Item | Value |
---|---|
geneid | 54823 |
ensemblid | ENSG00000116668.13 |
hgncid | 16785 |
symbol | SWT1 |
name | SWT1 RNA endoribonuclease homolog |
refseq_nuc | NM_017673.7 |
refseq_prot | NP_060143.4 |
ensembl_nuc | ENST00000367500.9 |
ensembl_prot | ENSP00000356470.4 |
mane_status | MANE Select |
chr | chr1 |
start | 185157167 |
end | 185291781 |
strand | + |
ver | v1.2 |
region | chr1:185157167-185291781 |
region5000 | chr1:185152167-185296781 |
regionname0 | SWT1_chr1_185157167_185291781 |
regionname5000 | SWT1_chr1_185152167_185296781 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 900 | 122 | 11 | 28 | 65 | 6 | 10 | 45 | SWT1_chr1_185152167_185296781 | SWT1 | MSSKE others(895): Show |
chr1 | 185152167 | 185296781 |
a0002 | 0/0 | 900 | 72 | 16 | 19 | 25 | 4 | 8 | 22 | SWT1_chr1_185152167_185296781 | SWT1 | MSSKE others(895): Show |
chr1 | 185152167 | 185296781 |
a0003 | 0/0 | 900 | 68 | 42 | 7 | 17 | 1 | 1 | 11 | SWT1_chr1_185152167_185296781 | SWT1 | MSSKE others(895): Show |
chr1 | 185152167 | 185296781 |
a0004 | 0/0 | 900 | 27 | 7 | 10 | 5 | 1 | 4 | 5 | SWT1_chr1_185152167_185296781 | SWT1 | MSSKE others(895): Show |
chr1 | 185152167 | 185296781 |
a0005 | 0/0 | 900 | 10 | 0 | 0 | 10 | 0 | 0 | 10 | SWT1_chr1_185152167_185296781 | SWT1 | MSSKE others(895): Show |
chr1 | 185152167 | 185296781 |
a0006 | 0/0 | 900 | 9 | 6 | 0 | 3 | 0 | 0 | 3 | SWT1_chr1_185152167_185296781 | SWT1 | MSSKE others(895): Show |
chr1 | 185152167 | 185296781 |
a0007 | 0/0 | 900 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | MSSKE others(895): Show |
chr1 | 185152167 | 185296781 |
a0008 | 0/0 | 900 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | MSSKE others(895): Show |
chr1 | 185152167 | 185296781 |
a0009 | 0/0 | 900 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SWT1_chr1_185152167_185296781 | SWT1 | MSSKE others(895): Show |
chr1 | 185152167 | 185296781 |
a0010 | 0/0 | 900 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | MSSKE others(895): Show |
chr1 | 185152167 | 185296781 |
a0011 | 0/0 | 900 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | MSSKE others(895): Show |
chr1 | 185152167 | 185296781 |
a0012 | 0/0 | 900 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | MSSKE others(895): Show |
chr1 | 185152167 | 185296781 |
a0013 | 0/0 | 900 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | MSSKE others(895): Show |
chr1 | 185152167 | 185296781 |
a0014 | 0/0 | 900 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | MSSKE others(895): Show |
chr1 | 185152167 | 185296781 |
a0015 | 0/0 | 900 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | MSSKE others(895): Show |
chr1 | 185152167 | 185296781 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2700 | 117 | 10 | 26 | 63 | 6 | 10 | SWT1_chr1_185152167_185296781 | SWT1 | ATGTC others(2695): Show |
chr1 | 185152167 | 185296781 | ||
a0001c0011 | 0/0 | 2700 | 4 | 1 | 2 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | ATGTC others(2695): Show |
chr1 | 185152167 | 185296781 | ||
a0001c0019 | 0/0 | 2700 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | ATGTC others(2695): Show |
chr1 | 185152167 | 185296781 | ||
a0002c0002 | 0/0 | 2700 | 44 | 13 | 10 | 14 | 4 | 3 | SWT1_chr1_185152167_185296781 | SWT1 | ATGTC others(2695): Show |
chr1 | 185152167 | 185296781 | ||
a0002c0004 | 0/0 | 2700 | 28 | 3 | 9 | 11 | 0 | 5 | SWT1_chr1_185152167_185296781 | SWT1 | ATGTC others(2695): Show |
chr1 | 185152167 | 185296781 | ||
a0003c0003 | 0/0 | 2700 | 41 | 16 | 6 | 17 | 1 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | ATGTC others(2695): Show |
chr1 | 185152167 | 185296781 | ||
a0003c0005 | 0/0 | 2700 | 26 | 25 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | ATGTC others(2695): Show |
chr1 | 185152167 | 185296781 | ||
a0003c0021 | 0/0 | 2700 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | ATGTC others(2695): Show |
chr1 | 185152167 | 185296781 | ||
a0004c0006 | 0/0 | 2700 | 21 | 7 | 8 | 4 | 0 | 2 | SWT1_chr1_185152167_185296781 | SWT1 | ATGTC others(2695): Show |
chr1 | 185152167 | 185296781 | ||
a0004c0009 | 0/0 | 2700 | 6 | 0 | 2 | 1 | 1 | 2 | SWT1_chr1_185152167_185296781 | SWT1 | ATGTC others(2695): Show |
chr1 | 185152167 | 185296781 | ||
a0005c0007 | 0/0 | 2700 | 10 | 0 | 0 | 10 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | ATGTC others(2695): Show |
chr1 | 185152167 | 185296781 | ||
a0006c0008 | 0/0 | 2700 | 7 | 6 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | ATGTC others(2695): Show |
chr1 | 185152167 | 185296781 | ||
a0006c0014 | 0/0 | 2700 | 2 | 0 | 0 | 2 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | ATGTC others(2695): Show |
chr1 | 185152167 | 185296781 | ||
a0007c0010 | 0/0 | 2700 | 5 | 5 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | ATGTC others(2695): Show |
chr1 | 185152167 | 185296781 | ||
a0007c0012 | 0/0 | 2700 | 3 | 3 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | ATGTC others(2695): Show |
chr1 | 185152167 | 185296781 | ||
a0008c0017 | 0/0 | 2700 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | ATGTC others(2695): Show |
chr1 | 185152167 | 185296781 | ||
a0008c0023 | 0/0 | 2700 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | ATGTC others(2695): Show |
chr1 | 185152167 | 185296781 | ||
a0009c0013 | 0/0 | 2700 | 2 | 0 | 0 | 2 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | ATGTC others(2695): Show |
chr1 | 185152167 | 185296781 | ||
a0010c0015 | 0/0 | 2700 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | ATGTC others(2695): Show |
chr1 | 185152167 | 185296781 | ||
a0011c0018 | 0/0 | 2700 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | ATGTC others(2695): Show |
chr1 | 185152167 | 185296781 | ||
a0012c0020 | 0/0 | 2700 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | ATGTC others(2695): Show |
chr1 | 185152167 | 185296781 | ||
a0013c0022 | 0/0 | 2700 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | ATGTC others(2695): Show |
chr1 | 185152167 | 185296781 | ||
a0014c0024 | 0/0 | 2700 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | ATGTC others(2695): Show |
chr1 | 185152167 | 185296781 | ||
a0015c0016 | 0/0 | 2700 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | ATGTC others(2695): Show |
chr1 | 185152167 | 185296781 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 3838 | 93 | 8 | 25 | 44 | 6 | 8 | SWT1_chr1_185152167_185296781 | SWT1 | GAGTA others(3833): Show |
chr1 | 185152167 | 185296781 |
a0001c0001t0002 | 0/0 | 3838 | 20 | 0 | 0 | 18 | 0 | 2 | SWT1_chr1_185152167_185296781 | SWT1 | GAGTA others(3833): Show |
chr1 | 185152167 | 185296781 |
a0001c0001t0004 | 0/0 | 3838 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | GAGTA others(3833): Show |
chr1 | 185152167 | 185296781 |
a0001c0001t0005 | 0/0 | 3838 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | GAGTA others(3833): Show |
chr1 | 185152167 | 185296781 |
a0001c0001t0006 | 0/0 | 3838 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | GAGTA others(3833): Show |
chr1 | 185152167 | 185296781 |
a0001c0001t0007 | 0/0 | 3838 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | GAGTA others(3833): Show |
chr1 | 185152167 | 185296781 |
a0001c0011t0001 | 0/0 | 3838 | 3 | 0 | 2 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | GAGTA others(3833): Show |
chr1 | 185152167 | 185296781 |
a0001c0011t0008 | 0/0 | 3838 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | GAGTA others(3833): Show |
chr1 | 185152167 | 185296781 |
a0001c0019t0001 | 0/0 | 3838 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | GAGTA others(3833): Show |
chr1 | 185152167 | 185296781 |
a0002c0002t0001 | 0/0 | 3838 | 44 | 13 | 10 | 14 | 4 | 3 | SWT1_chr1_185152167_185296781 | SWT1 | GAGTA others(3833): Show |
chr1 | 185152167 | 185296781 |
a0002c0004t0001 | 0/0 | 3838 | 28 | 3 | 9 | 11 | 0 | 5 | SWT1_chr1_185152167_185296781 | SWT1 | GAGTA others(3833): Show |
chr1 | 185152167 | 185296781 |
a0003c0003t0001 | 0/0 | 3838 | 39 | 14 | 6 | 17 | 1 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | GAGTA others(3833): Show |
chr1 | 185152167 | 185296781 |
a0003c0003t0004 | 0/0 | 3838 | 2 | 2 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | GAGTA others(3833): Show |
chr1 | 185152167 | 185296781 |
a0003c0005t0001 | 0/0 | 3838 | 3 | 2 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | GAGTA others(3833): Show |
chr1 | 185152167 | 185296781 |
a0003c0005t0003 | 0/0 | 3838 | 13 | 13 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | GAGTA others(3833): Show |
chr1 | 185152167 | 185296781 |
a0003c0005t0004 | 0/0 | 3838 | 9 | 9 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | GAGTA others(3833): Show |
chr1 | 185152167 | 185296781 |
a0003c0005t0009 | 0/0 | 3838 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | GAGTA others(3833): Show |
chr1 | 185152167 | 185296781 |
a0003c0021t0011 | 0/0 | 3838 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | GAGTA others(3833): Show |
chr1 | 185152167 | 185296781 |
a0004c0006t0001 | 0/0 | 3838 | 21 | 7 | 8 | 4 | 0 | 2 | SWT1_chr1_185152167_185296781 | SWT1 | GAGTA others(3833): Show |
chr1 | 185152167 | 185296781 |
a0004c0009t0001 | 0/0 | 3838 | 6 | 0 | 2 | 1 | 1 | 2 | SWT1_chr1_185152167_185296781 | SWT1 | GAGTA others(3833): Show |
chr1 | 185152167 | 185296781 |
a0005c0007t0001 | 0/0 | 3838 | 10 | 0 | 0 | 10 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | GAGTA others(3833): Show |
chr1 | 185152167 | 185296781 |
a0006c0008t0001 | 0/0 | 3838 | 5 | 4 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | GAGTA others(3833): Show |
chr1 | 185152167 | 185296781 |
a0006c0008t0003 | 0/0 | 3838 | 2 | 2 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | GAGTA others(3833): Show |
chr1 | 185152167 | 185296781 |
a0006c0014t0001 | 0/0 | 3838 | 2 | 0 | 0 | 2 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | GAGTA others(3833): Show |
chr1 | 185152167 | 185296781 |
a0007c0010t0001 | 0/0 | 3838 | 4 | 4 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | GAGTA others(3833): Show |
chr1 | 185152167 | 185296781 |
a0007c0010t0010 | 0/0 | 3838 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | GAGTA others(3833): Show |
chr1 | 185152167 | 185296781 |
a0007c0012t0001 | 0/0 | 3838 | 3 | 3 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | GAGTA others(3833): Show |
chr1 | 185152167 | 185296781 |
a0008c0017t0001 | 0/0 | 3838 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | GAGTA others(3833): Show |
chr1 | 185152167 | 185296781 |
a0008c0023t0001 | 0/0 | 3838 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | GAGTA others(3833): Show |
chr1 | 185152167 | 185296781 |
a0009c0013t0001 | 0/0 | 3838 | 2 | 0 | 0 | 2 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | GAGTA others(3833): Show |
chr1 | 185152167 | 185296781 |
a0010c0015t0001 | 0/0 | 3838 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | GAGTA others(3833): Show |
chr1 | 185152167 | 185296781 |
a0011c0018t0001 | 0/0 | 3838 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | GAGTA others(3833): Show |
chr1 | 185152167 | 185296781 |
a0012c0020t0001 | 0/0 | 3838 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | GAGTA others(3833): Show |
chr1 | 185152167 | 185296781 |
a0013c0022t0001 | 0/0 | 3838 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | GAGTA others(3833): Show |
chr1 | 185152167 | 185296781 |
a0014c0024t0001 | 0/0 | 3838 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | GAGTA others(3833): Show |
chr1 | 185152167 | 185296781 |
a0015c0016t0001 | 0/0 | 3838 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | GAGTA others(3833): Show |
chr1 | 185152167 | 185296781 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0083 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0323 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0005g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0006g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0007g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0011t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0011t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0011t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0011t0008g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0019t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0003g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0004g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0004g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0004g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0004g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0009g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0021t0011g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0006t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0006t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0006t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0006t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0006t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0006t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0006t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0006t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0006t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0006t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0006t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0006t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0006t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0006t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0006t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0006t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0006t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0006t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0006t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0006t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0006t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0009t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0009t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0009t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0009t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0009t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0009t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0005c0007t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0005c0007t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0005c0007t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0005c0007t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0005c0007t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0005c0007t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0005c0007t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0005c0007t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0005c0007t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0005c0007t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0006c0008t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0006c0008t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0006c0008t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0006c0008t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0006c0008t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0006c0008t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0006c0008t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0006c0014t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0006c0014t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0007c0010t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0007c0010t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0007c0010t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0007c0010t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0007c0010t0010g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0007c0012t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0007c0012t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0007c0012t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0008c0017t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0008c0023t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0009c0013t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0009c0013t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0010c0015t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0011c0018t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0012c0020t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0013c0022t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0014c0024t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0015c0016t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0105 | EUR | GBR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0078 | EUR | GBR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0038 | EUR | FIN | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00280 | hp2 | a0004 | c0009 | t0001 | g0060 | EUR | FIN | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00323 | hp1 | a0003 | c0003 | t0001 | g0197 | EUR | FIN | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0184 | EUR | FIN | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00408 | hp2 | a0003 | c0003 | t0001 | g0193 | EAS | CHS | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | CHS | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00544 | hp2 | a0003 | c0003 | t0001 | g0208 | EAS | CHS | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00558 | hp2 | a0003 | c0003 | t0001 | g0219 | EAS | CHS | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00597 | hp2 | a0001 | c0001 | t0006 | g0125 | EAS | CHS | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00609 | hp2 | a0003 | c0003 | t0001 | g0202 | EAS | CHS | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00621 | hp2 | a0010 | c0015 | t0001 | g0090 | EAS | CHS | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00639 | hp2 | a0004 | c0009 | t0001 | g0129 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00738 | hp2 | a0004 | c0006 | t0001 | g0143 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00741 | hp1 | a0002 | c0002 | t0001 | g0176 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01069 | hp1 | a0002 | c0002 | t0001 | g0287 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01069 | hp2 | a0011 | c0018 | t0001 | g0028 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01070 | hp1 | a0004 | c0009 | t0001 | g0067 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01070 | hp2 | a0001 | c0011 | t0001 | g0160 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0286 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01074 | hp2 | a0002 | c0002 | t0001 | g0177 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01081 | hp1 | a0004 | c0006 | t0001 | g0164 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01081 | hp2 | a0001 | c0001 | t0005 | g0100 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01099 | hp2 | a0003 | c0003 | t0001 | g0239 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01106 | hp1 | a0003 | c0003 | t0001 | g0210 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01167 | hp2 | a0002 | c0004 | t0001 | g0299 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01168 | hp1 | a0001 | c0011 | t0001 | g0157 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01168 | hp2 | a0008 | c0017 | t0001 | g0075 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01169 | hp1 | a0002 | c0004 | t0001 | g0300 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01169 | hp2 | a0008 | c0023 | t0001 | g0161 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0174 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01192 | hp1 | a0003 | c0003 | t0001 | g0203 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01192 | hp2 | a0004 | c0006 | t0001 | g0162 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01243 | hp1 | a0003 | c0005 | t0001 | g0230 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01255 | hp1 | a0002 | c0004 | t0001 | g0308 | AMR | CLM | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01256 | hp2 | a0002 | c0002 | t0001 | g0150 | AMR | CLM | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01257 | hp1 | a0003 | c0003 | t0001 | g0204 | AMR | CLM | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01257 | hp2 | a0004 | c0006 | t0001 | g0165 | AMR | CLM | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01346 | hp1 | a0004 | c0006 | t0001 | g0142 | AMR | CLM | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0169 | AMR | CLM | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01496 | hp1 | a0002 | c0004 | t0001 | g0288 | AMR | CLM | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0151 | EUR | IBS | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0084 | EUR | IBS | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01884 | hp1 | a0012 | c0020 | t0001 | g0130 | AFR | ACB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01884 | hp2 | a0013 | c0022 | t0001 | g0008 | AFR | ACB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01891 | hp1 | a0006 | c0008 | t0001 | g0139 | AFR | ACB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01891 | hp2 | a0003 | c0005 | t0004 | g0007 | AFR | ACB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01928 | hp1 | a0004 | c0006 | t0001 | g0222 | AMR | PEL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01928 | hp2 | a0002 | c0004 | t0001 | g0302 | AMR | PEL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01943 | hp1 | a0004 | c0006 | t0001 | g0144 | AMR | PEL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01943 | hp2 | a0002 | c0004 | t0001 | g0311 | AMR | PEL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01952 | hp1 | a0002 | c0004 | t0001 | g0303 | AMR | PEL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01975 | hp1 | a0002 | c0004 | t0001 | g0293 | AMR | PEL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01978 | hp1 | a0003 | c0003 | t0001 | g0205 | AMR | PEL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01981 | hp1 | a0002 | c0004 | t0001 | g0321 | AMR | PEL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02040 | hp1 | a0001 | c0019 | t0001 | g0046 | EAS | KHV | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02040 | hp2 | a0002 | c0004 | t0001 | g0314 | EAS | KHV | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02055 | hp1 | a0001 | c0011 | t0008 | g0260 | AFR | ACB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02055 | hp2 | a0003 | c0005 | t0003 | g0248 | AFR | ACB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | KHV | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | KHV | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02080 | hp1 | a0003 | c0003 | t0001 | g0207 | EAS | KHV | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0179 | EAS | KHV | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02145 | hp2 | a0007 | c0012 | t0001 | g0020 | AFR | ACB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02148 | hp1 | a0014 | c0024 | t0001 | g0175 | AMR | PEL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02148 | hp2 | a0004 | c0006 | t0001 | g0158 | AMR | PEL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02165 | hp1 | a0003 | c0003 | t0001 | g0200 | EAS | CDX | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | CDX | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02258 | hp1 | a0003 | c0003 | t0001 | g0262 | AFR | ACB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02258 | hp2 | a0003 | c0003 | t0001 | g0238 | AFR | ACB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02280 | hp1 | a0001 | c0001 | t0004 | g0037 | AFR | ACB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02280 | hp2 | a0006 | c0008 | t0001 | g0140 | AFR | ACB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02293 | hp1 | a0003 | c0003 | t0001 | g0196 | AMR | PEL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02451 | hp1 | a0003 | c0005 | t0003 | g0253 | AFR | ACB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02451 | hp2 | a0002 | c0002 | t0001 | g0135 | AFR | ACB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02572 | hp1 | a0007 | c0010 | t0001 | g0228 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02572 | hp2 | a0002 | c0002 | t0001 | g0257 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02615 | hp2 | a0002 | c0002 | t0001 | g0215 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02622 | hp1 | a0003 | c0003 | t0001 | g0234 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02622 | hp2 | a0006 | c0008 | t0003 | g0243 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02630 | hp1 | a0004 | c0006 | t0001 | g0225 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02630 | hp2 | a0002 | c0002 | t0001 | g0255 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02647 | hp1 | a0003 | c0005 | t0004 | g0268 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02647 | hp2 | a0004 | c0006 | t0001 | g0226 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02717 | hp1 | a0003 | c0005 | t0004 | g0265 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02717 | hp2 | a0006 | c0008 | t0003 | g0244 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02723 | hp1 | a0002 | c0002 | t0001 | g0258 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02723 | hp2 | a0003 | c0005 | t0003 | g0247 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02809 | hp1 | a0003 | c0003 | t0001 | g0211 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02809 | hp2 | a0003 | c0003 | t0004 | g0232 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02818 | hp1 | a0003 | c0005 | t0003 | g0252 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02818 | hp2 | a0007 | c0010 | t0001 | g0070 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02886 | hp1 | a0004 | c0006 | t0001 | g0224 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02886 | hp2 | a0003 | c0005 | t0004 | g0006 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02895 | hp1 | a0007 | c0012 | t0001 | g0019 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02895 | hp2 | a0003 | c0003 | t0001 | g0271 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02896 | hp1 | a0002 | c0002 | t0001 | g0153 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02896 | hp2 | a0003 | c0005 | t0003 | g0246 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02897 | hp1 | a0003 | c0005 | t0003 | g0003 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02897 | hp2 | a0003 | c0003 | t0001 | g0270 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02922 | hp1 | a0003 | c0005 | t0004 | g0269 | AFR | ESN | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02922 | hp2 | a0002 | c0002 | t0001 | g0136 | AFR | ESN | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02965 | hp1 | a0003 | c0003 | t0001 | g0240 | AFR | ESN | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02965 | hp2 | a0003 | c0003 | t0001 | g0263 | AFR | ESN | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02970 | hp1 | a0003 | c0005 | t0001 | g0013 | AFR | ESN | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02970 | hp2 | a0002 | c0002 | t0001 | g0256 | AFR | ESN | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02976 | hp2 | a0003 | c0005 | t0004 | g0229 | AFR | ESN | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03041 | hp1 | a0003 | c0021 | t0011 | g0131 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03041 | hp2 | a0003 | c0003 | t0001 | g0235 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03098 | hp2 | a0003 | c0003 | t0004 | g0233 | AFR | MSL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03130 | hp1 | a0004 | c0006 | t0001 | g0159 | AFR | ESN | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03130 | hp2 | a0003 | c0005 | t0001 | g0231 | AFR | ESN | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03139 | hp1 | a0003 | c0003 | t0001 | g0236 | AFR | ESN | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03139 | hp2 | a0003 | c0005 | t0003 | g0227 | AFR | ESN | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03195 | hp1 | a0006 | c0008 | t0001 | g0141 | AFR | ESN | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03195 | hp2 | a0003 | c0003 | t0001 | g0237 | AFR | ESN | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03209 | hp1 | a0003 | c0005 | t0004 | g0267 | AFR | MSL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03209 | hp2 | a0007 | c0010 | t0010 | g0085 | AFR | MSL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03225 | hp1 | a0003 | c0005 | t0003 | g0003 | AFR | MSL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03225 | hp2 | a0004 | c0006 | t0001 | g0166 | AFR | MSL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03239 | hp1 | a0002 | c0002 | t0001 | g0213 | SAS | PJL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03453 | hp1 | a0003 | c0005 | t0004 | g0264 | AFR | MSL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03453 | hp2 | a0007 | c0010 | t0001 | g0072 | AFR | MSL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03486 | hp1 | a0002 | c0002 | t0001 | g0272 | AFR | MSL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03486 | hp2 | a0001 | c0001 | t0007 | g0094 | AFR | MSL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03490 | hp1 | a0004 | c0009 | t0001 | g0113 | SAS | PJL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03490 | hp2 | a0004 | c0006 | t0001 | g0152 | SAS | PJL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03491 | hp2 | a0002 | c0004 | t0001 | g0026 | SAS | PJL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03492 | hp1 | a0004 | c0009 | t0001 | g0114 | SAS | PJL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03492 | hp2 | a0002 | c0004 | t0001 | g0027 | SAS | PJL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03516 | hp1 | a0003 | c0005 | t0003 | g0245 | AFR | ESN | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03516 | hp2 | a0002 | c0002 | t0001 | g0137 | AFR | ESN | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03540 | hp1 | a0002 | c0002 | t0001 | g0259 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03540 | hp2 | a0003 | c0005 | t0003 | g0254 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03579 | hp1 | a0003 | c0005 | t0004 | g0266 | AFR | MSL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | MSL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0276 | SAS | PJL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03654 | hp2 | a0004 | c0006 | t0001 | g0163 | SAS | PJL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03669 | hp1 | a0002 | c0002 | t0001 | g0178 | SAS | PJL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03688 | hp1 | a0002 | c0004 | t0001 | g0014 | SAS | STU | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03688 | hp2 | a0002 | c0004 | t0001 | g0296 | SAS | STU | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03704 | hp1 | a0015 | c0016 | t0001 | g0017 | SAS | PJL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0029 | SAS | PJL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0186 | SAS | BEB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | BEB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | BEB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03927 | hp1 | a0003 | c0003 | t0001 | g0189 | SAS | BEB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | BEB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | STU | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG04228 | hp2 | a0002 | c0004 | t0001 | g0307 | SAS | STU | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18522 | hp1 | a0003 | c0005 | t0003 | g0251 | AFR | YRI | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18522 | hp2 | a0003 | c0003 | t0001 | g0212 | AFR | YRI | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18612 | hp1 | a0002 | c0004 | t0001 | g0310 | EAS | CHB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | CHB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18906 | hp1 | a0002 | c0002 | t0001 | g0214 | AFR | YRI | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18906 | hp2 | a0003 | c0005 | t0003 | g0249 | AFR | YRI | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18939 | hp2 | a0004 | c0006 | t0001 | g0149 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18941 | hp1 | a0005 | c0007 | t0001 | g0295 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18942 | hp2 | a0003 | c0003 | t0001 | g0190 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18943 | hp1 | a0003 | c0003 | t0001 | g0195 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18944 | hp1 | a0002 | c0002 | t0001 | g0167 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18946 | hp2 | a0003 | c0003 | t0001 | g0201 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18948 | hp1 | a0006 | c0014 | t0001 | g0292 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18948 | hp2 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18949 | hp1 | a0003 | c0003 | t0001 | g0192 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18950 | hp1 | a0002 | c0004 | t0001 | g0087 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18951 | hp2 | a0003 | c0003 | t0001 | g0198 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0180 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18954 | hp1 | a0002 | c0004 | t0001 | g0313 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18961 | hp1 | a0003 | c0003 | t0001 | g0199 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18961 | hp2 | a0002 | c0002 | t0001 | g0218 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18967 | hp1 | a0002 | c0004 | t0001 | g0320 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18969 | hp1 | a0006 | c0008 | t0001 | g0188 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18970 | hp1 | a0005 | c0007 | t0001 | g0306 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18971 | hp2 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18972 | hp2 | a0002 | c0002 | t0001 | g0220 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18973 | hp2 | a0004 | c0006 | t0001 | g0147 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18977 | hp1 | a0009 | c0013 | t0001 | g0073 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18977 | hp2 | a0003 | c0003 | t0001 | g0194 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18983 | hp1 | a0002 | c0004 | t0001 | g0319 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18983 | hp2 | a0004 | c0006 | t0001 | g0145 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18989 | hp1 | a0005 | c0007 | t0001 | g0322 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18989 | hp2 | a0006 | c0014 | t0001 | g0294 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18992 | hp1 | a0003 | c0003 | t0001 | g0206 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18992 | hp2 | a0005 | c0007 | t0001 | g0298 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0181 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18999 | hp1 | a0003 | c0003 | t0001 | g0209 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18999 | hp2 | a0002 | c0002 | t0001 | g0185 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19000 | hp1 | a0005 | c0007 | t0001 | g0304 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19000 | hp2 | a0003 | c0003 | t0001 | g0221 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19002 | hp1 | a0004 | c0006 | t0001 | g0146 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19005 | hp2 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19006 | hp1 | a0002 | c0004 | t0001 | g0317 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19007 | hp2 | a0002 | c0002 | t0001 | g0173 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19009 | hp1 | a0005 | c0007 | t0001 | g0241 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19011 | hp2 | a0009 | c0013 | t0001 | g0074 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19030 | hp1 | a0007 | c0012 | t0001 | g0018 | AFR | LWK | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19030 | hp2 | a0003 | c0003 | t0001 | g0154 | AFR | LWK | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19043 | hp1 | a0002 | c0004 | t0001 | g0291 | AFR | LWK | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19043 | hp2 | a0003 | c0005 | t0003 | g0250 | AFR | LWK | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19056 | hp1 | a0005 | c0007 | t0001 | g0242 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19057 | hp2 | a0005 | c0007 | t0001 | g0297 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19066 | hp1 | a0002 | c0004 | t0001 | g0316 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19068 | hp1 | a0004 | c0009 | t0001 | g0080 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19068 | hp2 | a0001 | c0011 | t0001 | g0148 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19072 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19072 | hp2 | a0005 | c0007 | t0001 | g0312 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19074 | hp1 | a0002 | c0004 | t0001 | g0318 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19079 | hp2 | a0003 | c0003 | t0001 | g0191 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19081 | hp2 | a0005 | c0007 | t0001 | g0305 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19082 | hp1 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19083 | hp2 | a0002 | c0002 | t0001 | g0217 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19085 | hp2 | a0002 | c0002 | t0001 | g0216 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19090 | hp1 | a0002 | c0004 | t0001 | g0301 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19091 | hp2 | a0002 | c0004 | t0001 | g0315 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19240 | hp1 | a0002 | c0002 | t0001 | g0171 | AFR | YRI | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19240 | hp2 | a0004 | c0006 | t0001 | g0223 | AFR | YRI | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0063 | EUR | TSI | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA20752 | hp2 | a0002 | c0002 | t0001 | g0156 | EUR | TSI | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0182 | EUR | TSI | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0092 | EUR | TSI | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0183 | AMR | CLM | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02109 | hp2 | a0003 | c0005 | t0009 | g0004 | AFR | ACB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02559 | hp1 | a0003 | c0003 | t0001 | g0155 | AFR | ACB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02559 | hp2 | a0006 | c0008 | t0001 | g0138 | AFR | ACB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG06807 | hp1 | a0002 | c0004 | t0001 | g0009 | AFR | USA | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | USA | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA20300 | hp1 | a0002 | c0004 | t0001 | g0309 | AFR | USA | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA20300 | hp2 | a0007 | c0010 | t0001 | g0071 | AFR | USA | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | LWK | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA21309 | hp2 | a0004 | c0006 | t0001 | g0261 | AFR | LWK | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0323 | REF | REF | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0083 | REF | REF | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:185174589 | A | G | 6 | a0002 a0003 a0005 others(3): Show |
161 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(158): Show |
missense_variant | MODERATE | c.442A>G | p.Ile148Val | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/19 | 599/3838 | 442/2703 | 148/900 | chr1 | 185174589 | |||
chr1:185174607 | C | A | 1 | a0014 | 1 | HG02148.hp1 | missense_variant | MODERATE | c.460C>A | p.Pro154Thr | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/19 | 617/3838 | 460/2703 | 154/900 | chr1 | 185174607 | |||
