Item | Value |
---|---|
geneid | 22937 |
ensemblid | ENSG00000114650.21 |
hgncid | 30634 |
symbol | SCAP |
name | SREBF chaperone |
refseq_nuc | NM_012235.4 |
refseq_prot | NP_036367.2 |
ensembl_nuc | ENST00000265565.10 |
ensembl_prot | ENSP00000265565.5 |
mane_status | MANE Select |
chr | chr3 |
start | 47413681 |
end | 47475941 |
strand | - |
ver | v1.2 |
region | chr3:47413681-47475941 |
region5000 | chr3:47408681-47480941 |
regionname0 | SCAP_chr3_47413681_47475941 |
regionname5000 | SCAP_chr3_47408681_47480941 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 1279 | 176 | 67 | 27 | 57 | 7 | 17 | 39 | SCAP_chr3_47408681_47480941 | SCAP | MTLTE others(1274): Show |
chr3 | 47408681 | 47480941 |
a0002 | 0/1 | 1279 | 113 | 15 | 30 | 46 | 3 | 18 | 37 | SCAP_chr3_47408681_47480941 | SCAP | MTLTE others(1274): Show |
chr3 | 47408681 | 47480941 |
a0003 | 0/0 | 1279 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | SCAP_chr3_47408681_47480941 | SCAP | MTLTE others(1274): Show |
chr3 | 47408681 | 47480941 |
a0004 | 0/0 | 1279 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | MTLTE others(1274): Show |
chr3 | 47408681 | 47480941 |
a0005 | 0/0 | 1279 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SCAP_chr3_47408681_47480941 | SCAP | MTLTE others(1274): Show |
chr3 | 47408681 | 47480941 |
a0006 | 0/0 | 1279 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | MTLTE others(1274): Show |
chr3 | 47408681 | 47480941 |
a0007 | 0/0 | 1279 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | MTLTE others(1274): Show |
chr3 | 47408681 | 47480941 |
a0008 | 0/0 | 1279 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SCAP_chr3_47408681_47480941 | SCAP | MTLTE others(1274): Show |
chr3 | 47408681 | 47480941 |
a0009 | 0/0 | 1279 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | MTLTE others(1274): Show |
chr3 | 47408681 | 47480941 |
a0010 | 0/0 | 1279 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | MTLTE others(1274): Show |
chr3 | 47408681 | 47480941 |
a0011 | 0/0 | 1279 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | MTLTE others(1274): Show |
chr3 | 47408681 | 47480941 |
a0012 | 0/0 | 1279 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | MTLTE others(1274): Show |
chr3 | 47408681 | 47480941 |
a0013 | 0/0 | 1279 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | MTLTE others(1274): Show |
chr3 | 47408681 | 47480941 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 3837 | 151 | 45 | 26 | 57 | 7 | 16 | SCAP_chr3_47408681_47480941 | SCAP | ATGAC others(3832): Show |
chr3 | 47408681 | 47480941 | ||
a0001c0003 | 1/0 | 3837 | 15 | 14 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | ATGAC others(3832): Show |
chr3 | 47408681 | 47480941 | ||
a0001c0005 | 0/0 | 3837 | 3 | 3 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | ATGAC others(3832): Show |
chr3 | 47408681 | 47480941 | ||
a0001c0008 | 0/0 | 3837 | 2 | 1 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | ATGAC others(3832): Show |
chr3 | 47408681 | 47480941 | ||
a0001c0009 | 0/0 | 3837 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | ATGAC others(3832): Show |
chr3 | 47408681 | 47480941 | ||
a0001c0010 | 0/0 | 3837 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | ATGAC others(3832): Show |
chr3 | 47408681 | 47480941 | ||
a0001c0018 | 0/0 | 3837 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | ATGAC others(3832): Show |
chr3 | 47408681 | 47480941 | ||
a0001c0019 | 0/0 | 3837 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | ATGAC others(3832): Show |
chr3 | 47408681 | 47480941 | ||
a0001c0022 | 0/0 | 3837 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | ATGAC others(3832): Show |
chr3 | 47408681 | 47480941 | ||
a0002c0002 | 0/1 | 3837 | 112 | 15 | 30 | 46 | 3 | 17 | SCAP_chr3_47408681_47480941 | SCAP | ATGAC others(3832): Show |
chr3 | 47408681 | 47480941 | ||
a0002c0011 | 0/0 | 3837 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | ATGAC others(3832): Show |
chr3 | 47408681 | 47480941 | ||
a0003c0004 | 0/0 | 3837 | 3 | 0 | 0 | 3 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | ATGAC others(3832): Show |
chr3 | 47408681 | 47480941 | ||
a0004c0006 | 0/0 | 3837 | 2 | 0 | 0 | 2 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | ATGAC others(3832): Show |
chr3 | 47408681 | 47480941 | ||
a0005c0007 | 0/0 | 3837 | 2 | 0 | 0 | 2 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | ATGAC others(3832): Show |
chr3 | 47408681 | 47480941 | ||
a0006c0013 | 0/0 | 3837 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | ATGAC others(3832): Show |
chr3 | 47408681 | 47480941 | ||
a0007c0014 | 0/0 | 3837 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | ATGAC others(3832): Show |
chr3 | 47408681 | 47480941 | ||
a0008c0021 | 0/0 | 3837 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | ATGAC others(3832): Show |
chr3 | 47408681 | 47480941 | ||
a0009c0015 | 0/0 | 3837 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | ATGAC others(3832): Show |
chr3 | 47408681 | 47480941 | ||
a0010c0012 | 0/0 | 3837 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | ATGAC others(3832): Show |
chr3 | 47408681 | 47480941 | ||
a0011c0017 | 0/0 | 3837 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | ATGAC others(3832): Show |
chr3 | 47408681 | 47480941 | ||
a0012c0020 | 0/0 | 3837 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | ATGAC others(3832): Show |
chr3 | 47408681 | 47480941 | ||
a0013c0016 | 0/0 | 3837 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | ATGAC others(3832): Show |
chr3 | 47408681 | 47480941 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4254 | 116 | 41 | 16 | 45 | 3 | 11 | SCAP_chr3_47408681_47480941 | SCAP | GGGCA others(4249): Show |
chr3 | 47408681 | 47480941 |
a0001c0001t0002 | 0/0 | 4254 | 16 | 1 | 6 | 0 | 4 | 5 | SCAP_chr3_47408681_47480941 | SCAP | GGGCA others(4249): Show |
chr3 | 47408681 | 47480941 |
a0001c0001t0003 | 0/0 | 4259 | 15 | 0 | 3 | 12 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | GGGCA others(4254): Show |
chr3 | 47408681 | 47480941 |
a0001c0001t0005 | 0/0 | 4254 | 2 | 1 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | GGGCA others(4249): Show |
chr3 | 47408681 | 47480941 |
a0001c0001t0006 | 0/0 | 4254 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | GGGCA others(4249): Show |
chr3 | 47408681 | 47480941 |
a0001c0001t0007 | 0/0 | 4254 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | GGGCA others(4249): Show |
chr3 | 47408681 | 47480941 |
a0001c0003t0001 | 1/0 | 4254 | 15 | 14 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | GGGCA others(4249): Show |
chr3 | 47408681 | 47480941 |
a0001c0005t0001 | 0/0 | 4254 | 3 | 3 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | GGGCA others(4249): Show |
chr3 | 47408681 | 47480941 |
a0001c0008t0001 | 0/0 | 4254 | 2 | 1 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | GGGCA others(4249): Show |
chr3 | 47408681 | 47480941 |
a0001c0009t0001 | 0/0 | 4254 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | GGGCA others(4249): Show |
chr3 | 47408681 | 47480941 |
a0001c0010t0001 | 0/0 | 4254 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | GGGCA others(4249): Show |
chr3 | 47408681 | 47480941 |
a0001c0018t0002 | 0/0 | 4254 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | GGGCA others(4249): Show |
chr3 | 47408681 | 47480941 |
a0001c0019t0001 | 0/0 | 4254 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | GGGCA others(4249): Show |
chr3 | 47408681 | 47480941 |
a0001c0022t0001 | 0/0 | 4254 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | GGGCA others(4249): Show |
chr3 | 47408681 | 47480941 |
a0002c0002t0001 | 0/1 | 4254 | 108 | 13 | 28 | 46 | 3 | 17 | SCAP_chr3_47408681_47480941 | SCAP | GGGCA others(4249): Show |
chr3 | 47408681 | 47480941 |
a0002c0002t0004 | 0/0 | 4257 | 3 | 2 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | GGGCA others(4252): Show |
chr3 | 47408681 | 47480941 |
a0002c0002t0008 | 0/0 | 4254 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | GGGCA others(4249): Show |
chr3 | 47408681 | 47480941 |
a0002c0011t0001 | 0/0 | 4254 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | GGGCA others(4249): Show |
chr3 | 47408681 | 47480941 |
a0003c0004t0001 | 0/0 | 4254 | 3 | 0 | 0 | 3 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | GGGCA others(4249): Show |
chr3 | 47408681 | 47480941 |
a0004c0006t0001 | 0/0 | 4254 | 2 | 0 | 0 | 2 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | GGGCA others(4249): Show |
chr3 | 47408681 | 47480941 |
a0005c0007t0001 | 0/0 | 4254 | 2 | 0 | 0 | 2 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | GGGCA others(4249): Show |
chr3 | 47408681 | 47480941 |
a0006c0013t0001 | 0/0 | 4254 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | GGGCA others(4249): Show |
chr3 | 47408681 | 47480941 |
a0007c0014t0001 | 0/0 | 4254 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | GGGCA others(4249): Show |
chr3 | 47408681 | 47480941 |
a0008c0021t0001 | 0/0 | 4254 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | GGGCA others(4249): Show |
chr3 | 47408681 | 47480941 |
a0009c0015t0001 | 0/0 | 4254 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | GGGCA others(4249): Show |
chr3 | 47408681 | 47480941 |
a0010c0012t0001 | 0/0 | 4254 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | GGGCA others(4249): Show |
chr3 | 47408681 | 47480941 |
a0011c0017t0001 | 0/0 | 4254 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | GGGCA others(4249): Show |
chr3 | 47408681 | 47480941 |
a0012c0020t0001 | 0/0 | 4254 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | GGGCA others(4249): Show |
chr3 | 47408681 | 47480941 |
a0013c0016t0001 | 0/0 | 4254 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | GGGCA others(4249): Show |
chr3 | 47408681 | 47480941 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0003g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0005g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0005g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0006g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0001t0007g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0003t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0003t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0003t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0003t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0003t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0003t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0003t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0003t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0003t0001g0012 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0003t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0003t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0003t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0003t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0003t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0005t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0005t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0005t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0008t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0008t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0009t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0010t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0018t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0019t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0001c0022t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0162 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0004g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0004g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0002t0008g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0002c0011t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0003c0004t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0003c0004t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0003c0004t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0004c0006t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0004c0006t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0005c0007t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0005c0007t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0006c0013t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0007c0014t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0008c0021t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0009c0015t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0010c0012t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0011c0017t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0012c0020t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
a0013c0016t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0290 | EUR | GBR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0082 | EUR | GBR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0292 | EUR | GBR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0105 | EUR | GBR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG00408 | hp1 | a0003 | c0004 | t0001 | g0071 | EAS | CHS | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0242 | EAS | CHS | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG00544 | hp2 | a0004 | c0006 | t0001 | g0070 | EAS | CHS | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0128 | EAS | CHS | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | CHS | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG00597 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | CHS | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG00609 | hp1 | a0002 | c0002 | t0001 | g0155 | EAS | CHS | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG00621 | hp1 | a0002 | c0002 | t0001 | g0121 | EAS | CHS | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | CHS | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG00639 | hp2 | a0002 | c0002 | t0001 | g0164 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0297 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG00642 | hp2 | a0002 | c0002 | t0001 | g0091 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0117 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0296 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG00738 | hp2 | a0002 | c0002 | t0001 | g0145 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG00741 | hp1 | a0002 | c0002 | t0001 | g0156 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01069 | hp1 | a0002 | c0002 | t0001 | g0129 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01069 | hp2 | a0006 | c0013 | t0001 | g0265 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01070 | hp1 | a0002 | c0002 | t0001 | g0167 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01074 | hp1 | a0002 | c0002 | t0004 | g0285 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01074 | hp2 | a0002 | c0002 | t0001 | g0154 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0067 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01106 | hp2 | a0002 | c0002 | t0008 | g0115 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01168 | hp2 | a0002 | c0002 | t0001 | g0077 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0126 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0150 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0303 | AMR | PUR | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01256 | hp1 | a0002 | c0002 | t0001 | g0123 | AMR | CLM | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0293 | AMR | CLM | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0124 | AMR | CLM | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0141 | AMR | CLM | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0101 | AMR | CLM | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01261 | hp2 | a0001 | c0001 | t0005 | g0237 | AMR | CLM | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0153 | AMR | CLM | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0090 | AMR | CLM | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0299 | AMR | CLM | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0170 | AMR | CLM | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0289 | EUR | IBS | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0219 | EUR | IBS | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01928 | hp1 | a0002 | c0002 | t0001 | g0151 | AMR | PEL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0245 | AMR | PEL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01934 | hp1 | a0001 | c0008 | t0001 | g0022 | AMR | PEL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01934 | hp2 | a0002 | c0002 | t0001 | g0127 | AMR | PEL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01943 | hp1 | a0002 | c0002 | t0001 | g0081 | AMR | PEL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0217 | AMR | PEL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01952 | hp2 | a0002 | c0002 | t0001 | g0120 | AMR | PEL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01975 | hp2 | a0002 | c0002 | t0001 | g0052 | AMR | PEL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01981 | hp1 | a0002 | c0002 | t0001 | g0109 | AMR | PEL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PEL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02004 | hp1 | a0001 | c0001 | t0003 | g0269 | AMR | PEL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02004 | hp2 | a0002 | c0002 | t0001 | g0089 | AMR | PEL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02027 | hp1 | a0007 | c0014 | t0001 | g0130 | EAS | KHV | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02055 | hp2 | a0001 | c0018 | t0002 | g0300 | AFR | ACB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | KHV | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0113 | EAS | KHV | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02071 | hp1 | a0002 | c0002 | t0001 | g0100 | EAS | KHV | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0273 | EAS | KHV | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0272 | EAS | KHV | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02083 | hp2 | a0002 | c0002 | t0001 | g0125 | EAS | KHV | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0092 | EAS | KHV | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0138 | EAS | KHV | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02145 | hp2 | a0002 | c0002 | t0001 | g0157 | AFR | ACB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02148 | hp1 | a0002 | c0002 | t0001 | g0063 | AMR | PEL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PEL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | CDX | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CDX | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02257 | hp1 | a0001 | c0001 | t0005 | g0235 | AFR | ACB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02257 | hp2 | a0002 | c0002 | t0001 | g0147 | AFR | ACB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02258 | hp1 | a0001 | c0005 | t0001 | g0187 | AFR | ACB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02280 | hp2 | a0002 | c0002 | t0001 | g0095 | AFR | ACB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0161 | AMR | PEL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02451 | hp2 | a0002 | c0002 | t0001 | g0051 | AFR | ACB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02572 | hp1 | a0001 | c0003 | t0001 | g0009 | AFR | GWD | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0301 | SAS | PJL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02602 | hp2 | a0002 | c0002 | t0001 | g0112 | SAS | PJL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02622 | hp1 | a0001 | c0003 | t0001 | g0017 | AFR | GWD | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02630 | hp2 | a0002 | c0002 | t0001 | g0098 | AFR | GWD | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02647 | hp2 | a0002 | c0002 | t0001 | g0163 | AFR | GWD | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0288 | SAS | PJL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02698 | hp2 | a0002 | c0002 | t0001 | g0088 | SAS | PJL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02717 | hp2 | a0002 | c0002 | t0001 | g0104 | AFR | GWD | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02735 | hp1 | a0002 | c0002 | t0001 | g0076 | SAS | PJL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0302 | SAS | PJL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02738 | hp2 | a0002 | c0002 | t0001 | g0066 | SAS | PJL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02886 | hp1 | a0002 | c0002 | t0001 | g0146 | AFR | GWD | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02886 | hp2 | a0001 | c0003 | t0001 | g0008 | AFR | GWD | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02896 | hp1 | a0001 | c0003 | t0001 | g0001 | AFR | GWD | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ESN | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02965 | hp1 | a0002 | c0002 | t0004 | g0286 | AFR | ESN | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02970 | hp2 | a0001 | c0003 | t0001 | g0010 | AFR | ESN | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02976 | hp1 | a0001 | c0003 | t0001 | g0001 | AFR | ESN | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG03017 | hp2 | a0002 | c0002 | t0001 | g0169 | SAS | PJL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG03041 | hp2 | a0002 | c0002 | t0001 | g0062 | AFR | GWD | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG03098 | hp1 | a0001 | c0005 | t0001 | g0195 | AFR | MSL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG03098 | hp2 | a0001 | c0003 | t0001 | g0013 | AFR | MSL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG03130 | hp1 | a0002 | c0002 | t0001 | g0096 | AFR | ESN | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG03139 | hp2 | a0001 | c0005 | t0001 | g0194 | AFR | ESN | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | MSL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG03239 | hp1 | a0002 | c0002 | t0001 | g0078 | SAS | PJL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0087 | SAS | PJL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG03453 | hp1 | a0001 | c0022 | t0001 | g0196 | AFR | MSL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG03453 | hp2 | a0001 | c0019 | t0001 | g0045 | AFR | MSL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG03492 | hp2 | a0002 | c0002 | t0001 | g0079 | SAS | PJL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG03516 | hp2 | a0001 | c0010 | t0001 | g0179 | AFR | ESN | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG03540 | hp1 | a0001 | c0003 | t0001 | g0007 | AFR | GWD | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG03579 | hp2 | a0001 | c0003 | t0001 | g0015 | AFR | MSL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0116 | SAS | PJL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG03669 | hp1 | a0002 | c0002 | t0001 | g0171 | SAS | PJL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0291 | SAS | PJL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG03704 | hp2 | a0008 | c0021 | t0001 | g0210 | SAS | PJL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG03710 | hp1 | a0002 | c0002 | t0001 | g0069 | SAS | PJL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG03710 | hp2 | a0002 | c0011 | t0001 | g0097 | SAS | PJL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0099 | SAS | BEB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0287 | SAS | BEB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG03942 | hp1 | a0001 | c0009 | t0001 | g0266 | SAS | BEB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0142 | SAS | BEB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | STU | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0086 | SAS | STU | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | STU | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | STU | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0085 | SAS | STU | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | STU | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0282 | SAS | STU | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG04228 | hp2 | a0002 | c0002 | t0001 | g0111 | SAS | STU | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | YRI | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18522 | hp2 | a0001 | c0003 | t0001 | g0011 | AFR | YRI | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | YRI | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18906 | hp2 | a0002 | c0002 | t0004 | g0284 | AFR | YRI | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18943 | hp1 | a0002 | c0002 | t0001 | g0049 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18944 | hp2 | a0003 | c0004 | t0001 | g0158 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18947 | hp2 | a0009 | c0015 | t0001 | g0072 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18951 | hp2 | a0002 | c0002 | t0001 | g0152 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18952 | hp1 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0259 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18953 | hp1 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18954 | hp1 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18960 | hp1 | a0002 | c0002 | t0001 | g0114 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18961 | hp1 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18964 | hp1 | a0002 | c0002 | t0001 | g0225 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0132 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18966 | hp2 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18967 | hp1 | a0010 | c0012 | t0001 | g0084 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18969 | hp1 | a0005 | c0007 | t0001 | g0118 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18969 | hp2 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18972 | hp1 | a0002 | c0002 | t0001 | g0251 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0106 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18979 | hp2 | a0003 | c0004 | t0001 | g0139 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18984 | hp1 | a0005 | c0007 | t0001 | g0054 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18988 | hp1 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18988 | hp2 | a0001 | c0001 | t0003 | g0258 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18989 | hp1 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18997 | hp1 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA18999 | hp2 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA19000 | hp2 | a0002 | c0002 | t0001 | g0160 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA19001 | hp1 | a0002 | c0002 | t0001 | g0119 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA19001 | hp2 | a0011 | c0017 | t0001 | g0260 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA19002 | hp2 | a0012 | c0020 | t0001 | g0224 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA19004 | hp1 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA19005 | hp1 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA19010 | hp2 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | LWK | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | LWK | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | LWK | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | LWK | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA19055 | hp2 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA19058 | hp1 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0283 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA19060 | hp2 | a0004 | c0006 | t0001 | g0074 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA19063 | hp1 | a0002 | c0002 | t0001 | g0068 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA19063 | hp2 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA19066 | hp2 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA19067 | hp1 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA19079 | hp2 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA19080 | hp1 | a0001 | c0001 | t0003 | g0243 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA19080 | hp2 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA19081 | hp1 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA19084 | hp1 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA19084 | hp2 | a0013 | c0016 | t0001 | g0246 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA19240 | hp1 | a0002 | c0002 | t0001 | g0134 | AFR | YRI | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | YRI | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA20129 | hp1 | a0002 | c0002 | t0001 | g0103 | AFR | ASW | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ASW | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0270 | EUR | TSI | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA20752 | hp2 | a0002 | c0002 | t0001 | g0166 | EUR | TSI | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0294 | EUR | TSI | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA20805 | hp2 | a0002 | c0002 | t0001 | g0165 | EUR | TSI | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA20905 | hp1 | a0002 | c0002 | t0001 | g0108 | SAS | GIH | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | GIH | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0295 | AMR | CLM | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0298 | AFR | ACB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02486 | hp1 | a0001 | c0008 | t0001 | g0023 | AFR | ACB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02486 | hp2 | a0001 | c0003 | t0001 | g0014 | AFR | ACB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02559 | hp1 | a0001 | c0001 | t0007 | g0003 | AFR | ACB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG02559 | hp2 | a0002 | c0002 | t0001 | g0144 | AFR | ACB | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | MSL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | MSL | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | USA | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
HG06807 | hp2 | a0001 | c0003 | t0001 | g0005 | AFR | USA | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | USA | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA20300 | hp2 | a0001 | c0003 | t0001 | g0006 | AFR | USA | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA21309 | hp1 | a0001 | c0003 | t0001 | g0016 | AFR | LWK | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
NA21309 | hp2 | a0001 | c0001 | t0006 | g0002 | AFR | LWK | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0162 | REF | REF | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
homoSapiens | grch38p0 | a0001 | c0003 | t0001 | g0012 | REF | REF | SCAP_chr3_47408681_47480941 | SCAP | chr3 | 47408681 | 47480941 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:47413976 | T | C | 1 | a0013 | 1 | NA19084.hp2 | missense_variant | MODERATE | c.3718A>G | p.Lys1240Glu | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 23/23 | 3959/4254 | 3718/3840 | 1240/1279 | chr3 | 47413976 | |||
chr3:47417135 | A | G | 1 | a0009 | 1 | NA18947.hp2 | missense_variant | MODERATE | c.3043T>C | p.Phe1015Leu | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/23 | 3284/4254 | 3043/3840 | 1015/1279 | chr3 | 47417135 | |||
chr3:47417443 | T | G | 1 | a0011 | 1 | NA19001.hp2 | missense_variant | MODERATE | c.2831A>C | p.Gln944Pro | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 17/23 | 3072/4254 | 2831/3840 | 944/1279 | chr3 | 47417443 | |||
chr3:47417456 | G | A | 1 | a0004 | 2 | HG00544.hp2 NA19060.hp2 |
missense_variant | MODERATE | c.2818C>T | p.Pro940Ser | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 17/23 | 3059/4254 | 2818/3840 | 940/1279 | chr3 | 47417456 | |||
chr3:47417497 | G | A | 1 | a0005 | 2 | NA18969.hp1 NA18984.hp1 |
missense_variant | MODERATE | c.2777C>T | p.Ala926Val | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 17/23 | 3018/4254 | 2777/3840 | 926/1279 | chr3 | 47417497 | |||
chr3:47417560 | C | T | 2 | a0003 a0004 |
5 | HG00408.hp1 HG00544.hp2 NA18944.hp2 others(2): Show |
missense_variant | MODERATE | c.2714G>A | p.Arg905Gln | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 17/23 | 2955/4254 | 2714/3840 | 905/1279 | chr3 | 47417560 | |||
chr3:47418189 | C | T | 7 | a0002 a0003 a0004 others(4): Show |
122 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(119): Show |
missense_variant | MODERATE | c.2392G>A | p.Val798Ile | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/23 | 2633/4254 | 2392/3840 | 798/1279 | chr3 | 47418189 | |||
chr3:47419469 | C | T | 1 | a0007 | 1 | HG02027.hp1 | missense_variant | MODERATE | c.1799G>A | p.Arg600His | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 13/23 | 2040/4254 | 1799/3840 | 600/1279 | chr3 | 47419469 | |||
chr3:47420690 | C | T | 1 | a0006 | 1 | HG01069.hp2 | missense_variant | MODERATE | c.1427G>A | p.Arg476Gln | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 12/23 | 1668/4254 | 1427/3840 | 476/1279 | chr3 | 47420690 | |||
chr3:47420693 | T | A | 1 | a0010 | 1 | NA18967.hp1 | missense_variant | MODERATE | c.1424A>T | p.Glu475Val | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 12/23 | 1665/4254 | 1424/3840 | 475/1279 | chr3 | 47420693 | |||
chr3:47420694 | C | G | 1 | a0010 | 1 | NA18967.hp1 | missense_variant | MODERATE | c.1423G>C | p.Glu475Gln | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 12/23 | 1664/4254 | 1423/3840 | 475/1279 | chr3 | 47420694 | |||
chr3:47420697 | A | C | 1 | a0010 | 1 | NA18967.hp1 | missense_variant | MODERATE | c.1420T>G | p.Tyr474Asp | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 12/23 | 1661/4254 | 1420/3840 | 474/1279 | chr3 | 47420697 | |||
chr3:47428637 | T | C | 1 | a0012 | 1 | NA19002.hp2 | missense_variant | MODERATE | c.286A>G | p.Ile96Val | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 4/23 | 527/4254 | 286/3840 | 96/1279 | chr3 | 47428637 | |||
chr3:47435087 | G | A | 1 | a0008 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.173C>T | p.Thr58Ile | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/23 | 414/4254 | 173/3840 | 58/1279 | chr3 | 47435087 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:47414240 | C | T | 1 | a0001c0005 | 3 | HG02258.hp1 HG03098.hp1 HG03139.hp2 |
synonymous_variant | LOW | c.3534G>A | p.Leu1178Leu | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 22/23 | 3775/4254 | 3534/3840 | 1178/1279 | chr3 | 47414240 | |||
chr3:47418357 | C | T | 1 | a0001c0008 | 2 | HG01934.hp1 HG02486.hp1 |
synonymous_variant | LOW | c.2295G>A | p.Thr765Thr | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 15/23 | 2536/4254 | 2295/3840 | 765/1279 | chr3 | 47418357 | |||
chr3:47418402 | G | A | 1 | a0001c0018 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.2250C>T | p.Arg750Arg | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 15/23 | 2491/4254 | 2250/3840 | 750/1279 | chr3 | 47418402 | |||
chr3:47419387 | T | C | 1 | a0001c0019 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.1881A>G | p.Lys627Lys | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 13/23 | 2122/4254 | 1881/3840 | 627/1279 | chr3 | 47419387 | |||
chr3:47419582 | G | A | 1 | a0001c0008 | 2 | HG01934.hp1 HG02486.hp1 |
synonymous_variant | LOW | c.1686C>T | p.Pro562Pro | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 13/23 | 1927/4254 | 1686/3840 | 562/1279 | chr3 | 47419582 | |||
chr3:47420692 | C | T | 1 | a0010c0012 | 1 | NA18967.hp1 | synonymous_variant | LOW | c.1425G>A | p.Glu475Glu | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 12/23 | 1666/4254 | 1425/3840 | 475/1279 | chr3 | 47420692 | |||
chr3:47420695 | G | A | 1 | a0010c0012 | 1 | NA18967.hp1 | synonymous_variant | LOW | c.1422C>T | p.Tyr474Tyr | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 12/23 | 1663/4254 | 1422/3840 | 474/1279 | chr3 | 47420695 | |||
chr3:47420701 | C | T | 1 | a0010c0012 | 1 | NA18967.hp1 | synonymous_variant | LOW | c.1416G>A | p.Thr472Thr | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 12/23 | 1657/4254 | 1416/3840 | 472/1279 | chr3 | 47420701 | |||
chr3:47420710 | T | C | 21 | a0001c0001 a0001c0005 a0001c0008 others(18): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
synonymous_variant | LOW | c.1407A>G | p.Gly469Gly | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 12/23 | 1648/4254 | 1407/3840 | 469/1279 | chr3 | 47420710 | |||
chr3:47423979 | C | T | 1 | a0002c0011 | 1 | HG03710.hp2 | synonymous_variant | LOW | c.1104G>A | p.Val368Val | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 9/23 | 1345/4254 | 1104/3840 | 368/1279 | chr3 | 47423979 | |||
chr3:47427562 | C | G | 1 | a0001c0010 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.516G>C | p.Leu172Leu | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 5/23 | 757/4254 | 516/3840 | 172/1279 | chr3 | 47427562 | |||
chr3:47428545 | C | T | 1 | a0001c0009 | 1 | HG03942.hp1 | synonymous_variant | LOW | c.378G>A | p.Val126Val | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 4/23 | 619/4254 | 378/3840 | 126/1279 | chr3 | 47428545 | |||
chr3:47442883 | G | A | 1 | a0001c0022 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.111C>T | p.Ile37Ile | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/23 | 352/4254 | 111/3840 | 37/1279 | chr3 | 47442883 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:47413771 | G | A | 1 | a0001c0001t0005 | 2 | HG01261.hp2 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*83C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 23/23 | 83 | chr3 | 47413771 | ||||||
chr3:47413783 | C | A | 1 | a0002c0002t0008 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*71G>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 23/23 | 71 | chr3 | 47413783 | ||||||
chr3:47413804 | G | GGCCCC | 1 | a0001c0001t0003 | 15 | HG00408.hp2 HG01928.hp2 HG01952.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*45_*49dupGGGGC | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 23/23 | 49 | chr3 | 47413804 | ||||||
chr3:47475809 | A | T | 1 | a0001c0001t0007 | 1 | HG02559.hp1 | 5_prime_UTR_variant | MODIFIER | c.-109T>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/23 | 32816 | chr3 | 47475809 | ||||||
chr3:47475812 | A | T | 1 | a0001c0001t0006 | 1 | NA21309.hp2 | 5_prime_UTR_variant | MODIFIER | c.-112T>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/23 | 32819 | chr3 | 47475812 | ||||||
chr3:47475823 | T | TGCG | 1 | a0002c0002t0004 | 3 | HG01074.hp1 HG02965.hp1 NA18906.hp2 |
5_prime_UTR_variant | MODIFIER | c.-126_-124dupCGC | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/23 | 32831 | chr3 | 47475823 | ||||||
chr3:47475926 | T | C | 2 | a0001c0001t0002 a0001c0018t0002 |
17 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(14): Show |
5_prime_UTR_variant | MODIFIER | c.-226A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/23 | 32933 | chr3 | 47475926 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:47414448 | T | G | 1 | a0001c0005t0001g0187 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3388-62A>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 21/22 | chr3 | 47414448 | |||||||
chr3:47414566 | G | A | 2 | a0002c0002t0001g0154 a0002c0002t0001g0167 |
2 | HG01070.hp1 HG01074.hp2 |
splice_region_variant&intron_variant | LOW | c.3387+6C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 21/22 | chr3 | 47414566 | |||||||
chr3:47414735 | T | C | 295 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(292): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.3307-83A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 20/22 | chr3 | 47414735 | |||||||
chr3:47414761 | C | T | 1 | a0001c0001t0002g0294 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3306+66G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 20/22 | chr3 | 47414761 | |||||||
chr3:47414800 | G | GCACCCAA others(4): Show |
1 | a0002c0002t0001g0136 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.3306+16_3306+26dup others(11): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 20/22 | chr3 | 47414800 | |||||||
chr3:47415068 | T | C | 2 | a0001c0001t0001g0043 a0001c0019t0001g0045 |
2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3139+30A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 19/22 | chr3 | 47415068 | |||||||
chr3:47415199 | T | C | 3 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0001g0176 |
3 | HG04199.hp2 NA19010.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.3057-19A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47415199 | |||||||
chr3:47415384 | G | A | 2 | a0001c0001t0001g0234 a0001c0001t0001g0256 |
2 | HG03017.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.3057-204C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47415384 | |||||||
