hp1 HG03704.hp2 |
synonymous_variant | LOW | c.1479G>A | p.Ser493Ser | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/9 | 1813/4109 | 1479/3048 | 493/1015 | chr18 | 47247705 | |||
| chr18:47247759 | G | T | 1 | a0001c0014 | 1 | NA18957.hp1 | synonymous_variant | LOW | c.1425C>A | p.Thr475Thr | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/9 | 1759/4109 | 1425/3048 | 475/1015 | chr18 | 47247759 | |||
| chr18:47247909 | C | T | 1 | a0003c0010 | 2 | HG03139.hp2 HG03516.hp2 |
synonymous_variant | LOW | c.1275G>A | p.Glu425Glu | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/9 | 1609/4109 | 1275/3048 | 425/1015 | chr18 | 47247909 | |||
| chr18:47248089 | G | A | 1 | a0001c0020 | 1 | HG00438.hp1 | synonymous_variant | LOW | c.1095C>T | p.Gly365Gly | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/9 | 1429/4109 | 1095/3048 | 365/1015 | chr18 | 47248089 | |||
| chr18:47248317 | C | T | 1 | a0002c0008 | 2 | HG02698.hp2 NA20905.hp2 |
synonymous_variant | LOW | c.867G>A | p.Pro289Pro | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/9 | 1201/4109 | 867/3048 | 289/1015 | chr18 | 47248317 | |||
| chr18:47248344 | G | A | 1 | a0001c0021 | 1 | HG01934.hp1 | synonymous_variant | LOW | c.840C>T | p.His280His | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/9 | 1174/4109 | 840/3048 | 280/1015 | chr18 | 47248344 | |||
| chr18:47248812 | C | T | 1 | a0002c0012 | 1 | NA19064.hp2 | synonymous_variant | LOW | c.372G>A | p.Glu124Glu | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/9 | 706/4109 | 372/3048 | 124/1015 | chr18 | 47248812 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:47206316 | T | C | 6 | a0001c0001t0003 a0001c0001t0004 a0001c0006t0003 others(3): Show |
52 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*580A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 9/9 | 5773 | chr18 | 47206316 | ||||||
| chr18:47206428 | G | A | 1 | a0002c0002t0008 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*468C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 9/9 | 5661 | chr18 | 47206428 | ||||||
| chr18:47206696 | C | T | 1 | a0001c0001t0007 | 1 | NA18947.hp2 | 3_prime_UTR_variant | MODIFIER | c.*200G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 9/9 | 5393 | chr18 | 47206696 | ||||||
| chr18:47249200 | C | G | 1 | a0003c0010t0005 | 2 | HG03139.hp2 HG03516.hp2 |
5_prime_UTR_variant | MODIFIER | c.-17G>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/9 | 17 | chr18 | 47249200 | ||||||
| chr18:47251385 | T | C | 1 | a0001c0001t0006 | 2 | HG03098.hp2 HG03471.hp2 |
5_prime_UTR_variant | MODIFIER | c.-59A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/9 | 2202 | chr18 | 47251385 | ||||||
| chr18:47251510 | G | C | 19 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(16): Show |
190 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(187): Show |
5_prime_UTR_variant | MODIFIER | c.-184C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/9 | 2327 | chr18 | 47251510 | ||||||
| chr18:47251603 | G | C | 1 | a0001c0001t0009 | 1 | HG01255.hp2 | 5_prime_UTR_variant | MODIFIER | c.-277C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/9 | 2420 | chr18 | 47251603 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:47206904 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.*4-12G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47206904 | |||||||
| chr18:47207153 | C | A | 4 | a0001c0001t0001g0041 a0001c0001t0001g0045 a0001c0001t0001g0046 others(1): Show |
4 | HG01884.hp1 HG02257.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.*4-261G>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47207153 | |||||||
| chr18:47207243 | T | C | 5 | a0001c0001t0001g0048 a0001c0001t0001g0131 a0001c0001t0001g0134 others(2): Show |
5 | HG02572.hp1 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.*4-351A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47207243 | |||||||
| chr18:47207244 | G | A | 3 | a0001c0006t0003g0154 a0001c0006t0003g0155 a0001c0006t0003g0156 |
3 | HG01361.hp1 HG01515.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.*4-352C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47207244 | |||||||
| chr18:47207351 | G | A | 3 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 |
3 | HG03225.hp1 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.*4-459C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47207351 | |||||||
| chr18:47207397 | A | G | 3 | a0001c0001t0003g0233 a0001c0001t0004g0123 a0001c0001t0004g0124 |
3 | HG01891.hp2 HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.*4-505T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47207397 | |||||||
| chr18:47207569 | G | A | 1 | a0002c0002t0002g0162 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.*4-677C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47207569 | |||||||
| chr18:47207632 | C | G | 3 | a0001c0006t0003g0154 a0001c0006t0003g0155 a0001c0006t0003g0156 |
3 | HG01361.hp1 HG01515.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.*4-740G>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47207632 | |||||||
| chr18:47207769 | G | A | 2 | a0002c0008t0002g0147 a0002c0008t0002g0148 |
2 | HG02698.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.*4-877C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47207769 | |||||||
| chr18:47207875 | G | A | 6 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0072 others(3): Show |
6 | HG00673.hp1 HG02027.hp2 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.*4-983C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47207875 | |||||||
| chr18:47207931 | C | T | 3 | a0001c0001t0001g0078 a0001c0001t0002g0145 a0001c0001t0002g0146 |
3 | HG02109.hp1 HG02723.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.*4-1039G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47207931 | |||||||
| chr18:47208093 | AGAGT | A | 4 | a0001c0001t0002g0030 a0001c0001t0002g0238 a0001c0001t0002g0255 others(1): Show |
5 | HG02056.hp2 HG02129.hp2 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.*4-1205_*4-1202del others(4): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47208093 | |||||||
| chr18:47208165 | A | G | 1 | a0001c0001t0002g0254 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.*4-1273T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47208165 | |||||||
| chr18:47208194 | A | G | 37 | a0001c0001t0003g0028 a0001c0001t0003g0229 a0001c0001t0003g0230 others(34): Show |
52 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.*4-1302T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47208194 | |||||||
| chr18:47208329 | G | T | 1 | a0002c0002t0002g0172 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.*4-1437C>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47208329 | |||||||
| chr18:47208554 | A | C | 2 | a0001c0001t0006g0272 a0001c0001t0006g0273 |
2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.*4-1662T>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47208554 | |||||||
| chr18:47208566 | A | G | 4 | a0001c0001t0001g0010 a0001c0001t0001g0076 a0001c0001t0001g0095 others(1): Show |
6 | HG00408.hp1 HG00438.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.*4-1674T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47208566 | |||||||
| chr18:47208946 | A | C | 3 | a0001c0006t0003g0154 a0001c0006t0003g0155 a0001c0006t0003g0156 |
3 | HG01361.hp1 HG01515.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.*4-2054T>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47208946 | |||||||
| chr18:47209008 | G | C | 5 | a0001c0001t0003g0028 a0001c0001t0003g0229 a0001c0001t0003g0230 others(2): Show |
6 | HG00099.hp2 HG01123.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.*4-2116C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47209008 | |||||||
| chr18:47209151 | C | CAA | 26 | a0002c0002t0003g0004 a0002c0002t0003g0007 a0002c0002t0003g0013 others(23): Show |
40 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.*4-2261_*4-2260dup others(2): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47209151 | |||||||
| chr18:47209180 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.*4-2288C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47209180 | |||||||
| chr18:47209243 | A | C | 1 | a0002c0008t0002g0147 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.*4-2351T>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47209243 | |||||||
| chr18:47209409 | C | T | 1 | a0001c0001t0002g0145 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.*4-2517G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47209409 | |||||||
| chr18:47209874 | T | G | 2 | a0002c0002t0002g0226 a0002c0002t0002g0227 |
2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.*3+2212A>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47209874 | |||||||
| chr18:47209934 | A | G | 37 | a0001c0001t0003g0028 a0001c0001t0003g0229 a0001c0001t0003g0230 others(34): Show |
52 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.*3+2152T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47209934 | |||||||
| chr18:47209965 | C | T | 94 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0041 others(91): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.*3+2121G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47209965 | |||||||
| chr18:47210070 | C | A | 3 | a0003c0007t0002g0157 a0003c0007t0002g0158 a0003c0007t0002g0159 |
3 | HG00544.hp1 NA18747.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.*3+2016G>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47210070 | |||||||
| chr18:47210221 | G | A | 3 | a0001c0001t0001g0122 a0001c0001t0006g0272 a0001c0001t0006g0273 |
3 | HG03098.hp2 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.*3+1865C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47210221 | |||||||
| chr18:47210395 | C | T | 37 | a0001c0001t0003g0028 a0001c0001t0003g0229 a0001c0001t0003g0230 others(34): Show |
52 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.*3+1691G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47210395 | |||||||
| chr18:47210396 | G | A | 3 | a0001c0001t0001g0122 a0001c0001t0006g0272 a0001c0001t0006g0273 |
3 | HG03098.hp2 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.*3+1690C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47210396 | |||||||
| chr18:47210447 | G | A | 2 | a0001c0001t0001g0073 a0001c0001t0001g0085 |
2 | NA18969.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.*3+1639C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47210447 | |||||||
| chr18:47210606 | A | T | 3 | a0001c0006t0003g0154 a0001c0006t0003g0155 a0001c0006t0003g0156 |
3 | HG01361.hp1 HG01515.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.*3+1480T>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47210606 | |||||||
| chr18:47210708 | G | T | 1 | a0001c0001t0002g0256 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.*3+1378C>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47210708 | |||||||
| chr18:47210713 | G | C | 1 | a0001c0006t0003g0156 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.*3+1373C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47210713 | |||||||
| chr18:47210726 | G | A | 37 | a0001c0001t0003g0028 a0001c0001t0003g0229 a0001c0001t0003g0230 others(34): Show |
52 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.*3+1360C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47210726 | |||||||
| chr18:47210859 | A | G | 139 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0041 others(136): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.*3+1227T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47210859 | |||||||
| chr18:47210938 | C | T | 2 | a0003c0005t0001g0036 a0011c0018t0001g0105 |
2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.*3+1148G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47210938 | |||||||
| chr18:47211019 | AATT | A | 11 | a0001c0001t0003g0028 a0001c0001t0003g0229 a0001c0001t0003g0230 others(8): Show |