chr1:185174692 | A | G | 1 | a0007 | 5 | HG02572.hp1 HG02818.hp2 HG03209.hp2 others(2): Show |
missense_variant | MODERATE | c.545A>G | p.Lys182Arg | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/19 | 702/3838 | 545/2703 | 182/900 | chr1 | 185174692 | |||
chr1:185174693 | G | T | 1 | a0007 | 3 | HG02145.hp2 HG02895.hp1 NA19030.hp1 |
missense_variant | MODERATE | c.546G>T | p.Lys182Asn | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/19 | 703/3838 | 546/2703 | 182/900 | chr1 | 185174693 | |||
chr1:185184329 | A | G | 1 | a0012 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.1225A>G | p.Thr409Ala | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 8/19 | 1382/3838 | 1225/2703 | 409/900 | chr1 | 185184329 | |||
chr1:185202737 | A | G | 5 | a0002 a0005 a0006 others(2): Show |
94 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(91): Show |
missense_variant | MODERATE | c.1607A>G | p.His536Arg | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 11/19 | 1764/3838 | 1607/2703 | 536/900 | chr1 | 185202737 | |||
chr1:185204702 | A | G | 1 | a0011 | 1 | HG01069.hp2 | missense_variant&splice_region_variant | MODERATE | c.1672A>G | p.Thr558Ala | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 12/19 | 1829/3838 | 1672/2703 | 558/900 | chr1 | 185204702 | |||
chr1:185204724 | A | G | 1 | a0008 | 2 | HG01168.hp2 HG01169.hp2 |
missense_variant | MODERATE | c.1694A>G | p.Tyr565Cys | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 12/19 | 1851/3838 | 1694/2703 | 565/900 | chr1 | 185204724 | |||
chr1:185206667 | C | G | 1 | a0015 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.1876C>G | p.Gln626Glu | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/19 | 2033/3838 | 1876/2703 | 626/900 | chr1 | 185206667 | |||
chr1:185206705 | A | C | 1 | a0005 | 10 | NA18941.hp1 NA18970.hp1 NA18989.hp1 others(7): Show |
missense_variant | MODERATE | c.1914A>C | p.Leu638Phe | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/19 | 2071/3838 | 1914/2703 | 638/900 | chr1 | 185206705 | |||
chr1:185221934 | A | C | 1 | a0010 | 1 | HG00621.hp2 | missense_variant | MODERATE | c.2207A>C | p.Gln736Pro | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/19 | 2364/3838 | 2207/2703 | 736/900 | chr1 | 185221934 | |||
chr1:185271342 | A | G | 7 | a0002 a0004 a0005 others(4): Show |
115 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(112): Show |
missense_variant | MODERATE | c.2461A>G | p.Asn821Asp | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/19 | 2618/3838 | 2461/2703 | 821/900 | chr1 | 185271342 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:185166613 | A | G | 7 | a0001c0011 a0002c0002 a0003c0003 others(4): Show |
119 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(116): Show |
synonymous_variant | LOW | c.126A>G | p.Ser42Ser | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 3/19 | 283/3838 | 126/2703 | 42/900 | chr1 | 185166613 | |||
chr1:185174627 | G | A | 2 | a0003c0021 a0013c0022 |
2 | HG01884.hp2 HG03041.hp1 |
synonymous_variant | LOW | c.480G>A | p.Val160Val | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/19 | 637/3838 | 480/2703 | 160/900 | chr1 | 185174627 | |||
chr1:185202738 | C | T | 1 | a0001c0019 | 1 | HG02040.hp1 | synonymous_variant | LOW | c.1608C>T | p.His536His | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 11/19 | 1765/3838 | 1608/2703 | 536/900 | chr1 | 185202738 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:185290819 | T | G | 1 | a0001c0001t0005 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*16T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 19/19 | 16 | chr1 | 185290819 | ||||||
chr1:185290873 | A | G | 1 | a0003c0021t0011 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*70A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 19/19 | 70 | chr1 | 185290873 | ||||||
chr1:185290939 | A | G | 1 | a0001c0001t0002 | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*136A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 19/19 | 136 | chr1 | 185290939 | ||||||
chr1:185290974 | A | C | 1 | a0007c0010t0010 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*171A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 19/19 | 171 | chr1 | 185290974 | ||||||
chr1:185291071 | G | C | 1 | a0001c0001t0006 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*268G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 19/19 | 268 | chr1 | 185291071 | ||||||
chr1:185291229 | C | T | 1 | a0003c0005t0009 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*426C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 19/19 | 426 | chr1 | 185291229 | ||||||
chr1:185291283 | T | G | 2 | a0003c0005t0003 a0006c0008t0003 |
15 | HG02055.hp2 HG02451.hp1 HG02622.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*480T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 19/19 | 480 | chr1 | 185291283 | ||||||
chr1:185291331 | C | T | 3 | a0001c0001t0004 a0003c0003t0004 a0003c0005t0004 |
12 | HG01891.hp2 HG02280.hp1 HG02647.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*528C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 19/19 | 528 | chr1 | 185291331 | ||||||
chr1:185291383 | T | A | 3 | a0001c0001t0007 a0003c0005t0009 a0003c0021t0011 |
3 | HG02109.hp2 HG03041.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*580T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 19/19 | 580 | chr1 | 185291383 | ||||||
chr1:185291536 | A | C | 1 | a0001c0011t0008 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*733A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 19/19 | 733 | chr1 | 185291536 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:185157511 | G | A | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-10+197G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185157511 | |||||||
chr1:185157690 | A | G | 1 | a0005c0007t0001g0322 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-10+376A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185157690 | |||||||
chr1:185157734 | G | T | 35 | a0001c0001t0002g0289 a0001c0001t0002g0290 a0002c0004t0001g0288 others(32): Show |
35 | HG00438.hp1 HG01167.hp2 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.-10+420G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185157734 | |||||||
chr1:185158093 | G | A | 4 | a0001c0001t0001g0005 a0003c0005t0004g0006 a0003c0005t0004g0007 others(1): Show |
4 | HG01884.hp2 HG01891.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+779G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185158093 | |||||||
chr1:185158223 | G | A | 1 | a0002c0004t0001g0009 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-10+909G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185158223 | |||||||
chr1:185158259 | A | G | 2 | a0002c0002t0001g0286 a0002c0002t0001g0287 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-10+945A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185158259 | |||||||
chr1:185158261 | C | T | 13 | a0001c0001t0002g0273 a0001c0001t0002g0274 a0001c0001t0002g0275 others(10): Show |
13 | HG02071.hp2 HG03654.hp1 NA18949.hp2 others(10): Show |
intron_variant | MODIFIER | c.-10+947C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185158261 | |||||||
chr1:185158361 | G | T | 1 | a0002c0002t0001g0272 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-10+1047G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185158361 | |||||||
chr1:185158383 | C | T | 10 | a0003c0003t0001g0262 a0003c0003t0001g0263 a0003c0003t0001g0270 others(7): Show |
10 | HG02258.hp1 HG02647.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.-10+1069C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185158383 | |||||||
chr1:185158417 | C | CA | 3 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 |
3 | NA18972.hp1 NA19006.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.-10+1105dupA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 185158417 | ||||||
chr1:185158509 | C | CT | 52 | a0001c0001t0002g0289 a0001c0001t0002g0290 a0001c0011t0008g0260 others(49): Show |
53 | HG00438.hp1 HG01167.hp2 HG01169.hp1 others(50): Show |
intron_variant | MODIFIER | c.-10+1209dupT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 185158509 | ||||||
chr1:185158684 | A | G | 2 | a0006c0008t0003g0243 a0006c0008t0003g0244 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-10+1370A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185158684 | |||||||
chr1:185158979 | T | C | 15 | a0001c0001t0002g0273 a0001c0001t0002g0274 a0001c0001t0002g0275 others(12): Show |
15 | HG00438.hp1 HG02071.hp2 HG03654.hp1 others(12): Show |
intron_variant | MODIFIER | c.-10+1665T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185158979 | |||||||
chr1:185159118 | C | T | 134 | a0001c0011t0001g0148 a0001c0011t0001g0157 a0001c0011t0001g0160 others(131): Show |
135 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.-9-1715C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185159118 | |||||||
chr1:185159158 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-9-1675C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185159158 | |||||||
chr1:185159173 | G | A | 1 | a0003c0005t0001g0013 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-9-1660G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185159173 | |||||||
chr1:185159327 | T | A | 1 | a0002c0004t0001g0014 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-9-1506T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185159327 | |||||||
chr1:185159359 | G | A | 2 | a0002c0002t0001g0135 a0002c0002t0001g0136 |
2 | HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-9-1474G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185159359 | |||||||
chr1:185159413 | C | G | 47 | a0002c0004t0001g0009 a0002c0004t0001g0288 a0002c0004t0001g0291 others(44): Show |
48 | HG01167.hp2 HG01169.hp1 HG01255.hp1 others(45): Show |
intron_variant | MODIFIER | c.-9-1420C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185159413 | |||||||
chr1:185159475 | A | G | 12 | a0003c0003t0001g0234 a0003c0003t0001g0235 a0003c0003t0001g0236 others(9): Show |
12 | HG01099.hp2 HG02258.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-9-1358A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185159475 | |||||||
chr1:185159549 | C | A | 5 | a0002c0002t0001g0137 a0006c0008t0001g0138 a0006c0008t0001g0139 others(2): Show |
5 | HG01891.hp1 HG02280.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-1284C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185159549 | |||||||
chr1:185159696 | C | CAT | 3 | a0004c0006t0001g0142 a0004c0006t0001g0143 a0004c0006t0001g0144 |
3 | HG00738.hp2 HG01346.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.-9-1128_-9-1127dup others(2): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 185159696 | ||||||
chr1:185159755 | C | T | 5 | a0003c0003t0001g0236 a0003c0003t0001g0237 a0003c0003t0001g0238 others(2): Show |
5 | HG01099.hp2 HG02258.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-1078C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185159755 | |||||||
chr1:185159809 | C | G | 47 | a0002c0004t0001g0009 a0002c0004t0001g0288 a0002c0004t0001g0291 others(44): Show |
48 | HG01167.hp2 HG01169.hp1 HG01255.hp1 others(45): Show |
intron_variant | MODIFIER | c.-9-1024C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185159809 | |||||||
chr1:185160028 | A | G | 1 | a0001c0001t0001g0133 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-9-805A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185160028 | |||||||
chr1:185160513 | C | T | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-9-320C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185160513 | |||||||
chr1:185160631 | G | C | 118 | a0001c0011t0001g0148 a0001c0011t0001g0157 a0001c0011t0001g0160 others(115): Show |
119 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.-9-202G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185160631 | |||||||
chr1:185160757 | A | G | 5 | a0001c0001t0001g0132 a0004c0006t0001g0223 a0004c0006t0001g0224 others(2): Show |
5 | HG02630.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-76A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185160757 | |||||||
chr1:185160944 | T | C | 1 | a0003c0005t0001g0013 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.84+19T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185160944 | |||||||
chr1:185160993 | C | G | 2 | a0003c0021t0011g0131 a0013c0022t0001g0008 |
2 | HG01884.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.84+68C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185160993 | |||||||
chr1:185161221 | T | TA | 5 | a0001c0011t0001g0148 a0004c0006t0001g0145 a0004c0006t0001g0146 others(2): Show |
5 | NA18939.hp2 NA18973.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.84+299dupA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 185161221 | ||||||
chr1:185161274 | C | G | 1 | a0012c0020t0001g0130 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.84+349C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185161274 | |||||||
chr1:185161285 | A | G | 12 | a0003c0003t0001g0234 a0003c0003t0001g0235 a0003c0003t0001g0236 others(9): Show |
12 | HG01099.hp2 HG02258.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.84+360A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185161285 | |||||||
chr1:185161627 | G | A | 1 | a0002c0002t0001g0150 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.84+702G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185161627 | |||||||
chr1:185161716 | A | G | 1 | a0004c0006t0001g0149 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.84+791A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185161716 | |||||||
chr1:185162288 | A | C | 1 | a0004c0009t0001g0129 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.84+1363A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185162288 | |||||||
chr1:185162361 | C | T | 34 | a0002c0004t0001g0288 a0002c0004t0001g0293 a0002c0004t0001g0296 others(31): Show |
34 | HG01167.hp2 HG01169.hp1 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.84+1436C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185162361 | |||||||
chr1:185162417 | A | G | 1 | a0001c0011t0008g0260 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.84+1492A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185162417 | |||||||
chr1:185162707 | G | C | 1 | a0001c0001t0001g0015 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.84+1782G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185162707 | |||||||
chr1:185162730 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.84+1805C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185162730 | |||||||
chr1:185162742 | T | C | 1 | a0002c0002t0001g0151 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.84+1817T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185162742 | |||||||
chr1:185162811 | A | G | 1 | a0004c0006t0001g0222 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.84+1886A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185162811 | |||||||
chr1:185163037 | C | T | 13 | a0003c0005t0001g0230 a0003c0005t0001g0231 a0003c0005t0004g0006 others(10): Show |
13 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.84+2112C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185163037 | |||||||
chr1:185163153 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.84+2228T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185163153 | |||||||
chr1:185163214 | A | G | 18 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(15): Show |
18 | HG00438.hp1 HG02071.hp2 HG03654.hp1 others(15): Show |
intron_variant | MODIFIER | c.84+2289A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185163214 | |||||||
chr1:185163393 | C | CT | 11 | a0001c0001t0001g0005 a0001c0001t0001g0124 a0001c0001t0001g0126 others(8): Show |
11 | HG00597.hp2 HG00741.hp2 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.84+2486dupT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 185163393 | ||||||
chr1:185163393 | CT | C | 7 | a0002c0002t0001g0153 a0002c0004t0001g0293 a0004c0006t0001g0152 others(4): Show |
7 | HG01975.hp1 HG02896.hp1 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.84+2486delT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 185163393 | ||||||
chr1:185163432 | C | T | 2 | a0003c0003t0001g0270 a0003c0003t0001g0271 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.84+2507C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185163432 | |||||||
chr1:185163487 | G | A | 34 | a0002c0004t0001g0288 a0002c0004t0001g0293 a0002c0004t0001g0296 others(31): Show |
34 | HG01167.hp2 HG01169.hp1 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.84+2562G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185163487 | |||||||
chr1:185163708 | A | G | 18 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(15): Show |
18 | HG00438.hp1 HG02071.hp2 HG03654.hp1 others(15): Show |
intron_variant | MODIFIER | c.84+2783A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185163708 | |||||||
chr1:185163710 | T | C | 203 | a0001c0001t0001g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(200): Show |
205 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.84+2785T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185163710 | |||||||
chr1:185163723 | A | G | 1 | a0001c0001t0001g0123 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.84+2798A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185163723 | |||||||
chr1:185163899 | A | G | 2 | a0001c0001t0002g0283 a0001c0001t0002g0284 |
2 | NA18973.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.85-2673A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185163899 | |||||||
chr1:185164328 | T | G | 2 | a0003c0003t0001g0154 a0003c0003t0001g0155 |
2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.85-2244T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185164328 | |||||||
chr1:185164663 | G | A | 2 | a0003c0005t0001g0013 a0003c0005t0003g0227 |
2 | HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.85-1909G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185164663 | |||||||
chr1:185164753 | A | C | 2 | a0007c0012t0001g0019 a0007c0012t0001g0020 |
2 | HG02145.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.85-1819A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185164753 | |||||||
chr1:185164892 | A | C | 37 | a0001c0001t0001g0015 a0001c0001t0001g0088 a0001c0001t0001g0089 others(34): Show |
37 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-1680A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185164892 | |||||||
chr1:185165133 | G | A | 3 | a0003c0005t0003g0003 a0003c0005t0003g0245 a0003c0005t0003g0246 |
4 | HG02896.hp2 HG02897.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.85-1439G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185165133 | |||||||
chr1:185165337 | A | G | 1 | a0003c0003t0001g0219 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.85-1235A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185165337 | |||||||
chr1:185165374 | C | T | 2 | a0003c0005t0001g0230 a0003c0005t0001g0231 |
2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.85-1198C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185165374 | |||||||
chr1:185165464 | T | C | 1 | a0003c0003t0001g0219 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.85-1108T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185165464 | |||||||
chr1:185165535 | C | T | 2 | a0003c0021t0011g0131 a0013c0022t0001g0008 |
2 | HG01884.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.85-1037C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185165535 | |||||||
chr1:185165739 | C | T | 3 | a0002c0002t0001g0216 a0002c0002t0001g0217 a0002c0002t0001g0218 |
3 | NA18961.hp2 NA19083.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.85-833C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185165739 | |||||||
chr1:185165800 | G | A | 1 | a0002c0004t0001g0296 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.85-772G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185165800 | |||||||
chr1:185165920 | C | T | 1 | a0002c0004t0001g0087 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.85-652C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185165920 | |||||||
chr1:185166121 | C | A | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.85-451C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185166121 | |||||||
chr1:185166309 | A | G | 9 | a0003c0005t0004g0006 a0003c0005t0004g0007 a0003c0005t0004g0229 others(6): Show |
9 | HG01891.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.85-263A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185166309 | |||||||
chr1:185166436 | C | G | 1 | a0015c0016t0001g0017 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.85-136C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185166436 | |||||||
chr1:185166916 | A | T | 1 | a0002c0002t0001g0272 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.165+264A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 3/18 | chr1 | 185166916 | |||||||
chr1:185166918 | T | A | 52 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0002c0004t0001g0009 others(49): Show |
53 | HG01167.hp2 HG01169.hp1 HG01255.hp1 others(50): Show |
intron_variant | MODIFIER | c.165+266T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 3/18 | chr1 | 185166918 | |||||||
chr1:185167167 | C | T | 47 | a0002c0004t0001g0009 a0002c0004t0001g0288 a0002c0004t0001g0291 others(44): Show |
48 | HG01167.hp2 HG01169.hp1 HG01255.hp1 others(45): Show |
intron_variant | MODIFIER | c.165+515C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 3/18 | chr1 | 185167167 | |||||||
chr1:185167226 | A | G | 9 | a0003c0005t0004g0006 a0003c0005t0004g0007 a0003c0005t0004g0229 others(6): Show |
9 | HG01891.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.165+574A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 3/18 | chr1 | 185167226 | |||||||
chr1:185167232 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.165+580A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 3/18 | chr1 | 185167232 | |||||||
chr1:185167326 | C | A | 184 | a0001c0011t0001g0148 a0001c0011t0001g0157 a0001c0011t0001g0160 others(181): Show |
186 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.165+674C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 3/18 | chr1 | 185167326 | |||||||
chr1:185167366 | G | A | 3 | a0007c0012t0001g0018 a0007c0012t0001g0019 a0007c0012t0001g0020 |
3 | HG02145.hp2 HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.165+714G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 3/18 | chr1 | 185167366 | |||||||
chr1:185167417 | T | C | 9 | a0003c0005t0004g0006 a0003c0005t0004g0007 a0003c0005t0004g0229 others(6): Show |
9 | HG01891.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.165+765T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 3/18 | chr1 | 185167417 | |||||||
chr1:185167695 | C | A | 1 | a0002c0002t0001g0135 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.166-645C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 3/18 | chr1 | 185167695 | |||||||
chr1:185167872 | T | G | 1 | a0002c0002t0001g0156 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.166-468T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 3/18 | chr1 | 185167872 | |||||||
chr1:185168234 | G | A | 1 | a0001c0011t0008g0260 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.166-106G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 3/18 | chr1 | 185168234 | |||||||
chr1:185168322 | T | TAAATGAT others(4): Show |
203 | a0001c0001t0001g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(200): Show |
205 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.166-18_166-17insAA others(9): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 3/18 | chr1 | 185168322 | |||||||
chr1:185168329 | A | T | 203 | a0001c0001t0001g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(200): Show |
205 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.166-11A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 3/18 | chr1 | 185168329 | |||||||
chr1:185168332 | T | TAA | 203 | a0001c0001t0001g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(200): Show |
205 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(202): Show |
splice_region_variant&intron_variant | LOW | c.166-7_166-6insAA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr1 | 185168332 | ||||||
chr1:185168453 | A | G | 1 | a0001c0001t0001g0005 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.224+55A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185168453 | |||||||
chr1:185168496 | C | T | 203 | a0001c0001t0001g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(200): Show |
205 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.224+98C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185168496 | |||||||
chr1:185168541 | G | A | 2 | a0003c0005t0004g0264 a0003c0005t0004g0265 |
2 | HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.224+143G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185168541 | |||||||
chr1:185168889 | A | G | 18 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(15): Show |
18 | HG00438.hp1 HG02071.hp2 HG03654.hp1 others(15): Show |
intron_variant | MODIFIER | c.224+491A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185168889 | |||||||
chr1:185168937 | C | T | 2 | a0002c0002t0001g0214 a0002c0002t0001g0215 |
2 | HG02615.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.224+539C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185168937 | |||||||
chr1:185168973 | C | T | 2 | a0003c0005t0001g0230 a0003c0005t0001g0231 |
2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.224+575C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185168973 | |||||||
chr1:185169003 | T | A | 2 | a0001c0001t0001g0022 a0001c0001t0001g0023 |
2 | HG00438.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.224+605T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185169003 | |||||||
chr1:185169194 | G | T | 1 | a0002c0002t0001g0213 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.224+796G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185169194 | |||||||
chr1:185169196 | A | C | 2 | a0002c0004t0001g0009 a0002c0004t0001g0291 |
2 | HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.224+798A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185169196 | |||||||
chr1:185169227 | C | G | 2 | a0003c0005t0001g0230 a0003c0005t0001g0231 |
2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.224+829C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185169227 | |||||||
chr1:185169276 | A | G | 1 | a0002c0002t0001g0272 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.224+878A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185169276 | |||||||
chr1:185169279 | CT | C | 18 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0088 others(15): Show |
18 | HG00621.hp2 HG01123.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.224+898delT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 185169279 | ||||||
chr1:185169540 | A | G | 1 | a0003c0003t0001g0212 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.224+1142A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185169540 | |||||||
chr1:185169780 | AT | A | 19 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(16): Show |
19 | HG00438.hp1 HG02071.hp2 HG03486.hp2 others(16): Show |
intron_variant | MODIFIER | c.224+1397delT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 185169780 | ||||||
chr1:185170074 | C | T | 18 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(15): Show |
18 | HG00438.hp1 HG02071.hp2 HG03654.hp1 others(15): Show |
intron_variant | MODIFIER | c.224+1676C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185170074 | |||||||
chr1:185170183 | G | A | 1 | a0002c0004t0001g0296 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.224+1785G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185170183 | |||||||
chr1:185170221 | G | A | 47 | a0002c0004t0001g0009 a0002c0004t0001g0288 a0002c0004t0001g0291 others(44): Show |
48 | HG01167.hp2 HG01169.hp1 HG01255.hp1 others(45): Show |
intron_variant | MODIFIER | c.224+1823G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185170221 | |||||||
chr1:185170249 | T | C | 18 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(15): Show |
18 | HG00438.hp1 HG02071.hp2 HG03654.hp1 others(15): Show |
intron_variant | MODIFIER | c.224+1851T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185170249 | |||||||
chr1:185170400 | C | T | 1 | a0007c0010t0010g0085 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.224+2002C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185170400 | |||||||
chr1:185170402 | A | G | 1 | a0003c0005t0003g0227 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.224+2004A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185170402 | |||||||
chr1:185170519 | A | G | 1 | a0002c0002t0001g0218 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.224+2121A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185170519 | |||||||
chr1:185170732 | G | A | 320 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(317): Show |
323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.224+2334G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185170732 | |||||||
chr1:185170797 | C | T | 5 | a0003c0005t0001g0013 a0003c0005t0003g0227 a0007c0012t0001g0018 others(2): Show |
5 | HG02145.hp2 HG02895.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.224+2399C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185170797 | |||||||
chr1:185170830 | T | G | 1 | a0005c0007t0001g0322 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.224+2432T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185170830 | |||||||
chr1:185170971 | T | C | 1 | a0002c0004t0001g0296 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.224+2573T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185170971 | |||||||
chr1:185171160 | GA | G | 121 | a0001c0001t0001g0082 a0001c0001t0001g0122 a0001c0001t0002g0282 others(118): Show |
122 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.224+2774delA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 185171160 | ||||||
chr1:185171162 | A | G | 2 | a0003c0003t0001g0262 a0003c0003t0001g0263 |
2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.224+2764A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185171162 | |||||||
chr1:185171203 | G | A | 1 | a0002c0004t0001g0087 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.224+2805G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185171203 | |||||||
chr1:185171265 | G | C | 1 | a0006c0014t0001g0292 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.224+2867G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185171265 | |||||||
chr1:185171322 | C | A | 1 | a0001c0001t0002g0282 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.224+2924C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185171322 | |||||||
chr1:185171323 | A | T | 1 | a0001c0001t0002g0282 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.224+2925A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185171323 | |||||||
chr1:185171530 | A | G | 61 | a0001c0001t0001g0025 a0001c0001t0002g0121 a0002c0004t0001g0009 others(58): Show |
62 | HG01099.hp2 HG01167.hp2 HG01169.hp1 others(59): Show |
intron_variant | MODIFIER | c.225-2842A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185171530 | |||||||
chr1:185171609 | A | G | 12 | a0003c0005t0004g0006 a0003c0005t0004g0007 a0003c0005t0004g0229 others(9): Show |
12 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.225-2763A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185171609 | |||||||
chr1:185171663 | T | G | 3 | a0003c0005t0001g0230 a0003c0005t0001g0231 a0003c0005t0009g0004 |
3 | HG01243.hp1 HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.225-2709T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185171663 | |||||||
chr1:185171735 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.225-2637A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185171735 | |||||||
chr1:185171799 | A | G | 3 | a0003c0005t0003g0003 a0003c0005t0003g0245 a0003c0005t0003g0246 |
4 | HG02896.hp2 HG02897.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.225-2573A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185171799 | |||||||
chr1:185171981 | T | C | 1 | a0001c0001t0002g0121 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.225-2391T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185171981 | |||||||
chr1:185172183 | TC | T | 7 | a0002c0004t0001g0315 a0002c0004t0001g0316 a0002c0004t0001g0317 others(4): Show |
7 | NA18948.hp1 NA18967.hp1 NA18983.hp1 others(4): Show |
intron_variant | MODIFIER | c.225-2185delC | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 185172183 | ||||||
chr1:185172192 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.225-2180T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185172192 | |||||||
chr1:185172276 | G | T | 26 | a0003c0003t0001g0189 a0003c0003t0001g0190 a0003c0003t0001g0191 others(23): Show |
26 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.225-2096G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185172276 | |||||||
chr1:185172382 | T | C | 1 | a0004c0006t0001g0145 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.225-1990T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185172382 | |||||||
chr1:185172603 | G | C | 2 | a0001c0001t0001g0128 a0011c0018t0001g0028 |
2 | HG01069.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.225-1769G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185172603 | |||||||
chr1:185172695 | A | G | 161 | a0001c0001t0001g0081 a0002c0002t0001g0002 a0002c0002t0001g0135 others(158): Show |
163 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.225-1677A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185172695 | |||||||
chr1:185172711 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.225-1661C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185172711 | |||||||
chr1:185172831 | G | A | 2 | a0002c0004t0001g0299 a0002c0004t0001g0300 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.225-1541G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185172831 | |||||||
chr1:185173020 | G | A | 160 | a0001c0001t0001g0081 a0002c0002t0001g0002 a0002c0002t0001g0135 others(157): Show |
162 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.225-1352G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185173020 | |||||||
chr1:185173042 | C | CA | 160 | a0001c0001t0001g0030 a0001c0001t0001g0097 a0001c0001t0001g0122 others(157): Show |
162 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.225-1311dupA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 185173042 | ||||||
chr1:185173042 | C | CAA | 6 | a0001c0001t0001g0096 a0001c0001t0002g0010 a0001c0001t0002g0121 others(3): Show |
6 | HG01361.hp1 HG02074.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.225-1312_225-1311d others(4): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 185173042 | ||||||
chr1:185173200 | G | A | 179 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(176): Show |
181 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.225-1172G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185173200 | |||||||
chr1:185173376 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.225-996G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185173376 | |||||||
chr1:185173379 | T | C | 1 | a0001c0001t0001g0099 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.225-993T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185173379 | |||||||
chr1:185173412 | G | A | 3 | a0002c0002t0001g0135 a0002c0002t0001g0136 a0002c0002t0001g0255 |
3 | HG02451.hp2 HG02630.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.225-960G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185173412 | |||||||
chr1:185173456 | A | T | 40 | a0002c0002t0001g0214 a0002c0002t0001g0215 a0002c0004t0001g0009 others(37): Show |
40 | HG01167.hp2 HG01169.hp1 HG01255.hp1 others(37): Show |
intron_variant | MODIFIER | c.225-916A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185173456 | |||||||
chr1:185173492 | C | T | 1 | a0007c0012t0001g0020 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.225-880C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185173492 | |||||||
chr1:185173530 | C | CA | 11 | a0001c0001t0001g0022 a0001c0001t0001g0031 a0001c0001t0001g0032 others(8): Show |
11 | HG00597.hp2 HG01081.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.225-821dupA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 185173530 | ||||||
chr1:185173530 | CA | C | 46 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0029 others(43): Show |
47 | HG00438.hp1 HG01243.hp1 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.225-821delA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 185173530 | ||||||
chr1:185173530 | CAA | C | 128 | a0002c0002t0001g0002 a0002c0002t0001g0135 a0002c0002t0001g0136 others(125): Show |
129 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.225-822_225-821del others(2): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 185173530 | ||||||
chr1:185173582 | A | G | 1 | a0001c0001t0001g0081 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.225-790A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185173582 | |||||||
chr1:185173638 | T | C | 2 | a0003c0005t0001g0230 a0003c0005t0001g0231 |
2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.225-734T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185173638 | |||||||
chr1:185173681 | C | T | 2 | a0002c0004t0001g0313 a0002c0004t0001g0314 |
2 | HG02040.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.225-691C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185173681 | |||||||
chr1:185173738 | G | A | 2 | a0003c0005t0001g0230 a0003c0005t0001g0231 |
2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.225-634G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185173738 | |||||||
chr1:185175202 | G | GT | 19 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0002g0029 others(16): Show |
19 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(16): Show |
intron_variant | MODIFIER | c.966+104dupT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr1 | 185175202 | ||||||
chr1:185175202 | GT | G | 8 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0003c0003t0001g0154 others(5): Show |
8 | HG02559.hp1 HG02615.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.966+104delT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr1 | 185175202 | ||||||
chr1:185175215 | T | G | 168 | a0001c0001t0001g0021 a0001c0001t0001g0030 a0001c0001t0001g0035 others(165): Show |
170 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.966+102T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185175215 | |||||||
chr1:185175215 | T | TG | 4 | a0001c0001t0002g0283 a0002c0002t0001g0216 a0002c0002t0001g0217 others(1): Show |
4 | NA18961.hp2 NA19001.hp1 NA19083.hp2 others(1): Show |
intron_variant | MODIFIER | c.966+102_966+103ins others(1): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185175215 | |||||||
chr1:185175228 | G | T | 2 | a0003c0005t0001g0230 a0003c0005t0001g0231 |
2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.966+115G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185175228 | |||||||
chr1:185175381 | C | T | 1 | a0002c0002t0001g0255 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.966+268C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185175381 | |||||||
chr1:185175414 | A | T | 2 | a0001c0001t0001g0079 a0004c0009t0001g0080 |
2 | NA18954.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.966+301A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185175414 | |||||||