chr3:47415386 | A | G | 2 | a0002c0002t0001g0128 a0002c0002t0001g0131 |
2 | HG00558.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.3057-206T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47415386 | |||||||
chr3:47415399 | G | A | 1 | a0002c0002t0001g0088 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3057-219C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47415399 | |||||||
chr3:47415465 | A | G | 1 | a0001c0001t0002g0297 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3057-285T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47415465 | |||||||
chr3:47415544 | A | C | 2 | a0001c0001t0001g0175 a0001c0001t0001g0176 |
2 | NA19010.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.3057-364T>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47415544 | |||||||
chr3:47415614 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3057-434G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47415614 | |||||||
chr3:47415917 | C | T | 1 | a0002c0002t0001g0087 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3057-737G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47415917 | |||||||
chr3:47416098 | C | T | 3 | a0001c0001t0001g0227 a0001c0005t0001g0194 a0001c0005t0001g0195 |
3 | HG02132.hp1 HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.3057-918G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47416098 | |||||||
chr3:47416099 | G | A | 2 | a0001c0001t0005g0235 a0001c0001t0005g0237 |
2 | HG01261.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.3057-919C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47416099 | |||||||
chr3:47416228 | C | G | 2 | a0001c0001t0001g0231 a0001c0001t0001g0270 |
2 | HG00738.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.3056+894G>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47416228 | |||||||
chr3:47416311 | C | T | 3 | a0001c0001t0001g0202 a0001c0001t0001g0207 a0011c0017t0001g0260 |
3 | HG02155.hp2 NA18966.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.3056+811G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47416311 | |||||||
chr3:47416613 | C | T | 1 | a0002c0002t0001g0114 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.3056+509G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47416613 | |||||||
chr3:47416615 | C | CT | 13 | a0001c0001t0001g0254 a0001c0001t0001g0270 a0001c0001t0001g0282 others(10): Show |
13 | HG01981.hp2 HG02486.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.3056+506dupA | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47416615 | |||||||
chr3:47416615 | C | CTTTTTTT others(167): Show |
1 | a0002c0002t0001g0062 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3056+506_3056+507i others(176): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47416615 | |||||||
chr3:47416615 | C | CTTTTTTT others(178): Show |
1 | a0002c0002t0001g0098 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3056+506_3056+507i others(187): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47416615 | |||||||
chr3:47416615 | CT | C | 72 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(69): Show |
72 | HG00544.hp1 HG00642.hp1 HG00673.hp1 others(69): Show |
intron_variant | MODIFIER | c.3056+506delA | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47416615 | |||||||
chr3:47416615 | CTT | C | 74 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0001g0025 others(71): Show |
74 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.3056+505_3056+506d others(4): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47416615 | |||||||
chr3:47416615 | CTTTTTTT others(1): Show |
C | 41 | a0002c0002t0001g0049 a0002c0002t0001g0058 a0002c0002t0001g0059 others(38): Show |
41 | HG00544.hp2 HG00642.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.3056+499_3056+506d others(10): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47416615 | |||||||
chr3:47416615 | CTTTTTTT others(2): Show |
C | 77 | a0001c0001t0001g0093 a0001c0001t0001g0105 a0002c0002t0001g0050 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.3056+498_3056+506d others(11): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47416615 | |||||||
chr3:47416615 | CTTTTTTT others(3): Show |
C | 2 | a0002c0002t0001g0080 a0002c0002t0001g0166 |
2 | HG00597.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.3056+497_3056+506d others(12): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47416615 | |||||||
chr3:47416696 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3056+426C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47416696 | |||||||
chr3:47416712 | C | T | 1 | a0002c0002t0001g0053 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.3056+410G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47416712 | |||||||
chr3:47416749 | C | A | 1 | a0001c0001t0007g0003 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3056+373G>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47416749 | |||||||
chr3:47416784 | G | GCCCGGCT others(134): Show |
2 | a0002c0002t0001g0062 a0002c0002t0001g0098 |
2 | HG02630.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.3056+337_3056+338i others(143): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47416784 | |||||||
chr3:47416787 | C | T | 1 | a0002c0002t0008g0115 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3056+335G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47416787 | |||||||
chr3:47416788 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3056+334C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47416788 | |||||||
chr3:47416820 | G | T | 1 | a0011c0017t0001g0260 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.3056+302C>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47416820 | |||||||
chr3:47416869 | G | A | 1 | a0001c0022t0001g0196 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3056+253C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 18/22 | chr3 | 47416869 | |||||||
chr3:47417260 | C | T | 12 | a0002c0002t0001g0049 a0002c0002t0001g0052 a0002c0002t0001g0063 others(9): Show |
12 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(9): Show |
intron_variant | MODIFIER | c.2970+44G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 17/22 | chr3 | 47417260 | |||||||
chr3:47417850 | A | AGAGGGGG others(4): Show |
1 | a0011c0017t0001g0260 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2448-35_2448-25dup others(11): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417850 | |||||||
chr3:47417860 | C | T | 1 | a0001c0019t0001g0045 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2448-34G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417860 | |||||||
chr3:47417866 | A | AG | 9 | a0001c0001t0001g0206 a0001c0001t0001g0232 a0001c0001t0001g0255 others(6): Show |
9 | HG00597.hp2 HG01433.hp1 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.2448-41dupC | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417866 | |||||||
chr3:47417882 | G | GCA | 122 | a0001c0001t0001g0093 a0001c0001t0001g0105 a0002c0002t0001g0049 others(119): Show |
122 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.2448-57_2448-56ins others(2): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417882 | |||||||
chr3:47417890 | C | G | 287 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(284): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.2448-64G>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417890 | |||||||
chr3:47417893 | G | A | 2 | a0001c0001t0001g0271 a0001c0001t0007g0003 |
2 | HG02559.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2448-67C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417893 | |||||||
chr3:47417894 | G | A | 2 | a0001c0001t0001g0271 a0001c0001t0007g0003 |
2 | HG02559.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2448-68C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417894 | |||||||
chr3:47417894 | G | GGGTGAGA others(15): Show |
2 | a0001c0001t0001g0254 a0001c0001t0002g0302 |
2 | HG01981.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.2448-69_2448-68ins others(22): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417894 | |||||||
chr3:47417894 | G | GGGTGAGA others(39): Show |
1 | a0002c0002t0001g0171 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2448-69_2448-68ins others(46): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417894 | |||||||
chr3:47417894 | G | GGGTGAGA others(38): Show |
2 | a0002c0002t0001g0094 a0002c0002t0001g0142 |
2 | HG03942.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.2448-69_2448-68ins others(45): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417894 | |||||||
chr3:47417894 | G | GGTGAGAG others(14): Show |
153 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(150): Show |
153 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.2448-69_2448-68ins others(21): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417894 | |||||||
chr3:47417894 | G | GGTGAGAG others(35): Show |
1 | a0001c0001t0001g0229 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2448-69_2448-68ins others(42): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417894 | |||||||
chr3:47417894 | G | GGTGAGAG others(38): Show |
2 | a0002c0002t0001g0122 a0002c0002t0001g0148 |
2 | NA18961.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.2448-69_2448-68ins others(45): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417894 | |||||||
chr3:47417894 | G | GGTGAGAG others(37): Show |
101 | a0001c0001t0001g0093 a0001c0001t0001g0105 a0001c0001t0001g0214 others(98): Show |
101 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.2448-69_2448-68ins others(44): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417894 | |||||||
chr3:47417894 | G | GGTGAGAG others(60): Show |
1 | a0002c0002t0001g0134 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2448-69_2448-68ins others(67): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417894 | |||||||
chr3:47417894 | G | GGTGAGAG others(38): Show |
2 | a0002c0002t0001g0058 a0002c0002t0001g0125 |
2 | HG02083.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.2448-69_2448-68ins others(45): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417894 | |||||||
chr3:47417894 | G | GGTGAGAG others(38): Show |
6 | a0002c0002t0001g0069 a0002c0002t0001g0107 a0002c0002t0001g0123 others(3): Show |
6 | HG01256.hp1 HG01934.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.2448-69_2448-68ins others(45): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417894 | |||||||
chr3:47417894 | G | GGTGAGAG others(15): Show |
1 | a0001c0001t0002g0303 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2448-69_2448-68ins others(22): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417894 | |||||||
chr3:47417894 | G | GGTGAGAG others(15): Show |
1 | a0001c0001t0001g0239 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2448-69_2448-68ins others(22): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417894 | |||||||
chr3:47417894 | G | GGTGAGAG others(39): Show |
2 | a0002c0002t0001g0066 a0007c0014t0001g0130 |
2 | HG02027.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.2448-69_2448-68ins others(46): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417894 | |||||||
chr3:47417894 | G | GGTGAGAG others(38): Show |
3 | a0002c0002t0001g0063 a0002c0002t0001g0090 a0002c0002t0001g0102 |
3 | HG01433.hp1 HG02148.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.2448-69_2448-68ins others(45): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417894 | |||||||
chr3:47417894 | G | GGTGAGAT others(38): Show |
1 | a0002c0002t0001g0106 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2448-69_2448-68ins others(45): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417894 | |||||||
chr3:47417894 | G | GGTGAGGG others(35): Show |
2 | a0002c0002t0001g0085 a0002c0002t0001g0086 |
2 | HG04115.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.2448-69_2448-68ins others(42): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417894 | |||||||
chr3:47417900 | A | AGGGGGCG others(15): Show |
1 | a0001c0001t0001g0267 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.2448-75_2448-74ins others(22): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417900 | |||||||
chr3:47417901 | G | GGGGGCGG others(13): Show |
2 | a0001c0001t0001g0135 a0011c0017t0001g0260 |
2 | NA18972.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.2448-76_2448-75ins others(20): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417901 | |||||||
chr3:47417903 | G | GGGCGGGG others(15): Show |
1 | a0002c0002t0001g0225 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2448-78_2448-77ins others(22): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417903 | |||||||
chr3:47417908 | T | G | 1 | a0002c0002t0001g0131 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2448-82A>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417908 | |||||||
chr3:47417909 | G | GGGAGGGG others(36): Show |
1 | a0002c0002t0001g0131 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2448-84_2448-83ins others(43): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417909 | |||||||
chr3:47417933 | A | AG | 17 | a0001c0001t0001g0039 a0001c0001t0001g0135 a0001c0001t0001g0173 others(14): Show |
17 | HG00558.hp2 HG00621.hp2 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.2448-108dupC | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417933 | |||||||
chr3:47417939 | T | G | 3 | a0002c0002t0001g0064 a0002c0002t0001g0066 a0002c0002t0001g0125 |
3 | HG02083.hp2 HG02738.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.2448-113A>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417939 | |||||||
chr3:47417939 | T | TG | 18 | a0001c0001t0001g0004 a0001c0001t0001g0038 a0001c0001t0001g0177 others(15): Show |
18 | HG00673.hp1 HG00741.hp2 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.2448-114dupC | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417939 | |||||||
chr3:47417939 | T | TGGGGGGA others(15): Show |
2 | a0001c0005t0001g0194 a0001c0005t0001g0195 |
2 | HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2448-135_2448-114d others(24): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417939 | |||||||
chr3:47417957 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2448-131G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417957 | |||||||
chr3:47417958 | G | A | 2 | a0002c0002t0001g0095 a0002c0002t0001g0096 |
2 | HG02280.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2448-132C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417958 | |||||||
chr3:47417962 | T | G | 1 | a0002c0002t0001g0160 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2448-136A>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417962 | |||||||
chr3:47417969 | A | AG | 13 | a0001c0001t0001g0221 a0001c0001t0001g0239 a0001c0001t0001g0240 others(10): Show |
13 | HG00642.hp1 HG01192.hp1 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.2448-144dupC | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417969 | |||||||
chr3:47417970 | G | A | 1 | a0002c0002t0001g0077 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2448-144C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417970 | |||||||
chr3:47417978 | C | CG | 8 | a0001c0001t0001g0135 a0001c0001t0001g0221 a0001c0001t0001g0238 others(5): Show |
8 | HG00621.hp2 HG01175.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.2448-153dupC | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417978 | |||||||
chr3:47417990 | A | AG | 6 | a0001c0001t0001g0026 a0001c0001t0001g0191 a0001c0001t0001g0207 others(3): Show |
6 | HG01496.hp1 HG02027.hp1 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.2447+143dupC | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417990 | |||||||
chr3:47417995 | G | C | 1 | a0001c0001t0001g0231 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2447+139C>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417995 | |||||||
chr3:47417998 | C | CG | 15 | a0001c0001t0001g0033 a0001c0001t0001g0135 a0001c0001t0001g0204 others(12): Show |
15 | HG00741.hp1 HG00741.hp2 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.2447+135dupC | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47417998 | |||||||
chr3:47418004 | T | G | 4 | a0001c0001t0001g0180 a0001c0001t0001g0184 a0001c0001t0001g0206 others(1): Show |
4 | HG00597.hp2 HG01261.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.2447+130A>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47418004 | |||||||
chr3:47418004 | T | TG | 19 | a0001c0001t0001g0093 a0001c0001t0001g0236 a0001c0001t0001g0241 others(16): Show |
19 | HG00642.hp2 HG01109.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.2447+129dupC | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47418004 | |||||||
chr3:47418039 | C | T | 1 | a0001c0001t0007g0003 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2447+95G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47418039 | |||||||
chr3:47418074 | C | CG | 9 | a0001c0001t0001g0026 a0002c0002t0001g0080 a0002c0002t0001g0090 others(6): Show |
9 | HG00597.hp1 HG00621.hp1 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.2447+59dupC | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47418074 | |||||||
chr3:47418074 | CG | C | 124 | a0001c0001t0001g0032 a0001c0001t0001g0135 a0001c0001t0001g0172 others(121): Show |
124 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.2447+59delC | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47418074 | |||||||
chr3:47418080 | G | T | 2 | a0001c0001t0001g0280 a0011c0017t0001g0260 |
2 | HG00558.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.2447+54C>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47418080 | |||||||
chr3:47418081 | T | G | 2 | a0001c0001t0001g0280 a0011c0017t0001g0260 |
2 | HG00558.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.2447+53A>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47418081 | |||||||
chr3:47418084 | G | T | 1 | a0011c0017t0001g0260 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2447+50C>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 16/22 | chr3 | 47418084 | |||||||
chr3:47418852 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1941-9C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 13/22 | chr3 | 47418852 | |||||||
chr3:47419064 | G | A | 1 | a0001c0022t0001g0196 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1941-221C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 13/22 | chr3 | 47419064 | |||||||
chr3:47419136 | AGT | A | 12 | a0002c0002t0001g0049 a0002c0002t0001g0052 a0002c0002t0001g0063 others(9): Show |
12 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(9): Show |
intron_variant | MODIFIER | c.1940+190_1940+191d others(4): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 13/22 | chr3 | 47419136 | |||||||
chr3:47419140 | A | C | 12 | a0002c0002t0001g0049 a0002c0002t0001g0052 a0002c0002t0001g0063 others(9): Show |
12 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(9): Show |
intron_variant | MODIFIER | c.1940+188T>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 13/22 | chr3 | 47419140 | |||||||
chr3:47419231 | T | C | 1 | a0001c0001t0001g0268 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1940+97A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 13/22 | chr3 | 47419231 | |||||||
chr3:47419974 | C | A | 1 | a0002c0002t0001g0129 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1564-270G>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 12/22 | chr3 | 47419974 | |||||||
chr3:47420240 | G | A | 1 | a0002c0002t0001g0063 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1563+314C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 12/22 | chr3 | 47420240 | |||||||
chr3:47420329 | T | C | 1 | a0001c0001t0001g0214 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1563+225A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 12/22 | chr3 | 47420329 | |||||||
chr3:47420409 | G | A | 1 | a0001c0001t0001g0040 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1563+145C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 12/22 | chr3 | 47420409 | |||||||
chr3:47420823 | C | T | 1 | a0005c0007t0001g0118 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1345-51G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 11/22 | chr3 | 47420823 | |||||||
chr3:47421084 | C | T | 1 | a0002c0002t0001g0119 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1246-55G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 10/22 | chr3 | 47421084 | |||||||