12 | HG00099.hp2 HG01123.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.*3+1064_*3+1066del others(3): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47211019 | |||||||
| chr18:47211089 | A | G | 2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.*3+997T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47211089 | |||||||
| chr18:47211209 | G | A | 3 | a0001c0006t0003g0154 a0001c0006t0003g0155 a0001c0006t0003g0156 |
3 | HG01361.hp1 HG01515.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.*3+877C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47211209 | |||||||
| chr18:47211242 | C | T | 26 | a0002c0002t0003g0004 a0002c0002t0003g0007 a0002c0002t0003g0013 others(23): Show |
40 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.*3+844G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47211242 | |||||||
| chr18:47211649 | G | A | 1 | a0001c0021t0001g0111 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.*3+437C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47211649 | |||||||
| chr18:47211789 | T | A | 1 | a0002c0002t0001g0022 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.*3+297A>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47211789 | |||||||
| chr18:47212041 | A | G | 1 | a0001c0001t0002g0228 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.*3+45T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47212041 | |||||||
| chr18:47212455 | A | T | 3 | a0001c0001t0001g0122 a0001c0001t0006g0272 a0001c0001t0006g0273 |
3 | HG03098.hp2 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2986-304T>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47212455 | |||||||
| chr18:47212749 | G | C | 1 | a0001c0001t0001g0078 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2986-598C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47212749 | |||||||
| chr18:47212902 | G | A | 3 | a0001c0001t0001g0061 a0001c0001t0001g0125 a0001c0001t0009g0274 |
3 | HG01243.hp2 HG01255.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.2986-751C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47212902 | |||||||
| chr18:47212998 | T | C | 1 | a0002c0002t0002g0204 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2986-847A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47212998 | |||||||
| chr18:47213278 | C | G | 1 | a0002c0002t0002g0184 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2986-1127G>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47213278 | |||||||
| chr18:47213382 | T | TATATTTA others(30): Show |
2 | a0002c0008t0002g0147 a0002c0008t0002g0148 |
2 | HG02698.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2986-1268_2986-123 others(41): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47213382 | |||||||
| chr18:47213457 | C | T | 1 | a0001c0001t0001g0011 | 3 | HG03041.hp2 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2986-1306G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47213457 | |||||||
| chr18:47213519 | C | T | 1 | a0002c0002t0003g0161 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2986-1368G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47213519 | |||||||
| chr18:47213606 | A | C | 11 | a0001c0001t0003g0028 a0001c0001t0003g0229 a0001c0001t0003g0230 others(8): Show |
12 | HG00099.hp2 HG01123.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.2986-1455T>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47213606 | |||||||
| chr18:47213632 | G | A | 187 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0017 others(184): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.2986-1481C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47213632 | |||||||
| chr18:47213923 | C | T | 3 | a0001c0006t0003g0154 a0001c0006t0003g0155 a0001c0006t0003g0156 |
3 | HG01361.hp1 HG01515.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2986-1772G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47213923 | |||||||
| chr18:47214577 | C | G | 1 | a0001c0001t0001g0127 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2986-2426G>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47214577 | |||||||
| chr18:47214583 | T | A | 1 | a0002c0002t0008g0185 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2986-2432A>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47214583 | |||||||
| chr18:47214592 | A | G | 8 | a0001c0001t0003g0028 a0001c0001t0003g0229 a0001c0001t0003g0230 others(5): Show |
9 | HG00099.hp2 HG01123.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.2986-2441T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47214592 | |||||||
| chr18:47214692 | A | G | 26 | a0002c0002t0003g0004 a0002c0002t0003g0007 a0002c0002t0003g0013 others(23): Show |
40 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.2986-2541T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47214692 | |||||||
| chr18:47214789 | A | T | 3 | a0001c0006t0003g0154 a0001c0006t0003g0155 a0001c0006t0003g0156 |
3 | HG01361.hp1 HG01515.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2986-2638T>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47214789 | |||||||
| chr18:47214844 | C | A | 2 | a0001c0001t0001g0101 a0002c0002t0002g0192 |
2 | HG00558.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.2986-2693G>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47214844 | |||||||
| chr18:47214958 | C | T | 1 | a0002c0002t0003g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2986-2807G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47214958 | |||||||
| chr18:47214991 | G | GT | 36 | a0001c0001t0003g0028 a0001c0001t0003g0229 a0001c0001t0003g0230 others(33): Show |
51 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.2986-2841dupA | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47214991 | |||||||
| chr18:47214994 | T | TA | 103 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0041 others(100): Show |
126 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.2986-2844dupT | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47214994 | |||||||
| chr18:47214995 | A | T | 33 | a0001c0001t0003g0028 a0001c0001t0003g0229 a0001c0001t0003g0230 others(30): Show |
48 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.2986-2844T>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47214995 | |||||||
| chr18:47215177 | C | A | 1 | a0002c0002t0002g0186 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2986-3026G>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47215177 | |||||||
| chr18:47215211 | A | G | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG02486.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.2986-3060T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47215211 | |||||||
| chr18:47215255 | A | G | 2 | a0003c0005t0001g0036 a0011c0018t0001g0105 |
2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2986-3104T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47215255 | |||||||
| chr18:47215367 | T | A | 2 | a0001c0001t0002g0240 a0007c0019t0002g0259 |
2 | HG01257.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.2986-3216A>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47215367 | |||||||
| chr18:47215368 | A | T | 9 | a0001c0001t0001g0048 a0001c0001t0001g0087 a0001c0001t0001g0131 others(6): Show |
9 | HG01361.hp1 HG01515.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2986-3217T>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47215368 | |||||||
| chr18:47215684 | G | C | 3 | a0003c0007t0002g0157 a0003c0007t0002g0158 a0003c0007t0002g0159 |
3 | HG00544.hp1 NA18747.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.2986-3533C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47215684 | |||||||
| chr18:47215695 | C | A | 77 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0068 others(74): Show |
99 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.2986-3544G>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47215695 | |||||||
| chr18:47215718 | A | C | 37 | a0001c0001t0003g0028 a0001c0001t0003g0229 a0001c0001t0003g0230 others(34): Show |
52 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.2986-3567T>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47215718 | |||||||
| chr18:47216037 | T | C | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0002g0228 others(1): Show |
4 | HG02976.hp1 HG03098.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2986-3886A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47216037 | |||||||
| chr18:47216128 | T | G | 1 | a0002c0002t0002g0219 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2985+3815A>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47216128 | |||||||
| chr18:47216226 | A | T | 2 | a0001c0001t0004g0123 a0001c0001t0004g0124 |
2 | HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2985+3717T>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47216226 | |||||||
| chr18:47216497 | A | C | 97 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0045 others(94): Show |
129 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.2985+3446T>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47216497 | |||||||
| chr18:47216544 | C | T | 2 | a0001c0001t0003g0028 a0008c0013t0003g0141 |
3 | HG01243.hp1 HG01884.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.2985+3399G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47216544 | |||||||
| chr18:47216559 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2985+3384T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47216559 | |||||||
| chr18:47216815 | C | A | 2 | a0001c0001t0002g0228 a0002c0002t0002g0162 |
2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2985+3128G>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47216815 | |||||||
| chr18:47216855 | A | G | 5 | a0001c0003t0001g0008 a0001c0003t0001g0031 a0001c0003t0001g0032 others(2): Show |
7 | HG02451.hp1 HG02559.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2985+3088T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47216855 | |||||||
| chr18:47217344 | G | A | 13 | a0001c0001t0003g0028 a0001c0001t0003g0229 a0001c0001t0003g0230 others(10): Show |
16 | HG00099.hp2 HG01123.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.2985+2599C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47217344 | |||||||
| chr18:47217357 | G | A | 5 | a0001c0003t0001g0008 a0001c0003t0001g0031 a0001c0003t0001g0032 others(2): Show |
7 | HG02451.hp1 HG02559.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2985+2586C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47217357 | |||||||
| chr18:47217399 | C | A | 2 | a0003c0005t0001g0037 a0003c0005t0001g0038 |
2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2985+2544G>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47217399 | |||||||
| chr18:47217926 | G | C | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0002g0140 |
3 | HG02922.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2985+2017C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47217926 | |||||||
| chr18:47218019 | C | T | 2 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2985+1924G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47218019 | |||||||
| chr18:47218051 | G | A | 20 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0002g0140 others(17): Show |
24 | HG00140.hp2 HG00639.hp2 HG01952.hp1 others(21): Show |
intron_variant | MODIFIER | c.2985+1892C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47218051 | |||||||
| chr18:47218183 | C | G | 2 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2985+1760G>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47218183 | |||||||
| chr18:47218589 | C | CA | 44 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0042 others(41): Show |
52 | HG00673.hp2 HG01243.hp2 HG02056.hp1 others(49): Show |
intron_variant | MODIFIER | c.2985+1353dupT | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47218589 | |||||||
| chr18:47218589 | C | CAA | 12 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0043 others(9): Show |