chr1:185175496 | G | A | 1 | a0006c0008t0003g0243 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.966+383G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185175496 | |||||||
chr1:185175507 | C | T | 1 | a0007c0012t0001g0018 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.966+394C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185175507 | |||||||
chr1:185175522 | A | G | 14 | a0003c0005t0001g0013 a0003c0005t0003g0227 a0003c0005t0004g0006 others(11): Show |
14 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.966+409A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185175522 | |||||||
chr1:185175616 | C | A | 4 | a0001c0001t0001g0005 a0007c0012t0001g0018 a0007c0012t0001g0019 others(1): Show |
4 | HG02145.hp2 HG02615.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.966+503C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185175616 | |||||||
chr1:185175752 | C | CAG | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.966+639_966+640ins others(2): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185175752 | |||||||
chr1:185175826 | A | G | 1 | a0003c0003t0001g0210 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.966+713A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185175826 | |||||||
chr1:185176286 | CA | C | 173 | a0001c0001t0001g0015 a0001c0001t0001g0021 a0001c0001t0001g0030 others(170): Show |
174 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.966+1201delA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr1 | 185176286 | ||||||
chr1:185176286 | CAA | C | 42 | a0001c0001t0001g0119 a0001c0001t0001g0128 a0001c0001t0002g0011 others(39): Show |
42 | HG00438.hp1 HG01167.hp1 HG01167.hp2 others(39): Show |
intron_variant | MODIFIER | c.966+1200_966+1201d others(4): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr1 | 185176286 | ||||||
chr1:185176286 | CAAAAAAA others(6): Show |
C | 1 | a0004c0006t0001g0166 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.966+1189_966+1201d others(15): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr1 | 185176286 | ||||||
chr1:185176286 | CAAAAAAA others(8): Show |
C | 24 | a0003c0003t0001g0189 a0003c0003t0001g0190 a0003c0003t0001g0191 others(21): Show |
24 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.966+1187_966+1201d others(17): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr1 | 185176286 | ||||||
chr1:185176347 | AAC | A | 9 | a0003c0005t0004g0006 a0003c0005t0004g0007 a0003c0005t0004g0229 others(6): Show |
9 | HG01891.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.966+1236_966+1237d others(4): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr1 | 185176347 | ||||||
chr1:185176385 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.966+1272G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185176385 | |||||||
chr1:185176798 | C | T | 3 | a0007c0012t0001g0018 a0007c0012t0001g0019 a0007c0012t0001g0020 |
3 | HG02145.hp2 HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.966+1685C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185176798 | |||||||
chr1:185176978 | C | T | 1 | a0003c0003t0001g0189 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.966+1865C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185176978 | |||||||
chr1:185176983 | T | TA | 107 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(104): Show |
108 | HG00323.hp2 HG00438.hp1 HG00639.hp1 others(105): Show |
intron_variant | MODIFIER | c.966+1888dupA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr1 | 185176983 | ||||||
chr1:185177266 | T | A | 3 | a0007c0012t0001g0018 a0007c0012t0001g0019 a0007c0012t0001g0020 |
3 | HG02145.hp2 HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.966+2153T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185177266 | |||||||
chr1:185177412 | T | A | 1 | a0003c0005t0004g0006 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.966+2299T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185177412 | |||||||
chr1:185177649 | T | C | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.966+2536T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185177649 | |||||||
chr1:185177653 | C | A | 11 | a0003c0005t0003g0003 a0003c0005t0003g0245 a0003c0005t0003g0246 others(8): Show |
12 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.966+2540C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185177653 | |||||||
chr1:185177804 | A | G | 1 | a0001c0001t0001g0134 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.967-2587A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185177804 | |||||||
chr1:185178142 | A | G | 179 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(176): Show |
181 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.967-2249A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185178142 | |||||||
chr1:185178162 | T | G | 1 | a0001c0001t0001g0005 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.967-2229T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185178162 | |||||||
chr1:185178207 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.967-2184T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185178207 | |||||||
chr1:185178410 | C | T | 1 | a0001c0001t0002g0290 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.967-1981C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185178410 | |||||||
chr1:185178466 | G | A | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.967-1925G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185178466 | |||||||
chr1:185178602 | T | C | 9 | a0003c0005t0004g0006 a0003c0005t0004g0007 a0003c0005t0004g0229 others(6): Show |
9 | HG01891.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.967-1789T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185178602 | |||||||
chr1:185178715 | T | A | 320 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(317): Show |
323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.967-1676T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185178715 | |||||||
chr1:185178737 | GCACTTCT others(43): Show |
G | 1 | a0012c0020t0001g0130 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.967-1653_967-1604d others(52): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185178737 | |||||||
chr1:185178828 | A | T | 11 | a0003c0005t0003g0003 a0003c0005t0003g0245 a0003c0005t0003g0246 others(8): Show |
12 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.967-1563A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185178828 | |||||||
chr1:185179140 | G | A | 2 | a0003c0003t0001g0154 a0003c0003t0001g0155 |
2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.967-1251G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185179140 | |||||||
chr1:185179255 | C | T | 1 | a0001c0001t0001g0005 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.967-1136C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185179255 | |||||||
chr1:185179367 | A | G | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.967-1024A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185179367 | |||||||
chr1:185179377 | C | T | 11 | a0003c0005t0003g0003 a0003c0005t0003g0245 a0003c0005t0003g0246 others(8): Show |
12 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.967-1014C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185179377 | |||||||
chr1:185179557 | A | G | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.967-834A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185179557 | |||||||
chr1:185179760 | T | G | 2 | a0003c0003t0001g0262 a0003c0003t0001g0263 |
2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.967-631T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185179760 | |||||||
chr1:185180004 | G | C | 1 | a0004c0006t0001g0147 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.967-387G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185180004 | |||||||
chr1:185180131 | T | C | 183 | a0001c0001t0001g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(180): Show |
185 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.967-260T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185180131 | |||||||
chr1:185180221 | A | G | 2 | a0006c0008t0003g0243 a0006c0008t0003g0244 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.967-170A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185180221 | |||||||
chr1:185180813 | A | T | 11 | a0003c0005t0003g0003 a0003c0005t0003g0245 a0003c0005t0003g0246 others(8): Show |
12 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1026+363A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 6/18 | chr1 | 185180813 | |||||||
chr1:185181478 | A | G | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1027-468A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 6/18 | chr1 | 185181478 | |||||||
chr1:185182246 | T | G | 28 | a0001c0001t0001g0015 a0001c0001t0001g0095 a0001c0001t0001g0096 others(25): Show |
28 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.1138+189T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | chr1 | 185182246 | |||||||
chr1:185182266 | G | C | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1138+209G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | chr1 | 185182266 | |||||||
chr1:185182379 | T | C | 1 | a0001c0001t0001g0124 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1138+322T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | chr1 | 185182379 | |||||||
chr1:185182538 | G | A | 91 | a0002c0002t0001g0002 a0002c0002t0001g0135 a0002c0002t0001g0136 others(88): Show |
92 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(89): Show |
intron_variant | MODIFIER | c.1138+481G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | chr1 | 185182538 | |||||||
chr1:185182664 | C | G | 4 | a0003c0003t0001g0154 a0003c0003t0001g0155 a0003c0003t0001g0211 others(1): Show |
4 | HG02559.hp1 HG02809.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1138+607C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | chr1 | 185182664 | |||||||
chr1:185182668 | CA | C | 136 | a0001c0001t0001g0059 a0001c0001t0002g0010 a0001c0001t0002g0011 others(133): Show |
137 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.1138+635delA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr1 | 185182668 | ||||||
chr1:185182668 | CAA | C | 39 | a0002c0002t0001g0215 a0002c0002t0001g0287 a0002c0004t0001g0300 others(36): Show |
39 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.1138+634_1138+635d others(4): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr1 | 185182668 | ||||||
chr1:185182689 | AAAAG | A | 7 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0038 others(4): Show |
7 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.1138+639_1138+642d others(6): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr1 | 185182689 | ||||||
chr1:185182862 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1138+805A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | chr1 | 185182862 | |||||||
chr1:185182873 | C | T | 4 | a0003c0003t0001g0154 a0003c0003t0001g0155 a0003c0003t0001g0211 others(1): Show |
4 | HG02559.hp1 HG02809.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1138+816C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | chr1 | 185182873 | |||||||
chr1:185182983 | A | G | 2 | a0002c0004t0001g0026 a0002c0004t0001g0027 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1138+926A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | chr1 | 185182983 | |||||||
chr1:185183028 | T | G | 3 | a0007c0012t0001g0018 a0007c0012t0001g0019 a0007c0012t0001g0020 |
3 | HG02145.hp2 HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1138+971T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | chr1 | 185183028 | |||||||
chr1:185183059 | C | A | 2 | a0003c0003t0001g0270 a0003c0003t0001g0271 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1138+1002C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | chr1 | 185183059 | |||||||
chr1:185183137 | CA | C | 18 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(15): Show |
18 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(15): Show |
intron_variant | MODIFIER | c.1139-1091delA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr1 | 185183137 | ||||||
chr1:185183287 | G | T | 9 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(6): Show |
9 | NA18949.hp2 NA18964.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.1139-956G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | chr1 | 185183287 | |||||||
chr1:185183318 | G | A | 137 | a0002c0002t0001g0002 a0002c0002t0001g0135 a0002c0002t0001g0136 others(134): Show |
138 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.1139-925G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | chr1 | 185183318 | |||||||
chr1:185183470 | C | A | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1139-773C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | chr1 | 185183470 | |||||||
chr1:185183527 | C | T | 1 | a0004c0006t0001g0147 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1139-716C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | chr1 | 185183527 | |||||||
chr1:185183634 | G | A | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1139-609G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | chr1 | 185183634 | |||||||
chr1:185183868 | A | G | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1139-375A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | chr1 | 185183868 | |||||||
chr1:185183945 | T | G | 1 | a0001c0001t0001g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1139-298T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | chr1 | 185183945 | |||||||
chr1:185183975 | C | T | 6 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(3): Show |
6 | NA18964.hp2 NA18972.hp1 NA19006.hp2 others(3): Show |
intron_variant | MODIFIER | c.1139-268C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | chr1 | 185183975 | |||||||
chr1:185184068 | C | T | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1139-175C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | chr1 | 185184068 | |||||||
chr1:185184070 | G | T | 1 | a0003c0003t0001g0263 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1139-173G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | chr1 | 185184070 | |||||||
chr1:185184413 | G | GT | 179 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(176): Show |
181 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.1240+69_1240+70ins others(1): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 8/18 | chr1 | 185184413 | |||||||
chr1:185184433 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1240+89A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 8/18 | chr1 | 185184433 | |||||||
chr1:185184514 | T | G | 1 | a0001c0001t0001g0062 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1240+170T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 8/18 | chr1 | 185184514 | |||||||
chr1:185184942 | T | G | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1429+11T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185184942 | |||||||
chr1:185184993 | T | C | 2 | a0003c0021t0011g0131 a0013c0022t0001g0008 |
2 | HG01884.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1429+62T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185184993 | |||||||
chr1:185185015 | T | C | 1 | a0001c0001t0001g0103 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1429+84T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185185015 | |||||||
chr1:185185191 | G | C | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1429+260G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185185191 | |||||||
chr1:185185217 | A | G | 11 | a0003c0005t0003g0003 a0003c0005t0003g0245 a0003c0005t0003g0246 others(8): Show |
12 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1429+286A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185185217 | |||||||
chr1:185185365 | T | C | 4 | a0001c0001t0001g0088 a0001c0001t0001g0091 a0001c0001t0001g0092 others(1): Show |
4 | HG01099.hp1 HG01256.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.1429+434T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185185365 | |||||||
chr1:185185996 | G | C | 11 | a0003c0005t0003g0003 a0003c0005t0003g0245 a0003c0005t0003g0246 others(8): Show |
12 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1429+1065G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185185996 | |||||||
chr1:185186139 | T | A | 4 | a0001c0001t0001g0015 a0001c0001t0001g0104 a0001c0001t0001g0105 others(1): Show |
4 | HG00140.hp1 HG01081.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.1429+1208T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185186139 | |||||||
chr1:185186383 | A | G | 1 | a0004c0006t0001g0144 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1429+1452A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185186383 | |||||||
chr1:185186418 | G | A | 2 | a0002c0004t0001g0009 a0002c0004t0001g0291 |
2 | HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1429+1487G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185186418 | |||||||
chr1:185186683 | G | A | 11 | a0003c0005t0003g0003 a0003c0005t0003g0245 a0003c0005t0003g0246 others(8): Show |
12 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1429+1752G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185186683 | |||||||
chr1:185186795 | C | T | 2 | a0001c0001t0002g0029 a0001c0001t0002g0276 |
2 | HG03654.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1429+1864C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185186795 | |||||||
chr1:185186916 | G | A | 2 | a0003c0003t0001g0262 a0003c0003t0001g0263 |
2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1429+1985G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185186916 | |||||||
chr1:185187029 | A | G | 33 | a0003c0003t0001g0189 a0003c0003t0001g0190 a0003c0003t0001g0191 others(30): Show |
33 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.1429+2098A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185187029 | |||||||
chr1:185187053 | C | CT | 283 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(280): Show |
286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.1429+2141dupT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 185187053 | ||||||
chr1:185187053 | C | CTT | 11 | a0001c0001t0001g0036 a0001c0011t0001g0148 a0001c0011t0008g0260 others(8): Show |
11 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1429+2140_1429+214 others(6): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 185187053 | ||||||
chr1:185187062 | T | TTTTTTTT others(288): Show |
15 | a0001c0001t0002g0012 a0001c0001t0002g0029 a0001c0001t0002g0273 others(12): Show |
15 | HG00438.hp1 HG02071.hp2 HG03654.hp1 others(12): Show |
intron_variant | MODIFIER | c.1429+2141_1429+214 others(299): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 185187062 | ||||||
chr1:185187062 | T | TTTTTTTT others(289): Show |
4 | a0001c0001t0002g0010 a0001c0001t0002g0121 a0001c0001t0002g0275 others(1): Show |
4 | HG02074.hp1 NA18949.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.1429+2141_1429+214 others(300): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 185187062 | ||||||
chr1:185187062 | T | TTTTTTTT others(290): Show |
1 | a0001c0001t0002g0011 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1429+2141_1429+214 others(301): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 185187062 | ||||||
chr1:185187073 | A | T | 28 | a0001c0001t0001g0021 a0003c0003t0001g0154 a0003c0003t0001g0155 others(25): Show |
28 | HG00738.hp2 HG01081.hp1 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.1429+2142A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185187073 | |||||||
chr1:185187241 | G | A | 1 | a0006c0014t0001g0294 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1429+2310G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185187241 | |||||||
chr1:185187248 | T | G | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1429+2317T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185187248 | |||||||
chr1:185187342 | G | A | 1 | a0013c0022t0001g0008 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1429+2411G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185187342 | |||||||
chr1:185187711 | T | G | 1 | a0003c0003t0001g0191 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1429+2780T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185187711 | |||||||
chr1:185187771 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1430-2778G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185187771 | |||||||
chr1:185187832 | G | A | 3 | a0001c0001t0001g0001 a0001c0001t0001g0040 a0001c0001t0001g0041 |
4 | HG00738.hp1 HG01261.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.1430-2717G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185187832 | |||||||
chr1:185187984 | C | T | 3 | a0007c0012t0001g0018 a0007c0012t0001g0019 a0007c0012t0001g0020 |
3 | HG02145.hp2 HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1430-2565C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185187984 | |||||||
chr1:185187999 | C | A | 183 | a0001c0001t0001g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(180): Show |
185 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.1430-2550C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185187999 | |||||||
chr1:185188050 | A | G | 1 | a0002c0002t0001g0150 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1430-2499A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185188050 | |||||||
chr1:185188172 | TCTTTATT others(7): Show |
T | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1430-2361_1430-234 others(18): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 185188172 | ||||||
chr1:185188227 | T | C | 1 | a0001c0001t0001g0102 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1430-2322T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185188227 | |||||||
chr1:185188337 | G | A | 2 | a0001c0001t0002g0279 a0001c0001t0002g0280 |
2 | NA18964.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1430-2212G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185188337 | |||||||
chr1:185188568 | T | C | 179 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(176): Show |
181 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.1430-1981T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185188568 | |||||||
chr1:185188633 | G | A | 2 | a0003c0003t0001g0154 a0003c0003t0001g0155 |
2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1430-1916G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185188633 | |||||||
chr1:185188710 | G | A | 5 | a0003c0005t0001g0013 a0003c0005t0003g0227 a0003c0005t0009g0004 others(2): Show |
5 | HG01884.hp2 HG02109.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1430-1839G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185188710 | |||||||
chr1:185188917 | A | G | 1 | a0006c0014t0001g0294 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1430-1632A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185188917 | |||||||
chr1:185189232 | C | T | 2 | a0001c0001t0001g0040 a0001c0001t0001g0041 |
2 | HG00738.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1430-1317C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185189232 | |||||||
chr1:185189422 | C | A | 24 | a0003c0003t0001g0189 a0003c0003t0001g0190 a0003c0003t0001g0191 others(21): Show |
24 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.1430-1127C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185189422 | |||||||
chr1:185190341 | A | G | 1 | a0002c0002t0001g0185 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1430-208A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185190341 | |||||||
chr1:185190862 | G | A | 1 | a0001c0001t0001g0042 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1523+220G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185190862 | |||||||
chr1:185190910 | C | A | 1 | a0001c0001t0001g0042 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1523+268C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185190910 | |||||||
chr1:185191023 | A | G | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1523+381A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185191023 | |||||||
chr1:185191067 | T | C | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1523+425T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185191067 | |||||||
chr1:185191255 | G | A | 5 | a0003c0005t0001g0013 a0003c0005t0003g0227 a0003c0005t0009g0004 others(2): Show |
5 | HG01884.hp2 HG02109.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1523+613G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185191255 | |||||||
chr1:185191304 | C | G | 1 | a0004c0006t0001g0162 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1523+662C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185191304 | |||||||
chr1:185191337 | T | A | 4 | a0003c0003t0001g0154 a0003c0003t0001g0155 a0003c0003t0001g0211 others(1): Show |
4 | HG02559.hp1 HG02809.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1523+695T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185191337 | |||||||
chr1:185191467 | T | C | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1523+825T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185191467 | |||||||
chr1:185191669 | T | C | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1523+1027T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185191669 | |||||||
chr1:185191744 | A | G | 1 | a0002c0004t0001g0310 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1523+1102A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185191744 | |||||||
chr1:185191805 | A | C | 1 | a0001c0001t0001g0005 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1523+1163A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185191805 | |||||||
chr1:185191857 | A | G | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1523+1215A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185191857 | |||||||
chr1:185191905 | C | A | 1 | a0004c0006t0001g0224 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1523+1263C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185191905 | |||||||
chr1:185192278 | C | T | 4 | a0001c0001t0001g0088 a0001c0001t0001g0091 a0001c0001t0001g0092 others(1): Show |
4 | HG01099.hp1 HG01256.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.1523+1636C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185192278 | |||||||
chr1:185192380 | G | T | 1 | a0003c0003t0001g0208 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1523+1738G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185192380 | |||||||
chr1:185192396 | C | T | 11 | a0003c0005t0003g0003 a0003c0005t0003g0245 a0003c0005t0003g0246 others(8): Show |
12 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1523+1754C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185192396 | |||||||
chr1:185192451 | T | C | 4 | a0003c0003t0001g0154 a0003c0003t0001g0155 a0003c0003t0001g0211 others(1): Show |
4 | HG02559.hp1 HG02809.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1523+1809T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185192451 | |||||||
chr1:185192535 | C | T | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1523+1893C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185192535 | |||||||
chr1:185192586 | C | G | 3 | a0007c0012t0001g0018 a0007c0012t0001g0019 a0007c0012t0001g0020 |
3 | HG02145.hp2 HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1523+1944C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185192586 | |||||||
chr1:185192738 | C | T | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1523+2096C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185192738 | |||||||
chr1:185192891 | G | A | 4 | a0003c0005t0003g0247 a0003c0005t0003g0248 a0003c0005t0003g0249 others(1): Show |
4 | HG02055.hp2 HG02723.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1523+2249G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185192891 | |||||||
chr1:185192925 | A | G | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1523+2283A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185192925 | |||||||
chr1:185193097 | G | A | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1523+2455G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185193097 | |||||||
chr1:185193462 | C | A | 2 | a0001c0001t0002g0029 a0001c0001t0002g0276 |
2 | HG03654.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1523+2820C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185193462 | |||||||
chr1:185193467 | C | CT | 17 | a0003c0005t0003g0003 a0003c0005t0003g0245 a0003c0005t0003g0246 others(14): Show |
18 | HG02055.hp2 HG02451.hp1 HG02647.hp1 others(15): Show |
intron_variant | MODIFIER | c.1523+2839dupT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr1 | 185193467 | ||||||
chr1:185193467 | C | CTT | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1523+2838_1523+283 others(6): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr1 | 185193467 | ||||||
chr1:185193472 | T | C | 4 | a0003c0003t0001g0154 a0003c0003t0001g0155 a0003c0003t0001g0211 others(1): Show |
4 | HG02559.hp1 HG02809.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1523+2830T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185193472 | |||||||
chr1:185193501 | T | C | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1523+2859T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185193501 | |||||||
chr1:185193562 | A | G | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1523+2920A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185193562 | |||||||
chr1:185193630 | A | G | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1523+2988A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185193630 | |||||||
chr1:185193657 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1523+3015G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185193657 | |||||||
chr1:185193687 | G | T | 131 | a0001c0001t0002g0121 a0001c0001t0002g0278 a0001c0011t0001g0148 others(128): Show |
132 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1523+3045G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185193687 | |||||||
chr1:185193751 | C | T | 1 | a0002c0002t0001g0184 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1523+3109C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185193751 | |||||||
chr1:185193963 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1523+3321T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185193963 | |||||||
chr1:185193969 | G | T | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1523+3327G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185193969 | |||||||
chr1:185194190 | A | G | 4 | a0003c0003t0001g0154 a0003c0003t0001g0155 a0003c0003t0001g0211 others(1): Show |
4 | HG02559.hp1 HG02809.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1523+3548A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185194190 | |||||||
chr1:185194324 | T | A | 1 | a0003c0021t0011g0131 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1523+3682T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185194324 | |||||||
chr1:185194366 | G | T | 178 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(175): Show |
180 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.1523+3724G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185194366 | |||||||
chr1:185194527 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1523+3885G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185194527 | |||||||
chr1:185194532 | T | TTGCTGTT others(12): Show |
1 | a0005c0007t0001g0312 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1523+3891_1523+390 others(23): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr1 | 185194532 | ||||||
chr1:185194571 | T | TAA | 18 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(15): Show |
18 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(15): Show |
intron_variant | MODIFIER | c.1523+3940_1523+394 others(6): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr1 | 185194571 | ||||||
chr1:185194576 | A | T | 1 | a0005c0007t0001g0312 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1523+3934A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185194576 | |||||||
chr1:185194577 | AAAAAAAG others(8): Show |
A | 1 | a0005c0007t0001g0312 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1523+3936_1523+395 others(19): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185194577 | |||||||
chr1:185194603 | T | G | 1 | a0005c0007t0001g0312 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1523+3961T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185194603 | |||||||
chr1:185194664 | A | G | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1523+4022A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185194664 | |||||||
chr1:185194752 | T | C | 2 | a0001c0001t0002g0029 a0001c0001t0002g0276 |
2 | HG03654.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1523+4110T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185194752 | |||||||
chr1:185194975 | C | A | 1 | a0001c0001t0001g0120 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1523+4333C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185194975 | |||||||
chr1:185195128 | C | G | 1 | a0007c0012t0001g0019 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1523+4486C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185195128 | |||||||
chr1:185195172 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1523+4530C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185195172 | |||||||
chr1:185195246 | G | A | 160 | a0002c0002t0001g0002 a0002c0002t0001g0135 a0002c0002t0001g0136 others(157): Show |
162 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.1523+4604G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185195246 | |||||||
chr1:185195447 | C | T | 2 | a0008c0017t0001g0075 a0008c0023t0001g0161 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1523+4805C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185195447 | |||||||
chr1:185195661 | T | A | 1 | a0001c0001t0001g0043 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1523+5019T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185195661 | |||||||
chr1:185195713 | C | A | 2 | a0003c0003t0001g0262 a0003c0003t0001g0263 |
2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1523+5071C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185195713 | |||||||
chr1:185195714 | A | G | 2 | a0003c0003t0001g0262 a0003c0003t0001g0263 |
2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1523+5072A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185195714 | |||||||
chr1:185195771 | T | C | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1523+5129T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185195771 | |||||||
chr1:185195785 | T | C | 1 | a0003c0003t0001g0236 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1523+5143T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185195785 | |||||||
chr1:185195843 | T | G | 1 | a0003c0005t0001g0013 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1523+5201T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185195843 | |||||||
chr1:185195978 | C | A | 1 | a0001c0001t0001g0044 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1523+5336C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185195978 | |||||||
chr1:185196085 | G | T | 1 | a0003c0003t0001g0208 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1523+5443G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185196085 | |||||||
chr1:185196133 | G | A | 2 | a0001c0001t0001g0079 a0004c0009t0001g0080 |
2 | NA18954.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1523+5491G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185196133 | |||||||
chr1:185196291 | T | A | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1523+5649T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185196291 | |||||||
chr1:185196323 | C | G | 1 | a0002c0002t0001g0185 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1523+5681C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185196323 | |||||||
chr1:185196408 | G | T | 1 | a0004c0009t0001g0060 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1523+5766G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185196408 | |||||||
chr1:185196725 | A | G | 2 | a0003c0003t0001g0154 a0003c0003t0001g0155 |
2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1524-5929A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185196725 | |||||||
chr1:185196842 | T | C | 1 | a0001c0001t0002g0289 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1524-5812T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185196842 | |||||||
chr1:185196996 | A | G | 4 | a0003c0003t0001g0154 a0003c0003t0001g0155 a0003c0003t0001g0211 others(1): Show |
4 | HG02559.hp1 HG02809.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1524-5658A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185196996 | |||||||
chr1:185197194 | G | A | 1 | a0002c0004t0001g0310 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1524-5460G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185197194 | |||||||
chr1:185197430 | T | TC | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1524-5224_1524-522 others(5): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185197430 | |||||||
chr1:185197484 | G | C | 1 | a0001c0001t0001g0076 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1524-5170G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185197484 | |||||||
chr1:185197534 | G | T | 4 | a0001c0001t0001g0005 a0007c0012t0001g0018 a0007c0012t0001g0019 others(1): Show |
4 | HG02145.hp2 HG02615.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1524-5120G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185197534 | |||||||
chr1:185197558 | T | C | 1 | a0001c0001t0006g0125 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1524-5096T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185197558 | |||||||
chr1:185197653 | A | G | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1524-5001A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185197653 | |||||||
chr1:185197685 | T | G | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1524-4969T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185197685 | |||||||
chr1:185197791 | T | C | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1524-4863T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185197791 | |||||||
chr1:185197819 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1524-4835T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185197819 | |||||||
chr1:185197879 | A | G | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | HG00597.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.1524-4775A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185197879 | |||||||
chr1:185198010 | C | T | 4 | a0007c0010t0001g0070 a0007c0010t0001g0071 a0007c0010t0001g0072 others(1): Show |
4 | HG02572.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1524-4644C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185198010 | |||||||
chr1:185198075 | A | G | 1 | a0003c0005t0003g0245 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1524-4579A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185198075 | |||||||
chr1:185198111 | G | A | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1524-4543G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185198111 | |||||||
chr1:185198213 | A | G | 1 | a0001c0001t0001g0023 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1524-4441A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185198213 | |||||||
chr1:185198224 | C | T | 1 | a0004c0006t0001g0145 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1524-4430C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185198224 | |||||||
chr1:185198236 | C | T | 1 | a0003c0005t0004g0266 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1524-4418C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185198236 | |||||||