chr3:47421097 | A | G | 293 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(290): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1246-68T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 10/22 | chr3 | 47421097 | |||||||
chr3:47421236 | C | G | 1 | a0001c0001t0001g0209 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1246-207G>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 10/22 | chr3 | 47421236 | |||||||
chr3:47421277 | T | C | 1 | a0001c0001t0007g0003 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1246-248A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 10/22 | chr3 | 47421277 | |||||||
chr3:47421324 | A | C | 1 | a0001c0001t0001g0240 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1246-295T>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 10/22 | chr3 | 47421324 | |||||||
chr3:47421326 | C | A | 1 | a0001c0001t0001g0240 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1246-297G>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 10/22 | chr3 | 47421326 | |||||||
chr3:47421371 | C | T | 1 | a0001c0001t0001g0220 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1246-342G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 10/22 | chr3 | 47421371 | |||||||
chr3:47421386 | G | A | 10 | a0002c0002t0001g0058 a0002c0002t0001g0059 a0002c0002t0001g0060 others(7): Show |
10 | HG00408.hp1 HG00544.hp2 NA18969.hp2 others(7): Show |
intron_variant | MODIFIER | c.1246-357C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 10/22 | chr3 | 47421386 | |||||||
chr3:47421531 | T | C | 1 | a0002c0002t0001g0055 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1246-502A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 10/22 | chr3 | 47421531 | |||||||
chr3:47421790 | A | T | 2 | a0002c0002t0001g0062 a0002c0002t0001g0098 |
2 | HG02630.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1245+652T>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 10/22 | chr3 | 47421790 | |||||||
chr3:47421794 | G | A | 30 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(27): Show |
30 | HG01109.hp1 HG01934.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1245+648C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 10/22 | chr3 | 47421794 | |||||||
chr3:47421795 | C | G | 288 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(285): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.1245+647G>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 10/22 | chr3 | 47421795 | |||||||
chr3:47421870 | T | G | 1 | a0001c0001t0001g0042 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1245+572A>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 10/22 | chr3 | 47421870 | |||||||
chr3:47422004 | C | T | 2 | a0001c0001t0001g0234 a0001c0001t0001g0256 |
2 | HG03017.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1245+438G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 10/22 | chr3 | 47422004 | |||||||
chr3:47422018 | G | A | 1 | a0001c0022t0001g0196 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1245+424C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 10/22 | chr3 | 47422018 | |||||||
chr3:47422077 | T | C | 130 | a0001c0001t0001g0135 a0001c0001t0001g0172 a0001c0001t0001g0173 others(127): Show |
130 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.1245+365A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 10/22 | chr3 | 47422077 | |||||||
chr3:47422369 | C | T | 2 | a0001c0001t0005g0235 a0001c0001t0005g0237 |
2 | HG01261.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1245+73G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 10/22 | chr3 | 47422369 | |||||||
chr3:47422612 | C | T | 3 | a0001c0005t0001g0187 a0001c0005t0001g0194 a0001c0005t0001g0195 |
3 | HG02258.hp1 HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1151-76G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 9/22 | chr3 | 47422612 | |||||||
chr3:47422628 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1151-92A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 9/22 | chr3 | 47422628 | |||||||
chr3:47422632 | A | G | 122 | a0001c0001t0001g0093 a0001c0001t0001g0105 a0002c0002t0001g0049 others(119): Show |
122 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.1151-96T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 9/22 | chr3 | 47422632 | |||||||
chr3:47422654 | G | T | 1 | a0001c0001t0001g0168 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1151-118C>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 9/22 | chr3 | 47422654 | |||||||
chr3:47422739 | G | T | 1 | a0001c0022t0001g0196 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1151-203C>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 9/22 | chr3 | 47422739 | |||||||
chr3:47423029 | TCTAAGGC others(38): Show |
T | 1 | a0002c0002t0001g0251 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1151-538_1151-494d others(47): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 9/22 | chr3 | 47423029 | |||||||
chr3:47423126 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1151-590T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 9/22 | chr3 | 47423126 | |||||||
chr3:47423267 | T | C | 288 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(285): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.1150+666A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 9/22 | chr3 | 47423267 | |||||||
chr3:47423375 | G | A | 1 | a0001c0001t0003g0243 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1150+558C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 9/22 | chr3 | 47423375 | |||||||
chr3:47423603 | A | C | 1 | a0001c0001t0001g0275 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1150+330T>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 9/22 | chr3 | 47423603 | |||||||
chr3:47423690 | A | C | 1 | a0002c0002t0001g0055 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1150+243T>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 9/22 | chr3 | 47423690 | |||||||
chr3:47423691 | G | A | 1 | a0002c0002t0001g0055 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1150+242C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 9/22 | chr3 | 47423691 | |||||||
chr3:47423692 | C | G | 1 | a0002c0002t0001g0055 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1150+241G>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 9/22 | chr3 | 47423692 | |||||||
chr3:47423727 | C | G | 1 | a0001c0001t0001g0188 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1150+206G>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 9/22 | chr3 | 47423727 | |||||||
chr3:47424179 | C | A | 1 | a0002c0002t0008g0115 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1038-134G>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 8/22 | chr3 | 47424179 | |||||||
chr3:47424549 | C | G | 1 | a0002c0002t0001g0090 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1038-504G>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 8/22 | chr3 | 47424549 | |||||||
chr3:47424671 | A | G | 288 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(285): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.1038-626T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 8/22 | chr3 | 47424671 | |||||||
chr3:47424678 | T | C | 1 | a0001c0001t0003g0269 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1038-633A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 8/22 | chr3 | 47424678 | |||||||
chr3:47424695 | G | A | 5 | a0002c0002t0001g0108 a0002c0002t0001g0111 a0002c0002t0001g0116 others(2): Show |
5 | HG03654.hp2 HG03710.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.1038-650C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 8/22 | chr3 | 47424695 | |||||||
chr3:47425036 | G | A | 1 | a0001c0003t0001g0017 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1037+449C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 8/22 | chr3 | 47425036 | |||||||
chr3:47425639 | C | A | 1 | a0001c0001t0002g0288 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.911-28G>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 7/22 | chr3 | 47425639 | |||||||
chr3:47425659 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.911-48C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 7/22 | chr3 | 47425659 | |||||||
chr3:47425779 | T | C | 2 | a0001c0001t0001g0043 a0001c0019t0001g0045 |
2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.911-168A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 7/22 | chr3 | 47425779 | |||||||
chr3:47425795 | C | CAGGAAGG others(10): Show |
1 | a0001c0001t0001g0168 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.910+185_911-185dup others(17): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 7/22 | chr3 | 47425795 | |||||||
chr3:47426290 | T | A | 1 | a0001c0001t0007g0003 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.738-121A>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 6/22 | chr3 | 47426290 | |||||||
chr3:47426771 | C | T | 123 | a0001c0001t0001g0093 a0001c0001t0001g0105 a0002c0002t0001g0049 others(120): Show |
123 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.737+386G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 6/22 | chr3 | 47426771 | |||||||
chr3:47426854 | G | A | 1 | a0001c0001t0007g0003 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.737+303C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 6/22 | chr3 | 47426854 | |||||||
chr3:47427877 | G | C | 1 | a0002c0002t0001g0122 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.411-210C>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 4/22 | chr3 | 47427877 | |||||||
chr3:47428029 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.411-362G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 4/22 | chr3 | 47428029 | |||||||
chr3:47428182 | G | A | 1 | a0001c0003t0001g0006 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.410+331C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 4/22 | chr3 | 47428182 | |||||||
chr3:47428239 | G | A | 2 | a0002c0002t0001g0073 a0009c0015t0001g0072 |
2 | NA18947.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.410+274C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 4/22 | chr3 | 47428239 | |||||||
chr3:47428345 | G | A | 1 | a0002c0002t0001g0166 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.410+168C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 4/22 | chr3 | 47428345 | |||||||
chr3:47428994 | G | A | 129 | a0001c0001t0001g0135 a0001c0001t0001g0172 a0001c0001t0001g0173 others(126): Show |
129 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.253-324C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47428994 | |||||||
chr3:47429079 | T | C | 288 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(285): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.253-409A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47429079 | |||||||
chr3:47429297 | T | A | 158 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(155): Show |
158 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.253-627A>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47429297 | |||||||
chr3:47429354 | G | C | 1 | a0001c0001t0001g0257 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.253-684C>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47429354 | |||||||
chr3:47429381 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.253-711G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47429381 | |||||||
chr3:47430232 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.253-1562G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47430232 | |||||||
chr3:47430288 | T | C | 2 | a0001c0008t0001g0022 a0001c0008t0001g0023 |
2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.253-1618A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47430288 | |||||||
chr3:47430368 | C | G | 1 | a0001c0001t0001g0133 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.253-1698G>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47430368 | |||||||
chr3:47430513 | C | A | 1 | a0001c0022t0001g0196 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.253-1843G>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47430513 | |||||||
chr3:47430710 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.253-2040G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47430710 | |||||||
chr3:47430743 | T | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0002c0002t0001g0056 |
3 | HG02109.hp2 NA18522.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.253-2073A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47430743 | |||||||
chr3:47431004 | C | T | 1 | a0002c0002t0001g0066 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.253-2334G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47431004 | |||||||
chr3:47431267 | T | TACTTAAT others(2661): Show |
2 | a0001c0008t0001g0022 a0001c0008t0001g0023 |
2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.253-2598_253-2597i others(2670): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47431267 | |||||||
chr3:47431267 | T | TACTTAAT others(2661): Show |
1 | a0002c0002t0001g0169 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.253-2598_253-2597i others(2670): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47431267 | |||||||
chr3:47431267 | T | TACTTAAT others(2661): Show |
1 | a0001c0009t0001g0266 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.253-2598_253-2597i others(2670): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47431267 | |||||||
chr3:47431267 | T | TACTTAAT others(2661): Show |
1 | a0001c0001t0001g0039 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.253-2598_253-2597i others(2670): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47431267 | |||||||
chr3:47431267 | T | TACTTAAT others(2661): Show |
150 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(147): Show |
150 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.253-2598_253-2597i others(2670): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47431267 | |||||||
chr3:47431267 | T | TACTTAAT others(2661): Show |
9 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0001g0176 others(6): Show |
9 | HG01070.hp2 HG01175.hp2 HG03017.hp1 others(6): Show |
intron_variant | MODIFIER | c.253-2598_253-2597i others(2670): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47431267 | |||||||
chr3:47431267 | T | TACTTAAT others(2661): Show |
1 | a0002c0002t0001g0225 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.253-2598_253-2597i others(2670): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47431267 | |||||||
chr3:47431267 | T | TACTTAAT others(2661): Show |
1 | a0001c0001t0001g0133 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.253-2598_253-2597i others(2670): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47431267 | |||||||
chr3:47431267 | T | TACTTAAT others(2661): Show |
1 | a0002c0002t0001g0151 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.253-2598_253-2597i others(2670): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47431267 | |||||||
chr3:47431267 | T | TACTTAAT others(2661): Show |
1 | a0002c0002t0001g0059 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.253-2598_253-2597i others(2670): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47431267 | |||||||
chr3:47431267 | T | TACTTAAT others(2661): Show |
2 | a0002c0002t0001g0073 a0009c0015t0001g0072 |
2 | NA18947.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.253-2598_253-2597i others(2670): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47431267 | |||||||
chr3:47431267 | T | TACTTAAT others(2661): Show |
1 | a0002c0002t0001g0144 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.253-2598_253-2597i others(2670): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47431267 | |||||||
chr3:47431267 | T | TACTTAAT others(2661): Show |
30 | a0002c0002t0001g0058 a0002c0002t0001g0060 a0002c0002t0001g0061 others(27): Show |
30 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.253-2598_253-2597i others(2670): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47431267 | |||||||
chr3:47431267 | T | TACTTAAT others(2661): Show |
1 | a0002c0002t0001g0153 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.253-2598_253-2597i others(2670): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47431267 | |||||||
chr3:47431267 | T | TACTTAAT others(2661): Show |
3 | a0002c0002t0001g0106 a0002c0002t0001g0107 a0002c0002t0001g0110 |
3 | NA18977.hp1 NA18999.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.253-2598_253-2597i others(2670): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47431267 | |||||||
chr3:47431267 | T | TACTTAAT others(2661): Show |
83 | a0001c0001t0001g0093 a0001c0001t0001g0105 a0002c0002t0001g0049 others(80): Show |
83 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.253-2598_253-2597i others(2670): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47431267 | |||||||
chr3:47431450 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.253-2780G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47431450 | |||||||
chr3:47431491 | G | A | 30 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(27): Show |
30 | HG01109.hp1 HG01934.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.253-2821C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47431491 | |||||||
chr3:47431678 | C | T | 130 | a0001c0001t0001g0135 a0001c0001t0001g0172 a0001c0001t0001g0173 others(127): Show |
130 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.253-3008G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47431678 | |||||||
chr3:47431756 | A | C | 5 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0031 others(2): Show |
5 | HG02055.hp1 HG02976.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.253-3086T>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47431756 | |||||||
chr3:47432272 | G | A | 1 | a0002c0002t0001g0087 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.252+2736C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47432272 | |||||||
chr3:47432314 | GA | G | 277 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(274): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.252+2693delT | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47432314 | |||||||
chr3:47432420 | T | C | 1 | a0002c0002t0001g0225 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.252+2588A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47432420 | |||||||
chr3:47432614 | A | G | 3 | a0002c0002t0004g0284 a0002c0002t0004g0285 a0002c0002t0004g0286 |
3 | HG01074.hp1 HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.252+2394T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47432614 | |||||||
chr3:47432634 | T | C | 16 | a0001c0001t0001g0214 a0001c0001t0001g0220 a0001c0001t0003g0215 others(13): Show |
16 | HG00408.hp2 HG01928.hp2 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.252+2374A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47432634 | |||||||
chr3:47432669 | A | T | 2 | a0001c0001t0001g0208 a0001c0001t0001g0238 |
2 | HG01070.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.252+2339T>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47432669 | |||||||
chr3:47432842 | C | G | 1 | a0001c0001t0001g0177 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.252+2166G>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47432842 | |||||||
chr3:47432890 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.252+2118T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47432890 | |||||||
chr3:47433101 | A | G | 1 | a0002c0002t0001g0057 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.252+1907T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47433101 | |||||||
chr3:47433259 | C | T | 288 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(285): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.252+1749G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47433259 | |||||||
chr3:47433499 | C | T | 1 | a0001c0001t0001g0040 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.252+1509G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47433499 | |||||||
chr3:47433782 | C | T | 1 | a0002c0002t0001g0065 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.252+1226G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47433782 | |||||||
chr3:47433953 | C | G | 1 | a0001c0001t0001g0275 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.252+1055G>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47433953 | |||||||