13 | HG00544.hp1 HG01361.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.2985+1352_2985+135 others(6): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47218589 | |||||||
| chr18:47218589 | C | CAAA | 76 | a0001c0001t0001g0019 a0001c0001t0001g0046 a0001c0001t0001g0047 others(73): Show |
107 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.2985+1351_2985+135 others(7): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47218589 | |||||||
| chr18:47218589 | C | CAAAA | 12 | a0001c0001t0001g0041 a0001c0001t0001g0045 a0001c0001t0004g0124 others(9): Show |
12 | HG00735.hp2 HG01884.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.2985+1350_2985+135 others(8): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47218589 | |||||||
| chr18:47218589 | C | CAAAAA | 19 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0002g0140 others(16): Show |
20 | HG00140.hp2 HG00639.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.2985+1349_2985+135 others(9): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47218589 | |||||||
| chr18:47218589 | C | CAAAAAA | 13 | a0001c0001t0003g0028 a0001c0001t0003g0229 a0001c0001t0003g0230 others(10): Show |
17 | HG00099.hp2 HG01123.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.2985+1348_2985+135 others(10): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47218589 | |||||||
| chr18:47218589 | CA | C | 8 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0059 others(5): Show |
8 | HG00558.hp2 HG01069.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.2985+1353delT | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47218589 | |||||||
| chr18:47218685 | A | G | 133 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0045 others(130): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.2985+1258T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47218685 | |||||||
| chr18:47218814 | A | C | 133 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0045 others(130): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.2985+1129T>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47218814 | |||||||
| chr18:47218907 | C | T | 3 | a0001c0006t0003g0154 a0001c0006t0003g0155 a0001c0006t0003g0156 |
3 | HG01361.hp1 HG01515.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2985+1036G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47218907 | |||||||
| chr18:47219175 | T | C | 17 | a0002c0002t0002g0171 a0002c0002t0003g0013 a0002c0002t0003g0024 others(14): Show |
21 | HG00140.hp2 HG00639.hp2 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.2985+768A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47219175 | |||||||
| chr18:47219350 | C | G | 102 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0045 others(99): Show |
134 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.2985+593G>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47219350 | |||||||
| chr18:47219372 | T | C | 1 | a0001c0001t0001g0130 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2985+571A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47219372 | |||||||
| chr18:47219398 | GT | G | 133 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0045 others(130): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.2985+544delA | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47219398 | |||||||
| chr18:47219533 | C | T | 1 | a0002c0002t0002g0162 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2985+410G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47219533 | |||||||
| chr18:47219545 | G | A | 2 | a0002c0002t0003g0161 a0002c0002t0003g0163 |
2 | HG02258.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2985+398C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47219545 | |||||||
| chr18:47219662 | G | T | 3 | a0001c0001t0003g0233 a0001c0001t0004g0123 a0001c0001t0004g0124 |
3 | HG01891.hp2 HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2985+281C>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47219662 | |||||||
| chr18:47219663 | C | T | 3 | a0001c0001t0003g0233 a0001c0001t0004g0123 a0001c0001t0004g0124 |
3 | HG01891.hp2 HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2985+280G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47219663 | |||||||
| chr18:47219691 | G | T | 1 | a0001c0001t0001g0083 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2985+252C>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47219691 | |||||||
| chr18:47220089 | A | T | 92 | a0001c0001t0001g0019 a0001c0001t0001g0068 a0001c0001t0001g0082 others(89): Show |
124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.2918-79T>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47220089 | |||||||
| chr18:47220306 | G | C | 2 | a0002c0002t0003g0161 a0002c0002t0003g0163 |
2 | HG02258.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2918-296C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47220306 | |||||||
| chr18:47220368 | C | G | 133 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0045 others(130): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.2918-358G>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47220368 | |||||||
| chr18:47220416 | C | T | 4 | a0001c0001t0002g0242 a0001c0001t0002g0243 a0001c0001t0002g0244 others(1): Show |
4 | NA18968.hp1 NA18981.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.2918-406G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47220416 | |||||||
| chr18:47220576 | G | C | 118 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0045 others(115): Show |
151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.2918-566C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47220576 | |||||||
| chr18:47220626 | G | A | 87 | a0001c0001t0001g0019 a0001c0001t0002g0254 a0001c0021t0001g0111 others(84): Show |
119 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.2918-616C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47220626 | |||||||
| chr18:47220726 | G | C | 1 | a0001c0001t0002g0263 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2918-716C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47220726 | |||||||
| chr18:47220767 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2918-757C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47220767 | |||||||
| chr18:47220778 | T | A | 37 | a0001c0001t0001g0009 a0001c0001t0001g0039 a0001c0001t0001g0040 others(34): Show |
42 | HG00673.hp2 HG01243.hp2 HG01257.hp2 others(39): Show |
intron_variant | MODIFIER | c.2918-768A>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47220778 | |||||||
| chr18:47220822 | G | C | 1 | a0001c0001t0001g0121 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2918-812C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47220822 | |||||||
| chr18:47220928 | A | G | 25 | a0001c0001t0001g0057 a0001c0001t0001g0125 a0001c0001t0002g0015 others(22): Show |
28 | HG00673.hp2 HG01243.hp2 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.2918-918T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47220928 | |||||||
| chr18:47221012 | G | C | 1 | a0001c0001t0001g0086 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2918-1002C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47221012 | |||||||
| chr18:47221084 | A | C | 2 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2918-1074T>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47221084 | |||||||
| chr18:47221314 | A | T | 3 | a0001c0006t0003g0154 a0001c0006t0003g0155 a0001c0006t0003g0156 |
3 | HG01361.hp1 HG01515.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2918-1304T>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47221314 | |||||||
| chr18:47221374 | T | C | 3 | a0001c0006t0003g0154 a0001c0006t0003g0155 a0001c0006t0003g0156 |
3 | HG01361.hp1 HG01515.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2918-1364A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47221374 | |||||||
| chr18:47221395 | G | C | 2 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2918-1385C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47221395 | |||||||
| chr18:47221552 | C | A | 1 | a0001c0001t0002g0228 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2918-1542G>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47221552 | |||||||
| chr18:47221675 | A | AT | 47 | a0001c0001t0001g0054 a0001c0001t0001g0057 a0001c0001t0001g0078 others(44): Show |
52 | HG00673.hp2 HG01243.hp2 HG01257.hp2 others(49): Show |
intron_variant | MODIFIER | c.2918-1666dupA | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47221675 | |||||||
| chr18:47221693 | C | G | 6 | a0002c0002t0003g0024 a0002c0002t0003g0165 a0002c0002t0003g0166 others(3): Show |
7 | NA18940.hp2 NA18968.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.2918-1683G>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47221693 | |||||||
| chr18:47221708 | T | G | 137 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0039 others(134): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.2918-1698A>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47221708 | |||||||
| chr18:47221821 | A | T | 2 | a0001c0001t0001g0068 a0002c0002t0003g0025 |
3 | HG00140.hp1 HG00140.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.2918-1811T>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47221821 | |||||||
| chr18:47222096 | A | G | 143 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0039 others(140): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.2918-2086T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47222096 | |||||||
| chr18:47222174 | T | G | 182 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0039 others(179): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.2918-2164A>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47222174 | |||||||
| chr18:47222183 | A | T | 1 | a0001c0001t0001g0059 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2918-2173T>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47222183 | |||||||
| chr18:47222238 | C | T | 2 | a0003c0010t0005g0264 a0003c0010t0005g0265 |
2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2918-2228G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47222238 | |||||||
| chr18:47222249 | G | A | 2 | a0001c0001t0002g0232 a0002c0002t0002g0162 |
2 | HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2918-2239C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47222249 | |||||||
| chr18:47222289 | C | G | 1 | a0001c0001t0001g0076 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2918-2279G>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47222289 | |||||||
| chr18:47222312 | C | T | 188 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0039 others(185): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.2918-2302G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47222312 | |||||||
| chr18:47222315 | CA | C | 41 | a0001c0001t0001g0057 a0001c0001t0001g0078 a0001c0001t0001g0122 others(38): Show |
44 | HG00673.hp2 HG01243.hp2 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.2918-2306delT | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47222315 | |||||||
| chr18:47222521 | G | A | 1 | a0002c0002t0008g0185 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2918-2511C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47222521 | |||||||
| chr18:47222538 | C | G | 6 | a0001c0001t0001g0009 a0001c0001t0001g0039 a0001c0001t0001g0040 others(3): Show |
8 | HG02486.hp1 HG02717.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.2918-2528G>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47222538 | |||||||
| chr18:47222775 | G | C | 3 | a0001c0006t0003g0154 a0001c0006t0003g0155 a0001c0006t0003g0156 |
3 | HG01361.hp1 HG01515.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2918-2765C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47222775 | |||||||
| chr18:47223014 | A | G | 1 | a0002c0002t0003g0182 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2918-3004T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47223014 | |||||||