chr1:185198326 | T | C | 1 | a0001c0001t0001g0005 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1524-4328T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185198326 | |||||||
chr1:185198352 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1524-4302C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185198352 | |||||||
chr1:185198626 | C | T | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1524-4028C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185198626 | |||||||
chr1:185198680 | G | C | 11 | a0003c0005t0003g0003 a0003c0005t0003g0245 a0003c0005t0003g0246 others(8): Show |
12 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1524-3974G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185198680 | |||||||
chr1:185198707 | C | T | 4 | a0003c0003t0001g0154 a0003c0003t0001g0155 a0003c0003t0001g0211 others(1): Show |
4 | HG02559.hp1 HG02809.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1524-3947C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185198707 | |||||||
chr1:185198752 | G | A | 1 | a0004c0006t0001g0152 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1524-3902G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185198752 | |||||||
chr1:185198762 | G | GT | 15 | a0001c0001t0001g0025 a0001c0001t0001g0058 a0002c0002t0001g0151 others(12): Show |
15 | HG01069.hp1 HG01071.hp1 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.1524-3880dupT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr1 | 185198762 | ||||||
chr1:185198775 | G | T | 12 | a0001c0001t0001g0133 a0003c0005t0003g0003 a0003c0005t0003g0245 others(9): Show |
13 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1524-3879G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185198775 | |||||||
chr1:185198863 | G | T | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1524-3791G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185198863 | |||||||
chr1:185198938 | AT | A | 8 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0002g0029 others(5): Show |
8 | HG00438.hp2 HG01884.hp2 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.1524-3698delT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr1 | 185198938 | ||||||
chr1:185198938 | ATT | A | 17 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(14): Show |
17 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.1524-3699_1524-369 others(6): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr1 | 185198938 | ||||||
chr1:185199094 | T | G | 11 | a0003c0005t0003g0003 a0003c0005t0003g0245 a0003c0005t0003g0246 others(8): Show |
12 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1524-3560T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185199094 | |||||||
chr1:185199128 | G | A | 5 | a0003c0005t0001g0013 a0003c0005t0003g0227 a0003c0005t0009g0004 others(2): Show |
5 | HG01884.hp2 HG02109.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1524-3526G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185199128 | |||||||
chr1:185199171 | C | T | 5 | a0004c0006t0001g0158 a0004c0006t0001g0165 a0004c0006t0001g0222 others(2): Show |
5 | HG01168.hp2 HG01169.hp2 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1524-3483C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185199171 | |||||||
chr1:185199383 | G | A | 1 | a0002c0002t0001g0217 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1524-3271G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185199383 | |||||||
chr1:185199435 | G | A | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1524-3219G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185199435 | |||||||
chr1:185199469 | G | A | 2 | a0003c0003t0001g0192 a0003c0003t0001g0193 |
2 | HG00408.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.1524-3185G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185199469 | |||||||
chr1:185199523 | T | G | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1524-3131T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185199523 | |||||||
chr1:185199625 | C | A | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1524-3029C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185199625 | |||||||
chr1:185199662 | C | T | 4 | a0001c0001t0001g0005 a0007c0012t0001g0018 a0007c0012t0001g0019 others(1): Show |
4 | HG02145.hp2 HG02615.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1524-2992C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185199662 | |||||||
chr1:185199831 | A | C | 2 | a0002c0004t0001g0009 a0002c0004t0001g0291 |
2 | HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1524-2823A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185199831 | |||||||
chr1:185199901 | C | T | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1524-2753C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185199901 | |||||||
chr1:185200041 | G | A | 81 | a0001c0001t0001g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(78): Show |
82 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.1524-2613G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185200041 | |||||||
chr1:185200317 | G | A | 4 | a0001c0001t0001g0097 a0001c0001t0001g0106 a0001c0001t0001g0107 others(1): Show |
4 | HG00621.hp2 HG01952.hp2 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.1524-2337G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185200317 | |||||||
chr1:185200531 | G | T | 1 | a0003c0005t0003g0227 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1524-2123G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185200531 | |||||||
chr1:185200595 | G | A | 4 | a0003c0003t0001g0154 a0003c0003t0001g0155 a0003c0003t0001g0211 others(1): Show |
4 | HG02559.hp1 HG02809.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1524-2059G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185200595 | |||||||
chr1:185200673 | G | T | 11 | a0003c0005t0003g0003 a0003c0005t0003g0245 a0003c0005t0003g0246 others(8): Show |
12 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1524-1981G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185200673 | |||||||
chr1:185200768 | C | G | 1 | a0001c0001t0001g0115 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1524-1886C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185200768 | |||||||
chr1:185200805 | G | C | 4 | a0003c0003t0001g0154 a0003c0003t0001g0155 a0003c0003t0001g0211 others(1): Show |
4 | HG02559.hp1 HG02809.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1524-1849G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185200805 | |||||||
chr1:185200809 | C | T | 11 | a0003c0005t0003g0003 a0003c0005t0003g0245 a0003c0005t0003g0246 others(8): Show |
12 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1524-1845C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185200809 | |||||||
chr1:185200864 | C | T | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1524-1790C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185200864 | |||||||
chr1:185201002 | C | T | 2 | a0001c0001t0005g0100 a0003c0005t0004g0007 |
2 | HG01081.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.1524-1652C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185201002 | |||||||
chr1:185201015 | C | T | 1 | a0009c0013t0001g0074 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1524-1639C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185201015 | |||||||
chr1:185201227 | T | C | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1524-1427T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185201227 | |||||||
chr1:185201230 | G | A | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1524-1424G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185201230 | |||||||
chr1:185201244 | C | T | 2 | a0004c0009t0001g0113 a0004c0009t0001g0114 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1524-1410C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185201244 | |||||||
chr1:185201285 | C | T | 1 | a0007c0010t0010g0085 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1524-1369C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185201285 | |||||||
chr1:185201342 | C | T | 139 | a0002c0002t0001g0002 a0002c0002t0001g0135 a0002c0002t0001g0136 others(136): Show |
140 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.1524-1312C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185201342 | |||||||
chr1:185201406 | C | T | 1 | a0001c0011t0008g0260 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1524-1248C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185201406 | |||||||
chr1:185201415 | G | A | 1 | a0003c0005t0003g0251 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1524-1239G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185201415 | |||||||
chr1:185201539 | G | A | 4 | a0003c0003t0001g0154 a0003c0003t0001g0155 a0003c0003t0001g0211 others(1): Show |
4 | HG02559.hp1 HG02809.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1524-1115G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185201539 | |||||||
chr1:185201696 | T | A | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1524-958T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185201696 | |||||||
chr1:185201706 | C | T | 2 | a0001c0001t0001g0057 a0001c0001t0001g0059 |
2 | NA18612.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1524-948C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185201706 | |||||||
chr1:185201785 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1524-869C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185201785 | |||||||
chr1:185201946 | AT | A | 11 | a0003c0005t0003g0003 a0003c0005t0003g0245 a0003c0005t0003g0246 others(8): Show |
12 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1524-698delT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr1 | 185201946 | ||||||
chr1:185202135 | A | G | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1524-519A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185202135 | |||||||
chr1:185202455 | T | TTA | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1524-184_1524-183d others(4): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr1 | 185202455 | ||||||
chr1:185202547 | G | A | 2 | a0003c0005t0001g0230 a0003c0005t0001g0231 |
2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1524-107G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185202547 | |||||||
chr1:185202816 | A | C | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1669+17A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 11/18 | chr1 | 185202816 | |||||||
chr1:185203240 | C | CCTT | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1669+443_1669+444i others(5): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr1 | 185203240 | ||||||
chr1:185203352 | A | G | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1669+553A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 11/18 | chr1 | 185203352 | |||||||
chr1:185203362 | G | C | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1669+563G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 11/18 | chr1 | 185203362 | |||||||
chr1:185203428 | G | A | 22 | a0003c0003t0001g0189 a0003c0003t0001g0190 a0003c0003t0001g0191 others(19): Show |
22 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.1669+629G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 11/18 | chr1 | 185203428 | |||||||
chr1:185203443 | C | A | 185 | a0001c0001t0001g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(182): Show |
187 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.1669+644C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 11/18 | chr1 | 185203443 | |||||||
chr1:185203482 | G | A | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1669+683G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 11/18 | chr1 | 185203482 | |||||||
chr1:185203616 | C | T | 51 | a0002c0002t0001g0002 a0002c0002t0001g0135 a0002c0002t0001g0136 others(48): Show |
52 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.1669+817C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 11/18 | chr1 | 185203616 | |||||||
chr1:185203648 | A | G | 5 | a0003c0005t0001g0013 a0003c0005t0003g0227 a0003c0005t0009g0004 others(2): Show |
5 | HG01884.hp2 HG02109.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1669+849A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 11/18 | chr1 | 185203648 | |||||||
chr1:185203905 | A | G | 139 | a0002c0002t0001g0002 a0002c0002t0001g0135 a0002c0002t0001g0136 others(136): Show |
140 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.1670-795A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 11/18 | chr1 | 185203905 | |||||||
chr1:185204058 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1670-642C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 11/18 | chr1 | 185204058 | |||||||
chr1:185204171 | G | A | 2 | a0002c0004t0001g0009 a0002c0004t0001g0291 |
2 | HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1670-529G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 11/18 | chr1 | 185204171 | |||||||
chr1:185204263 | C | T | 4 | a0001c0001t0001g0005 a0007c0012t0001g0018 a0007c0012t0001g0019 others(1): Show |
4 | HG02145.hp2 HG02615.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1670-437C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 11/18 | chr1 | 185204263 | |||||||
chr1:185204575 | T | G | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1670-125T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 11/18 | chr1 | 185204575 | |||||||
chr1:185204585 | A | G | 1 | a0012c0020t0001g0130 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1670-115A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 11/18 | chr1 | 185204585 | |||||||
chr1:185204986 | T | C | 1 | a0002c0002t0001g0170 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1833+123T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 12/18 | chr1 | 185204986 | |||||||
chr1:185205075 | A | T | 62 | a0001c0001t0001g0021 a0001c0001t0001g0030 a0001c0001t0001g0032 others(59): Show |
62 | HG00140.hp2 HG00280.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.1833+212A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 12/18 | chr1 | 185205075 | |||||||
chr1:185205078 | CAG | C | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1833+217_1833+218d others(4): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 185205078 | ||||||
chr1:185205390 | C | T | 1 | a0003c0005t0004g0269 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1833+527C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 12/18 | chr1 | 185205390 | |||||||
chr1:185205406 | T | C | 6 | a0003c0005t0003g0247 a0003c0005t0003g0248 a0003c0005t0003g0249 others(3): Show |
6 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1833+543T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 12/18 | chr1 | 185205406 | |||||||
chr1:185205709 | A | T | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1833+846A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 12/18 | chr1 | 185205709 | |||||||
chr1:185205717 | T | A | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1833+854T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 12/18 | chr1 | 185205717 | |||||||
chr1:185205729 | A | T | 1 | a0001c0001t0002g0273 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1833+866A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 12/18 | chr1 | 185205729 | |||||||
chr1:185205884 | C | T | 35 | a0003c0003t0001g0189 a0003c0003t0001g0190 a0003c0003t0001g0191 others(32): Show |
35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.1834-741C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 12/18 | chr1 | 185205884 | |||||||
chr1:185205980 | T | C | 1 | a0001c0001t0001g0081 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1834-645T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 12/18 | chr1 | 185205980 | |||||||
chr1:185206131 | G | T | 1 | a0001c0001t0001g0038 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1834-494G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 12/18 | chr1 | 185206131 | |||||||
chr1:185206228 | A | G | 1 | a0004c0006t0001g0222 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1834-397A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 12/18 | chr1 | 185206228 | |||||||
chr1:185206412 | C | T | 1 | a0003c0005t0003g0253 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1834-213C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 12/18 | chr1 | 185206412 | |||||||
chr1:185206772 | C | G | 2 | a0003c0021t0011g0131 a0013c0022t0001g0008 |
2 | HG01884.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1972+9C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185206772 | |||||||
chr1:185206883 | A | G | 161 | a0002c0002t0001g0002 a0002c0002t0001g0135 a0002c0002t0001g0136 others(158): Show |
163 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.1972+120A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185206883 | |||||||
chr1:185207191 | G | C | 2 | a0002c0002t0001g0214 a0002c0002t0001g0215 |
2 | HG02615.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1972+428G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185207191 | |||||||
chr1:185207263 | G | A | 104 | a0002c0002t0001g0002 a0002c0002t0001g0135 a0002c0002t0001g0136 others(101): Show |
105 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(102): Show |
intron_variant | MODIFIER | c.1972+500G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185207263 | |||||||
chr1:185207373 | G | C | 1 | a0003c0003t0001g0211 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1972+610G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185207373 | |||||||
chr1:185207469 | A | G | 2 | a0009c0013t0001g0073 a0009c0013t0001g0074 |
2 | NA18977.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1972+706A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185207469 | |||||||
chr1:185207470 | A | C | 3 | a0007c0012t0001g0018 a0007c0012t0001g0019 a0007c0012t0001g0020 |
3 | HG02145.hp2 HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1972+707A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185207470 | |||||||
chr1:185207620 | G | A | 1 | a0007c0010t0010g0085 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1972+857G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185207620 | |||||||
chr1:185207761 | G | A | 1 | a0012c0020t0001g0130 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1972+998G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185207761 | |||||||
chr1:185207849 | C | T | 36 | a0002c0002t0001g0002 a0002c0002t0001g0150 a0002c0002t0001g0151 others(33): Show |
37 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.1972+1086C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185207849 | |||||||
chr1:185208187 | A | G | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1972+1424A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185208187 | |||||||
chr1:185208248 | A | G | 1 | a0003c0003t0001g0206 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1972+1485A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185208248 | |||||||
chr1:185208379 | A | G | 1 | a0002c0002t0001g0216 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1972+1616A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185208379 | |||||||
chr1:185208392 | A | G | 1 | a0003c0021t0011g0131 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1972+1629A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185208392 | |||||||
chr1:185208649 | AAAGT | A | 11 | a0002c0004t0001g0288 a0002c0004t0001g0293 a0002c0004t0001g0302 others(8): Show |
11 | HG01255.hp1 HG01496.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.1972+1891_1972+189 others(8): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr1 | 185208649 | ||||||
chr1:185208652 | G | C | 1 | a0001c0011t0008g0260 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1972+1889G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185208652 | |||||||
chr1:185208659 | G | A | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1972+1896G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185208659 | |||||||
chr1:185208675 | C | T | 4 | a0001c0001t0001g0005 a0007c0012t0001g0018 a0007c0012t0001g0019 others(1): Show |
4 | HG02145.hp2 HG02615.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1972+1912C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185208675 | |||||||
chr1:185208726 | G | A | 2 | a0008c0017t0001g0075 a0008c0023t0001g0161 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1972+1963G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185208726 | |||||||
chr1:185208742 | C | CT | 74 | a0002c0002t0001g0002 a0002c0002t0001g0135 a0002c0002t0001g0136 others(71): Show |
75 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(72): Show |
intron_variant | MODIFIER | c.1972+1993dupT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr1 | 185208742 | ||||||
chr1:185208742 | C | CTT | 35 | a0003c0003t0001g0189 a0003c0003t0001g0190 a0003c0003t0001g0191 others(32): Show |
35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.1972+1992_1972+199 others(6): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr1 | 185208742 | ||||||
chr1:185208759 | T | A | 36 | a0002c0002t0001g0002 a0002c0002t0001g0150 a0002c0002t0001g0151 others(33): Show |
37 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.1972+1996T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185208759 | |||||||
chr1:185208783 | A | G | 24 | a0001c0011t0001g0148 a0004c0006t0001g0142 a0004c0006t0001g0143 others(21): Show |
24 | HG00738.hp2 HG01081.hp1 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.1972+2020A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185208783 | |||||||
chr1:185208811 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1972+2048G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185208811 | |||||||
chr1:185208938 | T | C | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1972+2175T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185208938 | |||||||
chr1:185208968 | CACTGTT | C | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1972+2210_1972+221 others(10): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr1 | 185208968 | ||||||
chr1:185209019 | G | A | 181 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(178): Show |
183 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.1972+2256G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185209019 | |||||||
chr1:185209303 | C | T | 11 | a0003c0005t0003g0003 a0003c0005t0003g0245 a0003c0005t0003g0246 others(8): Show |
12 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1972+2540C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185209303 | |||||||
chr1:185209319 | G | T | 1 | a0001c0001t0001g0119 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1972+2556G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185209319 | |||||||
chr1:185209323 | C | T | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1972+2560C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185209323 | |||||||
chr1:185209331 | A | C | 1 | a0003c0003t0001g0207 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1972+2568A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185209331 | |||||||
chr1:185209601 | C | A | 1 | a0013c0022t0001g0008 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1972+2838C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185209601 | |||||||
chr1:185209685 | A | C | 3 | a0001c0001t0001g0001 a0001c0001t0001g0040 a0001c0001t0001g0041 |
4 | HG00738.hp1 HG01261.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.1972+2922A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185209685 | |||||||
chr1:185209727 | T | C | 1 | a0002c0004t0001g0313 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1972+2964T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185209727 | |||||||
chr1:185209730 | G | T | 5 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0054 others(2): Show |
5 | HG02165.hp2 NA18612.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.1972+2967G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185209730 | |||||||
chr1:185209800 | A | C | 161 | a0002c0002t0001g0002 a0002c0002t0001g0135 a0002c0002t0001g0136 others(158): Show |
163 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.1972+3037A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185209800 | |||||||
chr1:185209934 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1972+3171G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185209934 | |||||||
chr1:185210334 | C | T | 3 | a0007c0012t0001g0018 a0007c0012t0001g0019 a0007c0012t0001g0020 |
3 | HG02145.hp2 HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1972+3571C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185210334 | |||||||
chr1:185210420 | G | A | 2 | a0008c0017t0001g0075 a0008c0023t0001g0161 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1972+3657G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185210420 | |||||||
chr1:185210545 | A | G | 1 | a0003c0003t0004g0233 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1972+3782A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185210545 | |||||||
chr1:185210617 | T | G | 1 | a0001c0001t0001g0024 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1972+3854T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185210617 | |||||||
chr1:185210631 | C | A | 1 | a0003c0005t0003g0227 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1972+3868C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185210631 | |||||||
chr1:185210781 | G | A | 1 | a0001c0001t0002g0029 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1973-3726G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185210781 | |||||||
chr1:185211020 | C | CCGCT | 93 | a0002c0002t0001g0002 a0002c0002t0001g0135 a0002c0002t0001g0136 others(90): Show |
94 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(91): Show |
intron_variant | MODIFIER | c.1973-3486_1973-348 others(8): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr1 | 185211020 | ||||||
chr1:185211339 | A | G | 1 | a0001c0001t0001g0021 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1973-3168A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185211339 | |||||||
chr1:185211412 | C | T | 11 | a0003c0005t0003g0003 a0003c0005t0003g0245 a0003c0005t0003g0246 others(8): Show |
12 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1973-3095C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185211412 | |||||||
chr1:185211431 | A | G | 1 | a0002c0002t0001g0182 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1973-3076A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185211431 | |||||||
chr1:185211769 | T | C | 1 | a0002c0002t0001g0186 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1973-2738T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185211769 | |||||||
chr1:185211990 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1973-2517G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185211990 | |||||||
chr1:185212015 | G | A | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1973-2492G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185212015 | |||||||
chr1:185212352 | C | G | 161 | a0002c0002t0001g0002 a0002c0002t0001g0135 a0002c0002t0001g0136 others(158): Show |
163 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.1973-2155C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185212352 | |||||||
chr1:185212376 | A | C | 5 | a0003c0005t0004g0264 a0003c0005t0004g0265 a0003c0005t0004g0267 others(2): Show |
5 | HG02647.hp1 HG02717.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1973-2131A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185212376 | |||||||
chr1:185212382 | G | T | 5 | a0003c0005t0004g0264 a0003c0005t0004g0265 a0003c0005t0004g0267 others(2): Show |
5 | HG02647.hp1 HG02717.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1973-2125G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185212382 | |||||||
chr1:185212395 | C | T | 11 | a0003c0005t0003g0003 a0003c0005t0003g0245 a0003c0005t0003g0246 others(8): Show |
12 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1973-2112C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185212395 | |||||||
chr1:185212407 | G | A | 2 | a0002c0002t0001g0172 a0002c0002t0001g0173 |
2 | NA18971.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1973-2100G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185212407 | |||||||
chr1:185212539 | G | A | 1 | a0003c0005t0003g0247 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1973-1968G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185212539 | |||||||
chr1:185212589 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1973-1918C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185212589 | |||||||
chr1:185212608 | G | A | 1 | a0011c0018t0001g0028 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1973-1899G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185212608 | |||||||
chr1:185212695 | C | T | 1 | a0003c0003t0001g0208 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1973-1812C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185212695 | |||||||
chr1:185212725 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1973-1782C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185212725 | |||||||
chr1:185212803 | C | CA | 153 | a0001c0001t0001g0102 a0002c0002t0001g0002 a0002c0002t0001g0135 others(150): Show |
155 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.1973-1689dupA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr1 | 185212803 | ||||||
chr1:185212803 | C | CAA | 9 | a0002c0004t0001g0302 a0002c0004t0001g0317 a0003c0003t0001g0189 others(6): Show |
9 | HG01928.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1973-1690_1973-168 others(6): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr1 | 185212803 | ||||||
chr1:185212817 | A | AAAT | 19 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0029 others(16): Show |
19 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(16): Show |
intron_variant | MODIFIER | c.1973-1689_1973-168 others(7): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr1 | 185212817 | ||||||
chr1:185213086 | C | G | 1 | a0001c0001t0001g0056 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1973-1421C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185213086 | |||||||
chr1:185213138 | CT | C | 10 | a0005c0007t0001g0241 a0005c0007t0001g0242 a0005c0007t0001g0295 others(7): Show |
10 | NA18941.hp1 NA18970.hp1 NA18989.hp1 others(7): Show |
intron_variant | MODIFIER | c.1973-1365delT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr1 | 185213138 | ||||||
chr1:185213205 | G | T | 1 | a0001c0001t0001g0005 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1973-1302G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185213205 | |||||||
chr1:185213555 | A | G | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1973-952A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185213555 | |||||||
chr1:185213750 | A | ATTAG | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1973-754_1973-753i others(6): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr1 | 185213750 | ||||||
chr1:185213917 | A | G | 1 | a0001c0001t0002g0276 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1973-590A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185213917 | |||||||
chr1:185214166 | C | A | 2 | a0003c0003t0001g0191 a0003c0003t0001g0194 |
2 | NA18977.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1973-341C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185214166 | |||||||
chr1:185214169 | C | T | 2 | a0003c0003t0001g0191 a0003c0003t0001g0194 |
2 | NA18977.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1973-338C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185214169 | |||||||
chr1:185214269 | G | A | 1 | a0002c0002t0001g0272 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1973-238G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185214269 | |||||||
chr1:185214698 | A | G | 1 | a0001c0001t0001g0005 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2121+43A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185214698 | |||||||
chr1:185214743 | T | C | 2 | a0001c0001t0002g0029 a0001c0001t0002g0276 |
2 | HG03654.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2121+88T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185214743 | |||||||
chr1:185214776 | G | A | 21 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(18): Show |
21 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2121+121G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185214776 | |||||||
chr1:185214840 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2121+185C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185214840 | |||||||
chr1:185215029 | T | C | 14 | a0002c0004t0001g0296 a0002c0004t0001g0301 a0002c0004t0001g0307 others(11): Show |
14 | HG03688.hp2 HG04228.hp2 NA18612.hp1 others(11): Show |
intron_variant | MODIFIER | c.2121+374T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185215029 | |||||||
chr1:185215101 | T | C | 162 | a0002c0002t0001g0002 a0002c0002t0001g0135 a0002c0002t0001g0136 others(159): Show |
164 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.2121+446T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185215101 | |||||||
chr1:185215104 | C | T | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2121+449C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185215104 | |||||||
chr1:185215383 | A | G | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2121+728A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185215383 | |||||||
chr1:185215559 | A | T | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2121+904A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185215559 | |||||||
chr1:185215587 | C | T | 2 | a0002c0002t0001g0135 a0002c0002t0001g0136 |
2 | HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2121+932C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185215587 | |||||||
chr1:185215678 | A | G | 2 | a0002c0004t0001g0299 a0002c0004t0001g0300 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2121+1023A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185215678 | |||||||
chr1:185215691 | C | T | 157 | a0001c0011t0001g0148 a0002c0002t0001g0002 a0002c0002t0001g0135 others(154): Show |
159 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.2121+1036C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185215691 | |||||||
chr1:185215765 | C | T | 2 | a0004c0009t0001g0113 a0004c0009t0001g0114 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2121+1110C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185215765 | |||||||
chr1:185215806 | T | C | 1 | a0012c0020t0001g0130 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2121+1151T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185215806 | |||||||
chr1:185215922 | G | A | 5 | a0003c0005t0001g0013 a0003c0005t0003g0227 a0003c0005t0009g0004 others(2): Show |
5 | HG01884.hp2 HG02109.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2121+1267G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185215922 | |||||||
chr1:185215957 | T | G | 1 | a0002c0002t0001g0256 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2121+1302T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185215957 | |||||||
chr1:185215974 | C | CT | 4 | a0003c0003t0001g0154 a0003c0003t0001g0155 a0003c0003t0001g0211 others(1): Show |
4 | HG02559.hp1 HG02809.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.2121+1320dupT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr1 | 185215974 | ||||||
chr1:185216104 | C | CT | 11 | a0003c0003t0001g0234 a0003c0003t0001g0235 a0003c0003t0001g0236 others(8): Show |
11 | HG01099.hp2 HG02258.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.2121+1450dupT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr1 | 185216104 | ||||||
chr1:185216547 | C | T | 4 | a0003c0003t0001g0154 a0003c0003t0001g0155 a0003c0003t0001g0211 others(1): Show |
4 | HG02559.hp1 HG02809.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.2121+1892C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185216547 | |||||||
chr1:185216561 | A | G | 1 | a0003c0003t0001g0211 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2121+1906A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185216561 | |||||||
chr1:185216687 | C | T | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2121+2032C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185216687 | |||||||
chr1:185216831 | A | T | 1 | a0001c0001t0001g0034 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2121+2176A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185216831 | |||||||
chr1:185216951 | C | CA | 17 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(14): Show |
17 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.2121+2310dupA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr1 | 185216951 | ||||||
chr1:185216951 | CA | C | 13 | a0002c0004t0001g0291 a0002c0004t0001g0299 a0003c0003t0001g0235 others(10): Show |
13 | HG01099.hp2 HG01167.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2121+2310delA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr1 | 185216951 | ||||||
chr1:185216966 | G | A | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2121+2311G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185216966 | |||||||
chr1:185216968 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2121+2313A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185216968 | |||||||
chr1:185217017 | T | A | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2121+2362T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185217017 | |||||||
chr1:185217088 | A | G | 2 | a0003c0021t0011g0131 a0013c0022t0001g0008 |
2 | HG01884.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2121+2433A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185217088 | |||||||
chr1:185217266 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2121+2611G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185217266 | |||||||
chr1:185217302 | C | T | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2121+2647C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185217302 | |||||||
chr1:185217304 | A | G | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2121+2649A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185217304 | |||||||
chr1:185217369 | C | G | 2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | HG00140.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.2121+2714C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185217369 | |||||||
chr1:185217408 | T | C | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2121+2753T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185217408 | |||||||
chr1:185217419 | A | G | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2121+2764A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185217419 | |||||||
chr1:185217441 | C | T | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2121+2786C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185217441 | |||||||
chr1:185217743 | G | A | 2 | a0003c0005t0001g0230 a0003c0005t0001g0231 |
2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2121+3088G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185217743 | |||||||
chr1:185217869 | T | C | 1 | a0001c0001t0006g0125 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2121+3214T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185217869 | |||||||
chr1:185218069 | T | C | 1 | a0002c0002t0001g0218 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2121+3414T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185218069 | |||||||
chr1:185218265 | G | T | 2 | a0003c0003t0001g0154 a0003c0003t0001g0155 |
2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2122-3584G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185218265 | |||||||