chr3:47434234 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.252+774G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47434234 | |||||||
chr3:47434705 | C | T | 30 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(27): Show |
30 | HG01109.hp1 HG01934.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.252+303G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47434705 | |||||||
chr3:47434740 | G | C | 1 | a0001c0009t0001g0266 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.252+268C>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 3/22 | chr3 | 47434740 | |||||||
chr3:47435195 | G | A | 1 | a0002c0002t0001g0141 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.123-58C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435195 | |||||||
chr3:47435308 | T | C | 1 | a0001c0001t0001g0255 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.123-171A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435308 | |||||||
chr3:47435428 | TTATAACA others(5): Show |
T | 1 | a0001c0001t0003g0217 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.123-303_123-292del others(12): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435428 | |||||||
chr3:47435464 | AAAC | A | 3 | a0002c0002t0001g0094 a0002c0002t0001g0142 a0002c0002t0001g0145 |
3 | HG00738.hp2 HG03942.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.123-330_123-328del others(3): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435464 | |||||||
chr3:47435465 | AACAT | A | 38 | a0001c0001t0001g0105 a0002c0002t0001g0050 a0002c0002t0001g0051 others(35): Show |
38 | HG00140.hp2 HG00558.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.123-332_123-329del others(4): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435465 | |||||||
chr3:47435465 | AACATAC | A | 21 | a0002c0002t0001g0049 a0002c0002t0001g0058 a0002c0002t0001g0059 others(18): Show |
21 | HG00408.hp1 HG01106.hp1 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.123-334_123-329del others(6): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435465 | |||||||
chr3:47435465 | AACATACA others(1): Show |
A | 26 | a0002c0002t0001g0061 a0002c0002t0001g0064 a0002c0002t0001g0073 others(23): Show |
26 | HG00544.hp2 HG00639.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.123-336_123-329del others(8): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435465 | |||||||
chr3:47435465 | AACATACA others(3): Show |
A | 13 | a0002c0002t0001g0052 a0002c0002t0001g0063 a0002c0002t0001g0065 others(10): Show |
13 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.123-338_123-329del others(10): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435465 | |||||||
chr3:47435465 | AACATACA others(5): Show |
A | 2 | a0002c0002t0001g0156 a0003c0004t0001g0139 |
2 | HG00741.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.123-340_123-329del others(12): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435465 | |||||||
chr3:47435465 | AACATACA others(9): Show |
A | 1 | a0010c0012t0001g0084 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.123-344_123-329del others(16): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435465 | |||||||
chr3:47435467 | CAT | C | 12 | a0001c0001t0001g0093 a0002c0002t0001g0053 a0002c0002t0001g0057 others(9): Show |
12 | HG01346.hp1 HG01884.hp1 HG02602.hp2 others(9): Show |
intron_variant | MODIFIER | c.123-332_123-331del others(2): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435467 | |||||||
chr3:47435469 | T | C | 9 | a0002c0002t0001g0086 a0002c0002t0001g0087 a0002c0002t0001g0094 others(6): Show |
9 | HG00738.hp2 HG01106.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.123-332A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435469 | |||||||
chr3:47435469 | T | TAC | 9 | a0001c0001t0001g0180 a0001c0001t0001g0202 a0001c0001t0001g0219 others(6): Show |
10 | HG01515.hp2 HG02080.hp2 HG02155.hp2 others(7): Show |
intron_variant | MODIFIER | c.123-334_123-333dup others(2): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435469 | |||||||
chr3:47435469 | T | TACAC | 5 | a0001c0001t0001g0029 a0001c0001t0001g0048 a0001c0001t0001g0201 others(2): Show |
5 | HG01109.hp1 HG01934.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.123-336_123-333dup others(4): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435469 | |||||||
chr3:47435469 | T | TACACAC | 19 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0030 others(16): Show |
19 | HG01928.hp2 HG01952.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.123-338_123-333dup others(6): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435469 | |||||||
chr3:47435469 | T | TACACACA others(1): Show |
7 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(4): Show |
7 | HG02004.hp1 HG02056.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-340_123-333dup others(8): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435469 | |||||||
chr3:47435469 | T | TACACACA others(3): Show |
9 | a0001c0001t0001g0037 a0001c0001t0001g0042 a0001c0001t0001g0046 others(6): Show |
9 | HG00408.hp2 HG02559.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.123-342_123-333dup others(10): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435469 | |||||||
chr3:47435469 | T | TACACACA others(5): Show |
5 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0044 others(2): Show |
5 | HG02572.hp2 HG02717.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.123-344_123-333dup others(12): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435469 | |||||||
chr3:47435469 | T | TACACACA others(7): Show |
4 | a0001c0001t0001g0021 a0001c0001t0001g0034 a0001c0001t0001g0035 others(1): Show |
4 | HG02109.hp2 HG03130.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.123-346_123-333dup others(14): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435469 | |||||||
chr3:47435469 | T | TACACACA others(9): Show |
1 | a0001c0001t0001g0019 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.123-348_123-333dup others(16): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435469 | |||||||
chr3:47435469 | TAC | T | 50 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(47): Show |
50 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.123-334_123-333del others(2): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435469 | |||||||
chr3:47435469 | TACAC | T | 8 | a0001c0001t0001g0198 a0001c0001t0001g0232 a0001c0001t0001g0238 others(5): Show |
8 | HG01123.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.123-336_123-333del others(4): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435469 | |||||||
chr3:47435469 | TACACAC | T | 31 | a0001c0001t0001g0020 a0001c0001t0001g0135 a0001c0001t0001g0174 others(28): Show |
31 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.123-338_123-333del others(6): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435469 | |||||||
chr3:47435469 | TACACACA others(3): Show |
T | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG02083.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.123-342_123-333del others(10): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435469 | |||||||
chr3:47435493 | C | T | 1 | a0002c0002t0001g0057 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.123-356G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435493 | |||||||
chr3:47435494 | A | T | 1 | a0002c0002t0001g0057 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.123-357T>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435494 | |||||||
chr3:47435529 | C | T | 123 | a0001c0001t0001g0093 a0001c0001t0001g0105 a0002c0002t0001g0049 others(120): Show |
123 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.123-392G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435529 | |||||||
chr3:47435774 | C | T | 1 | a0001c0001t0003g0259 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.123-637G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47435774 | |||||||
chr3:47436038 | C | T | 4 | a0002c0002t0001g0108 a0002c0002t0001g0111 a0002c0002t0001g0116 others(1): Show |
4 | HG03654.hp2 HG03710.hp2 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.123-901G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47436038 | |||||||
chr3:47436325 | C | T | 1 | a0001c0001t0001g0253 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.123-1188G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47436325 | |||||||
chr3:47436408 | G | A | 1 | a0002c0002t0001g0094 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.123-1271C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47436408 | |||||||
chr3:47436413 | A | G | 1 | a0002c0002t0001g0083 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.123-1276T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47436413 | |||||||
chr3:47436504 | T | G | 1 | a0001c0001t0001g0262 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.123-1367A>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47436504 | |||||||
chr3:47436969 | T | C | 2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.123-1832A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47436969 | |||||||
chr3:47437213 | G | A | 3 | a0002c0002t0001g0108 a0002c0002t0001g0111 a0002c0002t0001g0144 |
3 | HG02559.hp2 HG04228.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.123-2076C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47437213 | |||||||
chr3:47437340 | G | A | 65 | a0001c0001t0001g0093 a0001c0001t0001g0105 a0001c0001t0003g0259 others(62): Show |
65 | HG00140.hp2 HG00558.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.123-2203C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47437340 | |||||||
chr3:47437419 | T | C | 1 | a0002c0002t0001g0160 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.123-2282A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47437419 | |||||||
chr3:47437422 | C | CA | 233 | a0001c0001t0001g0034 a0001c0001t0001g0093 a0001c0001t0001g0105 others(230): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.123-2286dupT | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47437422 | |||||||
chr3:47437422 | C | CAA | 16 | a0001c0001t0001g0240 a0001c0001t0001g0255 a0002c0002t0001g0050 others(13): Show |
16 | HG00597.hp1 HG01952.hp2 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.123-2287_123-2286d others(4): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47437422 | |||||||
chr3:47437585 | A | C | 2 | a0002c0002t0001g0095 a0002c0002t0001g0096 |
2 | HG02280.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.123-2448T>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47437585 | |||||||
chr3:47437688 | G | A | 2 | a0001c0001t0001g0043 a0001c0019t0001g0045 |
2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.123-2551C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47437688 | |||||||
chr3:47437777 | T | C | 1 | a0001c0001t0007g0003 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.123-2640A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47437777 | |||||||
chr3:47437860 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.123-2723C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47437860 | |||||||
chr3:47437862 | G | C | 1 | a0001c0001t0001g0200 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.123-2725C>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47437862 | |||||||
chr3:47437945 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.123-2808C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47437945 | |||||||
chr3:47438024 | C | T | 1 | a0001c0022t0001g0196 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.123-2887G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47438024 | |||||||
chr3:47438041 | G | A | 1 | a0002c0002t0001g0166 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.123-2904C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47438041 | |||||||
chr3:47438245 | A | C | 130 | a0001c0001t0001g0135 a0001c0001t0001g0172 a0001c0001t0001g0173 others(127): Show |
130 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.123-3108T>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47438245 | |||||||
chr3:47438429 | A | AGAGAAT | 288 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(285): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.123-3293_123-3292i others(8): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47438429 | |||||||
chr3:47438485 | T | C | 1 | a0001c0010t0001g0179 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.123-3348A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47438485 | |||||||
chr3:47438500 | AACTTGCT others(3): Show |
A | 3 | a0002c0002t0001g0108 a0002c0002t0001g0111 a0002c0002t0001g0116 |
3 | HG03654.hp2 HG04228.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.123-3373_123-3364d others(12): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47438500 | |||||||
chr3:47438580 | G | A | 1 | a0001c0001t0001g0213 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.123-3443C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47438580 | |||||||
chr3:47438867 | A | G | 24 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0207 others(21): Show |
24 | HG00408.hp2 HG01515.hp2 HG01928.hp2 others(21): Show |
intron_variant | MODIFIER | c.123-3730T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47438867 | |||||||
chr3:47439034 | G | C | 130 | a0001c0001t0001g0135 a0001c0001t0001g0172 a0001c0001t0001g0173 others(127): Show |
130 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.122+3838C>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47439034 | |||||||
chr3:47439036 | T | C | 288 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(285): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.122+3836A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47439036 | |||||||
chr3:47439148 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.122+3724G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47439148 | |||||||
chr3:47439170 | A | G | 1 | a0001c0001t0003g0258 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.122+3702T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47439170 | |||||||
chr3:47439171 | G | A | 1 | a0001c0001t0003g0258 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.122+3701C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47439171 | |||||||
chr3:47439621 | C | T | 2 | a0001c0001t0001g0234 a0001c0001t0001g0256 |
2 | HG03017.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.122+3251G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47439621 | |||||||
chr3:47440039 | T | C | 2 | a0001c0001t0001g0193 a0001c0001t0001g0268 |
2 | HG01884.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.122+2833A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47440039 | |||||||
chr3:47440436 | A | G | 1 | a0001c0001t0003g0258 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.122+2436T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47440436 | |||||||
chr3:47440437 | G | A | 1 | a0001c0001t0003g0258 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.122+2435C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47440437 | |||||||
chr3:47440448 | T | C | 1 | a0001c0001t0007g0003 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.122+2424A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47440448 | |||||||
chr3:47440609 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.122+2263T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47440609 | |||||||
chr3:47440658 | C | T | 1 | a0001c0001t0003g0258 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.122+2214G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47440658 | |||||||
chr3:47440732 | C | T | 85 | a0001c0001t0001g0093 a0001c0001t0001g0105 a0002c0002t0001g0049 others(82): Show |
85 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.122+2140G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47440732 | |||||||
chr3:47440774 | C | T | 1 | a0002c0002t0001g0063 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.122+2098G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47440774 | |||||||
chr3:47440879 | T | G | 1 | a0001c0001t0001g0198 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.122+1993A>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47440879 | |||||||
chr3:47440964 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.122+1908G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47440964 | |||||||
chr3:47441125 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.122+1747G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47441125 | |||||||
chr3:47441337 | G | A | 1 | a0001c0001t0002g0287 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.122+1535C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47441337 | |||||||
chr3:47441516 | G | A | 1 | a0002c0002t0001g0064 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.122+1356C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47441516 | |||||||
chr3:47441526 | C | T | 1 | a0002c0002t0001g0060 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.122+1346G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47441526 | |||||||
chr3:47441874 | C | CT | 150 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(147): Show |
150 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.122+997dupA | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47441874 | |||||||
chr3:47441874 | C | CTT | 16 | a0001c0001t0001g0040 a0001c0001t0001g0135 a0001c0001t0001g0174 others(13): Show |
16 | HG01175.hp2 HG01934.hp1 HG01981.hp2 others(13): Show |
intron_variant | MODIFIER | c.122+996_122+997dup others(2): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47441874 | |||||||
chr3:47442236 | A | C | 1 | a0001c0022t0001g0196 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.122+636T>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47442236 | |||||||
chr3:47442501 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.122+371G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47442501 | |||||||
chr3:47442525 | C | A | 1 | a0001c0001t0001g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.122+347G>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47442525 | |||||||
chr3:47442535 | G | C | 1 | a0002c0002t0001g0098 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.122+337C>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47442535 | |||||||
chr3:47442636 | G | C | 288 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(285): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.122+236C>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47442636 | |||||||
chr3:47442765 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.122+107A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47442765 | |||||||
chr3:47442840 | C | T | 1 | a0001c0001t0007g0003 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.122+32G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 2/22 | chr3 | 47442840 | |||||||
chr3:47443149 | C | A | 1 | a0001c0008t0001g0022 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-98-58G>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443149 | |||||||
chr3:47443233 | TAC | T | 14 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0035 others(11): Show |
14 | HG01975.hp1 HG02109.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-98-144_-98-143del others(2): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443233 | |||||||
chr3:47443233 | TACAC | T | 42 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(39): Show |
42 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(39): Show |
intron_variant | MODIFIER | c.-98-146_-98-143del others(4): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443233 | |||||||
chr3:47443233 | TACACAC | T | 110 | a0001c0001t0001g0093 a0001c0001t0001g0135 a0001c0001t0001g0172 others(107): Show |
110 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.-98-148_-98-143del others(6): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443233 | |||||||
chr3:47443233 | TACACACA others(1): Show |
T | 69 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0003t0001g0006 others(66): Show |
69 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.-98-150_-98-143del others(8): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443233 | |||||||
chr3:47443233 | TACACACA others(3): Show |
T | 8 | a0001c0001t0001g0004 a0001c0001t0001g0214 a0001c0001t0006g0002 others(5): Show |
8 | HG02027.hp1 HG02572.hp2 NA18966.hp2 others(5): Show |