| chr18:47223216 | C | T | 1 | a0002c0008t0002g0148 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2918-3206G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47223216 | |||||||
| chr18:47223374 | G | A | 3 | a0001c0006t0003g0154 a0001c0006t0003g0155 a0001c0006t0003g0156 |
3 | HG01361.hp1 HG01515.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2918-3364C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47223374 | |||||||
| chr18:47223513 | A | C | 76 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0039 others(73): Show |
106 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.2918-3503T>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47223513 | |||||||
| chr18:47223903 | CT | C | 180 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0039 others(177): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.2918-3894delA | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47223903 | |||||||
| chr18:47223917 | TA | T | 5 | a0001c0001t0001g0081 a0001c0001t0001g0094 a0001c0001t0001g0096 others(2): Show |
5 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.2918-3908delT | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47223917 | |||||||
| chr18:47223919 | A | T | 5 | a0001c0001t0001g0081 a0001c0001t0001g0094 a0001c0001t0001g0096 others(2): Show |
5 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.2918-3909T>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47223919 | |||||||
| chr18:47223932 | G | A | 3 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 |
3 | HG02257.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2918-3922C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47223932 | |||||||
| chr18:47223945 | G | A | 1 | a0001c0001t0002g0235 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2918-3935C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47223945 | |||||||
| chr18:47223994 | C | T | 166 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0041 others(163): Show |
209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.2918-3984G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47223994 | |||||||
| chr18:47224072 | C | CT | 5 | a0001c0001t0001g0041 a0001c0001t0001g0045 a0001c0001t0001g0046 others(2): Show |
5 | HG01884.hp1 HG02257.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2918-4063dupA | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47224072 | |||||||
| chr18:47224120 | G | C | 1 | a0013c0023t0002g0260 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2918-4110C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47224120 | |||||||
| chr18:47224434 | T | C | 1 | a0001c0001t0003g0233 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2918-4424A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47224434 | |||||||
| chr18:47224620 | C | CT | 181 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0039 others(178): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.2918-4611dupA | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47224620 | |||||||
| chr18:47224706 | C | T | 2 | a0001c0003t0001g0008 a0001c0003t0001g0033 |
4 | HG02451.hp1 HG02559.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2918-4696G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47224706 | |||||||
| chr18:47224962 | A | G | 1 | a0001c0001t0001g0080 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2918-4952T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47224962 | |||||||
| chr18:47225003 | A | G | 188 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0039 others(185): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.2918-4993T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47225003 | |||||||
| chr18:47225050 | A | G | 1 | a0002c0002t0002g0172 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2918-5040T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47225050 | |||||||
| chr18:47225053 | A | C | 1 | a0001c0001t0001g0122 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2918-5043T>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47225053 | |||||||
| chr18:47225485 | A | G | 188 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0039 others(185): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.2917+4974T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47225485 | |||||||
| chr18:47225499 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2917+4960G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47225499 | |||||||
| chr18:47225589 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2917+4870G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47225589 | |||||||
| chr18:47225633 | A | C | 1 | a0001c0001t0001g0079 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2917+4826T>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47225633 | |||||||
| chr18:47225670 | A | G | 188 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0039 others(185): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.2917+4789T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47225670 | |||||||
| chr18:47225754 | G | A | 185 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0039 others(182): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.2917+4705C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47225754 | |||||||
| chr18:47225754 | G | C | 3 | a0001c0001t0002g0228 a0002c0002t0002g0138 a0002c0002t0002g0162 |
3 | HG02486.hp2 HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2917+4705C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47225754 | |||||||
| chr18:47225867 | G | C | 182 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0039 others(179): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.2917+4592C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47225867 | |||||||
| chr18:47226139 | C | G | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0004g0123 |
3 | HG01891.hp2 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2917+4320G>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47226139 | |||||||
| chr18:47226522 | C | G | 1 | a0001c0001t0001g0122 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2917+3937G>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47226522 | |||||||
| chr18:47226870 | A | C | 3 | a0001c0001t0002g0228 a0002c0002t0002g0138 a0002c0002t0002g0162 |
3 | HG02486.hp2 HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2917+3589T>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47226870 | |||||||
| chr18:47226871 | A | G | 2 | a0003c0010t0005g0264 a0003c0010t0005g0265 |
2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2917+3588T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47226871 | |||||||
| chr18:47226968 | G | A | 2 | a0003c0010t0005g0264 a0003c0010t0005g0265 |
2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2917+3491C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47226968 | |||||||
| chr18:47227203 | C | T | 1 | a0001c0001t0002g0242 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2917+3256G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47227203 | |||||||
| chr18:47227206 | C | T | 1 | a0001c0001t0002g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2917+3253G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47227206 | |||||||
| chr18:47227326 | A | AT | 58 | a0001c0001t0001g0040 a0001c0001t0001g0049 a0001c0001t0001g0054 others(55): Show |
64 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.2917+3132dupA | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47227326 | |||||||
| chr18:47227326 | A | ATT | 10 | a0001c0001t0001g0039 a0001c0001t0006g0272 a0001c0001t0006g0273 others(7): Show |
11 | HG01070.hp2 HG01071.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.2917+3131_2917+313 others(6): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47227326 | |||||||
| chr18:47227326 | AT | A | 27 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(24): Show |
29 | HG01515.hp2 HG01517.hp1 HG01975.hp2 others(26): Show |
intron_variant | MODIFIER | c.2917+3132delA | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47227326 | |||||||
| chr18:47227326 | ATT | A | 7 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(4): Show |
9 | HG01884.hp1 HG02486.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.2917+3131_2917+313 others(6): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47227326 | |||||||
| chr18:47227326 | ATTTTTTT others(5): Show |
A | 3 | a0001c0006t0003g0154 a0001c0006t0003g0155 a0001c0006t0003g0156 |
3 | HG01361.hp1 HG01515.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2917+3121_2917+313 others(16): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47227326 | |||||||
| chr18:47227326 | ATTTTTTT others(7): Show |
A | 2 | a0001c0001t0001g0087 a0001c0001t0001g0088 |
2 | HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.2917+3119_2917+313 others(18): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47227326 | |||||||
| chr18:47227326 | ATTTTTTT others(8): Show |
A | 2 | a0002c0002t0002g0197 a0002c0002t0002g0221 |
2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2917+3118_2917+313 others(19): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47227326 | |||||||
| chr18:47227360 | C | T | 1 | a0001c0001t0002g0250 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2917+3099G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47227360 | |||||||
| chr18:47227374 | G | A | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0004g0123 |
3 | HG01891.hp2 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2917+3085C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47227374 | |||||||
| chr18:47227430 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2917+3029G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47227430 | |||||||
| chr18:47227447 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.2917+3012G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47227447 | |||||||
| chr18:47227658 | A | C | 1 | a0001c0001t0001g0137 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2917+2801T>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47227658 | |||||||
| chr18:47227732 | T | C | 166 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0122 others(163): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.2917+2727A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47227732 | |||||||
| chr18:47227793 | A | G | 7 | a0001c0001t0001g0009 a0001c0001t0001g0039 a0001c0001t0001g0040 others(4): Show |
9 | HG01884.hp1 HG02486.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.2917+2666T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47227793 | |||||||
| chr18:47227804 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2917+2655G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47227804 | |||||||
| chr18:47227891 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2917+2568C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47227891 | |||||||
| chr18:47228008 | T | C | 1 | a0001c0001t0001g0048 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2917+2451A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47228008 | |||||||
| chr18:47228280 | G | A | 74 | a0001c0006t0003g0154 a0001c0006t0003g0155 a0001c0006t0003g0156 others(71): Show |
100 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.2917+2179C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47228280 | |||||||
| chr18:47228502 | A | G | 5 | a0003c0005t0001g0035 a0003c0005t0001g0036 a0003c0005t0001g0037 others(2): Show |
5 | HG02559.hp2 HG02572.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2917+1957T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47228502 | |||||||
| chr18:47228645 | A | G | 1 | a0001c0001t0001g0053 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2917+1814T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47228645 | |||||||
| chr18:47228678 | A | G | 6 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.2917+1781T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47228678 | |||||||