chr1:185218289 | A | G | 1 | a0001c0001t0001g0062 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2122-3560A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185218289 | |||||||
chr1:185218404 | G | A | 4 | a0001c0001t0001g0088 a0001c0001t0001g0091 a0001c0001t0001g0092 others(1): Show |
4 | HG01099.hp1 HG01256.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.2122-3445G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185218404 | |||||||
chr1:185219576 | T | G | 1 | a0002c0002t0001g0215 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2122-2273T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185219576 | |||||||
chr1:185219635 | T | C | 24 | a0003c0003t0001g0189 a0003c0003t0001g0190 a0003c0003t0001g0191 others(21): Show |
24 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.2122-2214T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185219635 | |||||||
chr1:185219659 | G | C | 1 | a0001c0001t0001g0016 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2122-2190G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185219659 | |||||||
chr1:185219661 | T | C | 182 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(179): Show |
184 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.2122-2188T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185219661 | |||||||
chr1:185219980 | C | A | 2 | a0003c0005t0001g0230 a0003c0005t0001g0231 |
2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2122-1869C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185219980 | |||||||
chr1:185220138 | C | CA | 14 | a0001c0001t0001g0016 a0001c0001t0001g0023 a0001c0001t0001g0042 others(11): Show |
14 | HG00438.hp2 HG00558.hp1 HG00597.hp2 others(11): Show |
intron_variant | MODIFIER | c.2122-1685dupA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr1 | 185220138 | ||||||
chr1:185220138 | CA | C | 106 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0021 others(103): Show |
106 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.2122-1685delA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr1 | 185220138 | ||||||
chr1:185220138 | CAA | C | 148 | a0001c0001t0002g0011 a0001c0001t0002g0029 a0001c0001t0002g0121 others(145): Show |
150 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.2122-1686_2122-168 others(6): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr1 | 185220138 | ||||||
chr1:185220181 | T | C | 1 | a0001c0001t0001g0039 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2122-1668T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185220181 | |||||||
chr1:185220375 | A | G | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2122-1474A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185220375 | |||||||
chr1:185220479 | T | C | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2122-1370T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185220479 | |||||||
chr1:185220610 | T | G | 1 | a0001c0001t0001g0089 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2122-1239T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185220610 | |||||||
chr1:185220654 | A | G | 2 | a0001c0001t0001g0039 a0001c0001t0001g0102 |
2 | HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.2122-1195A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185220654 | |||||||
chr1:185220688 | T | C | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2122-1161T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185220688 | |||||||
chr1:185220746 | A | G | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2122-1103A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185220746 | |||||||
chr1:185220949 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2122-900G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185220949 | |||||||
chr1:185221010 | A | G | 5 | a0003c0005t0001g0013 a0003c0005t0003g0227 a0003c0005t0009g0004 others(2): Show |
5 | HG01884.hp2 HG02109.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2122-839A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185221010 | |||||||
chr1:185221040 | C | T | 1 | a0001c0001t0001g0062 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2122-809C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185221040 | |||||||
chr1:185221050 | G | GAC | 25 | a0001c0001t0001g0044 a0001c0001t0002g0010 a0001c0001t0002g0011 others(22): Show |
25 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(22): Show |
intron_variant | MODIFIER | c.2122-766_2122-765d others(4): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr1 | 185221050 | ||||||
chr1:185221050 | GAC | G | 98 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(95): Show |
99 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.2122-766_2122-765d others(4): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr1 | 185221050 | ||||||
chr1:185221050 | GACAC | G | 20 | a0001c0001t0001g0108 a0002c0002t0001g0151 a0003c0003t0001g0206 others(17): Show |
21 | HG00609.hp1 HG01515.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.2122-768_2122-765d others(6): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr1 | 185221050 | ||||||
chr1:185221050 | GACACAC | G | 139 | a0002c0002t0001g0002 a0002c0002t0001g0135 a0002c0002t0001g0136 others(136): Show |
140 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.2122-770_2122-765d others(8): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr1 | 185221050 | ||||||
chr1:185221050 | GACACACA others(3): Show |
G | 5 | a0002c0004t0001g0314 a0003c0003t0001g0195 a0003c0005t0001g0230 others(2): Show |
5 | HG01243.hp1 HG01884.hp1 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.2122-774_2122-765d others(12): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr1 | 185221050 | ||||||
chr1:185221083 | A | T | 4 | a0003c0003t0001g0154 a0003c0003t0001g0155 a0003c0003t0001g0211 others(1): Show |
4 | HG02559.hp1 HG02809.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.2122-766A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185221083 | |||||||
chr1:185221147 | G | T | 1 | a0003c0005t0004g0007 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2122-702G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185221147 | |||||||
chr1:185221436 | A | G | 4 | a0003c0003t0001g0154 a0003c0003t0001g0155 a0003c0003t0001g0211 others(1): Show |
4 | HG02559.hp1 HG02809.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.2122-413A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185221436 | |||||||
chr1:185221442 | A | AT | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2122-397dupT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr1 | 185221442 | ||||||
chr1:185221511 | G | A | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2122-338G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185221511 | |||||||
chr1:185221512 | C | A | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2122-337C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185221512 | |||||||
chr1:185221619 | C | T | 1 | a0003c0005t0003g0227 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2122-230C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185221619 | |||||||
chr1:185221678 | T | C | 7 | a0002c0002t0001g0187 a0002c0004t0001g0315 a0002c0004t0001g0316 others(4): Show |
7 | NA18948.hp2 NA18967.hp1 NA18983.hp1 others(4): Show |
intron_variant | MODIFIER | c.2122-171T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185221678 | |||||||
chr1:185222285 | G | T | 1 | a0001c0001t0001g0001 | 2 | HG01261.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.2309+249G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185222285 | |||||||
chr1:185222304 | A | G | 1 | a0012c0020t0001g0130 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2309+268A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185222304 | |||||||
chr1:185222366 | A | C | 2 | a0001c0001t0001g0111 a0001c0001t0001g0118 |
2 | HG00408.hp1 HG00544.hp1 |
intron_variant | MODIFIER | c.2309+330A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185222366 | |||||||
chr1:185222483 | G | A | 5 | a0003c0003t0001g0236 a0003c0003t0001g0237 a0003c0003t0001g0238 others(2): Show |
5 | HG01099.hp2 HG02258.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2309+447G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185222483 | |||||||
chr1:185222485 | G | C | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2309+449G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185222485 | |||||||
chr1:185222514 | C | T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0107 a0001c0001t0001g0123 |
3 | HG00558.hp1 HG01952.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.2309+478C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185222514 | |||||||
chr1:185222629 | A | G | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2309+593A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185222629 | |||||||
chr1:185222634 | G | A | 1 | a0004c0006t0001g0152 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2309+598G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185222634 | |||||||
chr1:185222638 | A | G | 2 | a0003c0005t0001g0013 a0003c0005t0003g0227 |
2 | HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2309+602A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185222638 | |||||||
chr1:185222762 | C | CA | 54 | a0001c0001t0001g0015 a0001c0001t0001g0025 a0001c0001t0001g0030 others(51): Show |
54 | HG00438.hp1 HG01106.hp2 HG01123.hp2 others(51): Show |
intron_variant | MODIFIER | c.2309+751dupA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185222762 | ||||||
chr1:185222762 | C | CAA | 38 | a0001c0001t0001g0108 a0003c0003t0001g0189 a0003c0003t0001g0190 others(35): Show |
39 | HG00323.hp1 HG00544.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.2309+750_2309+751d others(4): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185222762 | ||||||
chr1:185222762 | C | CAAA | 11 | a0003c0003t0001g0192 a0003c0003t0001g0193 a0003c0003t0001g0194 others(8): Show |
11 | HG00408.hp2 HG01106.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.2309+749_2309+751d others(5): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185222762 | ||||||
chr1:185222939 | C | T | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2309+903C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185222939 | |||||||
chr1:185222991 | T | A | 186 | a0001c0001t0001g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(183): Show |
188 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(185): Show |
intron_variant | MODIFIER | c.2309+955T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185222991 | |||||||
chr1:185223162 | T | C | 182 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(179): Show |
184 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.2309+1126T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185223162 | |||||||
chr1:185223279 | G | A | 26 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(23): Show |
26 | HG00140.hp2 HG00280.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.2309+1243G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185223279 | |||||||
chr1:185223470 | C | T | 4 | a0001c0001t0001g0032 a0001c0001t0001g0055 a0001c0001t0001g0077 others(1): Show |
4 | HG00140.hp2 HG00642.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.2309+1434C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185223470 | |||||||
chr1:185223471 | G | A | 1 | a0004c0006t0001g0152 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2309+1435G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185223471 | |||||||
chr1:185223722 | G | T | 2 | a0003c0005t0001g0230 a0003c0005t0001g0231 |
2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2309+1686G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185223722 | |||||||
chr1:185223815 | A | G | 4 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0052 others(1): Show |
4 | HG01168.hp1 HG01243.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.2309+1779A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185223815 | |||||||
chr1:185223895 | C | T | 3 | a0001c0001t0001g0005 a0003c0021t0011g0131 a0013c0022t0001g0008 |
3 | HG01884.hp2 HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2309+1859C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185223895 | |||||||
chr1:185224015 | G | A | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2309+1979G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185224015 | |||||||
chr1:185224322 | G | A | 24 | a0001c0011t0001g0148 a0004c0006t0001g0142 a0004c0006t0001g0143 others(21): Show |
24 | HG00738.hp2 HG01081.hp1 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.2309+2286G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185224322 | |||||||
chr1:185224399 | A | G | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2309+2363A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185224399 | |||||||
chr1:185224412 | A | G | 2 | a0003c0003t0001g0262 a0003c0003t0001g0263 |
2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2309+2376A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185224412 | |||||||
chr1:185224426 | C | T | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2309+2390C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185224426 | |||||||
chr1:185224492 | A | AT | 11 | a0003c0005t0003g0003 a0003c0005t0003g0245 a0003c0005t0003g0246 others(8): Show |
12 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.2309+2465dupT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185224492 | ||||||
chr1:185224555 | G | A | 1 | a0003c0003t0001g0193 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2309+2519G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185224555 | |||||||
chr1:185224692 | T | G | 2 | a0001c0001t0001g0034 a0001c0001t0001g0127 |
2 | HG00741.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.2309+2656T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185224692 | |||||||
chr1:185224858 | G | A | 6 | a0003c0005t0001g0013 a0003c0005t0003g0227 a0003c0005t0009g0004 others(3): Show |
6 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.2309+2822G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185224858 | |||||||
chr1:185224887 | C | T | 1 | a0001c0011t0008g0260 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2309+2851C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185224887 | |||||||
chr1:185225129 | G | A | 4 | a0003c0003t0001g0154 a0003c0003t0001g0155 a0003c0003t0001g0211 others(1): Show |
4 | HG02559.hp1 HG02809.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.2309+3093G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185225129 | |||||||
chr1:185225239 | C | G | 186 | a0001c0001t0001g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(183): Show |
188 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(185): Show |
intron_variant | MODIFIER | c.2309+3203C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185225239 | |||||||
chr1:185225277 | C | G | 104 | a0002c0002t0001g0002 a0002c0002t0001g0135 a0002c0002t0001g0136 others(101): Show |
105 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(102): Show |
intron_variant | MODIFIER | c.2309+3241C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185225277 | |||||||
chr1:185225467 | A | C | 1 | a0001c0001t0001g0048 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2309+3431A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185225467 | |||||||
chr1:185225548 | T | A | 4 | a0001c0001t0001g0005 a0007c0012t0001g0018 a0007c0012t0001g0019 others(1): Show |
4 | HG02145.hp2 HG02615.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2309+3512T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185225548 | |||||||
chr1:185225668 | G | C | 24 | a0003c0003t0001g0189 a0003c0003t0001g0190 a0003c0003t0001g0191 others(21): Show |
24 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.2309+3632G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185225668 | |||||||
chr1:185225832 | A | G | 1 | a0003c0003t0001g0205 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2309+3796A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185225832 | |||||||
chr1:185225909 | C | T | 1 | a0001c0001t0002g0273 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2309+3873C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185225909 | |||||||
chr1:185226357 | C | T | 2 | a0006c0008t0003g0243 a0006c0008t0003g0244 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2309+4321C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185226357 | |||||||
chr1:185226446 | C | T | 11 | a0003c0005t0003g0003 a0003c0005t0003g0245 a0003c0005t0003g0246 others(8): Show |
12 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.2309+4410C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185226446 | |||||||
chr1:185226679 | CA | C | 4 | a0003c0003t0001g0154 a0003c0003t0001g0155 a0003c0003t0001g0211 others(1): Show |
4 | HG02559.hp1 HG02809.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.2309+4648delA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185226679 | ||||||
chr1:185226732 | CT | C | 132 | a0001c0001t0001g0128 a0001c0001t0002g0273 a0001c0001t0002g0277 others(129): Show |
134 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(131): Show |
intron_variant | MODIFIER | c.2309+4712delT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185226732 | ||||||
chr1:185226732 | CTT | C | 35 | a0003c0003t0001g0189 a0003c0003t0001g0190 a0003c0003t0001g0191 others(32): Show |
35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2309+4711_2309+471 others(6): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185226732 | ||||||
chr1:185226821 | C | T | 162 | a0002c0002t0001g0002 a0002c0002t0001g0135 a0002c0002t0001g0136 others(159): Show |
164 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.2310-4756C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185226821 | |||||||
chr1:185226883 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2310-4694G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185226883 | |||||||
chr1:185226988 | C | T | 1 | a0004c0006t0001g0142 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2310-4589C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185226988 | |||||||
chr1:185227201 | A | T | 3 | a0007c0012t0001g0018 a0007c0012t0001g0019 a0007c0012t0001g0020 |
3 | HG02145.hp2 HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2310-4376A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185227201 | |||||||
chr1:185227247 | G | A | 1 | a0001c0001t0001g0044 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2310-4330G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185227247 | |||||||
chr1:185227429 | A | G | 35 | a0003c0003t0001g0189 a0003c0003t0001g0190 a0003c0003t0001g0191 others(32): Show |
35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2310-4148A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185227429 | |||||||
chr1:185227430 | G | A | 1 | a0003c0003t0001g0221 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2310-4147G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185227430 | |||||||
chr1:185227540 | G | A | 1 | a0006c0008t0001g0139 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2310-4037G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185227540 | |||||||
chr1:185227633 | C | T | 9 | a0003c0005t0004g0006 a0003c0005t0004g0007 a0003c0005t0004g0229 others(6): Show |
9 | HG01891.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.2310-3944C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185227633 | |||||||
chr1:185227634 | G | A | 11 | a0003c0005t0003g0003 a0003c0005t0003g0245 a0003c0005t0003g0246 others(8): Show |
12 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.2310-3943G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185227634 | |||||||
chr1:185227769 | G | A | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2310-3808G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185227769 | |||||||
chr1:185227854 | G | A | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2310-3723G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185227854 | |||||||
chr1:185227869 | T | C | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2310-3708T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185227869 | |||||||
chr1:185228016 | G | A | 3 | a0004c0006t0001g0159 a0004c0006t0001g0162 a0004c0006t0001g0166 |
3 | HG01192.hp2 HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2310-3561G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185228016 | |||||||
chr1:185228128 | G | A | 1 | a0001c0001t0001g0035 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2310-3449G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185228128 | |||||||
chr1:185228165 | ATG | A | 3 | a0003c0005t0003g0227 a0003c0005t0003g0251 a0003c0005t0003g0254 |
3 | HG03139.hp2 HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2310-3408_2310-340 others(6): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185228165 | ||||||
chr1:185228165 | ATGT | A | 11 | a0003c0003t0001g0234 a0003c0003t0001g0235 a0003c0003t0001g0236 others(8): Show |
11 | HG01099.hp2 HG02258.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.2310-3411_2310-340 others(7): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185228165 | |||||||
chr1:185228167 | G | GTATGTAT others(7): Show |
6 | a0001c0001t0002g0029 a0001c0001t0002g0275 a0001c0001t0002g0277 others(3): Show |
6 | HG00438.hp1 HG03704.hp2 NA18949.hp2 others(3): Show |
intron_variant | MODIFIER | c.2310-3409_2310-340 others(18): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185228167 | ||||||
chr1:185228167 | G | GTATGTAT others(9): Show |
6 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0121 others(3): Show |
6 | HG02071.hp2 HG02074.hp1 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.2310-3409_2310-340 others(20): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185228167 | ||||||
chr1:185228167 | G | GTATGTAT others(11): Show |
1 | a0001c0001t0002g0284 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2310-3409_2310-340 others(22): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185228167 | ||||||
chr1:185228167 | G | GTATGTAT others(13): Show |
2 | a0001c0001t0002g0276 a0001c0001t0002g0280 |
2 | HG03654.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.2310-3409_2310-340 others(24): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185228167 | ||||||
chr1:185228167 | G | GTATGTAT others(15): Show |
1 | a0001c0001t0002g0012 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2310-3409_2310-340 others(26): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185228167 | ||||||
chr1:185228167 | G | GTATGTAT others(17): Show |
2 | a0001c0001t0002g0279 a0001c0001t0002g0282 |
2 | NA18964.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.2310-3409_2310-340 others(28): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185228167 | ||||||
chr1:185228167 | G | GTATGTAT others(19): Show |
1 | a0001c0001t0002g0281 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2310-3409_2310-340 others(30): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185228167 | ||||||
chr1:185228167 | GTGTATA | G | 75 | a0002c0002t0001g0002 a0002c0002t0001g0137 a0002c0002t0001g0150 others(72): Show |
76 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(73): Show |
intron_variant | MODIFIER | c.2310-3408_2310-340 others(10): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185228167 | ||||||
chr1:185228169 | G | A | 89 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(86): Show |
90 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.2310-3408G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185228169 | |||||||
chr1:185228169 | G | GTA | 7 | a0001c0001t0001g0095 a0001c0001t0001g0106 a0001c0001t0001g0110 others(4): Show |
7 | HG00735.hp1 HG01496.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2310-3389_2310-338 others(6): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185228169 | ||||||
chr1:185228169 | G | GTATATAT others(3): Show |
1 | a0007c0012t0001g0018 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2310-3397_2310-338 others(14): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185228169 | ||||||
chr1:185228169 | G | GTATATAT others(5): Show |
1 | a0007c0012t0001g0020 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2310-3399_2310-338 others(16): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185228169 | ||||||
chr1:185228169 | G | GTATATAT others(9): Show |
1 | a0001c0001t0001g0005 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2310-3403_2310-338 others(20): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185228169 | ||||||
chr1:185228184 | TATATAC | T | 11 | a0003c0003t0001g0234 a0003c0003t0001g0235 a0003c0003t0001g0236 others(8): Show |
11 | HG01099.hp2 HG02258.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.2310-3387_2310-338 others(10): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185228184 | ||||||
chr1:185228190 | C | T | 120 | a0001c0001t0001g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(117): Show |
122 | HG00323.hp2 HG00438.hp1 HG00639.hp1 others(119): Show |
intron_variant | MODIFIER | c.2310-3387C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185228190 | |||||||
chr1:185228190 | CATATAT | C | 3 | a0002c0002t0001g0256 a0002c0002t0001g0257 a0002c0002t0001g0259 |
3 | HG02572.hp2 HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2310-3381_2310-337 others(10): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185228190 | ||||||
chr1:185228190 | CATATATA others(1): Show |
C | 51 | a0002c0002t0001g0214 a0002c0002t0001g0215 a0002c0004t0001g0009 others(48): Show |
51 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.2310-3383_2310-337 others(12): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185228190 | ||||||
chr1:185228196 | T | C | 1 | a0002c0002t0001g0258 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2310-3381T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185228196 | |||||||
chr1:185228198 | T | C | 97 | a0002c0002t0001g0002 a0002c0002t0001g0135 a0002c0002t0001g0136 others(94): Show |
99 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(96): Show |
intron_variant | MODIFIER | c.2310-3379T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185228198 | |||||||
chr1:185228198 | T | TAC | 4 | a0003c0005t0001g0013 a0003c0005t0003g0248 a0003c0005t0003g0252 others(1): Show |
4 | HG02055.hp2 HG02451.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2310-3378_2310-337 others(6): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185228198 | ||||||
chr1:185228200 | T | C | 153 | a0002c0002t0001g0002 a0002c0002t0001g0135 a0002c0002t0001g0136 others(150): Show |
155 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.2310-3377T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185228200 | |||||||
chr1:185228200 | T | TACAC | 3 | a0003c0005t0003g0247 a0003c0005t0003g0249 a0003c0005t0009g0004 |
3 | HG02109.hp2 HG02723.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2310-3375_2310-337 others(8): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185228200 | ||||||
chr1:185228200 | T | TATACAC | 3 | a0003c0005t0003g0245 a0003c0021t0011g0131 a0013c0022t0001g0008 |
3 | HG01884.hp2 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2310-3376_2310-337 others(10): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185228200 | ||||||
chr1:185228200 | T | TATATATA others(3): Show |
2 | a0003c0005t0001g0230 a0003c0005t0001g0231 |
2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2310-3376_2310-337 others(14): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185228200 | ||||||
chr1:185228200 | T | TATATATA others(7): Show |
1 | a0001c0001t0002g0274 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2310-3376_2310-337 others(18): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185228200 | ||||||
chr1:185228200 | T | TATATATA others(15): Show |
1 | a0012c0020t0001g0130 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2310-3376_2310-337 others(26): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185228200 | ||||||
chr1:185228229 | A | T | 1 | a0002c0002t0001g0220 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2310-3348A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185228229 | |||||||
chr1:185229010 | G | A | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2310-2567G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185229010 | |||||||
chr1:185229061 | T | A | 2 | a0003c0003t0001g0270 a0003c0003t0001g0271 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2310-2516T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185229061 | |||||||
chr1:185229076 | G | T | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2310-2501G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185229076 | |||||||
chr1:185229228 | G | A | 7 | a0004c0006t0001g0223 a0004c0006t0001g0224 a0004c0006t0001g0225 others(4): Show |
7 | HG02622.hp2 HG02630.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2310-2349G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185229228 | |||||||
chr1:185229494 | T | A | 1 | a0002c0002t0001g0167 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2310-2083T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185229494 | |||||||
chr1:185229659 | T | G | 1 | a0003c0003t0001g0207 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2310-1918T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185229659 | |||||||
chr1:185229735 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2310-1842G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185229735 | |||||||
chr1:185229866 | C | G | 9 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(6): Show |
9 | HG02071.hp2 HG02074.hp1 NA18964.hp2 others(6): Show |
intron_variant | MODIFIER | c.2310-1711C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185229866 | |||||||
chr1:185230018 | A | T | 35 | a0003c0003t0001g0189 a0003c0003t0001g0190 a0003c0003t0001g0191 others(32): Show |
35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2310-1559A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185230018 | |||||||
chr1:185230730 | T | TTG | 59 | a0001c0001t0001g0016 a0001c0001t0002g0010 a0001c0001t0002g0011 others(56): Show |
59 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.2310-825_2310-824d others(4): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185230730 | ||||||
chr1:185230833 | G | A | 1 | a0003c0003t0001g0211 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2310-744G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185230833 | |||||||
chr1:185230941 | G | T | 1 | a0003c0005t0003g0251 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2310-636G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185230941 | |||||||
chr1:185231001 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2310-576G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185231001 | |||||||
chr1:185231036 | G | A | 1 | a0002c0002t0001g0136 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2310-541G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185231036 | |||||||
chr1:185231113 | T | C | 15 | a0003c0003t0001g0234 a0003c0003t0001g0235 a0003c0003t0001g0236 others(12): Show |
15 | HG01099.hp2 HG01891.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.2310-464T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185231113 | |||||||
chr1:185231183 | A | G | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2310-394A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185231183 | |||||||
chr1:185231358 | T | C | 2 | a0003c0005t0001g0230 a0003c0005t0001g0231 |
2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2310-219T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185231358 | |||||||
chr1:185231396 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2310-181C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185231396 | |||||||
chr1:185231407 | T | A | 1 | a0001c0001t0002g0273 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2310-170T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185231407 | |||||||
chr1:185231416 | T | G | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2310-161T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185231416 | |||||||
chr1:185231772 | C | G | 1 | a0001c0001t0007g0094 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2441+64C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185231772 | |||||||
chr1:185231929 | T | C | 188 | a0001c0001t0001g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(185): Show |
190 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.2441+221T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185231929 | |||||||
chr1:185231942 | C | T | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+234C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185231942 | |||||||
chr1:185232166 | G | A | 3 | a0007c0012t0001g0018 a0007c0012t0001g0019 a0007c0012t0001g0020 |
3 | HG02145.hp2 HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2441+458G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185232166 | |||||||
chr1:185232291 | G | A | 1 | a0003c0003t0004g0232 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2441+583G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185232291 | |||||||
chr1:185232292 | T | G | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+584T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185232292 | |||||||
chr1:185232979 | C | G | 1 | a0003c0005t0003g0248 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2441+1271C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185232979 | |||||||
chr1:185233048 | T | C | 1 | a0001c0001t0001g0123 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2441+1340T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185233048 | |||||||
chr1:185233241 | C | CA | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+1539dupA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185233241 | ||||||
chr1:185233351 | T | C | 1 | a0006c0008t0001g0140 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2441+1643T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185233351 | |||||||
chr1:185233372 | A | G | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+1664A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185233372 | |||||||
chr1:185233709 | T | C | 2 | a0003c0003t0001g0196 a0003c0003t0001g0205 |
2 | HG01978.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.2441+2001T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185233709 | |||||||
chr1:185233813 | A | G | 184 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(181): Show |
186 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.2441+2105A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185233813 | |||||||
chr1:185233829 | C | T | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+2121C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185233829 | |||||||
chr1:185233892 | C | T | 4 | a0001c0001t0001g0005 a0007c0012t0001g0018 a0007c0012t0001g0019 others(1): Show |
4 | HG02145.hp2 HG02615.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2441+2184C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185233892 | |||||||
chr1:185233905 | A | G | 21 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(18): Show |
21 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2441+2197A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185233905 | |||||||
chr1:185233935 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2441+2227C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185233935 | |||||||
chr1:185233954 | A | C | 3 | a0003c0003t0001g0203 a0003c0003t0001g0204 a0003c0003t0001g0210 |
3 | HG01106.hp1 HG01192.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.2441+2246A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185233954 | |||||||
chr1:185234060 | G | A | 6 | a0003c0003t0001g0154 a0003c0003t0001g0155 a0003c0003t0001g0211 others(3): Show |
6 | HG02258.hp1 HG02559.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2441+2352G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185234060 | |||||||
chr1:185234082 | G | A | 2 | a0003c0003t0001g0262 a0003c0003t0001g0263 |
2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2441+2374G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185234082 | |||||||
chr1:185234463 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2441+2755G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185234463 | |||||||
chr1:185234593 | T | G | 61 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(58): Show |
61 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.2441+2885T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185234593 | |||||||
chr1:185234708 | G | A | 41 | a0001c0001t0004g0037 a0003c0003t0001g0154 a0003c0003t0001g0155 others(38): Show |
41 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.2441+3000G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185234708 | |||||||
chr1:185234769 | A | G | 1 | a0001c0001t0001g0063 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2441+3061A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185234769 | |||||||
chr1:185234901 | T | TA | 41 | a0001c0001t0004g0037 a0003c0003t0001g0154 a0003c0003t0001g0155 others(38): Show |
41 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.2441+3194dupA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185234901 | ||||||
chr1:185235171 | T | C | 7 | a0001c0001t0001g0128 a0007c0010t0001g0070 a0007c0010t0001g0071 others(4): Show |
7 | HG01069.hp2 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2441+3463T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185235171 | |||||||
chr1:185235201 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2441+3493C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185235201 | |||||||
chr1:185235259 | A | G | 1 | a0012c0020t0001g0130 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2441+3551A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185235259 | |||||||
chr1:185235407 | C | T | 3 | a0001c0001t0007g0094 a0003c0005t0009g0004 a0003c0021t0011g0131 |
3 | HG02109.hp2 HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2441+3699C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185235407 | |||||||
chr1:185235416 | T | A | 296 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0016 others(293): Show |
299 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.2441+3708T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185235416 | |||||||
chr1:185235422 | A | C | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+3714A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185235422 | |||||||
chr1:185235434 | G | T | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+3726G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185235434 | |||||||
chr1:185235437 | T | C | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+3729T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185235437 | |||||||
chr1:185235447 | G | A | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+3739G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185235447 | |||||||
chr1:185235452 | A | T | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+3744A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185235452 | |||||||
chr1:185235453 | G | A | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+3745G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185235453 | |||||||
chr1:185235584 | C | T | 1 | a0004c0006t0001g0146 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2441+3876C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185235584 | |||||||
chr1:185235592 | C | T | 1 | a0003c0021t0011g0131 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2441+3884C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185235592 | |||||||
chr1:185235706 | A | G | 1 | a0001c0001t0006g0125 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2441+3998A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185235706 | |||||||