intron_variant | MODIFIER | c.-98-152_-98-143del others(10): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443233 | |||||||
chr3:47443233 | TACACACA others(5): Show |
T | 14 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0028 others(11): Show |
14 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.-98-154_-98-143del others(12): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443233 | |||||||
chr3:47443233 | TACACACA others(7): Show |
T | 2 | a0002c0002t0001g0092 a0002c0002t0001g0152 |
2 | HG02132.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.-98-156_-98-143del others(14): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443233 | |||||||
chr3:47443264 | ACACACAC others(9): Show |
A | 1 | a0001c0001t0001g0039 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-98-189_-98-174del others(16): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443264 | |||||||
chr3:47443266 | ACACACAC others(7): Show |
A | 1 | a0002c0002t0001g0098 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-98-189_-98-176del others(14): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443266 | |||||||
chr3:47443268 | A | T | 2 | a0001c0001t0001g0200 a0001c0001t0001g0264 |
2 | HG01975.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.-98-177T>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443268 | |||||||
chr3:47443268 | ACACACAC others(3): Show |
A | 1 | a0002c0002t0001g0163 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-98-187_-98-178del others(10): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443268 | |||||||
chr3:47443270 | A | T | 9 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0220 others(6): Show |
9 | HG00642.hp1 HG01975.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-98-179T>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443270 | |||||||
chr3:47443272 | A | T | 19 | a0001c0001t0001g0178 a0001c0001t0001g0199 a0001c0001t0001g0200 others(16): Show |
19 | HG00642.hp1 HG01168.hp1 HG01515.hp1 others(16): Show |
intron_variant | MODIFIER | c.-98-181T>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443272 | |||||||
chr3:47443272 | ACACACT | A | 6 | a0001c0003t0001g0005 a0002c0002t0001g0109 a0002c0002t0001g0117 others(3): Show |
6 | HG00735.hp1 HG01192.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.-98-187_-98-182del others(6): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443272 | |||||||
chr3:47443274 | A | T | 140 | a0001c0001t0001g0093 a0001c0001t0001g0133 a0001c0001t0001g0135 others(137): Show |
140 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.-98-183T>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443274 | |||||||
chr3:47443276 | A | T | 199 | a0001c0001t0001g0021 a0001c0001t0001g0048 a0001c0001t0001g0093 others(196): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.-98-185T>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443276 | |||||||
chr3:47443278 | T | A | 2 | a0001c0001t0001g0027 a0001c0008t0001g0023 |
2 | HG02486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-98-187A>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443278 | |||||||
chr3:47443306 | T | C | 271 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(268): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.-98-215A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443306 | |||||||
chr3:47443306 | T | TCC | 3 | a0001c0001t0001g0178 a0001c0001t0001g0255 a0001c0001t0001g0264 |
3 | HG01168.hp1 NA18977.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-98-216_-98-215ins others(2): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443306 | |||||||
chr3:47443306 | T | TCTCTCCC others(5): Show |
5 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0229 others(2): Show |
5 | HG01515.hp2 HG02056.hp1 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.-98-216_-98-215ins others(12): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443306 | |||||||
chr3:47443306 | T | TCTCTCTC others(7): Show |
3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0207 |
3 | HG02155.hp2 NA18966.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-98-216_-98-215ins others(14): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443306 | |||||||
chr3:47443306 | T | TCTCTCTC others(6): Show |
1 | a0001c0001t0001g0199 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-98-216_-98-215ins others(13): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443306 | |||||||
chr3:47443307 | C | T | 155 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(152): Show |
155 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.-98-216G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443307 | |||||||
chr3:47443462 | C | A | 1 | a0001c0001t0001g0199 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-98-371G>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443462 | |||||||
chr3:47443463 | C | A | 1 | a0001c0001t0001g0274 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-98-372G>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443463 | |||||||
chr3:47443463 | C | G | 123 | a0001c0001t0001g0093 a0001c0001t0001g0105 a0002c0002t0001g0049 others(120): Show |
123 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.-98-372G>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443463 | |||||||
chr3:47443539 | C | T | 77 | a0001c0001t0001g0135 a0001c0001t0001g0172 a0001c0001t0001g0173 others(74): Show |
77 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.-98-448G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47443539 | |||||||
chr3:47444156 | G | T | 1 | a0001c0001t0001g0093 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-98-1065C>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47444156 | |||||||
chr3:47444157 | A | C | 1 | a0001c0001t0001g0093 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-98-1066T>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47444157 | |||||||
chr3:47444857 | T | C | 288 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(285): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.-98-1766A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47444857 | |||||||
chr3:47445069 | G | A | 2 | a0001c0008t0001g0022 a0001c0008t0001g0023 |
2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-98-1978C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47445069 | |||||||
chr3:47445077 | A | G | 1 | a0001c0005t0001g0194 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-98-1986T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47445077 | |||||||
chr3:47445142 | T | C | 130 | a0001c0001t0001g0135 a0001c0001t0001g0172 a0001c0001t0001g0173 others(127): Show |
130 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.-98-2051A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47445142 | |||||||
chr3:47445243 | C | CT | 6 | a0001c0018t0002g0300 a0002c0002t0001g0066 a0002c0002t0001g0096 others(3): Show |
6 | HG00741.hp1 HG02055.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.-98-2153dupA | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47445243 | |||||||
chr3:47445243 | CT | C | 18 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(15): Show |
18 | HG01943.hp2 HG01952.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-98-2153delA | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47445243 | |||||||
chr3:47445292 | G | A | 2 | a0001c0001t0001g0043 a0001c0019t0001g0045 |
2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-98-2201C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47445292 | |||||||
chr3:47445328 | C | A | 1 | a0001c0001t0001g0133 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-98-2237G>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47445328 | |||||||
chr3:47445405 | C | G | 2 | a0001c0001t0001g0043 a0001c0019t0001g0045 |
2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-98-2314G>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47445405 | |||||||
chr3:47445492 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-98-2401C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47445492 | |||||||
chr3:47445657 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-98-2566G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47445657 | |||||||
chr3:47445874 | A | AT | 18 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0026 others(15): Show |
18 | HG00099.hp2 HG00741.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.-98-2784dupA | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47445874 | |||||||
chr3:47445876 | T | A | 1 | a0002c0002t0001g0099 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-98-2785A>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47445876 | |||||||
chr3:47445895 | G | A | 1 | a0002c0002t0001g0099 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-98-2804C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47445895 | |||||||
chr3:47445897 | G | A | 1 | a0002c0002t0001g0099 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-98-2806C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47445897 | |||||||
chr3:47445931 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-98-2840C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47445931 | |||||||
chr3:47446120 | C | T | 1 | a0001c0001t0006g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-98-3029G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47446120 | |||||||
chr3:47446583 | G | A | 1 | a0001c0008t0001g0022 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-98-3492C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47446583 | |||||||
chr3:47446765 | G | A | 1 | a0002c0002t0001g0075 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-98-3674C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47446765 | |||||||
chr3:47446806 | G | T | 1 | a0002c0002t0001g0122 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-98-3715C>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47446806 | |||||||
chr3:47447298 | C | T | 4 | a0003c0004t0001g0071 a0003c0004t0001g0139 a0004c0006t0001g0070 others(1): Show |
4 | HG00408.hp1 HG00544.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.-98-4207G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47447298 | |||||||
chr3:47447387 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-98-4296G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47447387 | |||||||
chr3:47447418 | G | A | 1 | a0002c0002t0001g0078 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-98-4327C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47447418 | |||||||
chr3:47447801 | G | A | 2 | a0001c0001t0001g0204 a0001c0001t0001g0233 |
2 | NA18967.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.-98-4710C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47447801 | |||||||
chr3:47448002 | C | CA | 18 | a0001c0001t0001g0040 a0001c0001t0001g0172 a0001c0001t0001g0173 others(15): Show |
19 | HG00597.hp2 HG01261.hp2 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.-98-4912dupT | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47448002 | |||||||
chr3:47448002 | CA | C | 90 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(87): Show |
90 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.-98-4912delT | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47448002 | |||||||
chr3:47448002 | CAA | C | 52 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0028 others(49): Show |
52 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.-98-4913_-98-4912d others(4): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47448002 | |||||||
chr3:47448002 | CAAA | C | 87 | a0001c0001t0001g0043 a0001c0001t0001g0093 a0001c0001t0001g0105 others(84): Show |
87 | HG00140.hp2 HG00621.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.-98-4914_-98-4912d others(5): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47448002 | |||||||
chr3:47448312 | G | C | 1 | a0001c0001t0001g0133 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-98-5221C>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47448312 | |||||||
chr3:47448330 | C | T | 123 | a0001c0001t0001g0093 a0001c0001t0001g0105 a0002c0002t0001g0049 others(120): Show |
123 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.-98-5239G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47448330 | |||||||
chr3:47448395 | G | C | 129 | a0001c0001t0001g0135 a0001c0001t0001g0172 a0001c0001t0001g0173 others(126): Show |
129 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.-98-5304C>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47448395 | |||||||
chr3:47448724 | GTTCAT | G | 130 | a0001c0001t0001g0135 a0001c0001t0001g0172 a0001c0001t0001g0173 others(127): Show |
130 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.-98-5638_-98-5634d others(7): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47448724 | |||||||
chr3:47448833 | G | A | 1 | a0002c0002t0001g0073 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-98-5742C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47448833 | |||||||
chr3:47448931 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-98-5840T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47448931 | |||||||
chr3:47449003 | G | A | 123 | a0001c0001t0001g0093 a0001c0001t0001g0105 a0002c0002t0001g0049 others(120): Show |
123 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.-98-5912C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47449003 | |||||||
chr3:47449177 | TGCTGTTT others(2766): Show |
T | 130 | a0001c0001t0001g0135 a0001c0001t0001g0172 a0001c0001t0001g0173 others(127): Show |
130 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.-98-8859_-98-6087d others(2): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47449177 | |||||||
chr3:47449199 | G | A | 1 | a0001c0008t0001g0022 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-98-6108C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47449199 | |||||||
chr3:47449222 | C | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0021 |
2 | HG02109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-98-6131G>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47449222 | |||||||
chr3:47449535 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-98-6444C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47449535 | |||||||
chr3:47449697 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-98-6606G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47449697 | |||||||
chr3:47449811 | T | A | 2 | a0002c0002t0001g0095 a0002c0002t0001g0096 |
2 | HG02280.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-98-6720A>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47449811 | |||||||
chr3:47450083 | C | T | 1 | a0001c0003t0001g0010 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-98-6992G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47450083 | |||||||
chr3:47450143 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-98-7052C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47450143 | |||||||
chr3:47450457 | G | C | 1 | a0002c0002t0001g0099 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-98-7366C>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47450457 | |||||||
chr3:47450511 | G | GT | 45 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(42): Show |
45 | HG01175.hp1 HG01934.hp1 HG01981.hp1 others(42): Show |
intron_variant | MODIFIER | c.-98-7421dupA | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47450511 | |||||||
chr3:47450647 | G | A | 1 | a0001c0003t0001g0010 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-98-7556C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47450647 | |||||||
chr3:47450772 | G | C | 1 | a0002c0002t0001g0073 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-98-7681C>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47450772 | |||||||
chr3:47450863 | T | G | 1 | a0001c0001t0001g0027 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-98-7772A>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47450863 | |||||||
chr3:47451143 | G | A | 2 | a0002c0002t0001g0073 a0009c0015t0001g0072 |
2 | NA18947.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.-98-8052C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47451143 | |||||||
chr3:47451201 | C | T | 158 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(155): Show |
158 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.-98-8110G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47451201 | |||||||
chr3:47451394 | CT | C | 143 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(140): Show |
143 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.-98-8304delA | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47451394 | |||||||
chr3:47452052 | C | T | 2 | a0001c0001t0001g0185 a0001c0001t0001g0186 |
2 | HG00544.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.-98-8961G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47452052 | |||||||
chr3:47452667 | T | C | 77 | a0001c0001t0001g0135 a0001c0001t0001g0172 a0001c0001t0001g0173 others(74): Show |
77 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.-98-9576A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47452667 | |||||||
chr3:47452813 | G | A | 130 | a0001c0001t0001g0135 a0001c0001t0001g0172 a0001c0001t0001g0173 others(127): Show |
130 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.-98-9722C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47452813 | |||||||
chr3:47452861 | G | A | 1 | a0002c0002t0001g0112 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-98-9770C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47452861 | |||||||
chr3:47452890 | G | C | 157 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(154): Show |
157 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.-98-9799C>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47452890 | |||||||
chr3:47452926 | CA | C | 286 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(283): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.-98-9836delT | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47452926 | |||||||
chr3:47453252 | C | T | 2 | a0001c0001t0002g0291 a0001c0001t0002g0292 |
2 | HG00140.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-98-10161G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47453252 | |||||||
chr3:47453379 | T | TA | 13 | a0002c0002t0001g0050 a0002c0002t0001g0052 a0002c0002t0001g0063 others(10): Show |
13 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.-98-10289dupT | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47453379 | |||||||
chr3:47453397 | G | GA | 287 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(284): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.-98-10307dupT | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47453397 | |||||||
chr3:47454065 | C | G | 2 | a0001c0001t0001g0043 a0001c0019t0001g0045 |
2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-98-10974G>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47454065 | |||||||
chr3:47454163 | T | C | 1 | a0003c0004t0001g0139 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-98-11072A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47454163 | |||||||
chr3:47454194 | T | C | 4 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0001g0176 others(1): Show |
4 | HG00597.hp2 HG04199.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.-98-11103A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47454194 | |||||||
chr3:47454205 | A | C | 1 | a0002c0002t0001g0066 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-98-11114T>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47454205 | |||||||
chr3:47454361 | C | G | 1 | a0001c0003t0001g0011 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-98-11270G>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47454361 | |||||||
chr3:47454688 | C | T | 3 | a0002c0002t0001g0061 a0002c0002t0001g0092 a0002c0002t0001g0152 |
3 | HG02132.hp2 NA18951.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.-98-11597G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47454688 | |||||||
chr3:47454748 | A | T | 6 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0034 others(3): Show |
6 | HG02280.hp1 HG03130.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-98-11657T>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47454748 | |||||||
chr3:47454792 | C | T | 2 | a0001c0001t0001g0043 a0001c0019t0001g0045 |
2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-98-11701G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47454792 | |||||||