| chr18:47228984 | C | T | 6 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.2917+1475G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47228984 | |||||||
| chr18:47230050 | A | C | 87 | a0001c0001t0001g0009 a0001c0001t0001g0039 a0001c0001t0001g0040 others(84): Show |
115 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.2917+409T>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47230050 | |||||||
| chr18:47230140 | A | G | 1 | a0002c0002t0003g0267 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2917+319T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47230140 | |||||||
| chr18:47230350 | CTG | C | 6 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.2917+107_2917+108d others(4): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47230350 | |||||||
| chr18:47230562 | TA | T | 6 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02647.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.2819-6delT | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 5/8 | chr18 | 47230562 | |||||||
| chr18:47230667 | A | C | 3 | a0001c0006t0003g0154 a0001c0006t0003g0155 a0001c0006t0003g0156 |
3 | HG01361.hp1 HG01515.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2819-110T>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 5/8 | chr18 | 47230667 | |||||||
| chr18:47230765 | T | C | 30 | a0001c0001t0001g0125 a0001c0001t0002g0015 a0001c0001t0002g0030 others(27): Show |
33 | HG00609.hp1 HG00609.hp2 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.2818+170A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 5/8 | chr18 | 47230765 | |||||||
| chr18:47230766 | T | G | 3 | a0003c0007t0002g0157 a0003c0007t0002g0158 a0003c0007t0002g0159 |
3 | HG00544.hp1 NA18747.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.2818+169A>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 5/8 | chr18 | 47230766 | |||||||
| chr18:47230855 | G | T | 76 | a0001c0006t0003g0154 a0001c0006t0003g0155 a0001c0006t0003g0156 others(73): Show |
102 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.2818+80C>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 5/8 | chr18 | 47230855 | |||||||
| chr18:47231184 | T | C | 6 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.2753-184A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47231184 | |||||||
| chr18:47231370 | G | T | 1 | a0001c0001t0002g0234 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2753-370C>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47231370 | |||||||
| chr18:47231371 | C | T | 1 | a0001c0001t0002g0234 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2753-371G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47231371 | |||||||
| chr18:47231407 | G | A | 1 | a0001c0001t0003g0233 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2753-407C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47231407 | |||||||
| chr18:47231447 | A | G | 6 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.2753-447T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47231447 | |||||||
| chr18:47231546 | T | A | 17 | a0001c0001t0001g0104 a0002c0002t0002g0006 a0002c0002t0002g0026 others(14): Show |
21 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.2753-546A>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47231546 | |||||||
| chr18:47231547 | A | T | 6 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.2753-547T>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47231547 | |||||||
| chr18:47231565 | C | T | 1 | a0003c0005t0001g0035 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2753-565G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47231565 | |||||||
| chr18:47231570 | G | A | 5 | a0001c0001t0001g0122 a0001c0001t0002g0228 a0001c0006t0003g0154 others(2): Show |
5 | HG01361.hp1 HG01515.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2753-570C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47231570 | |||||||
| chr18:47231689 | C | G | 2 | a0002c0002t0002g0138 a0002c0002t0002g0162 |
2 | HG02486.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2753-689G>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47231689 | |||||||
| chr18:47231843 | C | CA | 8 | a0001c0001t0001g0054 a0001c0001t0001g0063 a0001c0001t0001g0090 others(5): Show |
8 | HG02258.hp1 HG02486.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.2753-844dupT | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47231843 | |||||||
| chr18:47231843 | C | CAA | 32 | a0002c0002t0002g0006 a0002c0002t0002g0026 a0002c0002t0002g0160 others(29): Show |
40 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.2753-845_2753-844d others(4): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47231843 | |||||||
| chr18:47231843 | C | CAAAA | 5 | a0001c0003t0001g0008 a0001c0003t0001g0031 a0001c0003t0001g0032 others(2): Show |
7 | HG02451.hp1 HG02559.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2753-847_2753-844d others(6): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47231843 | |||||||
| chr18:47231843 | CA | C | 108 | a0001c0001t0001g0064 a0001c0001t0001g0100 a0001c0001t0001g0125 others(105): Show |
138 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.2753-844delT | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47231843 | |||||||
| chr18:47231911 | C | T | 1 | a0002c0002t0003g0270 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2753-911G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47231911 | |||||||
| chr18:47231948 | C | T | 1 | a0001c0001t0004g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2753-948G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47231948 | |||||||
| chr18:47232153 | TA | T | 3 | a0001c0006t0003g0154 a0001c0006t0003g0155 a0001c0006t0003g0156 |
3 | HG01361.hp1 HG01515.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2753-1154delT | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47232153 | |||||||
| chr18:47232225 | C | T | 1 | a0003c0005t0001g0036 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2753-1225G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47232225 | |||||||
| chr18:47232242 | A | G | 1 | a0001c0001t0002g0255 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2753-1242T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47232242 | |||||||
| chr18:47232294 | G | T | 74 | a0001c0006t0003g0154 a0001c0006t0003g0155 a0001c0006t0003g0156 others(71): Show |
100 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.2753-1294C>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47232294 | |||||||
| chr18:47232301 | C | T | 1 | a0001c0001t0004g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2753-1301G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47232301 | |||||||
| chr18:47232643 | G | A | 1 | a0002c0002t0002g0171 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2753-1643C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47232643 | |||||||
| chr18:47232704 | T | C | 3 | a0001c0006t0003g0154 a0001c0006t0003g0155 a0001c0006t0003g0156 |
3 | HG01361.hp1 HG01515.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2753-1704A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47232704 | |||||||
| chr18:47232779 | G | C | 1 | a0001c0001t0001g0101 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2753-1779C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47232779 | |||||||
| chr18:47232832 | C | G | 36 | a0002c0002t0002g0006 a0002c0002t0002g0026 a0002c0002t0002g0138 others(33): Show |
44 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.2753-1832G>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47232832 | |||||||
| chr18:47232850 | G | A | 1 | a0002c0002t0003g0270 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2753-1850C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47232850 | |||||||
| chr18:47233276 | A | C | 1 | a0002c0002t0002g0162 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2753-2276T>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47233276 | |||||||
| chr18:47233347 | C | A | 1 | a0001c0001t0001g0099 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2753-2347G>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47233347 | |||||||
| chr18:47233452 | G | A | 3 | a0001c0001t0002g0232 a0001c0001t0006g0272 a0001c0001t0006g0273 |
3 | HG02922.hp2 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2753-2452C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47233452 | |||||||
| chr18:47233842 | G | A | 3 | a0001c0006t0003g0154 a0001c0006t0003g0155 a0001c0006t0003g0156 |
3 | HG01361.hp1 HG01515.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2753-2842C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47233842 | |||||||
| chr18:47234110 | C | T | 1 | a0002c0002t0002g0184 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2753-3110G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47234110 | |||||||
| chr18:47234113 | T | C | 1 | a0002c0002t0002g0178 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2753-3113A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47234113 | |||||||
| chr18:47234149 | C | T | 2 | a0002c0002t0002g0138 a0002c0002t0002g0162 |
2 | HG02486.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2753-3149G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47234149 | |||||||
| chr18:47234165 | G | A | 2 | a0001c0001t0001g0122 a0001c0001t0002g0228 |
2 | HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2753-3165C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47234165 | |||||||
| chr18:47234256 | TA | T | 8 | a0001c0001t0001g0009 a0001c0001t0001g0039 a0001c0001t0001g0040 others(5): Show |
10 | HG01884.hp1 HG01891.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.2753-3257delT | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47234256 | |||||||
| chr18:47234292 | C | T | 39 | a0001c0001t0002g0232 a0001c0001t0006g0272 a0001c0001t0006g0273 others(36): Show |
47 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.2753-3292G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47234292 | |||||||
| chr18:47234355 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2753-3355T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47234355 | |||||||
| chr18:47234530 | G | A | 74 | a0001c0006t0003g0154 a0001c0006t0003g0155 a0001c0006t0003g0156 others(71): Show |
100 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.2753-3530C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47234530 | |||||||
| chr18:47234541 | G | C | 1 | a0003c0005t0001g0038 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2753-3541C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47234541 | |||||||
| chr18:47234864 | G | GAAAAAAA others(2): Show |
10 | a0001c0001t0001g0054 a0001c0001t0002g0239 a0001c0001t0002g0252 others(7): Show |
11 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.2753-3873_2753-386 others(13): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47234864 | |||||||
| chr18:47234864 | G | GAAAAAAA others(3): Show |
96 | a0001c0001t0001g0125 a0001c0001t0002g0015 a0001c0001t0002g0030 others(93): Show |
126 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.2753-3874_2753-386 others(14): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47234864 | |||||||
| chr18:47234864 | G | GAAAAAAA others(4): Show |
17 | a0001c0001t0001g0122 a0001c0001t0002g0140 a0001c0001t0002g0146 others(14): Show |
17 | HG00735.hp2 HG01361.hp1 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.2753-3875_2753-386 others(15): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47234864 | |||||||
| chr18:47234864 | G | GAAAAAAA others(5): Show |
1 | a0011c0018t0001g0105 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2753-3865_2753-386 others(16): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47234864 | |||||||
| chr18:47234879 | A | G | 2 | a0001c0001t0003g0028 a0008c0013t0003g0141 |
3 | HG01243.hp1 HG01884.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.2753-3879T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47234879 | |||||||