chr1:185235731 | G | T | 1 | a0003c0003t0001g0196 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2441+4023G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185235731 | |||||||
chr1:185235808 | C | A | 3 | a0002c0002t0001g0216 a0002c0002t0001g0217 a0002c0002t0001g0218 |
3 | NA18961.hp2 NA19083.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.2441+4100C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185235808 | |||||||
chr1:185235957 | A | C | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+4249A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185235957 | |||||||
chr1:185236077 | G | A | 35 | a0001c0001t0004g0037 a0003c0003t0001g0189 a0003c0003t0001g0190 others(32): Show |
35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2441+4369G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185236077 | |||||||
chr1:185236153 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2441+4445G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185236153 | |||||||
chr1:185236252 | C | CAAAAAAT | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+4552_2441+455 others(11): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185236252 | ||||||
chr1:185236348 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2441+4640A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185236348 | |||||||
chr1:185236356 | G | T | 1 | a0001c0001t0001g0039 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2441+4648G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185236356 | |||||||
chr1:185236665 | A | C | 1 | a0006c0008t0003g0243 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2441+4957A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185236665 | |||||||
chr1:185236700 | A | C | 1 | a0001c0001t0001g0039 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2441+4992A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185236700 | |||||||
chr1:185236763 | C | G | 1 | a0001c0001t0001g0107 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2441+5055C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185236763 | |||||||
chr1:185236842 | T | C | 123 | a0001c0001t0007g0094 a0002c0002t0001g0002 a0002c0002t0001g0135 others(120): Show |
125 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(122): Show |
intron_variant | MODIFIER | c.2441+5134T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185236842 | |||||||
chr1:185236867 | A | G | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+5159A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185236867 | |||||||
chr1:185236868 | G | GA | 10 | a0001c0001t0004g0037 a0003c0005t0004g0006 a0003c0005t0004g0007 others(7): Show |
10 | HG01891.hp2 HG02280.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.2441+5167dupA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185236868 | ||||||
chr1:185237003 | A | G | 88 | a0002c0002t0001g0002 a0002c0002t0001g0135 a0002c0002t0001g0136 others(85): Show |
89 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(86): Show |
intron_variant | MODIFIER | c.2441+5295A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185237003 | |||||||
chr1:185237020 | A | G | 61 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(58): Show |
61 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.2441+5312A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185237020 | |||||||
chr1:185237188 | A | G | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+5480A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185237188 | |||||||
chr1:185237197 | C | T | 3 | a0007c0012t0001g0018 a0007c0012t0001g0019 a0007c0012t0001g0020 |
3 | HG02145.hp2 HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2441+5489C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185237197 | |||||||
chr1:185237235 | T | C | 2 | a0009c0013t0001g0073 a0009c0013t0001g0074 |
2 | NA18977.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.2441+5527T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185237235 | |||||||
chr1:185237252 | A | G | 188 | a0001c0001t0001g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(185): Show |
190 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.2441+5544A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185237252 | |||||||
chr1:185237282 | C | T | 15 | a0003c0003t0001g0234 a0003c0003t0001g0235 a0003c0003t0001g0236 others(12): Show |
15 | HG01099.hp2 HG01891.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.2441+5574C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185237282 | |||||||
chr1:185237381 | A | T | 1 | a0006c0008t0003g0243 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2441+5673A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185237381 | |||||||
chr1:185237699 | A | AAATAAT | 61 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(58): Show |
61 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.2441+5999_2441+600 others(10): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185237699 | ||||||
chr1:185237802 | A | G | 1 | a0001c0001t0001g0063 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2441+6094A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185237802 | |||||||
chr1:185238009 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2441+6301C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185238009 | |||||||
chr1:185238123 | A | T | 2 | a0001c0001t0001g0098 a0001c0001t0001g0101 |
2 | NA18942.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.2441+6415A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185238123 | |||||||
chr1:185238222 | G | A | 1 | a0007c0010t0010g0085 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2441+6514G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185238222 | |||||||
chr1:185238295 | T | A | 5 | a0001c0001t0001g0001 a0001c0001t0001g0040 a0001c0001t0001g0041 others(2): Show |
6 | HG00738.hp1 HG01074.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.2441+6587T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185238295 | |||||||
chr1:185238366 | G | T | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+6658G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185238366 | |||||||
chr1:185238431 | T | A | 1 | a0001c0001t0001g0005 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2441+6723T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185238431 | |||||||
chr1:185238733 | G | C | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+7025G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185238733 | |||||||
chr1:185238734 | G | T | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+7026G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185238734 | |||||||
chr1:185238752 | A | C | 2 | a0003c0003t0001g0154 a0003c0003t0001g0155 |
2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2441+7044A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185238752 | |||||||
chr1:185238834 | T | G | 103 | a0002c0002t0001g0002 a0002c0002t0001g0135 a0002c0002t0001g0136 others(100): Show |
104 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(101): Show |
intron_variant | MODIFIER | c.2441+7126T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185238834 | |||||||
chr1:185238863 | T | A | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+7155T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185238863 | |||||||
chr1:185238880 | T | A | 184 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(181): Show |
186 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.2441+7172T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185238880 | |||||||
chr1:185238989 | T | C | 1 | a0006c0008t0003g0243 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2441+7281T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185238989 | |||||||
chr1:185239056 | G | A | 1 | a0012c0020t0001g0130 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2441+7348G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185239056 | |||||||
chr1:185239086 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2441+7378C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185239086 | |||||||
chr1:185239088 | A | G | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+7380A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185239088 | |||||||
chr1:185239449 | C | T | 103 | a0002c0002t0001g0002 a0002c0002t0001g0135 a0002c0002t0001g0136 others(100): Show |
104 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(101): Show |
intron_variant | MODIFIER | c.2441+7741C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185239449 | |||||||
chr1:185239505 | A | G | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+7797A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185239505 | |||||||
chr1:185239569 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2441+7861A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185239569 | |||||||
chr1:185239607 | C | T | 2 | a0003c0005t0001g0230 a0003c0005t0001g0231 |
2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2441+7899C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185239607 | |||||||
chr1:185239613 | C | G | 1 | a0003c0005t0004g0266 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2441+7905C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185239613 | |||||||
chr1:185239629 | A | G | 24 | a0003c0003t0001g0189 a0003c0003t0001g0190 a0003c0003t0001g0191 others(21): Show |
24 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.2441+7921A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185239629 | |||||||
chr1:185240099 | T | G | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+8391T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185240099 | |||||||
chr1:185240224 | A | G | 1 | a0004c0006t0001g0143 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2441+8516A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185240224 | |||||||
chr1:185240340 | T | G | 3 | a0007c0012t0001g0018 a0007c0012t0001g0019 a0007c0012t0001g0020 |
3 | HG02145.hp2 HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2441+8632T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185240340 | |||||||
chr1:185240473 | A | T | 1 | a0001c0001t0001g0005 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2441+8765A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185240473 | |||||||
chr1:185240745 | A | G | 1 | a0001c0001t0001g0051 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2441+9037A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185240745 | |||||||
chr1:185240898 | A | T | 1 | a0007c0012t0001g0019 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2441+9190A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185240898 | |||||||
chr1:185241251 | C | G | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+9543C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185241251 | |||||||
chr1:185241549 | C | G | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+9841C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185241549 | |||||||
chr1:185241625 | C | A | 8 | a0002c0004t0001g0288 a0002c0004t0001g0293 a0002c0004t0001g0302 others(5): Show |
8 | HG01255.hp1 HG01496.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.2441+9917C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185241625 | |||||||
chr1:185241656 | C | G | 1 | a0004c0006t0001g0149 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2441+9948C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185241656 | |||||||
chr1:185241741 | T | A | 1 | a0005c0007t0001g0295 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2441+10033T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185241741 | |||||||
chr1:185241881 | A | C | 41 | a0001c0001t0004g0037 a0003c0003t0001g0154 a0003c0003t0001g0155 others(38): Show |
41 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.2441+10173A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185241881 | |||||||
chr1:185242033 | C | T | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+10325C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185242033 | |||||||
chr1:185242102 | G | A | 1 | a0002c0002t0001g0172 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2441+10394G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185242102 | |||||||
chr1:185242114 | G | A | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+10406G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185242114 | |||||||
chr1:185242138 | C | T | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+10430C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185242138 | |||||||
chr1:185242146 | G | A | 1 | a0001c0001t0001g0015 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2441+10438G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185242146 | |||||||
chr1:185242367 | A | G | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+10659A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185242367 | |||||||
chr1:185242402 | G | C | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+10694G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185242402 | |||||||
chr1:185242413 | A | G | 48 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0022 others(45): Show |
49 | HG00438.hp2 HG00558.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.2441+10705A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185242413 | |||||||
chr1:185242444 | G | A | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+10736G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185242444 | |||||||
chr1:185242445 | C | A | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+10737C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185242445 | |||||||
chr1:185242484 | T | A | 41 | a0001c0001t0004g0037 a0003c0003t0001g0154 a0003c0003t0001g0155 others(38): Show |
41 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.2441+10776T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185242484 | |||||||
chr1:185242532 | C | T | 1 | a0004c0006t0001g0146 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2441+10824C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185242532 | |||||||
chr1:185242637 | A | C | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+10929A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185242637 | |||||||
chr1:185242772 | CCTGA | C | 3 | a0007c0012t0001g0018 a0007c0012t0001g0019 a0007c0012t0001g0020 |
3 | HG02145.hp2 HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2441+11067_2441+11 others(10): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185242772 | ||||||
chr1:185242919 | A | G | 4 | a0003c0003t0001g0154 a0003c0003t0001g0155 a0003c0003t0001g0211 others(1): Show |
4 | HG02559.hp1 HG02809.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.2441+11211A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185242919 | |||||||
chr1:185243007 | G | T | 1 | a0001c0001t0001g0062 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2441+11299G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185243007 | |||||||
chr1:185243076 | A | G | 41 | a0001c0001t0004g0037 a0003c0003t0001g0154 a0003c0003t0001g0155 others(38): Show |
41 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.2441+11368A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185243076 | |||||||
chr1:185243146 | A | T | 1 | a0003c0003t0001g0202 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2441+11438A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185243146 | |||||||
chr1:185243151 | C | A | 1 | a0001c0001t0001g0122 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2441+11443C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185243151 | |||||||
chr1:185243169 | T | C | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+11461T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185243169 | |||||||
chr1:185243216 | C | G | 1 | a0003c0003t0001g0202 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2441+11508C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185243216 | |||||||
chr1:185243230 | T | C | 1 | a0003c0003t0001g0202 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2441+11522T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185243230 | |||||||
chr1:185243237 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2441+11529T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185243237 | |||||||
chr1:185243275 | A | G | 1 | a0002c0002t0001g0168 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2441+11567A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185243275 | |||||||
chr1:185243301 | G | A | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+11593G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185243301 | |||||||
chr1:185243354 | T | C | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+11646T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185243354 | |||||||
chr1:185243367 | C | T | 1 | a0003c0003t0001g0190 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2441+11659C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185243367 | |||||||
chr1:185243512 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2441+11804A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185243512 | |||||||
chr1:185243547 | T | G | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+11839T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185243547 | |||||||
chr1:185243554 | T | C | 186 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(183): Show |
188 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(185): Show |
intron_variant | MODIFIER | c.2441+11846T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185243554 | |||||||
chr1:185243691 | A | G | 2 | a0001c0001t0001g0063 a0001c0001t0001g0066 |
2 | HG03669.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2441+11983A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185243691 | |||||||
chr1:185243728 | AT | A | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+12022delT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185243728 | ||||||
chr1:185243788 | A | T | 2 | a0001c0001t0007g0094 a0003c0005t0009g0004 |
2 | HG02109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2441+12080A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185243788 | |||||||
chr1:185243809 | T | C | 1 | a0004c0006t0001g0166 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2441+12101T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185243809 | |||||||
chr1:185243833 | T | C | 41 | a0001c0001t0004g0037 a0003c0003t0001g0154 a0003c0003t0001g0155 others(38): Show |
41 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.2441+12125T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185243833 | |||||||
chr1:185244028 | C | T | 103 | a0002c0002t0001g0002 a0002c0002t0001g0135 a0002c0002t0001g0136 others(100): Show |
104 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(101): Show |
intron_variant | MODIFIER | c.2441+12320C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185244028 | |||||||
chr1:185244231 | C | T | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2441+12523C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185244231 | |||||||
chr1:185244260 | G | A | 1 | a0002c0004t0001g0309 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2441+12552G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185244260 | |||||||
chr1:185244328 | A | G | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+12620A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185244328 | |||||||
chr1:185244392 | G | A | 41 | a0001c0001t0004g0037 a0003c0003t0001g0154 a0003c0003t0001g0155 others(38): Show |
41 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.2441+12684G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185244392 | |||||||
chr1:185244479 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2441+12771G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185244479 | |||||||
chr1:185244631 | A | G | 1 | a0003c0003t0001g0263 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2441+12923A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185244631 | |||||||
chr1:185244806 | C | G | 1 | a0002c0002t0001g0183 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2441+13098C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185244806 | |||||||
chr1:185244871 | C | A | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+13163C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185244871 | |||||||
chr1:185244910 | G | A | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+13202G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185244910 | |||||||
chr1:185244926 | A | G | 117 | a0001c0001t0001g0030 a0001c0011t0008g0260 a0002c0002t0001g0002 others(114): Show |
119 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(116): Show |
intron_variant | MODIFIER | c.2441+13218A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185244926 | |||||||
chr1:185244930 | T | C | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+13222T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185244930 | |||||||
chr1:185245052 | AG | A | 3 | a0001c0001t0001g0034 a0001c0001t0001g0076 a0001c0001t0001g0127 |
3 | HG00735.hp2 HG00741.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.2441+13345delG | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185245052 | |||||||
chr1:185245132 | T | G | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+13424T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185245132 | |||||||
chr1:185245380 | T | C | 131 | a0001c0001t0007g0094 a0002c0002t0001g0002 a0002c0002t0001g0135 others(128): Show |
133 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(130): Show |
intron_variant | MODIFIER | c.2441+13672T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185245380 | |||||||
chr1:185245394 | G | T | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+13686G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185245394 | |||||||
chr1:185245396 | G | A | 1 | a0003c0003t0001g0189 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2441+13688G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185245396 | |||||||
chr1:185245482 | G | C | 1 | a0003c0003t0001g0197 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2441+13774G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185245482 | |||||||
chr1:185245593 | G | A | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+13885G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185245593 | |||||||
chr1:185245624 | G | A | 2 | a0003c0005t0001g0230 a0003c0005t0001g0231 |
2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2441+13916G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185245624 | |||||||
chr1:185245638 | C | T | 2 | a0006c0008t0001g0139 a0006c0008t0001g0141 |
2 | HG01891.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2441+13930C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185245638 | |||||||
chr1:185245710 | T | A | 3 | a0003c0005t0004g0006 a0003c0005t0004g0007 a0003c0005t0004g0229 |
3 | HG01891.hp2 HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2441+14002T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185245710 | |||||||
chr1:185245737 | A | AT | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+14036dupT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185245737 | ||||||
chr1:185245820 | G | T | 1 | a0001c0001t0001g0065 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2441+14112G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185245820 | |||||||
chr1:185245821 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2441+14113C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185245821 | |||||||
chr1:185245837 | C | T | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+14129C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185245837 | |||||||
chr1:185246048 | G | A | 35 | a0001c0001t0004g0037 a0003c0003t0001g0189 a0003c0003t0001g0190 others(32): Show |
35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2441+14340G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185246048 | |||||||
chr1:185246347 | G | A | 35 | a0001c0001t0004g0037 a0003c0003t0001g0189 a0003c0003t0001g0190 others(32): Show |
35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2441+14639G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185246347 | |||||||
chr1:185246357 | G | A | 35 | a0001c0001t0004g0037 a0003c0003t0001g0189 a0003c0003t0001g0190 others(32): Show |
35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2441+14649G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185246357 | |||||||
chr1:185246623 | C | CT | 33 | a0001c0001t0001g0015 a0001c0001t0001g0033 a0001c0001t0001g0050 others(30): Show |
34 | HG01243.hp1 HG02040.hp1 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.2441+14936dupT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185246623 | ||||||
chr1:185246623 | C | CTT | 33 | a0001c0001t0004g0037 a0002c0002t0001g0218 a0003c0003t0001g0190 others(30): Show |
33 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.2441+14935_2441+14 others(8): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185246623 | ||||||
chr1:185246623 | C | CTTT | 91 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(88): Show |
92 | HG00323.hp2 HG00438.hp1 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.2441+14934_2441+14 others(9): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185246623 | ||||||
chr1:185246623 | C | CTTTT | 32 | a0002c0002t0001g0137 a0002c0002t0001g0174 a0002c0002t0001g0187 others(29): Show |
32 | HG01167.hp2 HG01169.hp1 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.2441+14933_2441+14 others(10): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185246623 | ||||||
chr1:185246623 | CT | C | 8 | a0001c0001t0001g0048 a0001c0001t0001g0051 a0001c0001t0001g0091 others(5): Show |
8 | HG01070.hp2 HG01256.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2441+14936delT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185246623 | ||||||
chr1:185246822 | T | A | 1 | a0003c0003t0001g0219 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2441+15114T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185246822 | |||||||
chr1:185247038 | C | T | 4 | a0003c0003t0001g0154 a0003c0003t0001g0155 a0003c0003t0001g0211 others(1): Show |
4 | HG02559.hp1 HG02809.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.2441+15330C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185247038 | |||||||
chr1:185247128 | A | G | 3 | a0007c0012t0001g0018 a0007c0012t0001g0019 a0007c0012t0001g0020 |
3 | HG02145.hp2 HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2441+15420A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185247128 | |||||||
chr1:185247179 | G | T | 2 | a0001c0001t0001g0124 a0001c0001t0001g0126 |
2 | NA18943.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.2441+15471G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185247179 | |||||||
chr1:185247648 | C | T | 2 | a0003c0005t0001g0230 a0003c0005t0001g0231 |
2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2441+15940C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185247648 | |||||||
chr1:185247696 | T | C | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+15988T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185247696 | |||||||
chr1:185248035 | T | A | 14 | a0003c0005t0003g0003 a0003c0005t0003g0227 a0003c0005t0003g0245 others(11): Show |
15 | HG02055.hp2 HG02451.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.2441+16327T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185248035 | |||||||
chr1:185248284 | AAAC | A | 14 | a0003c0005t0003g0003 a0003c0005t0003g0227 a0003c0005t0003g0245 others(11): Show |
15 | HG02055.hp2 HG02451.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.2441+16579_2441+16 others(9): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185248284 | ||||||
chr1:185248352 | A | G | 2 | a0006c0008t0003g0243 a0006c0008t0003g0244 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2441+16644A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185248352 | |||||||
chr1:185248606 | G | A | 8 | a0002c0004t0001g0288 a0002c0004t0001g0293 a0002c0004t0001g0302 others(5): Show |
8 | HG01255.hp1 HG01496.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.2441+16898G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185248606 | |||||||
chr1:185248775 | C | CA | 7 | a0001c0001t0001g0005 a0001c0001t0001g0112 a0001c0001t0001g0128 others(4): Show |
7 | HG02109.hp1 HG02132.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.2441+17085dupA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185248775 | ||||||
chr1:185248775 | CA | C | 26 | a0001c0001t0001g0025 a0001c0001t0001g0052 a0001c0001t0001g0062 others(23): Show |
26 | HG00438.hp1 HG01975.hp2 HG02071.hp2 others(23): Show |
intron_variant | MODIFIER | c.2441+17085delA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185248775 | ||||||
chr1:185248775 | CAA | C | 120 | a0001c0001t0007g0094 a0002c0002t0001g0002 a0002c0002t0001g0135 others(117): Show |
122 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(119): Show |
intron_variant | MODIFIER | c.2441+17084_2441+17 others(8): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185248775 | ||||||
chr1:185248775 | CAAA | C | 10 | a0003c0003t0001g0154 a0003c0003t0001g0155 a0003c0003t0001g0211 others(7): Show |
10 | HG02258.hp1 HG02559.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.2441+17083_2441+17 others(9): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185248775 | ||||||
chr1:185248860 | A | C | 1 | a0001c0001t0001g0064 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2441+17152A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185248860 | |||||||
chr1:185249049 | G | A | 1 | a0001c0011t0008g0260 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2441+17341G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185249049 | |||||||
chr1:185249551 | C | T | 2 | a0006c0008t0003g0243 a0006c0008t0003g0244 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2441+17843C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185249551 | |||||||
chr1:185249774 | G | T | 1 | a0002c0004t0001g0296 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2441+18066G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185249774 | |||||||
chr1:185249876 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2441+18168C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185249876 | |||||||
chr1:185250007 | A | G | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+18299A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185250007 | |||||||
chr1:185250103 | T | C | 6 | a0003c0003t0001g0154 a0003c0003t0001g0155 a0003c0003t0001g0211 others(3): Show |
6 | HG02258.hp1 HG02559.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2441+18395T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185250103 | |||||||
chr1:185250152 | G | A | 2 | a0001c0001t0001g0040 a0001c0001t0001g0041 |
2 | HG00738.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2441+18444G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185250152 | |||||||
chr1:185250164 | G | A | 185 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(182): Show |
187 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.2441+18456G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185250164 | |||||||
chr1:185250238 | T | C | 296 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0016 others(293): Show |
299 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.2441+18530T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185250238 | |||||||
chr1:185250415 | T | A | 1 | a0005c0007t0001g0312 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2441+18707T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185250415 | |||||||
chr1:185250528 | C | T | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+18820C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185250528 | |||||||
chr1:185250530 | C | A | 1 | a0001c0001t0002g0274 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2441+18822C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185250530 | |||||||
chr1:185250548 | C | T | 170 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(167): Show |
171 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.2441+18840C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185250548 | |||||||
chr1:185250622 | C | G | 1 | a0001c0001t0001g0082 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2441+18914C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185250622 | |||||||
chr1:185250642 | TATTTAAT others(4): Show |
T | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2441+18935_2441+18 others(17): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185250642 | |||||||
chr1:185250668 | A | T | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | HG00597.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.2441+18960A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185250668 | |||||||
chr1:185250749 | A | G | 35 | a0001c0001t0004g0037 a0003c0003t0001g0189 a0003c0003t0001g0190 others(32): Show |
35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2441+19041A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185250749 | |||||||
chr1:185250756 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2441+19048G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185250756 | |||||||
chr1:185250811 | C | T | 1 | a0003c0021t0011g0131 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2441+19103C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185250811 | |||||||
chr1:185250860 | G | A | 105 | a0002c0002t0001g0002 a0002c0002t0001g0135 a0002c0002t0001g0136 others(102): Show |
106 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(103): Show |
intron_variant | MODIFIER | c.2441+19152G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185250860 | |||||||
chr1:185250950 | A | G | 23 | a0001c0001t0001g0021 a0001c0001t0001g0030 a0001c0001t0001g0032 others(20): Show |
23 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.2441+19242A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185250950 | |||||||
chr1:185250955 | A | G | 186 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(183): Show |
188 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(185): Show |
intron_variant | MODIFIER | c.2441+19247A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185250955 | |||||||
chr1:185251553 | T | C | 1 | a0002c0002t0001g0257 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2442-19770T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185251553 | |||||||
chr1:185251797 | TA | T | 5 | a0002c0002t0001g0169 a0003c0003t0001g0154 a0003c0003t0001g0155 others(2): Show |
5 | HG01361.hp2 HG02559.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2442-19525delA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185251797 | |||||||
chr1:185251798 | A | T | 58 | a0001c0001t0004g0037 a0002c0004t0001g0303 a0002c0004t0001g0310 others(55): Show |
58 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.2442-19525A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185251798 | |||||||
chr1:185251800 | T | A | 2 | a0001c0001t0001g0103 a0002c0002t0001g0153 |
2 | HG02896.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.2442-19523T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185251800 | |||||||
chr1:185251838 | C | T | 1 | a0002c0002t0001g0181 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2442-19485C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185251838 | |||||||
chr1:185251863 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2442-19460A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185251863 | |||||||
chr1:185252014 | A | G | 3 | a0001c0001t0001g0061 a0001c0001t0001g0079 a0001c0011t0001g0148 |
3 | HG01106.hp2 NA18954.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.2442-19309A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185252014 | |||||||
chr1:185252092 | A | T | 5 | a0004c0006t0001g0223 a0004c0006t0001g0224 a0004c0006t0001g0225 others(2): Show |
5 | HG02630.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.2442-19231A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185252092 | |||||||
chr1:185252116 | A | T | 90 | a0002c0002t0001g0002 a0002c0002t0001g0135 a0002c0002t0001g0136 others(87): Show |
91 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(88): Show |
intron_variant | MODIFIER | c.2442-19207A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185252116 | |||||||
chr1:185252184 | G | T | 1 | a0001c0001t0002g0276 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2442-19139G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185252184 | |||||||
chr1:185252230 | T | C | 55 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(52): Show |
55 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.2442-19093T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185252230 | |||||||
chr1:185252231 | G | A | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2442-19092G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185252231 | |||||||
chr1:185252243 | C | T | 1 | a0005c0007t0001g0304 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2442-19080C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185252243 | |||||||
chr1:185252351 | T | C | 1 | a0001c0001t0001g0044 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2442-18972T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185252351 | |||||||
chr1:185252352 | G | A | 1 | a0001c0001t0001g0044 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2442-18971G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185252352 | |||||||
chr1:185252676 | A | G | 1 | a0003c0021t0011g0131 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2442-18647A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185252676 | |||||||
chr1:185252696 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2442-18627G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185252696 | |||||||
chr1:185252794 | C | T | 2 | a0001c0001t0002g0029 a0001c0001t0002g0276 |
2 | HG03654.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2442-18529C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185252794 | |||||||
chr1:185252860 | G | A | 1 | a0003c0005t0003g0248 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2442-18463G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185252860 | |||||||
chr1:185252861 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2442-18462C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185252861 | |||||||
chr1:185252899 | G | C | 16 | a0003c0005t0001g0230 a0003c0005t0001g0231 a0003c0005t0003g0003 others(13): Show |
17 | HG01243.hp1 HG02055.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.2442-18424G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185252899 | |||||||
chr1:185252923 | G | A | 2 | a0001c0001t0002g0029 a0001c0001t0002g0276 |
2 | HG03654.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2442-18400G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185252923 | |||||||
chr1:185252957 | G | C | 3 | a0001c0001t0001g0061 a0001c0001t0001g0079 a0001c0011t0001g0148 |
3 | HG01106.hp2 NA18954.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.2442-18366G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185252957 | |||||||
chr1:185252963 | G | T | 1 | a0005c0007t0001g0322 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2442-18360G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185252963 | |||||||
chr1:185253010 | G | T | 19 | a0001c0001t0007g0094 a0003c0005t0001g0230 a0003c0005t0001g0231 others(16): Show |
20 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.2442-18313G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185253010 | |||||||
chr1:185253037 | G | A | 1 | a0004c0006t0001g0159 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2442-18286G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185253037 | |||||||