chr3:47454880 | T | A | 1 | a0002c0002t0001g0113 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-98-11789A>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47454880 | |||||||
chr3:47454974 | G | A | 62 | a0001c0001t0001g0135 a0001c0001t0001g0172 a0001c0001t0001g0173 others(59): Show |
62 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-98-11883C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47454974 | |||||||
chr3:47455062 | C | CAT | 14 | a0001c0003t0001g0005 a0002c0002t0001g0060 a0002c0002t0001g0063 others(11): Show |
14 | HG00099.hp2 HG00621.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.-98-11973_-98-1197 others(6): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47455062 | |||||||
chr3:47455062 | C | CATAT | 5 | a0002c0002t0001g0080 a0002c0002t0001g0142 a0002c0002t0001g0144 others(2): Show |
5 | HG00597.hp1 HG02559.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.-98-11975_-98-1197 others(8): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47455062 | |||||||
chr3:47455062 | CAT | C | 30 | a0001c0001t0007g0003 a0001c0003t0001g0010 a0001c0003t0001g0013 others(27): Show |
30 | HG00408.hp1 HG00544.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.-98-11973_-98-1197 others(6): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47455062 | |||||||
chr3:47455062 | CATAT | C | 28 | a0001c0001t0001g0043 a0001c0001t0001g0093 a0001c0008t0001g0022 others(25): Show |
28 | HG00609.hp1 HG00639.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.-98-11975_-98-1197 others(8): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47455062 | |||||||
chr3:47455062 | CATATAT | C | 50 | a0001c0001t0001g0105 a0001c0001t0001g0180 a0001c0001t0001g0181 others(47): Show |
50 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.-98-11977_-98-1197 others(10): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47455062 | |||||||
chr3:47455062 | CATATATA others(1): Show |
C | 33 | a0001c0001t0001g0018 a0001c0001t0001g0178 a0001c0001t0001g0183 others(30): Show |
33 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.-98-11979_-98-1197 others(12): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47455062 | |||||||
chr3:47455062 | CATATATA others(3): Show |
C | 33 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(30): Show |
33 | HG00408.hp2 HG00673.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.-98-11981_-98-1197 others(14): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47455062 | |||||||
chr3:47455062 | CATATATA others(5): Show |
C | 85 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(82): Show |
85 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.-98-11983_-98-1197 others(16): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47455062 | |||||||
chr3:47455062 | CATATATA others(7): Show |
C | 2 | a0001c0001t0001g0168 a0001c0001t0001g0282 |
2 | HG02922.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-98-11985_-98-1197 others(18): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47455062 | |||||||
chr3:47455062 | CATATATA others(15): Show |
C | 1 | a0002c0002t0001g0052 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-98-11993_-98-1197 others(26): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47455062 | |||||||
chr3:47455084 | TATATATA others(4): Show |
T | 1 | a0001c0001t0001g0202 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-98-12004_-98-1199 others(15): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47455084 | |||||||
chr3:47455094 | T | A | 29 | a0001c0001t0001g0193 a0001c0001t0001g0197 a0001c0001t0001g0198 others(26): Show |
29 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.-98-12003A>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47455094 | |||||||
chr3:47455146 | A | G | 1 | a0002c0002t0001g0063 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-98-12055T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47455146 | |||||||
chr3:47455332 | C | T | 1 | a0002c0002t0001g0064 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-98-12241G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47455332 | |||||||
chr3:47455364 | A | G | 296 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(293): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.-98-12273T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47455364 | |||||||
chr3:47455517 | C | T | 21 | a0002c0002t0001g0049 a0002c0002t0001g0050 a0002c0002t0001g0052 others(18): Show |
21 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.-98-12426G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47455517 | |||||||
chr3:47455594 | C | CA | 25 | a0001c0001t0001g0043 a0001c0001t0001g0133 a0001c0001t0001g0174 others(22): Show |
25 | HG01106.hp2 HG01175.hp2 HG01934.hp1 others(22): Show |
intron_variant | MODIFIER | c.-98-12504dupT | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47455594 | |||||||
chr3:47455594 | CA | C | 13 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0034 others(10): Show |
13 | HG01069.hp1 HG02280.hp1 HG03017.hp1 others(10): Show |
intron_variant | MODIFIER | c.-98-12504delT | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47455594 | |||||||
chr3:47455759 | C | T | 1 | a0002c0002t0001g0134 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-98-12668G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47455759 | |||||||
chr3:47456041 | G | A | 2 | a0001c0001t0001g0213 a0001c0001t0001g0239 |
2 | HG02135.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.-98-12950C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47456041 | |||||||
chr3:47456362 | T | G | 1 | a0001c0001t0003g0272 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-98-13271A>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47456362 | |||||||
chr3:47456851 | A | G | 2 | a0002c0002t0001g0123 a0002c0002t0001g0124 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-98-13760T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47456851 | |||||||
chr3:47456857 | G | A | 2 | a0001c0001t0002g0303 a0001c0019t0001g0045 |
2 | HG01192.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-98-13766C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47456857 | |||||||
chr3:47457130 | T | C | 1 | a0002c0002t0001g0117 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-98-14039A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47457130 | |||||||
chr3:47457508 | T | C | 1 | a0004c0006t0001g0074 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-98-14417A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47457508 | |||||||
chr3:47457635 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-98-14544G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47457635 | |||||||
chr3:47457636 | G | A | 1 | a0001c0003t0001g0016 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-98-14545C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47457636 | |||||||
chr3:47457918 | A | G | 1 | a0002c0002t0001g0163 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-98-14827T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47457918 | |||||||
chr3:47458082 | G | A | 1 | a0002c0002t0001g0145 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-98-14991C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47458082 | |||||||
chr3:47458116 | C | T | 1 | a0001c0022t0001g0196 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-98-15025G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47458116 | |||||||
chr3:47458140 | T | C | 1 | a0001c0001t0001g0257 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-98-15049A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47458140 | |||||||
chr3:47458498 | T | G | 1 | a0001c0022t0001g0196 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-98-15407A>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47458498 | |||||||
chr3:47458647 | C | T | 1 | a0002c0002t0001g0145 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-98-15556G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47458647 | |||||||
chr3:47458811 | A | G | 1 | a0001c0001t0007g0003 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-98-15720T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47458811 | |||||||
chr3:47458962 | T | C | 30 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(27): Show |
30 | HG01109.hp1 HG01934.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.-98-15871A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47458962 | |||||||
chr3:47459080 | C | T | 1 | a0005c0007t0001g0118 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-98-15989G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47459080 | |||||||
chr3:47459172 | G | A | 121 | a0001c0001t0001g0093 a0001c0001t0001g0105 a0002c0002t0001g0049 others(118): Show |
121 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.-98-16081C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47459172 | |||||||
chr3:47459442 | T | G | 1 | a0005c0007t0001g0118 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-98-16351A>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47459442 | |||||||
chr3:47459759 | C | A | 1 | a0001c0001t0001g0168 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-99+16040G>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47459759 | |||||||
chr3:47459760 | G | A | 1 | a0002c0002t0001g0119 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-99+16039C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47459760 | |||||||
chr3:47459763 | T | C | 28 | a0001c0001t0001g0193 a0001c0001t0001g0197 a0001c0001t0001g0198 others(25): Show |
28 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.-99+16036A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47459763 | |||||||
chr3:47459947 | T | C | 2 | a0002c0002t0001g0123 a0002c0002t0001g0124 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-99+15852A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47459947 | |||||||
chr3:47460268 | A | G | 4 | a0001c0001t0001g0192 a0001c0001t0001g0250 a0001c0001t0001g0253 others(1): Show |
4 | HG02027.hp2 NA18947.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.-99+15531T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47460268 | |||||||
chr3:47460363 | G | A | 1 | a0001c0001t0003g0245 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-99+15436C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47460363 | |||||||
chr3:47460363 | G | T | 6 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0034 others(3): Show |
6 | HG02280.hp1 HG03130.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-99+15436C>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47460363 | |||||||
chr3:47460443 | A | G | 1 | a0002c0002t0001g0066 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-99+15356T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47460443 | |||||||
chr3:47460524 | A | G | 1 | a0001c0001t0001g0267 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-99+15275T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47460524 | |||||||
chr3:47460547 | G | T | 1 | a0002c0002t0001g0079 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-99+15252C>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47460547 | |||||||
chr3:47460576 | A | G | 288 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(285): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.-99+15223T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47460576 | |||||||
chr3:47460660 | C | T | 6 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0034 others(3): Show |
6 | HG02280.hp1 HG03130.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-99+15139G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47460660 | |||||||
chr3:47460910 | G | A | 1 | a0001c0001t0007g0003 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-99+14889C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47460910 | |||||||
chr3:47461693 | T | C | 1 | a0002c0002t0001g0120 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-99+14106A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47461693 | |||||||
chr3:47461859 | C | T | 132 | a0001c0001t0001g0135 a0001c0001t0001g0172 a0001c0001t0001g0173 others(129): Show |
132 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.-99+13940G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47461859 | |||||||
chr3:47461872 | A | T | 2 | a0002c0002t0001g0148 a0002c0002t0001g0149 |
2 | NA19004.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-99+13927T>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47461872 | |||||||
chr3:47461912 | T | C | 1 | a0001c0001t0001g0250 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-99+13887A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47461912 | |||||||
chr3:47462343 | A | G | 288 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(285): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.-99+13456T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47462343 | |||||||
chr3:47462610 | G | A | 15 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(12): Show |
15 | HG01109.hp1 HG02055.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.-99+13189C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47462610 | |||||||
chr3:47462704 | G | C | 1 | a0001c0001t0007g0003 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-99+13095C>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47462704 | |||||||
chr3:47462705 | A | G | 1 | a0001c0001t0002g0290 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-99+13094T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47462705 | |||||||
chr3:47462709 | C | T | 1 | a0002c0002t0001g0078 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-99+13090G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47462709 | |||||||
chr3:47462753 | C | CA | 8 | a0001c0001t0001g0027 a0001c0001t0001g0044 a0002c0002t0001g0121 others(5): Show |
8 | HG00621.hp1 HG01256.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-99+13045dupT | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47462753 | |||||||
chr3:47462753 | CA | C | 127 | a0001c0001t0001g0018 a0001c0001t0001g0043 a0001c0001t0001g0172 others(124): Show |
127 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.-99+13045delT | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47462753 | |||||||
chr3:47462767 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-99+13032T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47462767 | |||||||
chr3:47462771 | A | G | 54 | a0001c0001t0001g0188 a0001c0001t0001g0193 a0001c0001t0001g0197 others(51): Show |
54 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.-99+13028T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47462771 | |||||||
chr3:47463359 | G | A | 10 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0028 others(7): Show |
10 | HG01109.hp1 HG02055.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-99+12440C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47463359 | |||||||
chr3:47463430 | G | A | 2 | a0001c0022t0001g0196 a0002c0002t0001g0125 |
2 | HG02083.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-99+12369C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47463430 | |||||||
chr3:47463514 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-99+12285G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47463514 | |||||||
chr3:47464031 | T | C | 1 | a0001c0001t0001g0220 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-99+11768A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47464031 | |||||||
chr3:47464134 | G | C | 1 | a0001c0001t0001g0201 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-99+11665C>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47464134 | |||||||
chr3:47464204 | C | T | 8 | a0002c0002t0001g0051 a0002c0002t0001g0145 a0002c0002t0001g0146 others(5): Show |
8 | HG00738.hp2 HG01074.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-99+11595G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47464204 | |||||||
chr3:47464235 | T | C | 288 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(285): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.-99+11564A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47464235 | |||||||
chr3:47464332 | G | A | 1 | a0001c0001t0001g0228 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-99+11467C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47464332 | |||||||
chr3:47464481 | C | T | 3 | a0001c0005t0001g0187 a0001c0005t0001g0194 a0001c0005t0001g0195 |
3 | HG02258.hp1 HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-99+11318G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47464481 | |||||||
chr3:47464489 | T | C | 2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-99+11310A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47464489 | |||||||
chr3:47464740 | G | A | 3 | a0002c0002t0001g0126 a0002c0002t0001g0127 a0002c0002t0001g0161 |
3 | HG01175.hp1 HG01934.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.-99+11059C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47464740 | |||||||
chr3:47464837 | C | T | 1 | a0002c0002t0001g0062 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-99+10962G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47464837 | |||||||
chr3:47464921 | T | C | 5 | a0001c0001t0002g0288 a0001c0001t0002g0301 a0001c0001t0002g0302 others(2): Show |
5 | HG01192.hp2 HG02055.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.-99+10878A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47464921 | |||||||
chr3:47464951 | T | C | 1 | a0001c0003t0001g0017 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-99+10848A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47464951 | |||||||
chr3:47465168 | C | CT | 23 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(20): Show |
23 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.-99+10630dupA | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47465168 | |||||||
chr3:47465785 | T | C | 1 | a0001c0001t0001g0040 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-99+10014A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47465785 | |||||||
chr3:47465841 | C | CA | 116 | a0001c0001t0001g0093 a0001c0001t0001g0105 a0001c0001t0001g0174 others(113): Show |
116 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.-99+9957dupT | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47465841 | |||||||
chr3:47465841 | CA | C | 100 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0175 others(97): Show |
100 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.-99+9957delT | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47465841 | |||||||
chr3:47465844 | A | AC | 3 | a0002c0002t0001g0066 a0002c0002t0001g0067 a0002c0002t0001g0068 |
3 | HG01106.hp1 HG02738.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.-99+9954_-99+9955i others(3): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47465844 | |||||||
chr3:47465845 | A | C | 1 | a0001c0001t0007g0003 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-99+9954T>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47465845 | |||||||
chr3:47466129 | T | TA | 8 | a0001c0001t0001g0168 a0001c0001t0007g0003 a0002c0002t0001g0060 others(5): Show |
8 | HG00558.hp1 HG01069.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.-99+9669dupT | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47466129 | |||||||
chr3:47466135 | C | A | 292 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(289): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.-99+9664G>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47466135 | |||||||
chr3:47466136 | C | A | 11 | a0001c0001t0001g0168 a0001c0001t0007g0003 a0002c0002t0001g0060 others(8): Show |
11 | HG00558.hp1 HG01069.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.-99+9663G>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47466136 | |||||||
chr3:47466136 | CA | C | 7 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0032 others(4): Show |
7 | HG01168.hp1 HG01258.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.-99+9662delT | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47466136 | |||||||
chr3:47466138 | A | C | 1 | a0001c0001t0001g0133 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-99+9661T>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47466138 | |||||||
chr3:47466150 | A | G | 2 | a0001c0001t0001g0207 a0001c0001t0002g0296 |
2 | HG00735.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.-99+9649T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47466150 | |||||||