| chr18:47235298 | A | G | 6 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.2753-4298T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47235298 | |||||||
| chr18:47235447 | T | A | 1 | a0001c0001t0004g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2753-4447A>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47235447 | |||||||
| chr18:47235487 | G | T | 1 | a0001c0001t0001g0044 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2753-4487C>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47235487 | |||||||
| chr18:47235780 | C | CA | 49 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0045 others(46): Show |
56 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.2753-4781dupT | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47235780 | |||||||
| chr18:47235780 | C | CAA | 19 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(16): Show |
21 | HG01884.hp1 HG02486.hp1 HG02572.hp2 others(18): Show |
intron_variant | MODIFIER | c.2753-4782_2753-478 others(6): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47235780 | |||||||
| chr18:47235780 | CA | C | 13 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(10): Show |
13 | HG00673.hp1 HG00733.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.2753-4781delT | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47235780 | |||||||
| chr18:47235780 | CAA | C | 6 | a0001c0001t0001g0055 a0001c0001t0001g0130 a0001c0001t0001g0131 others(3): Show |
6 | HG01975.hp2 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.2753-4782_2753-478 others(6): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47235780 | |||||||
| chr18:47235793 | A | AC | 8 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 others(5): Show |
9 | HG01123.hp1 HG01243.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.2753-4794_2753-479 others(5): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47235793 | |||||||
| chr18:47235793 | A | C | 1 | a0001c0001t0003g0230 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2753-4793T>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47235793 | |||||||
| chr18:47235801 | AC | A | 8 | a0001c0006t0003g0154 a0001c0006t0003g0155 a0001c0006t0003g0156 others(5): Show |
8 | HG01361.hp1 HG01515.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.2753-4802delG | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47235801 | |||||||
| chr18:47235802 | C | A | 67 | a0002c0002t0001g0022 a0002c0002t0001g0113 a0002c0002t0001g0114 others(64): Show |
93 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.2753-4802G>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47235802 | |||||||
| chr18:47235805 | C | G | 2 | a0003c0010t0005g0264 a0003c0010t0005g0265 |
2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2753-4805G>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47235805 | |||||||
| chr18:47235936 | C | T | 77 | a0001c0006t0003g0154 a0001c0006t0003g0155 a0001c0006t0003g0156 others(74): Show |
103 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.2753-4936G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47235936 | |||||||
| chr18:47235964 | T | C | 5 | a0003c0005t0001g0035 a0003c0005t0001g0036 a0003c0005t0001g0037 others(2): Show |
5 | HG02559.hp2 HG02572.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2753-4964A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47235964 | |||||||
| chr18:47236016 | G | A | 35 | a0002c0002t0002g0006 a0002c0002t0002g0026 a0002c0002t0002g0138 others(32): Show |
43 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.2753-5016C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47236016 | |||||||
| chr18:47236037 | C | T | 77 | a0001c0006t0003g0154 a0001c0006t0003g0155 a0001c0006t0003g0156 others(74): Show |
103 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.2753-5037G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47236037 | |||||||
| chr18:47236038 | G | A | 16 | a0002c0002t0002g0006 a0002c0002t0002g0026 a0002c0002t0002g0160 others(13): Show |
20 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.2753-5038C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47236038 | |||||||
| chr18:47236071 | A | G | 1 | a0002c0002t0002g0181 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2753-5071T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47236071 | |||||||
| chr18:47236161 | G | C | 3 | a0001c0006t0003g0154 a0001c0006t0003g0155 a0001c0006t0003g0156 |
3 | HG01361.hp1 HG01515.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2753-5161C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47236161 | |||||||
| chr18:47236179 | C | T | 7 | a0001c0001t0001g0009 a0001c0001t0001g0039 a0001c0001t0001g0040 others(4): Show |
9 | HG01884.hp1 HG02486.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.2753-5179G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47236179 | |||||||
| chr18:47236205 | G | A | 1 | a0003c0005t0001g0036 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2753-5205C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47236205 | |||||||
| chr18:47236221 | G | T | 35 | a0002c0002t0002g0006 a0002c0002t0002g0026 a0002c0002t0002g0138 others(32): Show |
43 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.2753-5221C>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47236221 | |||||||
| chr18:47236269 | G | A | 9 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 others(6): Show |
10 | HG00099.hp2 HG01123.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.2753-5269C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47236269 | |||||||
| chr18:47236377 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2753-5377G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47236377 | |||||||
| chr18:47236581 | C | A | 1 | a0002c0002t0002g0186 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2753-5581G>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47236581 | |||||||
| chr18:47236674 | C | T | 1 | a0002c0002t0002g0172 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2753-5674G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47236674 | |||||||
| chr18:47236922 | T | C | 1 | a0001c0003t0001g0034 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2753-5922A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47236922 | |||||||
| chr18:47237223 | A | T | 3 | a0001c0001t0002g0232 a0001c0001t0006g0272 a0001c0001t0006g0273 |
3 | HG02922.hp2 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2753-6223T>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47237223 | |||||||
| chr18:47237428 | A | G | 2 | a0003c0010t0005g0264 a0003c0010t0005g0265 |
2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2753-6428T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47237428 | |||||||
| chr18:47237519 | C | T | 3 | a0001c0006t0003g0154 a0001c0006t0003g0155 a0001c0006t0003g0156 |
3 | HG01361.hp1 HG01515.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2753-6519G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47237519 | |||||||
| chr18:47237623 | T | G | 77 | a0001c0006t0003g0154 a0001c0006t0003g0155 a0001c0006t0003g0156 others(74): Show |
103 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.2753-6623A>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47237623 | |||||||
| chr18:47237624 | C | A | 1 | a0001c0001t0001g0098 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2753-6624G>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47237624 | |||||||
| chr18:47237699 | C | CT | 33 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0070 others(30): Show |
38 | HG00609.hp1 HG00609.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.2753-6700dupA | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47237699 | |||||||
| chr18:47237699 | CT | C | 87 | a0001c0001t0001g0064 a0001c0001t0001g0099 a0001c0001t0001g0100 others(84): Show |
114 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.2753-6700delA | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47237699 | |||||||
| chr18:47237704 | T | C | 2 | a0001c0006t0003g0154 a0001c0006t0003g0156 |
2 | HG01361.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2753-6704A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47237704 | |||||||
| chr18:47237785 | C | T | 2 | a0002c0002t0002g0197 a0002c0002t0002g0221 |
2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2753-6785G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47237785 | |||||||
| chr18:47237967 | T | C | 1 | a0012c0015t0002g0215 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2752+6941A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47237967 | |||||||
| chr18:47238000 | C | A | 3 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 |
3 | HG02257.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2752+6908G>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47238000 | |||||||
| chr18:47238018 | G | C | 2 | a0002c0002t0002g0138 a0002c0002t0002g0162 |
2 | HG02486.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2752+6890C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47238018 | |||||||
| chr18:47238191 | T | G | 1 | a0001c0001t0001g0069 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2752+6717A>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47238191 | |||||||
| chr18:47238196 | A | G | 1 | a0001c0001t0001g0069 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2752+6712T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47238196 | |||||||
| chr18:47238311 | T | G | 1 | a0002c0002t0002g0187 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2752+6597A>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47238311 | |||||||
| chr18:47238320 | CT | C | 65 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0039 others(62): Show |
72 | HG00099.hp2 HG00609.hp1 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.2752+6587delA | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47238320 | |||||||
| chr18:47238320 | CTT | C | 69 | a0002c0002t0001g0022 a0002c0002t0001g0113 a0002c0002t0001g0114 others(66): Show |
91 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.2752+6586_2752+658 others(6): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47238320 | |||||||
| chr18:47238325 | T | C | 30 | a0002c0002t0002g0006 a0002c0002t0002g0026 a0002c0002t0002g0160 others(27): Show |
38 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.2752+6583A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47238325 | |||||||
| chr18:47238326 | T | C | 1 | a0002c0002t0003g0180 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2752+6582A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47238326 | |||||||
| chr18:47238447 | C | T | 1 | a0001c0001t0003g0233 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2752+6461G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47238447 | |||||||
| chr18:47238448 | G | A | 1 | a0012c0015t0002g0215 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2752+6460C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47238448 | |||||||
| chr18:47238614 | C | T | 35 | a0002c0002t0002g0006 a0002c0002t0002g0026 a0002c0002t0002g0138 others(32): Show |
43 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.2752+6294G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47238614 | |||||||
| chr18:47238669 | G | A | 1 | a0001c0001t0002g0254 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2752+6239C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47238669 | |||||||
| chr18:47239098 | G | A | 74 | a0002c0002t0001g0022 a0002c0002t0001g0113 a0002c0002t0001g0114 others(71): Show |
100 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.2752+5810C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47239098 | |||||||
| chr18:47239306 | CT | C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0101 others(2): Show |
9 | HG00597.hp2 HG01070.hp1 HG02698.hp1 others(6): Show |
intron_variant | MODIFIER | c.2752+5601delA | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47239306 | |||||||