chr1:185253069 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2442-18254G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185253069 | |||||||
chr1:185253142 | A | G | 1 | a0003c0021t0011g0131 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2442-18181A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185253142 | |||||||
chr1:185253264 | A | G | 190 | a0001c0001t0001g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(187): Show |
192 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.2442-18059A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185253264 | |||||||
chr1:185253443 | T | C | 1 | a0002c0002t0001g0169 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2442-17880T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185253443 | |||||||
chr1:185253466 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2442-17857T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185253466 | |||||||
chr1:185253497 | A | G | 1 | a0002c0004t0001g0307 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2442-17826A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185253497 | |||||||
chr1:185253559 | T | A | 27 | a0002c0002t0001g0002 a0002c0002t0001g0150 a0002c0002t0001g0167 others(24): Show |
28 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.2442-17764T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185253559 | |||||||
chr1:185253583 | T | TTGTC | 55 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(52): Show |
55 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.2442-17737_2442-17 others(10): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185253583 | ||||||
chr1:185253677 | C | G | 1 | a0003c0003t0001g0211 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2442-17646C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185253677 | |||||||
chr1:185253677 | C | T | 5 | a0004c0006t0001g0223 a0004c0006t0001g0224 a0004c0006t0001g0225 others(2): Show |
5 | HG02630.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.2442-17646C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185253677 | |||||||
chr1:185253742 | T | TC | 55 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(52): Show |
55 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.2442-17580dupC | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185253742 | ||||||
chr1:185253785 | A | G | 1 | a0003c0005t0004g0264 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2442-17538A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185253785 | |||||||
chr1:185253858 | A | G | 37 | a0001c0001t0004g0037 a0003c0003t0001g0189 a0003c0003t0001g0190 others(34): Show |
37 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.2442-17465A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185253858 | |||||||
chr1:185253894 | A | G | 105 | a0002c0002t0001g0002 a0002c0002t0001g0135 a0002c0002t0001g0136 others(102): Show |
106 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(103): Show |
intron_variant | MODIFIER | c.2442-17429A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185253894 | |||||||
chr1:185253925 | T | C | 16 | a0003c0005t0001g0230 a0003c0005t0001g0231 a0003c0005t0003g0003 others(13): Show |
17 | HG01243.hp1 HG02055.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.2442-17398T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185253925 | |||||||
chr1:185254057 | C | T | 1 | a0003c0003t0001g0239 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2442-17266C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185254057 | |||||||
chr1:185254093 | G | A | 35 | a0001c0001t0004g0037 a0003c0003t0001g0189 a0003c0003t0001g0190 others(32): Show |
35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2442-17230G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185254093 | |||||||
chr1:185254174 | G | A | 2 | a0002c0002t0001g0135 a0002c0002t0001g0136 |
2 | HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2442-17149G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185254174 | |||||||
chr1:185254175 | T | G | 1 | a0001c0001t0007g0094 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2442-17148T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185254175 | |||||||
chr1:185254191 | T | C | 1 | a0002c0002t0001g0177 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2442-17132T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185254191 | |||||||
chr1:185254247 | T | G | 1 | a0001c0001t0007g0094 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2442-17076T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185254247 | |||||||
chr1:185254392 | G | A | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2442-16931G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185254392 | |||||||
chr1:185254404 | G | T | 35 | a0001c0001t0004g0037 a0003c0003t0001g0189 a0003c0003t0001g0190 others(32): Show |
35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2442-16919G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185254404 | |||||||
chr1:185254415 | CCT | C | 4 | a0003c0003t0001g0154 a0003c0003t0001g0155 a0003c0003t0001g0211 others(1): Show |
4 | HG02559.hp1 HG02809.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.2442-16907_2442-16 others(8): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185254415 | |||||||
chr1:185254416 | C | T | 186 | a0001c0001t0001g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(183): Show |
188 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(185): Show |
intron_variant | MODIFIER | c.2442-16907C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185254416 | |||||||
chr1:185254638 | T | C | 1 | a0005c0007t0001g0297 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2442-16685T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185254638 | |||||||
chr1:185254666 | T | C | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2442-16657T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185254666 | |||||||
chr1:185254680 | A | G | 4 | a0004c0009t0001g0060 a0004c0009t0001g0129 a0008c0017t0001g0075 others(1): Show |
4 | HG00280.hp2 HG00639.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.2442-16643A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185254680 | |||||||
chr1:185254771 | C | T | 259 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0016 others(256): Show |
262 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.2442-16552C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185254771 | |||||||
chr1:185254892 | T | C | 24 | a0004c0006t0001g0142 a0004c0006t0001g0143 a0004c0006t0001g0144 others(21): Show |
24 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.2442-16431T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185254892 | |||||||
chr1:185255030 | G | A | 1 | a0003c0021t0011g0131 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2442-16293G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185255030 | |||||||
chr1:185255243 | A | G | 1 | a0007c0012t0001g0018 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2442-16080A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185255243 | |||||||
chr1:185255387 | A | G | 190 | a0001c0001t0001g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(187): Show |
192 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.2442-15936A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185255387 | |||||||
chr1:185255394 | A | G | 3 | a0001c0001t0001g0124 a0001c0001t0001g0126 a0001c0001t0006g0125 |
3 | HG00597.hp2 NA18943.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.2442-15929A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185255394 | |||||||
chr1:185255435 | C | G | 3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0097 |
3 | HG00438.hp2 HG02056.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.2442-15888C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185255435 | |||||||
chr1:185255457 | G | T | 1 | a0002c0002t0001g0185 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2442-15866G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185255457 | |||||||
chr1:185255681 | C | T | 190 | a0001c0001t0001g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(187): Show |
192 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.2442-15642C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185255681 | |||||||
chr1:185255780 | G | A | 22 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(19): Show |
22 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(19): Show |
intron_variant | MODIFIER | c.2442-15543G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185255780 | |||||||
chr1:185255813 | C | A | 2 | a0002c0002t0001g0174 a0002c0002t0001g0213 |
2 | HG01175.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.2442-15510C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185255813 | |||||||
chr1:185255868 | C | G | 5 | a0003c0005t0003g0003 a0003c0005t0003g0245 a0003c0005t0003g0246 others(2): Show |
6 | HG02896.hp2 HG02897.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.2442-15455C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185255868 | |||||||
chr1:185255871 | A | G | 1 | a0005c0007t0001g0304 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2442-15452A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185255871 | |||||||
chr1:185255876 | T | C | 6 | a0003c0005t0003g0003 a0003c0005t0003g0245 a0003c0005t0003g0246 others(3): Show |
7 | HG02647.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.2442-15447T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185255876 | |||||||
chr1:185255881 | G | T | 5 | a0003c0005t0003g0003 a0003c0005t0003g0245 a0003c0005t0003g0246 others(2): Show |
6 | HG02896.hp2 HG02897.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.2442-15442G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185255881 | |||||||
chr1:185255883 | C | G | 1 | a0012c0020t0001g0130 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2442-15440C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185255883 | |||||||
chr1:185255928 | G | C | 55 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(52): Show |
55 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.2442-15395G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185255928 | |||||||
chr1:185255935 | T | C | 1 | a0002c0002t0001g0169 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2442-15388T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185255935 | |||||||
chr1:185255979 | A | G | 1 | a0003c0003t0001g0201 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2442-15344A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185255979 | |||||||
chr1:185256032 | G | A | 1 | a0003c0005t0001g0013 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2442-15291G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185256032 | |||||||
chr1:185256107 | C | A | 105 | a0002c0002t0001g0002 a0002c0002t0001g0135 a0002c0002t0001g0136 others(102): Show |
106 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(103): Show |
intron_variant | MODIFIER | c.2442-15216C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185256107 | |||||||
chr1:185256109 | C | A | 1 | a0003c0005t0003g0227 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2442-15214C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185256109 | |||||||
chr1:185256140 | C | T | 1 | a0002c0002t0001g0218 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2442-15183C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185256140 | |||||||
chr1:185256146 | A | T | 3 | a0001c0001t0007g0094 a0003c0005t0009g0004 a0003c0021t0011g0131 |
3 | HG02109.hp2 HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2442-15177A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185256146 | |||||||
chr1:185256149 | C | T | 2 | a0001c0001t0001g0082 a0001c0001t0001g0099 |
2 | HG02080.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.2442-15174C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185256149 | |||||||
chr1:185256210 | A | T | 15 | a0003c0003t0001g0234 a0003c0003t0001g0235 a0003c0003t0001g0236 others(12): Show |
15 | HG01099.hp2 HG01891.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.2442-15113A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185256210 | |||||||
chr1:185256227 | T | C | 1 | a0003c0005t0001g0013 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2442-15096T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185256227 | |||||||
chr1:185256232 | G | C | 18 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(15): Show |
18 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(15): Show |
intron_variant | MODIFIER | c.2442-15091G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185256232 | |||||||
chr1:185256508 | C | T | 2 | a0001c0001t0002g0029 a0001c0001t0002g0276 |
2 | HG03654.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2442-14815C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185256508 | |||||||
chr1:185256511 | C | T | 1 | a0004c0006t0001g0163 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2442-14812C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185256511 | |||||||
chr1:185256527 | C | G | 1 | a0001c0001t0001g0127 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2442-14796C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185256527 | |||||||
chr1:185256530 | T | G | 1 | a0001c0001t0001g0124 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2442-14793T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185256530 | |||||||
chr1:185256568 | C | T | 3 | a0007c0012t0001g0018 a0007c0012t0001g0019 a0007c0012t0001g0020 |
3 | HG02145.hp2 HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2442-14755C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185256568 | |||||||
chr1:185256569 | G | A | 1 | a0002c0002t0001g0184 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2442-14754G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185256569 | |||||||
chr1:185256573 | T | C | 296 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0016 others(293): Show |
299 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.2442-14750T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185256573 | |||||||
chr1:185256600 | C | T | 2 | a0002c0004t0001g0009 a0002c0004t0001g0291 |
2 | HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2442-14723C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185256600 | |||||||
chr1:185256694 | CA | C | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2442-14626delA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185256694 | ||||||
chr1:185256736 | G | C | 35 | a0001c0001t0004g0037 a0003c0003t0001g0189 a0003c0003t0001g0190 others(32): Show |
35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2442-14587G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185256736 | |||||||
chr1:185256766 | G | C | 186 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(183): Show |
188 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(185): Show |
intron_variant | MODIFIER | c.2442-14557G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185256766 | |||||||
chr1:185256905 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2442-14418T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185256905 | |||||||
chr1:185256946 | C | T | 22 | a0003c0003t0001g0189 a0003c0003t0001g0190 a0003c0003t0001g0191 others(19): Show |
22 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.2442-14377C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185256946 | |||||||
chr1:185257016 | T | G | 1 | a0002c0004t0001g0301 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2442-14307T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257016 | |||||||
chr1:185257022 | G | C | 1 | a0002c0004t0001g0301 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2442-14301G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257022 | |||||||
chr1:185257030 | A | C | 1 | a0003c0005t0003g0227 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2442-14293A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257030 | |||||||
chr1:185257038 | C | T | 4 | a0003c0003t0001g0154 a0003c0003t0001g0155 a0003c0003t0001g0211 others(1): Show |
4 | HG02559.hp1 HG02809.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.2442-14285C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257038 | |||||||
chr1:185257039 | C | T | 1 | a0015c0016t0001g0017 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2442-14284C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257039 | |||||||
chr1:185257049 | G | A | 1 | a0002c0004t0001g0301 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2442-14274G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257049 | |||||||
chr1:185257103 | T | G | 4 | a0002c0002t0001g0171 a0002c0002t0001g0272 a0002c0004t0001g0301 others(1): Show |
4 | HG03486.hp1 HG03704.hp1 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.2442-14220T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257103 | |||||||
chr1:185257109 | G | A | 2 | a0001c0001t0001g0105 a0001c0001t0005g0100 |
2 | HG00140.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.2442-14214G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257109 | |||||||
chr1:185257136 | G | A | 2 | a0001c0001t0001g0030 a0003c0005t0001g0013 |
2 | HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2442-14187G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257136 | |||||||
chr1:185257143 | T | G | 2 | a0002c0002t0001g0171 a0002c0002t0001g0272 |
2 | HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2442-14180T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257143 | |||||||
chr1:185257221 | C | T | 4 | a0001c0001t0001g0005 a0007c0012t0001g0018 a0007c0012t0001g0019 others(1): Show |
4 | HG02145.hp2 HG02615.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2442-14102C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257221 | |||||||
chr1:185257247 | C | G | 35 | a0001c0001t0004g0037 a0003c0003t0001g0189 a0003c0003t0001g0190 others(32): Show |
35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2442-14076C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257247 | |||||||
chr1:185257319 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2442-14004C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257319 | |||||||
chr1:185257324 | T | C | 5 | a0001c0001t0007g0094 a0002c0002t0001g0286 a0002c0002t0001g0287 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.2442-13999T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257324 | |||||||
chr1:185257338 | A | G | 3 | a0001c0001t0007g0094 a0003c0005t0009g0004 a0003c0021t0011g0131 |
3 | HG02109.hp2 HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2442-13985A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257338 | |||||||
chr1:185257352 | G | A | 2 | a0001c0001t0002g0029 a0001c0001t0002g0276 |
2 | HG03654.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2442-13971G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257352 | |||||||
chr1:185257357 | A | G | 2 | a0002c0002t0001g0137 a0002c0002t0001g0153 |
2 | HG02896.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2442-13966A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257357 | |||||||
chr1:185257361 | A | C | 1 | a0004c0006t0001g0226 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2442-13962A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257361 | |||||||
chr1:185257384 | C | T | 2 | a0001c0001t0001g0049 a0001c0001t0001g0051 |
2 | NA18962.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.2442-13939C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257384 | |||||||
chr1:185257410 | C | G | 105 | a0002c0002t0001g0002 a0002c0002t0001g0135 a0002c0002t0001g0136 others(102): Show |
106 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(103): Show |
intron_variant | MODIFIER | c.2442-13913C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257410 | |||||||
chr1:185257502 | G | C | 131 | a0001c0001t0007g0094 a0002c0002t0001g0002 a0002c0002t0001g0135 others(128): Show |
133 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(130): Show |
intron_variant | MODIFIER | c.2442-13821G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257502 | |||||||
chr1:185257506 | G | A | 2 | a0003c0005t0001g0013 a0003c0005t0004g0266 |
2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2442-13817G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257506 | |||||||
chr1:185257513 | C | T | 2 | a0006c0008t0003g0243 a0006c0008t0003g0244 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2442-13810C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257513 | |||||||
chr1:185257555 | T | C | 1 | a0001c0001t0001g0056 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2442-13768T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257555 | |||||||
chr1:185257561 | C | G | 1 | a0001c0001t0001g0056 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2442-13762C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257561 | |||||||
chr1:185257601 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2442-13722C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257601 | |||||||
chr1:185257619 | A | G | 190 | a0001c0001t0001g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(187): Show |
192 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.2442-13704A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257619 | |||||||
chr1:185257635 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2442-13688C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257635 | |||||||
chr1:185257683 | C | T | 3 | a0001c0001t0001g0021 a0001c0001t0001g0030 a0001c0001t0001g0036 |
3 | HG02145.hp1 HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2442-13640C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257683 | |||||||
chr1:185257705 | G | C | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2442-13618G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257705 | |||||||
chr1:185257706 | G | T | 131 | a0001c0001t0007g0094 a0002c0002t0001g0002 a0002c0002t0001g0135 others(128): Show |
133 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(130): Show |
intron_variant | MODIFIER | c.2442-13617G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257706 | |||||||
chr1:185257734 | C | T | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2442-13589C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257734 | |||||||
chr1:185257770 | A | G | 35 | a0001c0001t0004g0037 a0003c0003t0001g0189 a0003c0003t0001g0190 others(32): Show |
35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2442-13553A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257770 | |||||||
chr1:185257785 | C | T | 16 | a0003c0005t0001g0230 a0003c0005t0001g0231 a0003c0005t0003g0003 others(13): Show |
17 | HG01243.hp1 HG02055.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.2442-13538C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257785 | |||||||
chr1:185257932 | A | G | 1 | a0003c0021t0011g0131 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2442-13391A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257932 | |||||||
chr1:185258019 | C | G | 4 | a0001c0001t0001g0005 a0007c0012t0001g0018 a0007c0012t0001g0019 others(1): Show |
4 | HG02145.hp2 HG02615.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2442-13304C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185258019 | |||||||
chr1:185258272 | C | T | 3 | a0001c0001t0007g0094 a0003c0005t0009g0004 a0003c0021t0011g0131 |
3 | HG02109.hp2 HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2442-13051C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185258272 | |||||||
chr1:185258281 | C | T | 2 | a0001c0001t0002g0029 a0001c0001t0002g0276 |
2 | HG03654.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2442-13042C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185258281 | |||||||
chr1:185258394 | A | G | 2 | a0003c0003t0001g0192 a0003c0003t0001g0193 |
2 | HG00408.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.2442-12929A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185258394 | |||||||
chr1:185258405 | T | C | 35 | a0001c0001t0004g0037 a0003c0003t0001g0189 a0003c0003t0001g0190 others(32): Show |
35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2442-12918T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185258405 | |||||||
chr1:185258510 | A | C | 15 | a0003c0003t0001g0234 a0003c0003t0001g0235 a0003c0003t0001g0236 others(12): Show |
15 | HG01099.hp2 HG01891.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.2442-12813A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185258510 | |||||||
chr1:185258520 | T | G | 1 | a0002c0002t0001g0137 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2442-12803T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185258520 | |||||||
chr1:185258679 | A | G | 1 | a0002c0002t0001g0255 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2442-12644A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185258679 | |||||||
chr1:185258754 | G | A | 186 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(183): Show |
188 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(185): Show |
intron_variant | MODIFIER | c.2442-12569G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185258754 | |||||||
chr1:185258766 | C | G | 6 | a0003c0003t0001g0154 a0003c0003t0001g0155 a0003c0003t0001g0211 others(3): Show |
6 | HG02258.hp1 HG02559.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2442-12557C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185258766 | |||||||
chr1:185258778 | A | G | 35 | a0001c0001t0004g0037 a0003c0003t0001g0189 a0003c0003t0001g0190 others(32): Show |
35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2442-12545A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185258778 | |||||||
chr1:185258845 | A | C | 35 | a0001c0001t0004g0037 a0003c0003t0001g0189 a0003c0003t0001g0190 others(32): Show |
35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2442-12478A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185258845 | |||||||
chr1:185259114 | C | A | 1 | a0002c0004t0001g0293 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2442-12209C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185259114 | |||||||
chr1:185259304 | C | T | 3 | a0001c0001t0007g0094 a0003c0005t0009g0004 a0003c0021t0011g0131 |
3 | HG02109.hp2 HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2442-12019C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185259304 | |||||||
chr1:185259786 | T | C | 1 | a0003c0005t0003g0251 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2442-11537T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185259786 | |||||||
chr1:185259821 | A | G | 1 | a0003c0003t0001g0204 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2442-11502A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185259821 | |||||||
chr1:185259833 | A | G | 1 | a0003c0003t0001g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2442-11490A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185259833 | |||||||
chr1:185259866 | T | C | 3 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0010c0015t0001g0090 |
3 | HG00621.hp2 HG01952.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.2442-11457T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185259866 | |||||||
chr1:185260153 | G | A | 10 | a0001c0001t0004g0037 a0003c0005t0004g0006 a0003c0005t0004g0007 others(7): Show |
10 | HG01891.hp2 HG02280.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.2442-11170G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185260153 | |||||||
chr1:185260349 | C | T | 25 | a0003c0003t0001g0189 a0003c0003t0001g0190 a0003c0003t0001g0191 others(22): Show |
25 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.2442-10974C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185260349 | |||||||
chr1:185260669 | T | C | 186 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(183): Show |
188 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(185): Show |
intron_variant | MODIFIER | c.2442-10654T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185260669 | |||||||
chr1:185260792 | C | T | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2442-10531C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185260792 | |||||||
chr1:185261065 | T | G | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2442-10258T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185261065 | |||||||
chr1:185261519 | G | A | 2 | a0003c0003t0001g0270 a0003c0003t0001g0271 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2442-9804G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185261519 | |||||||
chr1:185261533 | C | T | 1 | a0009c0013t0001g0074 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2442-9790C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185261533 | |||||||
chr1:185261535 | T | C | 1 | a0001c0001t0001g0079 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2442-9788T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185261535 | |||||||
chr1:185261541 | A | G | 2 | a0001c0001t0001g0024 a0001c0001t0001g0054 |
2 | HG02165.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.2442-9782A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185261541 | |||||||
chr1:185261569 | A | G | 2 | a0002c0002t0001g0214 a0002c0002t0001g0215 |
2 | HG02615.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2442-9754A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185261569 | |||||||
chr1:185261673 | CTT | C | 143 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(140): Show |
145 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.2442-9636_2442-963 others(6): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185261673 | ||||||
chr1:185261673 | CTTT | C | 67 | a0002c0002t0001g0187 a0002c0002t0001g0214 a0002c0002t0001g0215 others(64): Show |
67 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.2442-9637_2442-963 others(7): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185261673 | ||||||
chr1:185261718 | G | T | 155 | a0001c0001t0007g0094 a0002c0002t0001g0002 a0002c0002t0001g0135 others(152): Show |
157 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(154): Show |
intron_variant | MODIFIER | c.2442-9605G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185261718 | |||||||
chr1:185261934 | G | A | 1 | a0012c0020t0001g0130 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2442-9389G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185261934 | |||||||
chr1:185261970 | A | G | 1 | a0001c0001t0001g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2442-9353A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185261970 | |||||||
chr1:185262007 | G | A | 7 | a0003c0003t0001g0154 a0003c0003t0001g0155 a0003c0003t0001g0211 others(4): Show |
7 | HG01884.hp1 HG02258.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.2442-9316G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185262007 | |||||||
chr1:185262066 | C | T | 2 | a0003c0005t0001g0230 a0003c0005t0001g0231 |
2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2442-9257C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185262066 | |||||||
chr1:185262183 | G | A | 10 | a0002c0004t0001g0288 a0002c0004t0001g0293 a0002c0004t0001g0302 others(7): Show |
10 | HG01255.hp1 HG01496.hp1 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.2442-9140G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185262183 | |||||||
chr1:185262190 | T | G | 1 | a0013c0022t0001g0008 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2442-9133T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185262190 | |||||||
chr1:185262386 | C | T | 35 | a0001c0001t0004g0037 a0003c0003t0001g0189 a0003c0003t0001g0190 others(32): Show |
35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2442-8937C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185262386 | |||||||
chr1:185262440 | C | T | 10 | a0001c0001t0004g0037 a0003c0005t0004g0006 a0003c0005t0004g0007 others(7): Show |
10 | HG01891.hp2 HG02280.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.2442-8883C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185262440 | |||||||
chr1:185262514 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2442-8809C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185262514 | |||||||
chr1:185262786 | C | CT | 27 | a0001c0001t0001g0095 a0001c0001t0001g0102 a0001c0001t0007g0094 others(24): Show |
27 | HG00735.hp1 HG01099.hp2 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.2442-8520dupT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185262786 | ||||||
chr1:185262786 | CT | C | 9 | a0001c0001t0001g0069 a0001c0001t0001g0084 a0001c0001t0001g0089 others(6): Show |
9 | HG01069.hp2 HG01123.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.2442-8520delT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185262786 | ||||||
chr1:185262810 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2442-8513G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185262810 | |||||||
chr1:185262855 | T | C | 210 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(207): Show |
212 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.2442-8468T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185262855 | |||||||
chr1:185262894 | T | A | 1 | a0004c0006t0001g0147 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2442-8429T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185262894 | |||||||
chr1:185262933 | G | A | 3 | a0001c0001t0007g0094 a0003c0005t0009g0004 a0003c0021t0011g0131 |
3 | HG02109.hp2 HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2442-8390G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185262933 | |||||||
chr1:185263024 | T | C | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2442-8299T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185263024 | |||||||
chr1:185263042 | C | T | 12 | a0003c0005t0003g0003 a0003c0005t0003g0227 a0003c0005t0003g0245 others(9): Show |
13 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.2442-8281C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185263042 | |||||||
chr1:185263119 | G | A | 155 | a0001c0001t0007g0094 a0002c0002t0001g0002 a0002c0002t0001g0135 others(152): Show |
157 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(154): Show |
intron_variant | MODIFIER | c.2442-8204G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185263119 | |||||||
chr1:185263284 | C | CA | 35 | a0001c0001t0004g0037 a0003c0003t0001g0189 a0003c0003t0001g0190 others(32): Show |
35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2442-8029dupA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185263284 | ||||||
chr1:185263372 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2442-7951T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185263372 | |||||||
chr1:185263403 | C | T | 6 | a0003c0003t0001g0154 a0003c0003t0001g0155 a0003c0003t0001g0211 others(3): Show |
6 | HG02258.hp1 HG02559.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2442-7920C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185263403 | |||||||
chr1:185264132 | T | C | 2 | a0003c0005t0001g0230 a0003c0005t0001g0231 |
2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2442-7191T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185264132 | |||||||
chr1:185264183 | G | A | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2442-7140G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185264183 | |||||||
chr1:185264227 | G | T | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2442-7096G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185264227 | |||||||
chr1:185264253 | T | C | 1 | a0013c0022t0001g0008 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2442-7070T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185264253 | |||||||
chr1:185264338 | C | T | 25 | a0003c0003t0001g0189 a0003c0003t0001g0190 a0003c0003t0001g0191 others(22): Show |
25 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.2442-6985C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185264338 | |||||||
chr1:185265108 | C | T | 1 | a0002c0002t0001g0187 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2442-6215C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185265108 | |||||||
chr1:185265284 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2442-6039A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185265284 | |||||||
chr1:185265351 | A | T | 1 | a0001c0001t0001g0065 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2442-5972A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185265351 | |||||||
chr1:185265411 | T | C | 3 | a0001c0001t0007g0094 a0003c0005t0009g0004 a0003c0021t0011g0131 |
3 | HG02109.hp2 HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2442-5912T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185265411 | |||||||
chr1:185265541 | C | T | 1 | a0002c0002t0001g0259 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2442-5782C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185265541 | |||||||
chr1:185265580 | C | T | 1 | a0001c0001t0006g0125 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2442-5743C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185265580 | |||||||
chr1:185265597 | A | G | 1 | a0003c0005t0004g0006 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2442-5726A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185265597 | |||||||
chr1:185266156 | C | G | 2 | a0003c0005t0001g0230 a0003c0005t0001g0231 |
2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2442-5167C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185266156 | |||||||
chr1:185266212 | C | T | 3 | a0001c0001t0001g0079 a0001c0001t0001g0089 a0001c0011t0001g0148 |
3 | HG01123.hp2 NA18954.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.2442-5111C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185266212 | |||||||
chr1:185266213 | G | A | 1 | a0004c0006t0001g0162 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2442-5110G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185266213 | |||||||
chr1:185266230 | AT | A | 45 | a0002c0002t0001g0002 a0002c0002t0001g0135 a0002c0002t0001g0136 others(42): Show |
46 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.2442-5086delT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185266230 | ||||||
chr1:185266265 | C | T | 2 | a0001c0001t0001g0044 a0011c0018t0001g0028 |
2 | HG01069.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.2442-5058C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185266265 | |||||||
chr1:185266403 | T | G | 14 | a0003c0005t0003g0003 a0003c0005t0003g0227 a0003c0005t0003g0245 others(11): Show |
15 | HG02055.hp2 HG02451.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.2442-4920T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185266403 | |||||||
chr1:185266908 | G | T | 1 | a0002c0002t0001g0002 | 2 | HG00639.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.2442-4415G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185266908 | |||||||
chr1:185267027 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2442-4296G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185267027 | |||||||
chr1:185267033 | G | A | 21 | a0002c0002t0001g0187 a0002c0004t0001g0026 a0002c0004t0001g0027 others(18): Show |
21 | HG01167.hp2 HG01169.hp1 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.2442-4290G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185267033 | |||||||
chr1:185267045 | T | G | 1 | a0001c0001t0001g0005 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2442-4278T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185267045 | |||||||
chr1:185267083 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2442-4240G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185267083 | |||||||
chr1:185267257 | C | T | 1 | a0001c0001t0007g0094 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2442-4066C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185267257 | |||||||