chr3:47466154 | A | AG | 35 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0001g0204 others(32): Show |
35 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.-99+9644_-99+9645i others(3): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47466154 | |||||||
chr3:47466154 | A | G | 98 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0175 others(95): Show |
98 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.-99+9645T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47466154 | |||||||
chr3:47466345 | C | T | 1 | a0001c0001t0002g0289 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-99+9454G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47466345 | |||||||
chr3:47466589 | T | C | 1 | a0002c0002t0001g0163 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-99+9210A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47466589 | |||||||
chr3:47466858 | C | A | 1 | a0001c0001t0001g0133 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-99+8941G>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47466858 | |||||||
chr3:47466886 | C | A | 8 | a0001c0001t0001g0177 a0001c0001t0001g0180 a0001c0001t0001g0181 others(5): Show |
8 | HG00544.hp1 HG00673.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.-99+8913G>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47466886 | |||||||
chr3:47466963 | T | A | 1 | a0002c0002t0001g0057 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-99+8836A>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47466963 | |||||||
chr3:47466979 | G | C | 1 | a0002c0002t0001g0134 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-99+8820C>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47466979 | |||||||
chr3:47467099 | GA | G | 8 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0034 others(5): Show |
8 | HG02280.hp1 HG02922.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.-99+8699delT | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47467099 | |||||||
chr3:47467327 | C | T | 1 | a0001c0003t0001g0005 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-99+8472G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47467327 | |||||||
chr3:47467434 | A | G | 1 | a0002c0002t0001g0062 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-99+8365T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47467434 | |||||||
chr3:47467605 | G | A | 288 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(285): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.-99+8194C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47467605 | |||||||
chr3:47467879 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-99+7920G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47467879 | |||||||
chr3:47467890 | G | A | 1 | a0001c0001t0001g0135 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-99+7909C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47467890 | |||||||
chr3:47468163 | A | C | 1 | a0001c0001t0001g0206 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-99+7636T>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47468163 | |||||||
chr3:47468285 | G | C | 1 | a0001c0001t0007g0003 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-99+7514C>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47468285 | |||||||
chr3:47468663 | G | T | 1 | a0001c0022t0001g0196 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-99+7136C>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47468663 | |||||||
chr3:47468921 | T | C | 1 | a0001c0001t0001g0229 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-99+6878A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47468921 | |||||||
chr3:47468962 | G | A | 3 | a0002c0002t0001g0136 a0002c0002t0001g0137 a0002c0002t0001g0138 |
3 | HG02135.hp2 NA19002.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.-99+6837C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47468962 | |||||||
chr3:47469003 | G | A | 1 | a0001c0001t0003g0230 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-99+6796C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47469003 | |||||||
chr3:47469075 | C | T | 1 | a0002c0002t0001g0061 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-99+6724G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47469075 | |||||||
chr3:47469090 | G | A | 3 | a0001c0001t0001g0231 a0001c0001t0001g0254 a0001c0001t0001g0270 |
3 | HG00738.hp1 HG01981.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-99+6709C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47469090 | |||||||
chr3:47469156 | T | C | 1 | a0001c0022t0001g0196 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-99+6643A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47469156 | |||||||
chr3:47469288 | G | A | 10 | a0001c0001t0002g0289 a0001c0001t0002g0290 a0001c0001t0002g0291 others(7): Show |
10 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.-99+6511C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47469288 | |||||||
chr3:47469339 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-99+6460G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47469339 | |||||||
chr3:47469401 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-99+6398T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47469401 | |||||||
chr3:47469957 | C | T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0033 |
3 | HG02055.hp1 HG02976.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-99+5842G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47469957 | |||||||
chr3:47470208 | T | C | 17 | a0001c0001t0002g0287 a0001c0001t0002g0288 a0001c0001t0002g0289 others(14): Show |
17 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.-99+5591A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47470208 | |||||||
chr3:47470600 | C | T | 27 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(24): Show |
27 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.-99+5199G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47470600 | |||||||
chr3:47470614 | A | G | 1 | a0002c0002t0001g0052 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-99+5185T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47470614 | |||||||
chr3:47470675 | C | G | 1 | a0001c0001t0001g0205 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-99+5124G>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47470675 | |||||||
chr3:47470841 | G | A | 30 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(27): Show |
30 | HG01109.hp1 HG01934.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.-99+4958C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47470841 | |||||||
chr3:47470865 | G | GA | 4 | a0002c0002t0001g0164 a0002c0002t0001g0165 a0002c0002t0001g0166 others(1): Show |
4 | HG00639.hp2 HG01070.hp1 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.-99+4933dupT | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47470865 | |||||||
chr3:47470965 | A | C | 2 | a0001c0001t0001g0197 a0001c0001t0001g0199 |
2 | HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-99+4834T>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47470965 | |||||||
chr3:47471070 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-99+4729A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47471070 | |||||||
chr3:47471189 | G | T | 1 | a0001c0001t0001g0198 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-99+4610C>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47471189 | |||||||
chr3:47471418 | C | A | 1 | a0003c0004t0001g0139 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-99+4381G>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47471418 | |||||||
chr3:47471436 | C | G | 1 | a0001c0001t0001g0267 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-99+4363G>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47471436 | |||||||
chr3:47471844 | T | C | 1 | a0001c0001t0001g0275 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-99+3955A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47471844 | |||||||
chr3:47471928 | G | A | 1 | a0001c0001t0001g0232 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-99+3871C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47471928 | |||||||
chr3:47472055 | A | C | 1 | a0002c0002t0001g0144 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-99+3744T>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47472055 | |||||||
chr3:47472268 | C | A | 1 | a0001c0001t0001g0168 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-99+3531G>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47472268 | |||||||
chr3:47472291 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-99+3508C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47472291 | |||||||
chr3:47472398 | C | T | 4 | a0002c0002t0001g0058 a0002c0002t0001g0059 a0002c0002t0001g0060 others(1): Show |
4 | NA18969.hp2 NA18988.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.-99+3401G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47472398 | |||||||
chr3:47472431 | A | G | 1 | a0002c0002t0001g0057 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-99+3368T>C | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47472431 | |||||||
chr3:47472453 | T | A | 2 | a0001c0001t0001g0198 a0002c0002t0001g0140 |
2 | HG02300.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.-99+3346A>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47472453 | |||||||
chr3:47472460 | A | AAAT | 259 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(256): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.-99+3336_-99+3338d others(5): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47472460 | |||||||
chr3:47472460 | A | AAATAAT | 5 | a0001c0001t0001g0168 a0001c0005t0001g0187 a0001c0022t0001g0196 others(2): Show |
5 | HG02258.hp1 HG02922.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-99+3333_-99+3338d others(8): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47472460 | |||||||
chr3:47472460 | AAAT | A | 22 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(19): Show |
22 | HG01109.hp1 HG02055.hp1 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.-99+3336_-99+3338d others(5): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47472460 | |||||||
chr3:47472846 | C | A | 1 | a0002c0002t0001g0141 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-99+2953G>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47472846 | |||||||
chr3:47472914 | C | T | 2 | a0001c0001t0001g0204 a0001c0001t0001g0233 |
2 | NA18967.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.-99+2885G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47472914 | |||||||
chr3:47473079 | T | TCAAAAAA others(15): Show |
2 | a0001c0001t0001g0190 a0001c0001t0001g0191 |
2 | HG01346.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.-99+2719_-99+2720i others(24): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473079 | |||||||
chr3:47473080 | C | CAAA | 7 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0002c0002t0001g0052 others(4): Show |
7 | HG01884.hp2 HG01975.hp2 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.-99+2716_-99+2718d others(5): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473080 | |||||||
chr3:47473080 | C | CAAAA | 88 | a0001c0001t0001g0093 a0001c0001t0001g0105 a0001c0001t0001g0133 others(85): Show |
88 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.-99+2715_-99+2718d others(6): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473080 | |||||||
chr3:47473080 | C | CAAAAA | 32 | a0001c0001t0007g0003 a0001c0005t0001g0194 a0001c0005t0001g0195 others(29): Show |
32 | HG00609.hp1 HG00639.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.-99+2714_-99+2718d others(7): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473080 | |||||||
chr3:47473080 | C | CAAAAAAA | 6 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
6 | HG02109.hp2 HG02922.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-99+2712_-99+2718d others(9): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473080 | |||||||
chr3:47473080 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0197 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-99+2709_-99+2718d others(12): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473080 | |||||||
chr3:47473080 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0002g0287 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-99+2706_-99+2718d others(15): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473080 | |||||||
chr3:47473080 | C | CAAAAAAA others(10): Show |
4 | a0001c0001t0001g0048 a0001c0001t0001g0198 a0001c0008t0001g0022 others(1): Show |
4 | HG01934.hp1 HG02300.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-99+2702_-99+2718d others(19): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473080 | |||||||
chr3:47473080 | C | CAAAAAAA others(11): Show |
10 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(7): Show |
10 | HG01109.hp1 HG02922.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.-99+2701_-99+2718d others(20): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473080 | |||||||
chr3:47473080 | C | CAAAAAAA others(12): Show |
7 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(4): Show |
7 | HG02055.hp1 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-99+2700_-99+2718d others(21): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473080 | |||||||
chr3:47473080 | C | CAAAAAAA others(13): Show |
6 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0200 others(3): Show |
6 | HG01975.hp1 HG02155.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-99+2718_-99+2719i others(22): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473080 | |||||||
chr3:47473080 | C | CAAAAAAA others(14): Show |
34 | a0001c0001t0001g0172 a0001c0001t0001g0204 a0001c0001t0001g0205 others(31): Show |
34 | HG00597.hp2 HG00673.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.-99+2718_-99+2719i others(23): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473080 | |||||||
chr3:47473080 | C | CAAAAAAA others(15): Show |
26 | a0001c0001t0001g0042 a0001c0001t0001g0173 a0001c0001t0001g0174 others(23): Show |
26 | HG00408.hp2 HG00609.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.-99+2718_-99+2719i others(24): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473080 | |||||||
chr3:47473080 | C | CAAAAAAA others(16): Show |
11 | a0001c0001t0001g0004 a0001c0001t0001g0043 a0001c0001t0001g0044 others(8): Show |
11 | HG01123.hp2 HG02148.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-99+2718_-99+2719i others(25): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473080 | |||||||
chr3:47473080 | C | CAAAAAAA others(17): Show |
3 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0019t0001g0045 |
3 | HG03225.hp2 HG03453.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.-99+2718_-99+2719i others(26): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473080 | |||||||
chr3:47473080 | C | CAAAAAAA others(18): Show |
9 | a0001c0001t0002g0288 a0001c0001t0002g0289 a0001c0001t0002g0290 others(6): Show |
9 | HG00099.hp1 HG00140.hp1 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.-99+2718_-99+2719i others(27): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473080 | |||||||
chr3:47473080 | C | CAAAAAAA others(19): Show |
14 | a0001c0001t0001g0046 a0001c0001t0001g0267 a0001c0001t0001g0268 others(11): Show |
14 | HG00558.hp2 HG00642.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.-99+2718_-99+2719i others(28): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473080 | |||||||
chr3:47473080 | C | CAAAAAAA others(20): Show |
7 | a0001c0001t0001g0047 a0001c0001t0001g0175 a0001c0001t0001g0176 others(4): Show |
7 | HG02080.hp1 HG02080.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-99+2718_-99+2719i others(29): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473080 | |||||||
chr3:47473080 | C | CAAAAAAA others(21): Show |
1 | a0001c0018t0002g0300 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-99+2718_-99+2719i others(30): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473080 | |||||||
chr3:47473080 | C | CAAAAAAA others(25): Show |
2 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
2 | HG00741.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-99+2718_-99+2719i others(34): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473080 | |||||||
chr3:47473085 | A | AAAAAAAA others(14): Show |
2 | a0001c0001t0001g0185 a0001c0001t0001g0186 |
2 | HG00544.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.-99+2713_-99+2714i others(23): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473085 | |||||||
chr3:47473086 | A | AAAAAAAA others(14): Show |
1 | a0001c0001t0001g0184 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-99+2712_-99+2713i others(23): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473086 | |||||||
chr3:47473086 | A | AAAAAAAA others(13): Show |
4 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 others(1): Show |
4 | NA18951.hp1 NA18954.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.-99+2712_-99+2713i others(22): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473086 | |||||||
chr3:47473086 | A | AAAAAAAA others(13): Show |
1 | a0001c0001t0001g0177 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-99+2712_-99+2713i others(22): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473086 | |||||||
chr3:47473086 | A | AAAAAAAA others(13): Show |
2 | a0001c0001t0001g0178 a0001c0010t0001g0179 |
2 | HG01168.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-99+2712_-99+2713i others(22): Show |
SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473086 | |||||||
chr3:47473145 | T | C | 1 | a0001c0001t0001g0276 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-99+2654A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473145 | |||||||
chr3:47473273 | G | T | 1 | a0002c0002t0001g0049 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-99+2526C>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473273 | |||||||
chr3:47473933 | T | C | 1 | a0002c0002t0001g0169 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-99+1866A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47473933 | |||||||
chr3:47474060 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-99+1739A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47474060 | |||||||
chr3:47474067 | G | A | 125 | a0001c0001t0001g0093 a0001c0001t0001g0105 a0001c0001t0001g0133 others(122): Show |
125 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.-99+1732C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47474067 | |||||||
chr3:47474146 | T | C | 3 | a0001c0001t0002g0301 a0001c0001t0002g0302 a0001c0001t0002g0303 |
3 | HG01192.hp2 HG02602.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.-99+1653A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47474146 | |||||||
chr3:47474264 | C | CA | 126 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0180 others(123): Show |
126 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.-99+1534dupT | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47474264 | |||||||
chr3:47474371 | T | C | 1 | a0002c0002t0001g0171 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-99+1428A>G | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47474371 | |||||||
chr3:47474658 | G | A | 2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-99+1141C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47474658 | |||||||
chr3:47474782 | G | A | 2 | a0001c0001t0001g0279 a0001c0001t0001g0280 |
2 | HG00558.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.-99+1017C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47474782 | |||||||
chr3:47475238 | G | A | 130 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(127): Show |
130 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.-99+561C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47475238 | |||||||
chr3:47475268 | C | T | 1 | a0001c0001t0001g0004 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-99+531G>A | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47475268 | |||||||
chr3:47475548 | G | A | 2 | a0001c0001t0001g0281 a0001c0001t0001g0282 |
2 | HG00639.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-99+251C>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47475548 | |||||||
chr3:47475601 | C | A | 1 | a0001c0001t0003g0283 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-99+198G>T | SCAP | ENSG00000114650.21 | transcript | ENST00000265565.10 | protein_coding | 1/22 | chr3 | 47475601 |