| chr18:47239530 | G | A | 30 | a0002c0002t0002g0006 a0002c0002t0002g0026 a0002c0002t0002g0160 others(27): Show |
38 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.2752+5378C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47239530 | |||||||
| chr18:47239572 | G | A | 77 | a0001c0006t0003g0154 a0001c0006t0003g0155 a0001c0006t0003g0156 others(74): Show |
103 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.2752+5336C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47239572 | |||||||
| chr18:47239600 | G | A | 35 | a0002c0002t0002g0006 a0002c0002t0002g0026 a0002c0002t0002g0138 others(32): Show |
43 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.2752+5308C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47239600 | |||||||
| chr18:47239712 | A | G | 35 | a0002c0002t0002g0006 a0002c0002t0002g0026 a0002c0002t0002g0138 others(32): Show |
43 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.2752+5196T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47239712 | |||||||
| chr18:47239807 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2752+5101G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47239807 | |||||||
| chr18:47239982 | T | A | 2 | a0001c0001t0001g0102 a0001c0001t0001g0132 |
2 | HG02970.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.2752+4926A>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47239982 | |||||||
| chr18:47239982 | T | TA | 72 | a0002c0002t0001g0022 a0002c0002t0001g0113 a0002c0002t0001g0114 others(69): Show |
98 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.2752+4925dupT | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47239982 | |||||||
| chr18:47240162 | A | G | 7 | a0001c0001t0001g0009 a0001c0001t0001g0039 a0001c0001t0001g0040 others(4): Show |
9 | HG01884.hp1 HG02486.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.2752+4746T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47240162 | |||||||
| chr18:47240521 | G | C | 1 | a0001c0001t0001g0103 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2752+4387C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47240521 | |||||||
| chr18:47240539 | C | G | 2 | a0003c0010t0005g0264 a0003c0010t0005g0265 |
2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2752+4369G>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47240539 | |||||||
| chr18:47240584 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2752+4324G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47240584 | |||||||
| chr18:47240838 | C | T | 5 | a0003c0005t0001g0035 a0003c0005t0001g0036 a0003c0005t0001g0037 others(2): Show |
5 | HG02559.hp2 HG02572.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2752+4070G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47240838 | |||||||
| chr18:47241187 | C | T | 3 | a0002c0002t0003g0164 a0002c0002t0003g0169 a0002c0002t0003g0170 |
3 | HG01952.hp1 HG02293.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.2752+3721G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47241187 | |||||||
| chr18:47241231 | A | G | 2 | a0003c0010t0005g0264 a0003c0010t0005g0265 |
2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2752+3677T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47241231 | |||||||
| chr18:47241395 | G | T | 3 | a0001c0001t0002g0235 a0001c0001t0002g0236 a0001c0001t0002g0241 |
3 | HG00609.hp2 NA18952.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.2752+3513C>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47241395 | |||||||
| chr18:47241414 | A | G | 35 | a0002c0002t0002g0006 a0002c0002t0002g0026 a0002c0002t0002g0138 others(32): Show |
43 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.2752+3494T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47241414 | |||||||
| chr18:47241450 | T | G | 2 | a0002c0002t0002g0196 a0002c0002t0002g0216 |
2 | HG00639.hp1 HG00642.hp1 |
intron_variant | MODIFIER | c.2752+3458A>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47241450 | |||||||
| chr18:47241638 | CA | C | 74 | a0001c0001t0002g0140 a0002c0002t0001g0022 a0002c0002t0001g0113 others(71): Show |
100 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.2752+3269delT | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47241638 | |||||||
| chr18:47241642 | A | C | 36 | a0001c0006t0003g0154 a0001c0006t0003g0155 a0001c0006t0003g0156 others(33): Show |
44 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.2752+3266T>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47241642 | |||||||
| chr18:47241653 | T | C | 74 | a0002c0002t0001g0022 a0002c0002t0001g0113 a0002c0002t0001g0114 others(71): Show |
100 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.2752+3255A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47241653 | |||||||
| chr18:47241746 | A | G | 2 | a0001c0001t0001g0067 a0001c0001t0001g0068 |
2 | HG00140.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.2752+3162T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47241746 | |||||||
| chr18:47241924 | T | C | 31 | a0002c0002t0002g0006 a0002c0002t0002g0026 a0002c0002t0002g0160 others(28): Show |
39 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.2752+2984A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47241924 | |||||||
| chr18:47241970 | C | A | 7 | a0002c0002t0002g0218 a0002c0002t0002g0219 a0002c0002t0003g0217 others(4): Show |
8 | HG00639.hp2 HG02280.hp1 HG03490.hp2 others(5): Show |
intron_variant | MODIFIER | c.2752+2938G>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47241970 | |||||||
| chr18:47242030 | C | T | 1 | a0004c0004t0002g0151 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2752+2878G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47242030 | |||||||
| chr18:47242122 | A | G | 187 | a0001c0001t0001g0009 a0001c0001t0001g0039 a0001c0001t0001g0040 others(184): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.2752+2786T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47242122 | |||||||
| chr18:47242212 | A | T | 2 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2752+2696T>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47242212 | |||||||
| chr18:47242368 | G | C | 1 | a0001c0001t0001g0104 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2752+2540C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47242368 | |||||||
| chr18:47242718 | T | C | 1 | a0002c0002t0002g0220 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2752+2190A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47242718 | |||||||
| chr18:47242771 | G | C | 1 | a0001c0001t0001g0021 | 2 | HG01070.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.2752+2137C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47242771 | |||||||
| chr18:47243026 | A | G | 1 | a0002c0002t0002g0199 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2752+1882T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47243026 | |||||||
| chr18:47243060 | A | G | 1 | a0001c0001t0001g0066 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2752+1848T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47243060 | |||||||
| chr18:47243163 | T | A | 74 | a0002c0002t0001g0022 a0002c0002t0001g0113 a0002c0002t0001g0114 others(71): Show |
100 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.2752+1745A>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47243163 | |||||||
| chr18:47243449 | C | T | 187 | a0001c0001t0001g0009 a0001c0001t0001g0039 a0001c0001t0001g0040 others(184): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.2752+1459G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47243449 | |||||||
| chr18:47243886 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2752+1022A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47243886 | |||||||
| chr18:47243946 | C | A | 256 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 others(253): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.2752+962G>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47243946 | |||||||
| chr18:47244079 | A | G | 1 | a0001c0001t0003g0233 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2752+829T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47244079 | |||||||
| chr18:47244228 | A | G | 3 | a0002c0002t0002g0223 a0002c0002t0002g0224 a0002c0002t0002g0225 |
3 | HG03195.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2752+680T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47244228 | |||||||
| chr18:47244250 | T | G | 187 | a0001c0001t0001g0009 a0001c0001t0001g0039 a0001c0001t0001g0040 others(184): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.2752+658A>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47244250 | |||||||
| chr18:47244369 | A | G | 1 | a0001c0001t0002g0240 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2752+539T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47244369 | |||||||
| chr18:47244375 | T | C | 74 | a0002c0002t0001g0022 a0002c0002t0001g0113 a0002c0002t0001g0114 others(71): Show |
100 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.2752+533A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47244375 | |||||||
| chr18:47244590 | A | G | 1 | a0002c0002t0003g0169 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2752+318T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47244590 | |||||||
| chr18:47244593 | A | G | 2 | a0002c0002t0002g0198 a0002c0002t0002g0222 |
2 | NA18959.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.2752+315T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47244593 | |||||||
| chr18:47244594 | G | C | 3 | a0001c0001t0001g0011 a0001c0001t0001g0120 a0001c0001t0001g0121 |
5 | HG02922.hp1 HG03041.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.2752+314C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47244594 | |||||||
| chr18:47244788 | T | C | 11 | a0001c0001t0001g0122 a0001c0001t0002g0228 a0001c0001t0002g0261 others(8): Show |
12 | HG00099.hp2 HG01123.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.2752+120A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47244788 | |||||||
| chr18:47245048 | A | AT | 8 | a0001c0003t0001g0008 a0001c0003t0001g0031 a0001c0003t0001g0032 others(5): Show |
10 | HG00099.hp1 HG02145.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.2678-67dupA | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245048 | |||||||
| chr18:47245110 | C | T | 74 | a0002c0002t0001g0022 a0002c0002t0001g0113 a0002c0002t0001g0114 others(71): Show |
100 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.2678-128G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245110 | |||||||
| chr18:47245208 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2678-226T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245208 | |||||||
| chr18:47245478 | A | ATT | 6 | a0001c0001t0001g0009 a0001c0001t0001g0039 a0001c0001t0001g0040 others(3): Show |
8 | HG01884.hp1 HG02486.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2677+18_2677+19dup others(2): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245478 | |||||||
| chr18:47245478 | A | ATTTTTTT others(1): Show |
12 | a0002c0002t0001g0022 a0002c0002t0002g0012 a0002c0002t0002g0142 others(9): Show |
15 | HG01070.hp2 HG01071.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.2677+12_2677+19dup others(8): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245478 | |||||||
| chr18:47245478 | A | ATTTTTTT others(2): Show |
52 | a0001c0001t0003g0233 a0002c0002t0001g0114 a0002c0002t0001g0115 others(49): Show |
75 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.2677+11_2677+19dup others(9): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245478 | |||||||
| chr18:47245478 | A | ATTTTTTT others(3): Show |
14 | a0001c0001t0002g0255 a0001c0001t0002g0256 a0001c0001t0002g0257 others(11): Show |
14 | HG00558.hp1 HG00642.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.2677+10_2677+19dup others(10): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245478 | |||||||
| chr18:47245478 | A | ATTTTTTT others(4): Show |
20 | a0001c0001t0002g0015 a0001c0001t0002g0030 a0001c0001t0002g0146 others(17): Show |