chr1:185267352 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2442-3971C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185267352 | |||||||
chr1:185267380 | G | A | 210 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(207): Show |
212 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.2442-3943G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185267380 | |||||||
chr1:185267467 | A | G | 2 | a0006c0008t0001g0139 a0006c0008t0001g0141 |
2 | HG01891.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2442-3856A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185267467 | |||||||
chr1:185267649 | T | C | 1 | a0002c0002t0001g0187 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2442-3674T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185267649 | |||||||
chr1:185267798 | G | T | 3 | a0001c0001t0007g0094 a0003c0005t0009g0004 a0003c0021t0011g0131 |
3 | HG02109.hp2 HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2442-3525G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185267798 | |||||||
chr1:185268505 | A | G | 35 | a0001c0001t0004g0037 a0003c0003t0001g0189 a0003c0003t0001g0190 others(32): Show |
35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2442-2818A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185268505 | |||||||
chr1:185268757 | C | G | 1 | a0001c0001t0001g0062 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2442-2566C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185268757 | |||||||
chr1:185268853 | C | CT | 58 | a0001c0001t0001g0088 a0002c0002t0001g0002 a0002c0002t0001g0150 others(55): Show |
59 | HG00323.hp2 HG00621.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.2442-2453dupT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185268853 | ||||||
chr1:185268875 | C | T | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2442-2448C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185268875 | |||||||
chr1:185268892 | G | A | 1 | a0006c0008t0001g0188 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2442-2431G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185268892 | |||||||
chr1:185268937 | C | G | 6 | a0003c0003t0001g0154 a0003c0003t0001g0155 a0003c0003t0001g0211 others(3): Show |
6 | HG02258.hp1 HG02559.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2442-2386C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185268937 | |||||||
chr1:185269001 | C | T | 22 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(19): Show |
22 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(19): Show |
intron_variant | MODIFIER | c.2442-2322C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185269001 | |||||||
chr1:185269069 | G | T | 156 | a0001c0001t0001g0102 a0001c0001t0007g0094 a0002c0002t0001g0002 others(153): Show |
158 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(155): Show |
intron_variant | MODIFIER | c.2442-2254G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185269069 | |||||||
chr1:185269074 | G | C | 4 | a0001c0001t0001g0088 a0001c0001t0001g0091 a0001c0001t0001g0092 others(1): Show |
4 | HG01099.hp1 HG01256.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.2442-2249G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185269074 | |||||||
chr1:185269075 | A | G | 1 | a0001c0001t0001g0034 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2442-2248A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185269075 | |||||||
chr1:185269084 | C | T | 1 | a0001c0001t0007g0094 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2442-2239C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185269084 | |||||||
chr1:185269141 | C | T | 1 | a0012c0020t0001g0130 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2442-2182C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185269141 | |||||||
chr1:185269147 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2442-2176T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185269147 | |||||||
chr1:185269335 | T | C | 1 | a0003c0003t0001g0189 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2442-1988T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185269335 | |||||||
chr1:185269367 | G | GT | 10 | a0001c0001t0004g0037 a0003c0005t0004g0006 a0003c0005t0004g0007 others(7): Show |
10 | HG01891.hp2 HG02280.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.2442-1951dupT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185269367 | ||||||
chr1:185269367 | G | GTTT | 20 | a0003c0003t0001g0189 a0003c0003t0001g0190 a0003c0003t0001g0192 others(17): Show |
20 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(17): Show |
intron_variant | MODIFIER | c.2442-1953_2442-195 others(7): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185269367 | ||||||
chr1:185269373 | G | GT | 54 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0030 others(51): Show |
55 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.2442-1935dupT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185269373 | ||||||
chr1:185269373 | G | T | 35 | a0001c0001t0004g0037 a0003c0003t0001g0189 a0003c0003t0001g0190 others(32): Show |
35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2442-1950G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185269373 | |||||||
chr1:185269379 | T | G | 1 | a0001c0001t0007g0094 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2442-1944T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185269379 | |||||||
chr1:185269380 | T | G | 2 | a0001c0001t0001g0084 a0001c0001t0001g0089 |
2 | HG01123.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.2442-1943T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185269380 | |||||||
chr1:185269456 | T | C | 4 | a0002c0002t0001g0256 a0002c0002t0001g0257 a0002c0002t0001g0258 others(1): Show |
4 | HG02572.hp2 HG02723.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2442-1867T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185269456 | |||||||
chr1:185269516 | A | G | 2 | a0003c0005t0001g0013 a0012c0020t0001g0130 |
2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2442-1807A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185269516 | |||||||
chr1:185269537 | G | A | 210 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(207): Show |
212 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.2442-1786G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185269537 | |||||||
chr1:185269943 | T | A | 1 | a0003c0005t0004g0266 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2442-1380T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185269943 | |||||||
chr1:185270034 | T | A | 3 | a0004c0006t0001g0142 a0004c0006t0001g0143 a0004c0006t0001g0144 |
3 | HG00738.hp2 HG01346.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.2442-1289T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185270034 | |||||||
chr1:185270265 | A | G | 35 | a0001c0001t0004g0037 a0003c0003t0001g0189 a0003c0003t0001g0190 others(32): Show |
35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2442-1058A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185270265 | |||||||
chr1:185270302 | T | C | 4 | a0001c0001t0007g0094 a0003c0005t0003g0251 a0003c0005t0003g0254 others(1): Show |
4 | HG01257.hp2 HG03486.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2442-1021T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185270302 | |||||||
chr1:185270302 | T | TC | 203 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(200): Show |
205 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.2442-1019dupC | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185270302 | ||||||
chr1:185270358 | A | C | 35 | a0001c0001t0004g0037 a0003c0003t0001g0189 a0003c0003t0001g0190 others(32): Show |
35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2442-965A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185270358 | |||||||
chr1:185270566 | G | A | 1 | a0001c0001t0002g0283 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2442-757G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185270566 | |||||||
chr1:185270663 | C | T | 209 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(206): Show |
211 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.2442-660C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185270663 | |||||||
chr1:185270697 | A | G | 1 | a0002c0004t0001g0319 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2442-626A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185270697 | |||||||
chr1:185271018 | T | A | 2 | a0002c0004t0001g0009 a0002c0004t0001g0291 |
2 | HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2442-305T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185271018 | |||||||
chr1:185271044 | A | T | 1 | a0003c0005t0004g0267 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2442-279A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185271044 | |||||||
chr1:185271268 | T | C | 5 | a0007c0010t0001g0070 a0007c0010t0001g0071 a0007c0010t0001g0072 others(2): Show |
5 | HG02572.hp1 HG02818.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2442-55T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185271268 | |||||||
chr1:185271439 | T | G | 35 | a0001c0001t0004g0037 a0003c0003t0001g0189 a0003c0003t0001g0190 others(32): Show |
35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2508+50T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185271439 | |||||||
chr1:185271513 | T | C | 1 | a0004c0009t0001g0060 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2508+124T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185271513 | |||||||
chr1:185271530 | T | TTGTCAGT others(12): Show |
1 | a0001c0001t0001g0015 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2508+152_2508+153i others(21): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 185271530 | ||||||
chr1:185271538 | G | A | 12 | a0003c0005t0003g0003 a0003c0005t0003g0227 a0003c0005t0003g0245 others(9): Show |
13 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.2508+149G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185271538 | |||||||
chr1:185271591 | A | G | 3 | a0001c0001t0002g0121 a0001c0001t0002g0278 a0001c0001t0002g0282 |
3 | HG02071.hp2 HG02074.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.2508+202A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185271591 | |||||||
chr1:185271611 | A | G | 5 | a0004c0006t0001g0145 a0004c0006t0001g0146 a0004c0006t0001g0147 others(2): Show |
5 | NA18939.hp2 NA18973.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.2508+222A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185271611 | |||||||
chr1:185272044 | G | A | 24 | a0003c0003t0001g0189 a0003c0003t0001g0190 a0003c0003t0001g0191 others(21): Show |
24 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.2508+655G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185272044 | |||||||
chr1:185272055 | T | A | 3 | a0004c0006t0001g0142 a0004c0006t0001g0143 a0004c0006t0001g0144 |
3 | HG00738.hp2 HG01346.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.2508+666T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185272055 | |||||||
chr1:185272141 | G | C | 35 | a0001c0001t0004g0037 a0003c0003t0001g0189 a0003c0003t0001g0190 others(32): Show |
35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2508+752G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185272141 | |||||||
chr1:185272150 | G | T | 1 | a0003c0005t0004g0229 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2508+761G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185272150 | |||||||
chr1:185272278 | C | T | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2508+889C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185272278 | |||||||
chr1:185272295 | A | G | 1 | a0012c0020t0001g0130 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2508+906A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185272295 | |||||||
chr1:185272301 | G | C | 1 | a0002c0004t0001g0319 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2508+912G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185272301 | |||||||
chr1:185272661 | A | G | 66 | a0002c0002t0001g0187 a0002c0002t0001g0214 a0002c0002t0001g0215 others(63): Show |
66 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(63): Show |
intron_variant | MODIFIER | c.2508+1272A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185272661 | |||||||
chr1:185273133 | C | G | 1 | a0003c0005t0004g0229 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2508+1744C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185273133 | |||||||
chr1:185273224 | A | G | 1 | a0002c0004t0001g0317 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2508+1835A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185273224 | |||||||
chr1:185273431 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2508+2042G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185273431 | |||||||
chr1:185273492 | G | A | 1 | a0001c0001t0001g0044 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2508+2103G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185273492 | |||||||
chr1:185273571 | C | G | 1 | a0003c0003t0001g0221 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2508+2182C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185273571 | |||||||
chr1:185273606 | G | A | 2 | a0003c0005t0001g0230 a0003c0005t0001g0231 |
2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2508+2217G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185273606 | |||||||
chr1:185273920 | G | A | 3 | a0001c0001t0007g0094 a0003c0005t0009g0004 a0003c0021t0011g0131 |
3 | HG02109.hp2 HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2508+2531G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185273920 | |||||||
chr1:185274221 | A | G | 1 | a0003c0021t0011g0131 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2509-2383A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185274221 | |||||||
chr1:185274233 | CAT | C | 10 | a0001c0001t0004g0037 a0003c0005t0004g0006 a0003c0005t0004g0007 others(7): Show |
10 | HG01891.hp2 HG02280.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.2509-2368_2509-236 others(6): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 185274233 | ||||||
chr1:185274336 | G | GAT | 4 | a0001c0001t0001g0005 a0007c0012t0001g0018 a0007c0012t0001g0019 others(1): Show |
4 | HG02145.hp2 HG02615.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2509-2257_2509-225 others(6): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 185274336 | ||||||
chr1:185274454 | G | A | 1 | a0006c0008t0001g0140 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2509-2150G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185274454 | |||||||
chr1:185274455 | C | T | 1 | a0006c0008t0001g0140 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2509-2149C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185274455 | |||||||
chr1:185274457 | G | A | 1 | a0006c0008t0001g0140 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2509-2147G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185274457 | |||||||
chr1:185274459 | T | A | 1 | a0006c0008t0001g0140 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2509-2145T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185274459 | |||||||
chr1:185274648 | A | T | 5 | a0002c0002t0001g0168 a0002c0002t0001g0170 a0002c0002t0001g0172 others(2): Show |
5 | NA18952.hp2 NA18971.hp2 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.2509-1956A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185274648 | |||||||
chr1:185274721 | C | G | 1 | a0002c0002t0001g0177 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2509-1883C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185274721 | |||||||
chr1:185274749 | T | G | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2509-1855T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185274749 | |||||||
chr1:185275184 | C | T | 1 | a0004c0006t0001g0142 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2509-1420C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185275184 | |||||||
chr1:185275436 | A | C | 155 | a0001c0001t0007g0094 a0002c0002t0001g0002 a0002c0002t0001g0135 others(152): Show |
157 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(154): Show |
intron_variant | MODIFIER | c.2509-1168A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185275436 | |||||||
chr1:185275541 | T | C | 2 | a0003c0005t0003g0251 a0003c0005t0003g0254 |
2 | HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2509-1063T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185275541 | |||||||
chr1:185275543 | T | C | 5 | a0003c0005t0003g0003 a0003c0005t0003g0245 a0003c0005t0003g0246 others(2): Show |
6 | HG02896.hp2 HG02897.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.2509-1061T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185275543 | |||||||
chr1:185275687 | A | G | 2 | a0001c0001t0001g0098 a0001c0001t0001g0101 |
2 | NA18942.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.2509-917A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185275687 | |||||||
chr1:185275915 | G | A | 210 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(207): Show |
212 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.2509-689G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185275915 | |||||||
chr1:185276230 | G | T | 1 | a0002c0002t0001g0218 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2509-374G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185276230 | |||||||
chr1:185276253 | A | G | 4 | a0007c0010t0001g0070 a0007c0010t0001g0071 a0007c0010t0001g0072 others(1): Show |
4 | HG02572.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2509-351A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185276253 | |||||||
chr1:185276268 | G | A | 1 | a0003c0003t0001g0189 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2509-336G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185276268 | |||||||
chr1:185276314 | T | C | 2 | a0008c0017t0001g0075 a0008c0023t0001g0161 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2509-290T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185276314 | |||||||
chr1:185276816 | C | T | 2 | a0001c0001t0001g0068 a0001c0011t0001g0160 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2573+148C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185276816 | |||||||
chr1:185277248 | CTTTA | C | 35 | a0001c0001t0004g0037 a0003c0003t0001g0189 a0003c0003t0001g0190 others(32): Show |
35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2573+596_2573+599d others(6): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr1 | 185277248 | ||||||
chr1:185277289 | T | A | 2 | a0006c0008t0003g0243 a0006c0008t0003g0244 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2573+621T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185277289 | |||||||
chr1:185277352 | G | A | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2573+684G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185277352 | |||||||
chr1:185277361 | T | A | 1 | a0001c0001t0001g0111 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2573+693T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185277361 | |||||||
chr1:185277558 | G | A | 1 | a0002c0002t0001g0178 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2573+890G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185277558 | |||||||
chr1:185277612 | A | G | 6 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(3): Show |
6 | NA18964.hp2 NA18972.hp1 NA19006.hp2 others(3): Show |
intron_variant | MODIFIER | c.2573+944A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185277612 | |||||||
chr1:185277628 | T | A | 1 | a0002c0002t0001g0216 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2573+960T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185277628 | |||||||
chr1:185277672 | C | T | 3 | a0001c0001t0007g0094 a0003c0005t0009g0004 a0003c0021t0011g0131 |
3 | HG02109.hp2 HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2573+1004C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185277672 | |||||||
chr1:185277836 | G | C | 3 | a0007c0012t0001g0018 a0007c0012t0001g0019 a0007c0012t0001g0020 |
3 | HG02145.hp2 HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2573+1168G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185277836 | |||||||
chr1:185278024 | A | G | 15 | a0003c0003t0001g0234 a0003c0003t0001g0235 a0003c0003t0001g0236 others(12): Show |
15 | HG01099.hp2 HG01891.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.2573+1356A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185278024 | |||||||
chr1:185278050 | C | T | 2 | a0003c0003t0001g0262 a0003c0003t0001g0263 |
2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2573+1382C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185278050 | |||||||
chr1:185278119 | T | C | 210 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(207): Show |
212 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.2573+1451T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185278119 | |||||||
chr1:185278120 | G | A | 1 | a0002c0002t0001g0255 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2573+1452G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185278120 | |||||||
chr1:185278137 | A | G | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2573+1469A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185278137 | |||||||
chr1:185278336 | G | C | 210 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(207): Show |
212 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.2573+1668G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185278336 | |||||||
chr1:185278421 | A | T | 210 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(207): Show |
212 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.2573+1753A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185278421 | |||||||
chr1:185278662 | G | A | 214 | a0001c0001t0001g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(211): Show |
216 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.2573+1994G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185278662 | |||||||
chr1:185278927 | G | A | 2 | a0003c0005t0001g0230 a0003c0005t0001g0231 |
2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2573+2259G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185278927 | |||||||
chr1:185278969 | G | A | 1 | a0003c0003t0001g0262 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2573+2301G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185278969 | |||||||
chr1:185279061 | G | A | 3 | a0007c0012t0001g0018 a0007c0012t0001g0019 a0007c0012t0001g0020 |
3 | HG02145.hp2 HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2573+2393G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185279061 | |||||||
chr1:185279132 | A | G | 1 | a0002c0002t0001g0217 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2573+2464A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185279132 | |||||||
chr1:185279139 | C | T | 1 | a0003c0005t0001g0013 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2573+2471C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185279139 | |||||||
chr1:185279140 | G | T | 2 | a0001c0001t0001g0128 a0011c0018t0001g0028 |
2 | HG01069.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.2573+2472G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185279140 | |||||||
chr1:185279301 | C | T | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2573+2633C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185279301 | |||||||
chr1:185279302 | G | A | 3 | a0001c0001t0007g0094 a0003c0005t0009g0004 a0003c0021t0011g0131 |
3 | HG02109.hp2 HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2573+2634G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185279302 | |||||||
chr1:185279378 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2573+2710G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185279378 | |||||||
chr1:185279744 | G | A | 35 | a0001c0001t0004g0037 a0003c0003t0001g0189 a0003c0003t0001g0190 others(32): Show |
35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2573+3076G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185279744 | |||||||
chr1:185279918 | A | T | 1 | a0002c0004t0001g0307 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2573+3250A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185279918 | |||||||
chr1:185279926 | A | G | 1 | a0003c0003t0001g0210 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2573+3258A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185279926 | |||||||
chr1:185280082 | G | C | 210 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(207): Show |
212 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.2573+3414G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185280082 | |||||||
chr1:185280115 | T | C | 1 | a0001c0011t0008g0260 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2573+3447T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185280115 | |||||||
chr1:185280574 | G | A | 1 | a0003c0021t0011g0131 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2573+3906G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185280574 | |||||||
chr1:185280672 | A | G | 35 | a0001c0001t0004g0037 a0003c0003t0001g0189 a0003c0003t0001g0190 others(32): Show |
35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2573+4004A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185280672 | |||||||
chr1:185280699 | C | G | 1 | a0001c0001t0001g0082 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2573+4031C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185280699 | |||||||
chr1:185280868 | G | A | 1 | a0014c0024t0001g0175 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2573+4200G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185280868 | |||||||
chr1:185280950 | G | A | 3 | a0004c0006t0001g0163 a0004c0006t0001g0164 a0004c0009t0001g0067 |
3 | HG01070.hp1 HG01081.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.2573+4282G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185280950 | |||||||
chr1:185281222 | T | G | 3 | a0001c0001t0007g0094 a0003c0005t0009g0004 a0003c0021t0011g0131 |
3 | HG02109.hp2 HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2573+4554T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185281222 | |||||||
chr1:185281489 | G | A | 1 | a0002c0004t0001g0311 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2573+4821G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185281489 | |||||||
chr1:185281499 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2573+4831C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185281499 | |||||||
chr1:185281894 | C | G | 1 | a0002c0004t0001g0308 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2573+5226C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185281894 | |||||||
chr1:185282376 | TA | T | 15 | a0002c0002t0001g0137 a0002c0002t0001g0153 a0003c0005t0003g0003 others(12): Show |
16 | HG02055.hp2 HG02451.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.2573+5720delA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr1 | 185282376 | ||||||
chr1:185282596 | T | C | 10 | a0002c0002t0001g0167 a0002c0002t0001g0168 a0002c0002t0001g0170 others(7): Show |
10 | HG02132.hp2 NA18944.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.2573+5928T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185282596 | |||||||
chr1:185282793 | C | T | 3 | a0001c0001t0001g0095 a0003c0005t0001g0230 a0003c0005t0001g0231 |
3 | HG00735.hp1 HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2573+6125C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185282793 | |||||||
chr1:185282819 | A | T | 1 | a0003c0005t0003g0248 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2573+6151A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185282819 | |||||||
chr1:185282853 | G | A | 1 | a0001c0001t0001g0033 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2573+6185G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185282853 | |||||||
chr1:185283321 | C | G | 5 | a0002c0002t0001g0168 a0002c0002t0001g0170 a0002c0002t0001g0172 others(2): Show |
5 | NA18952.hp2 NA18971.hp2 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.2573+6653C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185283321 | |||||||
chr1:185283341 | G | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0066 |
2 | HG03669.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2573+6673G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185283341 | |||||||
chr1:185283426 | A | G | 14 | a0002c0002t0001g0002 a0002c0002t0001g0150 a0002c0002t0001g0169 others(11): Show |
15 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.2573+6758A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185283426 | |||||||
chr1:185283481 | A | C | 1 | a0001c0001t0001g0126 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2573+6813A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185283481 | |||||||
chr1:185283550 | T | TTTTG | 37 | a0001c0001t0004g0037 a0003c0003t0001g0189 a0003c0003t0001g0190 others(34): Show |
37 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.2573+6901_2573+690 others(8): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr1 | 185283550 | ||||||
chr1:185283550 | TTTTG | T | 11 | a0002c0002t0001g0002 a0002c0002t0001g0150 a0002c0002t0001g0169 others(8): Show |
12 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.2573+6901_2573+690 others(8): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr1 | 185283550 | ||||||
chr1:185283873 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2574-6801T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185283873 | |||||||
chr1:185284168 | C | T | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2574-6506C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185284168 | |||||||
chr1:185284456 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2574-6218C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185284456 | |||||||
chr1:185284478 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2574-6196C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185284478 | |||||||
chr1:185284658 | T | G | 217 | a0001c0001t0001g0005 a0001c0001t0001g0063 a0001c0001t0001g0065 others(214): Show |
219 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.2574-6016T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185284658 | |||||||
chr1:185284689 | T | G | 37 | a0001c0001t0004g0037 a0003c0003t0001g0189 a0003c0003t0001g0190 others(34): Show |
37 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.2574-5985T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185284689 | |||||||
chr1:185284734 | G | A | 37 | a0001c0001t0004g0037 a0003c0003t0001g0189 a0003c0003t0001g0190 others(34): Show |
37 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.2574-5940G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185284734 | |||||||
chr1:185284782 | C | T | 5 | a0007c0010t0001g0070 a0007c0010t0001g0071 a0007c0010t0001g0072 others(2): Show |
5 | HG02572.hp1 HG02818.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2574-5892C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185284782 | |||||||
chr1:185284876 | C | T | 6 | a0003c0003t0001g0154 a0003c0003t0001g0155 a0003c0003t0001g0211 others(3): Show |
6 | HG02258.hp1 HG02559.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2574-5798C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185284876 | |||||||
chr1:185284884 | A | C | 2 | a0003c0003t0001g0262 a0003c0003t0001g0263 |
2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2574-5790A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185284884 | |||||||
chr1:185284889 | C | CT | 6 | a0001c0001t0001g0039 a0001c0001t0001g0091 a0001c0001t0001g0105 others(3): Show |
6 | HG00140.hp1 HG00741.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.2574-5771dupT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr1 | 185284889 | ||||||
chr1:185284992 | G | C | 1 | a0015c0016t0001g0017 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2574-5682G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185284992 | |||||||
chr1:185285684 | T | C | 2 | a0003c0005t0001g0230 a0003c0005t0001g0231 |
2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2574-4990T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185285684 | |||||||
chr1:185285879 | T | A | 2 | a0003c0003t0001g0207 a0003c0003t0001g0221 |
2 | HG02080.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.2574-4795T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185285879 | |||||||
chr1:185285893 | T | C | 2 | a0003c0005t0001g0230 a0003c0005t0001g0231 |
2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2574-4781T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185285893 | |||||||
chr1:185286286 | C | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0118 a0004c0006t0001g0225 |
3 | HG00408.hp1 HG02630.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.2574-4388C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185286286 | |||||||
chr1:185286487 | G | A | 3 | a0002c0002t0001g0137 a0002c0002t0001g0153 a0013c0022t0001g0008 |
3 | HG01884.hp2 HG02896.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2574-4187G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185286487 | |||||||
chr1:185286563 | C | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0066 |
2 | HG03669.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2574-4111C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185286563 | |||||||
chr1:185286585 | G | T | 3 | a0003c0005t0004g0006 a0003c0005t0004g0007 a0003c0005t0004g0229 |
3 | HG01891.hp2 HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2574-4089G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185286585 | |||||||
chr1:185286653 | T | A | 1 | a0001c0001t0002g0273 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2574-4021T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185286653 | |||||||
chr1:185286734 | A | C | 2 | a0001c0001t0002g0283 a0001c0001t0002g0284 |
2 | NA18973.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.2574-3940A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185286734 | |||||||
chr1:185286831 | T | C | 1 | a0001c0001t0007g0094 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2574-3843T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185286831 | |||||||
chr1:185286936 | T | G | 1 | a0001c0001t0001g0005 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2574-3738T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185286936 | |||||||
chr1:185286960 | T | C | 2 | a0002c0004t0001g0299 a0002c0004t0001g0300 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2574-3714T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185286960 | |||||||
chr1:185287358 | G | A | 12 | a0001c0001t0004g0037 a0003c0003t0004g0232 a0003c0003t0004g0233 others(9): Show |
12 | HG01891.hp2 HG02280.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.2574-3316G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185287358 | |||||||
chr1:185287576 | G | A | 25 | a0003c0003t0001g0189 a0003c0003t0001g0190 a0003c0003t0001g0191 others(22): Show |
25 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.2574-3098G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185287576 | |||||||
chr1:185287617 | T | C | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2574-3057T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185287617 | |||||||
chr1:185287929 | T | C | 212 | a0001c0001t0001g0063 a0001c0001t0001g0066 a0001c0001t0002g0010 others(209): Show |
214 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(211): Show |
intron_variant | MODIFIER | c.2574-2745T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185287929 | |||||||
chr1:185287930 | T | C | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(17): Show |
20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2574-2744T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185287930 | |||||||
chr1:185288067 | C | T | 6 | a0003c0003t0001g0270 a0003c0003t0001g0271 a0006c0008t0001g0138 others(3): Show |
6 | HG01891.hp1 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2574-2607C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185288067 | |||||||
chr1:185288080 | G | A | 1 | a0003c0003t0001g0207 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2574-2594G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185288080 | |||||||
chr1:185288137 | T | A | 1 | a0002c0004t0001g0014 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2574-2537T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185288137 | |||||||
chr1:185288440 | A | G | 1 | a0005c0007t0001g0242 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2574-2234A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185288440 | |||||||
chr1:185288584 | T | C | 6 | a0001c0001t0001g0033 a0001c0001t0001g0062 a0001c0001t0001g0064 others(3): Show |
6 | HG00621.hp1 NA18970.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.2574-2090T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185288584 | |||||||
chr1:185288736 | A | G | 2 | a0001c0001t0001g0063 a0001c0001t0001g0066 |
2 | HG03669.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2574-1938A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185288736 | |||||||
chr1:185288773 | G | A | 2 | a0001c0001t0001g0124 a0001c0001t0001g0126 |
2 | NA18943.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.2574-1901G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185288773 | |||||||
chr1:185289395 | T | C | 38 | a0001c0001t0004g0037 a0003c0003t0001g0189 a0003c0003t0001g0190 others(35): Show |
38 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.2574-1279T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185289395 | |||||||
chr1:185289509 | A | G | 2 | a0001c0001t0001g0063 a0001c0001t0001g0066 |
2 | HG03669.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2574-1165A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185289509 | |||||||
chr1:185289560 | A | G | 1 | a0004c0006t0001g0222 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2574-1114A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185289560 | |||||||
chr1:185289731 | CATT | C | 14 | a0003c0005t0003g0003 a0003c0005t0003g0227 a0003c0005t0003g0245 others(11): Show |
15 | HG02055.hp2 HG02451.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.2574-941_2574-939d others(5): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr1 | 185289731 | ||||||
chr1:185289801 | T | C | 2 | a0001c0001t0001g0068 a0001c0011t0001g0160 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2574-873T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185289801 | |||||||
chr1:185290111 | GCAAAACA others(3): Show |
G | 1 | a0001c0001t0001g0065 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2574-552_2574-543d others(12): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr1 | 185290111 | ||||||
chr1:185290293 | A | G | 2 | a0003c0005t0001g0230 a0003c0005t0001g0231 |
2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2574-381A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185290293 | |||||||
chr1:185290299 | G | A | 1 | a0002c0002t0001g0153 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2574-375G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185290299 | |||||||
chr1:185290500 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2574-174G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185290500 | |||||||
chr1:185290576 | T | A | 8 | a0003c0003t0001g0154 a0003c0003t0001g0155 a0003c0003t0001g0211 others(5): Show |
8 | HG01884.hp1 HG02258.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.2574-98T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185290576 | |||||||
chr1:185290599 | A | G | 129 | a0001c0001t0001g0063 a0001c0001t0005g0100 a0002c0002t0001g0002 others(126): Show |
130 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(127): Show |
intron_variant | MODIFIER | c.2574-75A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185290599 |