23 | HG00609.hp1 HG00609.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.2677+9_2677+19dupA others(10): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245478 | |||||||
| chr18:47245478 | A | ATTTTTTT others(5): Show |
7 | a0001c0001t0001g0125 a0001c0001t0002g0145 a0001c0001t0002g0235 others(4): Show |
7 | HG01243.hp2 HG02109.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.2677+8_2677+19dupA others(11): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245478 | |||||||
| chr18:47245478 | A | ATTTTTTT others(6): Show |
13 | a0002c0002t0002g0006 a0002c0002t0002g0026 a0002c0002t0002g0160 others(10): Show |
20 | HG00140.hp2 HG00438.hp2 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.2677+7_2677+19dupA others(12): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245478 | |||||||
| chr18:47245478 | A | ATTTTTTT others(7): Show |
15 | a0001c0001t0001g0135 a0001c0006t0003g0156 a0002c0002t0002g0171 others(12): Show |
16 | HG01952.hp1 HG02080.hp1 HG02155.hp2 others(13): Show |
intron_variant | MODIFIER | c.2677+6_2677+19dupA others(13): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245478 | |||||||
| chr18:47245478 | A | ATTTTTTT others(8): Show |
11 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0003t0001g0034 others(8): Show |
12 | HG00408.hp2 HG01515.hp1 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.2677+5_2677+19dupA others(14): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245478 | |||||||
| chr18:47245478 | A | ATTTTTTT others(9): Show |
6 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0002g0232 others(3): Show |
8 | HG01361.hp1 HG02451.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.2677+4_2677+19dupA others(15): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245478 | |||||||
| chr18:47245478 | A | ATTTTTTT others(10): Show |
5 | a0001c0001t0001g0130 a0001c0001t0006g0273 a0001c0003t0001g0032 others(2): Show |
5 | HG03041.hp1 HG03471.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.2677+3_2677+19dupA others(16): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245478 | |||||||
| chr18:47245478 | A | ATTTTTTT others(11): Show |
2 | a0001c0001t0001g0048 a0001c0003t0001g0031 |
2 | HG03195.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2677+19_2677+20ins others(18): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245478 | |||||||
| chr18:47245478 | A | ATTTTTTT others(12): Show |
1 | a0001c0001t0006g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2677+19_2677+20ins others(19): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245478 | |||||||
| chr18:47245478 | A | ATTTTTTT others(14): Show |
2 | a0001c0001t0003g0230 a0001c0001t0003g0231 |
2 | HG00099.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.2677+19_2677+20ins others(21): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245478 | |||||||
| chr18:47245478 | A | ATTTTTTT others(15): Show |
2 | a0001c0001t0004g0123 a0002c0002t0002g0138 |
2 | HG01891.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.2677+19_2677+20ins others(22): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245478 | |||||||
| chr18:47245478 | A | ATTTTTTT others(17): Show |
3 | a0001c0001t0003g0028 a0001c0001t0003g0229 a0008c0013t0003g0141 |
4 | HG01123.hp1 HG01243.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.2677+19_2677+20ins others(24): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245478 | |||||||
| chr18:47245478 | A | ATTTTTTT others(22): Show |
3 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0002g0263 |
3 | HG02896.hp1 HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2677+19_2677+20ins others(29): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245478 | |||||||
| chr18:47245478 | A | ATTTTTTT others(23): Show |
2 | a0001c0001t0002g0261 a0001c0001t0002g0262 |
2 | HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2677+19_2677+20ins others(30): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245478 | |||||||
| chr18:47245478 | A | ATTTTTTT others(24): Show |
1 | a0001c0001t0002g0228 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2677+19_2677+20ins others(31): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245478 | |||||||
| chr18:47245478 | A | ATTTTTTT others(25): Show |
2 | a0001c0001t0001g0045 a0001c0001t0001g0122 |
2 | HG02257.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2677+19_2677+20ins others(32): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245478 | |||||||
| chr18:47245478 | AT | A | 8 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0049 others(5): Show |
12 | HG00673.hp1 HG01070.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.2677+19delA | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245478 | |||||||
| chr18:47245598 | C | G | 3 | a0001c0006t0003g0154 a0001c0006t0003g0155 a0001c0006t0003g0156 |
3 | HG01361.hp1 HG01515.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2614-37G>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/8 | chr18 | 47245598 | |||||||
| chr18:47245883 | C | A | 1 | a0001c0001t0001g0109 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2614-322G>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/8 | chr18 | 47245883 | |||||||
| chr18:47245956 | C | T | 2 | a0006c0009t0002g0149 a0006c0009t0002g0150 |
2 | NA18974.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.2614-395G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/8 | chr18 | 47245956 | |||||||
| chr18:47245997 | T | TGGAG | 74 | a0002c0002t0001g0022 a0002c0002t0001g0113 a0002c0002t0001g0114 others(71): Show |
100 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.2614-437_2614-436i others(6): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/8 | chr18 | 47245997 | |||||||
| chr18:47246000 | T | TGA | 74 | a0002c0002t0001g0022 a0002c0002t0001g0113 a0002c0002t0001g0114 others(71): Show |
100 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.2614-440_2614-439i others(4): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/8 | chr18 | 47246000 | |||||||
| chr18:47246236 | A | C | 1 | a0002c0002t0002g0160 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2613+335T>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/8 | chr18 | 47246236 | |||||||
| chr18:47246238 | T | C | 30 | a0001c0001t0001g0125 a0001c0001t0002g0015 a0001c0001t0002g0030 others(27): Show |
33 | HG00609.hp1 HG00609.hp2 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.2613+333A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/8 | chr18 | 47246238 | |||||||
| chr18:47246253 | G | C | 3 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 |
3 | HG02451.hp2 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2613+318C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/8 | chr18 | 47246253 | |||||||
| chr18:47246284 | C | G | 2 | a0001c0001t0001g0053 a0001c0001t0002g0144 |
2 | NA18959.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.2613+287G>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/8 | chr18 | 47246284 | |||||||
| chr18:47246449 | A | G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0120 a0001c0001t0001g0121 |
5 | HG02922.hp1 HG03041.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.2613+122T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/8 | chr18 | 47246449 | |||||||
| chr18:47249319 | A | G | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | HG00673.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.-47-89T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/8 | chr18 | 47249319 | |||||||
| chr18:47249526 | G | A | 192 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0039 others(189): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.-47-296C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/8 | chr18 | 47249526 | |||||||
| chr18:47249666 | G | A | 1 | a0001c0001t0001g0129 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-47-436C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/8 | chr18 | 47249666 | |||||||
| chr18:47249700 | C | A | 2 | a0003c0010t0005g0264 a0003c0010t0005g0265 |
2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-47-470G>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/8 | chr18 | 47249700 | |||||||
| chr18:47249743 | T | G | 6 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-47-513A>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/8 | chr18 | 47249743 | |||||||
| chr18:47249818 | A | G | 15 | a0001c0001t0001g0009 a0001c0001t0001g0039 a0001c0001t0001g0040 others(12): Show |
17 | HG01884.hp1 HG02257.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.-47-588T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/8 | chr18 | 47249818 | |||||||
| chr18:47249963 | T | G | 2 | a0003c0010t0005g0264 a0003c0010t0005g0265 |
2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-47-733A>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/8 | chr18 | 47249963 | |||||||
| chr18:47250182 | A | G | 15 | a0001c0001t0001g0009 a0001c0001t0001g0039 a0001c0001t0001g0040 others(12): Show |
17 | HG01884.hp1 HG02257.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.-47-952T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/8 | chr18 | 47250182 | |||||||
| chr18:47250511 | A | G | 7 | a0001c0001t0001g0009 a0001c0001t0001g0039 a0001c0001t0001g0040 others(4): Show |
9 | HG01884.hp1 HG02486.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-48+863T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/8 | chr18 | 47250511 | |||||||
| chr18:47250705 | G | A | 3 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 |
3 | HG03225.hp1 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-48+669C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/8 | chr18 | 47250705 | |||||||
| chr18:47250794 | G | A | 2 | a0003c0010t0005g0264 a0003c0010t0005g0265 |
2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-48+580C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/8 | chr18 | 47250794 | |||||||
| chr18:47250811 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-48+563A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/8 | chr18 | 47250811 | |||||||
| chr18:47250863 | C | T | 4 | a0002c0002t0002g0012 a0002c0002t0002g0142 a0002c0002t0002g0143 others(1): Show |
6 | HG01884.hp2 HG02647.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-48+511G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/8 | chr18 | 47250863 | |||||||
| chr18:47250913 | C | A | 7 | a0002c0002t0003g0004 a0002c0002t0003g0266 a0002c0002t0003g0267 others(4): Show |
14 | HG00597.hp1 NA18612.hp2 NA18939.hp2 others(11): Show |
intron_variant | MODIFIER | c.-48+461G>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/8 | chr18 | 47250913 | |||||||
| chr18:47250934 | A | G | 4 | a0003c0005t0001g0035 a0003c0005t0001g0036 a0003c0005t0001g0037 others(1): Show |
4 | HG02559.hp2 HG02630.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+440T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/8 | chr18 | 47250934 | |||||||
| chr18:47250984 | G | T | 5 | a0001c0003t0001g0008 a0001c0003t0001g0031 a0001c0003t0001g0032 others(2): Show |
7 | HG02451.hp1 HG02559.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-48+390C>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/8 | chr18 | 47250984 | |||||||
| chr18:47251109 | G | T | 1 | a0001c0001t0002g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-48+265C>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/8 | chr18 | 47251109 | |||||||
| chr18:47251161 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-48+213A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/8 | chr18 | 47251161 | |||||||
| chr18:47251186 | A | T | 1 | a0002c0012t0003g0139 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-48+188T>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/8 | chr18 | 47251186 | |||||||
| chr18:47251241 | C | T | 1 | a0002c0002t0002g0138 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-48+133G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/8 | chr18 | 47251241 |